Exact Mass: 432.0827

Exact Mass Matches: 432.0827

Found 500 metabolites which its exact mass value is equals to given mass value 432.0827, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Genistin

5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

C21H20O10 (432.1056)


Genistein 7-O-beta-D-glucoside is a 7-hydroxyisoflavones 7-O-beta-D-glucoside. It is functionally related to a genistein. It is a conjugate acid of a genistein 7-O-beta-D-glucoside(1-). Genistin is a natural product found in Ficus septica, Dalbergia sissoo, and other organisms with data available. Genistin is found in fruits. Genistin is present in soy foods. Potential nutriceutical. It is isolated from Prunus avium (wild cherry) Genistin is one of several known isoflavones. Genistin is found in a number of plants and herbs like soy Present in soy foods. Potential nutriceutical. Isolated from Prunus avium (wild cherry) Genistin (Genistine), an isoflavone belonging to the phytoestrogen family, is a potent anti-adipogenic and anti-lipogenic agent. Genistin attenuates cellular growth and promotes apoptotic cell death breast cancer cells through modulation of ERalpha signaling pathway[1][2][3]. Genistin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=529-59-9 (retrieved 2024-11-05) (CAS RN: 529-59-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

Isovitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O10 (432.1056)


Isovitexin is a C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. It has a role as an EC 3.2.1.20 (alpha-glucosidase) inhibitor and a metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of an isovitexin-7-olate. Isovitexin is a natural product found in Carex fraseriana, Rauhiella, and other organisms with data available. See also: Fenugreek seed (part of); Acai (part of); Crataegus monogyna flowering top (part of). [Raw Data] CBA25_Isovitexin_neg_20eV_1-7_01_1425.txt [Raw Data] CBA25_Isovitexin_neg_10eV_1-7_01_1369.txt [Raw Data] CBA25_Isovitexin_pos_30eV_1-7_01_1399.txt [Raw Data] CBA25_Isovitexin_neg_40eV_1-7_01_1427.txt [Raw Data] CBA25_Isovitexin_neg_30eV_1-7_01_1426.txt [Raw Data] CBA25_Isovitexin_neg_50eV_1-7_01_1428.txt [Raw Data] CBA25_Isovitexin_pos_20eV_1-7_01_1398.txt [Raw Data] CBA25_Isovitexin_pos_10eV_1-7_01_1358.txt [Raw Data] CBA25_Isovitexin_pos_40eV_1-7_01_1400.txt [Raw Data] CBA25_Isovitexin_pos_50eV_1-7_01_1401.txt Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB.

   

Cosmosiin

5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one;Apigenin 7-Glucoside

C21H20O10 (432.1056)


Cosmosiin, also known as apigenin 7-O-glucoside or apigetrin, is a member of the class of compounds known as flavonoid-7-O-glycosides. Flavonoid-7-O-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Cosmosiin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Cosmosiin can be found in a number of food items, such as common thyme, white lupine, common oregano, and orange mint. Cosmosiin can also be found in dandelion coffee and in Teucrium gnaphalodes (Wikipedia). Cosmosiin can also be found plants such as wild celery and anise. Cosmosiin has been shown to exhibit anti-platelet function (PMID: 21834233). Apigenin 7-O-beta-D-glucoside is a glycosyloxyflavone that is apigenin substituted by a beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. It has a role as a non-steroidal anti-inflammatory drug, a metabolite and an antibacterial agent. It is a beta-D-glucoside, a dihydroxyflavone, a glycosyloxyflavone and a monosaccharide derivative. It is functionally related to an apigenin. It is a conjugate acid of an apigenin 7-O-beta-D-glucoside(1-). It is an enantiomer of an apigenin 7-O-beta-L-glucoside. Cosmosiin is a natural product found in Galeopsis tetrahit, Carex fraseriana, and other organisms with data available. See also: Chamomile (part of). Apiumetrin, also known as 7-O-beta-D-glucosyl-5,7,4-trihydroxyflavone or cosmosiin, is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Apiumetrin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Apiumetrin can be found in wild celery, which makes apiumetrin a potential biomarker for the consumption of this food product. Acquisition and generation of the data is financially supported in part by CREST/JST. Annotation level-1 Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2]. Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2].

   

Vitexin 6'-O-malonyl 2'-O-xyloside

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O10 (432.1056)


Vitexin 6-o-malonyl 2-o-xyloside, also known as apigenin 8-C-glucoside or 8-glycosyl-apigenin, is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin 6-o-malonyl 2-o-xyloside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Vitexin 6-o-malonyl 2-o-xyloside can be synthesized from apigenin. Vitexin 6-o-malonyl 2-o-xyloside is also a parent compound for other transformation products, including but not limited to, vitexin 2-O-beta-L-rhamnoside, 7-O-methylvitexin 2-O-beta-L-rhamnoside, and vitexin 2-O-beta-D-glucoside. Vitexin 6-o-malonyl 2-o-xyloside can be found in common beet, which makes vitexin 6-o-malonyl 2-o-xyloside a potential biomarker for the consumption of this food product. Vitexin, also known as apigenin 8-C-glucoside or 8-glycosylapigenin, belongs to the class of organic compounds known as flavonoid 8-C-glycosides. Flavonoid 8-C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin is also described as an apigenin flavone glucoside. Vitexin has been found in passion flower, chasteberry, bamboo leaves, millet and Hawthorn. Vitexin has shown a wide range of pharmacological effects, such as antioxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects (PMID: 27693342). Vitexin has also been shown to directly inhibit thyroid peroxidase and potentially contributes to goiter (PMID: 1696490). It is sometimes called a goitrogen. Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CBA68_Vitexin_neg_10eV.txt [Raw Data] CBA68_Vitexin_neg_30eV.txt [Raw Data] CBA68_Vitexin_pos_20eV.txt [Raw Data] CBA68_Vitexin_neg_50eV.txt [Raw Data] CBA68_Vitexin_neg_40eV.txt [Raw Data] CBA68_Vitexin_pos_40eV.txt [Raw Data] CBA68_Vitexin_pos_30eV.txt [Raw Data] CBA68_Vitexin_pos_10eV.txt [Raw Data] CBA68_Vitexin_neg_20eV.txt Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Afzelin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C21H20O10 (432.1056)


Afzelin is a glycosyloxyflavone that is kaempferol attached to an alpha-L-rhamnosyl residue at position 3 via a glycosidic linkage. It has a role as a plant metabolite, an antibacterial agent and an anti-inflammatory agent. It is a glycosyloxyflavone, a trihydroxyflavone and a monosaccharide derivative. It is functionally related to a kaempferol. It is a conjugate acid of an afzelin(1-). Afzelin is a natural product found in Premna odorata, Vicia tenuifolia, and other organisms with data available. [Raw Data] CBA27_Afzelin_neg_30eV_1-1_01_1585.txt [Raw Data] CBA27_Afzelin_pos_20eV_1-1_01_1549.txt [Raw Data] CBA27_Afzelin_pos_10eV_1-1_01_1540.txt [Raw Data] CBA27_Afzelin_neg_10eV_1-1_01_1576.txt [Raw Data] CBA27_Afzelin_neg_20eV_1-1_01_1584.txt [Raw Data] CBA27_Afzelin_neg_40eV_1-1_01_1586.txt [Raw Data] CBA27_Afzelin_pos_30eV_1-1_01_1550.txt [Raw Data] CBA27_Afzelin_pos_50eV_1-1_01_1552.txt [Raw Data] CBA27_Afzelin_pos_40eV_1-1_01_1551.txt [Raw Data] CBA27_Afzelin_neg_50eV_1-1_01_1587.txt Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1]. Afzelin (Kaempferol-3-O-rhamnoside)It is a flavonol glycoside that has anti-inflammatory, anti-oxidative stress response, anti-apoptotic, and anti-cardiac cytotoxic effects. AfzelinIt can reduce mitochondrial damage, enhance mitochondrial biosynthesis, and reduce mitochondria-related proteins. Parkinand PTENinduced putative kinase 1 (putative kinase 1)s level. AfzelinCan be improved D-galactosamine(GalN)/LPSSurvival rate of mice treated with doxorubicin prophylaxis (HY-15142A)Induced cardiotoxicity and scopolamine (HY-N0296)-induced neurological injury. AfzelinAlso inhibits asthma and allergies caused by ovalbumin[1][2][3][4]. Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1].

   

Genistein 8-c-glucoside

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


Genistein 8-C-glucoside is a C-glycosyl compound that is genistein substituted by a beta-D-glucopyranosyl residue at position 8 via a C-glucosidic linkage. It has a role as a plant metabolite. It is a C-glycosyl compound and a member of 7-hydroxyisoflavones. It is functionally related to a genistein. Genistein 8-C-glucoside is a natural product found in Dalbergia sissoo, Genista ephedroides, and other organisms with data available. A C-glycosyl compound that is genistein substituted by a beta-D-glucopyranosyl residue at position 8 via a C-glucosidic linkage.

   

Glucocapangulin

1,6-dihydroxy-3-methyl-8-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


Glucocapangulin, also known as anthraglycoside b, is a member of the class of compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. Thus, glucocapangulin is considered to be an aromatic polyketide lipid molecule. Glucocapangulin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Glucocapangulin can be found in capers, which makes glucocapangulin a potential biomarker for the consumption of this food product. Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1]. Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1].

   

Se-Adenosylselenohomocysteine

2-amino-4-({[(2S,3S,4R,5S)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}selanyl)butanoic acid

C14H20N6O5Se (432.066)


Se-Adenosylselenohomocysteine is an intermediate in Selenoamino acid metabolism. Se-Adenosylselenohomocysteine is the second to last step in the synthesis of Selenohomocystine and is converted from Se-Adenosylselenomethionine via the enzyme Transferases (EC 2.1.1.-). It is then. converted to Selenohomocysteine via the enzyme adenosylhomocysteinase (EC 3.3.1.1). Se-Adenosylselenohomocysteine is an intermediate in Selenoamino acid metabolism. Se-Adenosylselenohomocysteine is the second to last step in the synthesis of Selenohomocystine and is converted from Se-Adenosylselenomethionine via the enzyme Transferases (EC 2.1.1.-). It is then

   

7a-Hydroxy-O-carbamoyl-deacetylcephalosporin C

7a-Hydroxy-O-carbamoyl-deacetylcephalosporin C

C15H20N4O9S (432.0951)


   

4-Aminoanhydrochlortetracycline

4-Aminoanhydro-7-chlorotetracycline

C20H17ClN2O7 (432.0724)


   

N-(3-Oxo-3-(4-(pyridin-4-yl)piperazin-1-yl)propyl)benzo[c][1,2,5]thiadiazole-4-sulfonamide

N-(3-Oxo-3-(4-(pyridin-4-yl)piperazin-1-yl)propyl)benzo[c][1,2,5]thiadiazole-4-sulfonamide

C18H20N6O3S2 (432.1038)


VU 0255035 is a highly selective, competitive and brain penetrant muscarinic M1 receptor antagonist with an IC50 of 130 nM. VU 0255035 reduces pilocarpine-induced seizures in mice. VU0255035 is used to examine the role of the M1 receptor in diverse situations[1].

   

Vitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O10 (432.1056)


Vitexin is an apigenin flavone glycoside, which is found in the passion flower, bamboo leaves and pearl millet It has a role as a platelet aggregation inhibitor, an EC 3.2.1.20 (alpha-glucosidase) inhibitor, an antineoplastic agent and a plant metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of a vitexin-7-olate. Vitexin is a natural product found in Itea chinensis, Salacia chinensis, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of); Cytisus scoparius flowering top (part of); Fenugreek seed (part of) ... View More ... An apigenin flavone glycoside, which is found in the passion flower, bamboo leaves and pearl millet Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Apigenin 4'-O-glucoside

5,7-dihydroxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxyphenyl]chromen-4-one

C21H20O10 (432.1056)


Apigenin 4-O-glucoside is also known as apigenin 4-O-beta-D-glucopyranoside. Apigenin 4-O-glucoside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Apigenin 4-O-glucoside is a constituent of many plant species [CCD]. Apigenin 4-O-glucoside is a glycoside and a member of flavonoids. Apigenin-4-glucoside is a natural product found in Chaerophyllum aureum, Gerbera jamesonii, and other organisms with data available.

   

Vitexin

8-beta-D-Glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

C21H20O10 (432.1056)


Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

17-Beta-Estradiol-3,17-beta-sulfate

[(1S,10R,11S,14S,15S)-15-methyl-5-(sulfooxy)tetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadeca-2,4,6-trien-14-yl]oxidanesulfonic acid

C18H24O8S2 (432.0913)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones 17-Beta-Estradiol-3,17-beta-sulfate is found in milk.

   

Kaempferol 7-rhamnoside

kaempferol 7-O-alpha-L-rhamnopyranoside

C21H20O10 (432.1056)


Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1]. Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1].

   

w-O-beta-D-Glucopyranosylaloeemodin

1,8-dihydroxy-3-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


w-O-beta-D-Glucopyranosylaloeemodin is found in green vegetables. w-O-beta-D-Glucopyranosylaloeemodin is isolated from Chinese rhubar Isolated from Chinese rhubarb. w-O-beta-D-Glucopyranosylaloeemodin is found in green vegetables.

   

Genistein 5-glucoside

7-hydroxy-3-(4-hydroxyphenyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

C21H20O10 (432.1056)


Genistein 5-glucoside is found in fruits. Genistein 5-glucoside is isolated from bark of morello cherry (Prunus cerasus). Isolated from bark of morello cherry (Prunus cerasus). Genistein 5-glucoside is found in fruits and sour cherry.

   

alpha-Rhamnorobin

7-{[3,4-dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


Isolated from bean Phaseolus atropurpureum, leaves of sloe (Prunus spinosa) and others. Kaempferol 7-rhamnofuranoside is found in many foods, some of which are pulses, mung bean, herbs and spices, and alcoholic beverages. alpha-Rhamnorobin is found in alcoholic beverages. alpha-Rhamnorobin is isolated from bean Phaseolus atropurpureum, leaves of sloe (Prunus spinosa) and other

   

Kaempferol 3-O-alpha-L-rhamnofuranoside

3-{[3,4-dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


Constituent of Prunus spinosa (sloe). Kaempferol 3-rhamnofuranoside is found in many foods, some of which are beverages, sweet bay, herbs and spices, and alcoholic beverages. Kaempferol 3-O-alpha-L-rhamnofuranoside is found in alcoholic beverages. Kaempferol 3-O-alpha-L-rhamnofuranoside is a constituent of Prunus spinosa (sloe).

   

1-O-beta-D-Glucopyranosylaloeemodin

8-hydroxy-3-(hydroxymethyl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


1-O-beta-D-Glucopyranosylaloeemodin is found in green vegetables. 1-O-beta-D-Glucopyranosylaloeemodin is a constituent of the rhizomes of Rheum undulatum (rhubarb). Constituent of the rhizomes of Rheum undulatum (rhubarb). 1-O-beta-D-Glucopyranosylaloeemodin is found in green vegetables.

   

Glucoemodin

1,8-dihydroxy-3-methyl-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


Glucoemodin is found in green vegetables. Glucoemodin is isolated from rhubarb. Isolated from rhubarb. Glucoemodin is found in green vegetables. Emodin-6-O-β-D-glucoside (Glucoemodin) is an active compound from Reynoutria japonica. Emodin-6-O-β-D-glucoside shows potent anti-inflammatory and barrier protective effects. Emodin-6-O-β-D-glucoside can be used for the research of diabetic complications and atherosclerosis[1].

   

1,8-Dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside

1-hydroxy-3-(hydroxymethyl)-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


1,8-Dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside is found in green vegetables. 1,8-Dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside is found in Chinese rhubarb (Rheum palmatum), cascara sagrada (Rhamnus purshiana) and Alexandria senna (Cassia acutifolia Aloe-emodin-8-O-β-D-glucopyranoside, a compound isolated from Saussrurea lappa, is a moderate inhibitor of human protein tyrosine phosphatase 1B (hPTP1B) with an IC50 of 26.6 μM[1]. Aloe-emodin-8-O-β-D-glucopyranoside, a compound isolated from Saussrurea lappa, is a moderate inhibitor of human protein tyrosine phosphatase 1B (hPTP1B) with an IC50 of 26.6 μM[1].

   

2-(3,4-dihydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

2-(3,4-dihydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

C21H20O10 (432.1056)


   

Mollicellin F

6-chloro-5,12-dihydroxy-7,15,15,19-tetramethyl-9,17-dioxo-2,10,14-trioxatetracyclo[9.8.0.0³,⁸.0¹³,¹⁸]nonadeca-1(11),3,5,7,12,18-hexaene-4-carbaldehyde

C21H17ClO8 (432.0612)


Mollicellin F is classified as a Food Contaminant (code WG) in the DFC.

   

3,4,5-trihydroxy-6-[(5-hydroxy-4-oxo-2-phenyl-3,4-dihydro-2H-1-benzopyran-7-yl)oxy]oxane-2-carboxylic acid

3,4,5-trihydroxy-6-[(5-hydroxy-4-oxo-2-phenyl-3,4-dihydro-2H-1-benzopyran-7-yl)oxy]oxane-2-carboxylic acid

C21H20O10 (432.1056)


   

6-C-Fucosylluteolin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)-4H-chromen-4-one

C21H20O10 (432.1056)


6-C-(6-Deoxygalactopyranosyl)-3,4,5,7-tetrahydroxyflavone is found in fruits. 6-C-(6-Deoxygalactopyranosyl)-3,4,5,7-tetrahydroxyflavone is a constituent of the juice of Passiflora edulis f. flavicarpa (yellow passion fruit). Constituent of the juice of Passiflora edulis f. flavicarpa (yellow passion fruit). 6-C-(6-Deoxygalactopyranosyl)-3,4,5,7-tetrahydroxyflavone is found in passion fruit and fruits.

   

Isogenistein 7-glucoside

5-hydroxy-3-(2-hydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

C21H20O10 (432.1056)


Isogenistein 7-glucoside is found in pigeon pea. Isogenistein 7-glucoside is isolated from rootbark of Cajanus cajan (pigeon pea). Isolated from rootbark of Cajanus cajan (pigeon pea). Isogenistein 7-glucoside is found in pigeon pea and pulses.

   

6-Hydroxydaidzein 4'-glucoside

6,7-dihydroxy-3-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


6-Hydroxydaidzein 4-glucoside is found in pulses. 6-Hydroxydaidzein 4-glucoside is isolated from seeds of Glycine ma

   

Dihydrodaidzein 7-O-glucuronide

(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[3-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}oxane-2-carboxylic acid

C21H20O10 (432.1056)


Dihydrodaidzein 7-O-glucuronide is a polyphenol metabolite detected in biological fluids (PMID: 20428313).

   

lamotrigine-2-N-glucuronide

3,5-diamino-2-[(2R,3R,4S,5S,6S)-6-carboxy-3,4,5-trihydroxyoxan-2-yl]-6-(2,3-dichlorophenyl)-1,2lambda5,4-triazin-2-ylium

C15H16Cl2N5O6 (432.0478)


lamotrigine-2-N-glucuronide is a metabolite of lamotrigine. Lamotrigine, marketed in the US and most of Europe as Lamictal by GlaxoSmithKline, is an anticonvulsant drug used in the treatment of epilepsy and bipolar disorder. It is also used as an adjunct in treating depression, though this is considered off-label usage. For epilepsy, it is used to treat focal seizures, primary and secondary tonic-clonic seizures, and seizures associated with Lennox-Gastaut syndrome. (Wikipedia)

   

Se-Adenosyl-L-selenohomocysteine

(2S)-2-amino-4-({[(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}selanyl)butanoic acid

C14H20N6O5Se (432.066)


Se-Adenosyl-L-selenohomocysteine is classified as a member of the 5-deoxyribonucleosides. 5-deoxyribonucleosides are nucleosides in which the oxygen atom at the 5position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives. Se-Adenosyl-L-selenohomocysteine is considered to be slightly soluble (in water) and acidic

   

1-(Perfluorohexyl)octane

1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorotetradecane

C14H17F13 (432.1123)


   

Pueraria glycoside

3-(3,4-dihydroxyphenyl)-7-hydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O10 (432.1056)


   

4-Fluoranyl-3-(4-Oxidanylpiperidin-1-Yl)sulfonyl-~{n}-[3,4,5-Tris(Fluoranyl)phenyl]benzamide

4-Fluoranyl-3-(4-oxidanylpiperidin-1-yl)sulphonyl-~{n}-[3,4,5-tris(fluoranyl)phenyl]benzamide

C18H16F4N2O4S (432.0767)


   

Afzelin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4H-chromen-4-one

C21H20O10 (432.1056)


5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4h-chromen-4-one is a member of the class of compounds known as flavonoid-3-o-glycosides. Flavonoid-3-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4h-chromen-4-one is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4h-chromen-4-one can be found in a number of food items such as endive, linden, peach, and ginkgo nuts, which makes 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4h-chromen-4-one a potential biomarker for the consumption of these food products. Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1]. Afzelin (Kaempferol-3-O-rhamnoside)It is a flavonol glycoside that has anti-inflammatory, anti-oxidative stress response, anti-apoptotic, and anti-cardiac cytotoxic effects. AfzelinIt can reduce mitochondrial damage, enhance mitochondrial biosynthesis, and reduce mitochondria-related proteins. Parkinand PTENinduced putative kinase 1 (putative kinase 1)s level. AfzelinCan be improved D-galactosamine(GalN)/LPSSurvival rate of mice treated with doxorubicin prophylaxis (HY-15142A)Induced cardiotoxicity and scopolamine (HY-N0296)-induced neurological injury. AfzelinAlso inhibits asthma and allergies caused by ovalbumin[1][2][3][4]. Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1].

   

Genistein 4'-O-glucoside

5,7-dihydroxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxyphenyl]chromen-4-one;Sophoricoside

C21H20O10 (432.1056)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.780 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.777 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.779 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.782

   

Isovitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O10 (432.1056)


   

7-Hydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one

7-Hydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one

C21H20O10 (432.1056)


   

Ulixertinib

4-{5-chloro-2-[(propan-2-yl)amino]pyridin-4-yl}-N-[1-(3-chlorophenyl)-2-hydroxyethyl]-1H-pyrrole-2-carboxamide

C21H22Cl2N4O2 (432.112)


   

Vitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O10 (432.1056)


Vitexin is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Vitexin can be found in a number of food items such as flaxseed, prairie turnip, mung bean, and tree fern, which makes vitexin a potential biomarker for the consumption of these food products. Vitexin is an apigenin flavone glucoside, a chemical compound found in the passion flower, Vitex agnus-castus (chaste tree or chasteberry), in the Phyllostachys nigra bamboo leaves, in the pearl millet (Pennisetum millet), and in Hawthorn . Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Demethyltexasin 4'-O-glucoside

6,7-dihydroxy-3-(4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


Demethyltexasin 4-o-glucoside is a member of the class of compounds known as isoflavonoid o-glycosides. Isoflavonoid o-glycosides are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one. Demethyltexasin 4-o-glucoside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Demethyltexasin 4-o-glucoside can be found in soy bean, which makes demethyltexasin 4-o-glucoside a potential biomarker for the consumption of this food product.

   

Calcium cyclamate

Calcium dihydric acid bis(N-cyclohexylsulphamic acid)

C12H28CaN2O8S2 (432.0913)


It is used as a food additive, prohibited .

   

Anthemoside

5-hydroxy-2-(4-hydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

C21H20O10 (432.1056)


Constituent of Anthemis nobilis (Roman chamomile). Anthemoside is found in herbs and spices.

   

Apigenin 5-glucoside

7-hydroxy-2-(4-hydroxyphenyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

C21H20O10 (432.1056)


Apigenin 5-glucoside is a member of the class of compounds known as flavonoid o-glycosides. Flavonoid o-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Apigenin 5-glucoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Apigenin 5-glucoside can be found in cumin, which makes apigenin 5-glucoside a potential biomarker for the consumption of this food product.

   

Emodin 1-glucoside

1,3-dihydroxy-6-methyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


Emodin 1-glucoside is a member of the class of compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. Emodin 1-glucoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Emodin 1-glucoside can be found in garden rhubarb, which makes emodin 1-glucoside a potential biomarker for the consumption of this food product. Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1]. Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1].

   

Emodin 8-glucoside

1,6-dihydroxy-3-methyl-8-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


Emodin 8-glucoside is a member of the class of compounds known as hydroxyanthraquinones. Hydroxyanthraquinones are compounds containing a hydroxyanthraquinone moiety, which consists of an anthracene bearing a quinone, and hydroxyl group. Emodin 8-glucoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Emodin 8-glucoside can be found in garden rhubarb, which makes emodin 8-glucoside a potential biomarker for the consumption of this food product. Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1]. Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1].

   

pelargonidin-3-O-beta-D-glucoside

5-hydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-7H-chromen-7-one

C21H20O10 (432.1056)


Pelargonidin-3-o-beta-d-glucoside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Pelargonidin-3-o-beta-d-glucoside can be found in a number of food items such as tea leaf willow, carob, sour cherry, and black cabbage, which makes pelargonidin-3-o-beta-d-glucoside a potential biomarker for the consumption of these food products.

   

pipecolic acid betaine

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-((3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yloxy)-4H-chromen-4-one

C21H20O10 (432.1056)


Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1]. Afzelin (Kaempferol-3-O-rhamnoside)It is a flavonol glycoside that has anti-inflammatory, anti-oxidative stress response, anti-apoptotic, and anti-cardiac cytotoxic effects. AfzelinIt can reduce mitochondrial damage, enhance mitochondrial biosynthesis, and reduce mitochondria-related proteins. Parkinand PTENinduced putative kinase 1 (putative kinase 1)s level. AfzelinCan be improved D-galactosamine(GalN)/LPSSurvival rate of mice treated with doxorubicin prophylaxis (HY-15142A)Induced cardiotoxicity and scopolamine (HY-N0296)-induced neurological injury. AfzelinAlso inhibits asthma and allergies caused by ovalbumin[1][2][3][4]. Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1].

   

Pueraria glycoside

3-(3,4-dihydroxyphenyl)-7-hydroxy-8-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O10 (432.1056)


Pueraria glycoside is a natural product found in Pueraria montana var. lobata with data available. 3'-Hydroxypuerarin is an isoflavone isolated from the roots of Pueraria lobata (Willd.) Ohwi. 3'-Hydroxypuerarin is a antioxidant, which shows marked ONOO(-), NO?, total ROS scavenging activities[1][2][3]. 3'-Hydroxypuerarin is an isoflavone isolated from the roots of Pueraria lobata (Willd.) Ohwi. 3'-Hydroxypuerarin is a antioxidant, which shows marked ONOO(-), NO?, total ROS scavenging activities[1][2][3].

   

OroxinA

5,6-Dihydroxy-2-phenyl-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C21H20O10 (432.1056)


Oroxin A is a natural product found in Scutellaria immaculata, Scutellaria glabrata, and other organisms with data available. Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2]. Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2]. Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2].

   

Aloe-emodin-8-O-β-D-glucoside

1-hydroxy-3-(hydroxymethyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione

C21H20O10 (432.1056)


Aloe-emodin-8-O-beta-D-glucopyranoside is a natural product found in Rheum officinale, Rheum palmatum, and Senna alexandrina with data available. Aloe-emodin-8-O-β-D-glucopyranoside, a compound isolated from Saussrurea lappa, is a moderate inhibitor of human protein tyrosine phosphatase 1B (hPTP1B) with an IC50 of 26.6 μM[1]. Aloe-emodin-8-O-β-D-glucopyranoside, a compound isolated from Saussrurea lappa, is a moderate inhibitor of human protein tyrosine phosphatase 1B (hPTP1B) with an IC50 of 26.6 μM[1].

   

anthraglycoside B

1,6-Dihydroxy-3-methyl-8-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)anthracene-9,10-dione

C21H20O10 (432.1056)


Emodin 8-glucoside is a dihydroxyanthraquinone. Emodin-8-glucoside is a natural product found in Rheum palmatum, Rumex patientia, and other organisms with data available. See also: Reynoutria multiflora root (has part). Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1]. Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1]. Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1]. Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1].

   

Emodin 1-glucoside

1,3-dihydroxy-6-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione

C21H20O10 (432.1056)


Emodin 1-O-beta-D-glucoside is a natural product found in Selaginella delicatula, Rheum palmatum, and other organisms with data available. Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1]. Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1].

   

Sophoricoside

3-{4-[(2S,4S,5S,3R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)(2H-3,4,5,6-tetrahydr opyran-2-yloxy)]phenyl}-5,7-dihydroxychromen-4-one

C21H20O10 (432.1056)


Sophoricoside is an isoflavonoid and an acrovestone. Sophoricoside is a natural product found in Oxytropis falcata, Lupinus polyphyllus, and other organisms with data available. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.780 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.782 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.779 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.777 Sophoricoside is an isoflavone glycoside isolated from Sophora japonica and has anti-inflammatory, anti-cancer and immunosuppressive effects. Sophoricoside is an isoflavone glycoside isolated from Sophora japonica and has anti-inflammatory, anti-cancer and immunosuppressive effects.

   

Oroxin

5,6-Dihydroxy-2-phenyl-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C21H20O10 (432.1056)


Oroxin A is a natural product found in Scutellaria immaculata, Scutellaria glabrata, and other organisms with data available. Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2]. Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2]. Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2].

   

Trichodermamide A

Trichodermamide A

C20H20N2O9 (432.1169)


CONFIDENCE Penicillium corvianum

   

Salipurpin

7-hydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

C21H20O10 (432.1056)


Apigenin 5-O-beta-D-glucopyranoside is a natural product found in Ligustrum vulgare, Prunus cerasus, and other organisms with data available.

   

Resokaempferol 7-glucoside

Resokaempferol 7-glucoside

C21H20O10 (432.1056)


   

Luteolin 7-rhamnoside

5,7,3,4-Tetrahydroxyflavone 7-rhamnoside

C21H20O10 (432.1056)


   

Kaempferide 3-alpha-L-arabinopyranoside

3,5,7-Trihydroxy-4-methoxyflavone 3-alpha-L-arabinopyranoside

C21H20O10 (432.1056)


   

Cimicifugic acid E

(+)-Cimicifugic acid E

C21H20O10 (432.1056)


   

8-C-Glucosyl-5-deoxykaempferol

8-beta-D-Glucopyranosyl-3,7-dihydroxy-2- (4-hydroxyphenyl) -4H-1-benzopyran-4-one

C21H20O10 (432.1056)


   

Kaempferol 5-rhamnoside

Kaempferol 5-rhamnoside

C21H20O10 (432.1056)


   

Aureusidin 6-rhamnoside

4,6,3,4-Tetrahydroxyaurone 6-rhamnoside

C21H20O10 (432.1056)


   

Galanginin

3,5,7-Trihydroxyflavone 3-glucoside

C21H20O10 (432.1056)


   

Cimicifugic acid F

(+)-Cimicifugic acid F

C21H20O10 (432.1056)


   

Luteolin 3-rhamnoside

Luteolin 3-rhamnoside

C21H20O10 (432.1056)


   

Baicalein 6-glucoside

Baicalein 6-glucoside

C21H20O10 (432.1056)


   

Scutellarein 7-rhamnoside

Scutellarein 7-rhamnoside

C21H20O10 (432.1056)


   

Resokaempferol 4-glucoside

3,7,4-Trihydroxyflavone 4-glucoside

C21H20O10 (432.1056)


   

7,3,4-Trihydroxyflavone 7-glucoside

7,3,4-Trihydroxyflavone 7-glucoside

C21H20O10 (432.1056)


   

7,3,4,5-Tetrahydroxyflavone 7-rhamnoside

7,3,4,5-Tetrahydroxyflavone 7-rhamnoside

C21H20O10 (432.1056)


   

5,7,8-Trihydroxyflavone 7-galactoside

5,7,8-Trihydroxyflavone 7-galactoside

C21H20O10 (432.1056)


   

5,7,8-Trihydroxyflavone 5-glucoside

5,7,8-Trihydroxyflavone 5-glucoside

C21H20O10 (432.1056)


   

Kaempferol 4-rhamnoside

Kaempferol 4-rhamnoside

C21H20O10 (432.1056)


   

8-C-Rhamnopyranosylluteolin

5,7,3,4-Tetrahydroxyflavone 8-C-rhamnoside

C21H20O10 (432.1056)


   

Galangin 7-glucoside

Galangin 7-glucoside

C21H20O10 (432.1056)


   
   

Luteolin 3-methyl ether 7-xyloside

Luteolin 3-methyl ether 7-xyloside

C21H20O10 (432.1056)


   

Resokaempferol 3-glucoside

3,7,4-Trihydroxyflavone 3-glucoside

C21H20O10 (432.1056)


   

Demethyltexasin 4-O-glucoside

6,7,4-Trihydroxyisoflavone 4-O-glucoside

C21H20O10 (432.1056)


   

5,7,2-Trihydroxy 7-glucoside

5,7,2-Trihydroxyflavone 7-glucoside

C21H20O10 (432.1056)


   

7,2,4-Trihydroxyisoflavone 4-O-glucoside

7,2,4-Trihydroxyisoflavone 4-O-glucoside

C21H20O10 (432.1056)


   

Acanthophorin A

Acanthophorin A

C21H20O10 (432.1056)


   

8-C-beta-D-Galactopyranosylapigenin

5,7,4-Trihydroxyflavone 8-C-beta-D-galactopyranoside

C21H20O10 (432.1056)


   

3-Hydroxy-3,5,8,4,5-pentamethoxy-6,7-methylenedioxyflavone

3-Hydroxy-3,5,8,4,5-pentamethoxy-6,7-methylenedioxyflavone

C21H20O10 (432.1056)


   

7,3,4-Trihydroxyflavone 7-galactoside

7,3,4-Trihydroxyflavone 7-galactoside

C21H20O10 (432.1056)


   

Emodin 8-glucoside

1-beta-D-Glucopyranosyloxy-3-methyl-6-hydroxy-8-hydroxy-9,10-anthraquinone

C21H20O10 (432.1056)


Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1]. Emodin-1-O-β-D-glucopyranoside, isolated from medicinal plant Polygonum cuspidatum Sieb. & Zucc, is a potent and noncompetitive bacterial neuraminidase (BNA) inhibitor with an IC50 of 0.85 μM[1]. Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1]. Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1].

   

Kaempferol 3-p-coumarate

3,5,7,4-Tetrahydroxyflavone 3-p-coumarate

C24H16O8 (432.0845)


   

3-O-cis-p-Coumaroylkaempferol

3-O-cis-p-Coumaroylkaempferol

C24H16O8 (432.0845)


   

Neovitexin

5,7,4-Trihydroxyflavone 8-C-alpha-D-glucoside

C21H20O10 (432.1056)


   

sulfurein

(Z) -2- [ (3,4-Dihydroxyphenyl) methylene ] -6- (beta-D-glucopyranosyloxy) -3 (2H) -benzofuranone

C21H20O10 (432.1056)


   

Afzelin

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C21H20O10 (432.1056)


Afzelin is a glycosyloxyflavone that is kaempferol attached to an alpha-L-rhamnosyl residue at position 3 via a glycosidic linkage. It has a role as a plant metabolite, an antibacterial agent and an anti-inflammatory agent. It is a glycosyloxyflavone, a trihydroxyflavone and a monosaccharide derivative. It is functionally related to a kaempferol. It is a conjugate acid of an afzelin(1-). Afzelin is a natural product found in Premna odorata, Vicia tenuifolia, and other organisms with data available. A glycosyloxyflavone that is kaempferol attached to an alpha-L-rhamnosyl residue at position 3 via a glycosidic linkage. Acquisition and generation of the data is financially supported in part by CREST/JST. Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1]. Afzelin (Kaempferol-3-O-rhamnoside)It is a flavonol glycoside that has anti-inflammatory, anti-oxidative stress response, anti-apoptotic, and anti-cardiac cytotoxic effects. AfzelinIt can reduce mitochondrial damage, enhance mitochondrial biosynthesis, and reduce mitochondria-related proteins. Parkinand PTENinduced putative kinase 1 (putative kinase 1)s level. AfzelinCan be improved D-galactosamine(GalN)/LPSSurvival rate of mice treated with doxorubicin prophylaxis (HY-15142A)Induced cardiotoxicity and scopolamine (HY-N0296)-induced neurological injury. AfzelinAlso inhibits asthma and allergies caused by ovalbumin[1][2][3][4]. Afzelin (Kaempferol-3-O-rhamnoside) is is a flavonol glycoside found in Houttuynia cordata Thunberg and is widely used in the preparation of antibacterial and antipyretic agents, detoxicants and for the treatment of inflammation. Afzelin attenuates the mitochondrial damage, enhances mitochondrial biogenesis and decreases the level of mitophagy-related proteins, parkin and PTEN-induced putative kinase 1. Afzelin improves the survival rate and reduces the serum levels of alanine aminotransferase and pro-inflammatory cytokines in D-galactosamine (GalN)/LPS -treated mice[1].

   

Vitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]chromen-4-one

C21H20O10 (432.1056)


Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Apigenin 7-galactoside

7- (beta-D-Galactopyranosyloxy) -4,5-dihydroxyflavone

C21H20O10 (432.1056)


   

Apigenin 4-glucoside

2- [ 4- (beta-D-Glucopyranosyloxy) phenyl ] -5,7-dihydroxy-4H-1-benzopyran-4-one

C21H20O10 (432.1056)


   

6-C-beta-D-Galactosylapigenin

5,7,4-Trihydroxyflavone 6-C-beta-D-galactoside

C21H20O10 (432.1056)


   

6-C-Chinovopyranosylluteolin

6-C-Chinovopyranosylluteolin

C21H20O10 (432.1056)


   

6-C-Fucopyranosylluteolin

5,7,3,4-Tetrahydroxyflavone 6-C-fucopyranoside

C21H20O10 (432.1056)


   

Genistein 5-O-glucoside

5,7,4-Trihydroxyisoflavone 5-O-glucoside

C21H20O10 (432.1056)


   

Isogenistein 7-O-glucoside

5,7,2-Trihydroxyisoflavone 7-O-glucoside

C21H20O10 (432.1056)


   

Kaempferol 7-rhamnoside

7- (alpha-L-Rhamnopyranosyloxy) -3,5-dihydroxy-2- (4-hydroxyphenyl) -4H-1-benzopyran-4-one

C21H20O10 (432.1056)


Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1]. Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1].

   

Maybridge1_006057

Maybridge1_006057

C24H21ClN4S (432.1175)


   

Pelargonidin O-hexoside

Pelargonidin O-hexoside

C21H20O10 (432.1056)


   

Cyanidin 3-rhamnoside

Cyanidin 3-rhamnoside

C21H20O10 (432.1056)


   

Peonidin-3-O-alpha-arabinoside

Peonidin-3-O-alpha-arabinoside

C21H20O10 (432.1056)


   

Genistein sophoricoside

Genistein sophoricoside

C21H20O10 (432.1056)


   

kaempferol 3-O-rhamnoside

kaempferol 3-O-rhamnoside

C21H20O10 (432.1056)


   

Genistin

5-hydroxy-3-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C21H20O10 (432.1056)


Genistein 7-O-beta-D-glucoside is a 7-hydroxyisoflavones 7-O-beta-D-glucoside. It is functionally related to a genistein. It is a conjugate acid of a genistein 7-O-beta-D-glucoside(1-). Genistin is a natural product found in Ficus septica, Dalbergia sissoo, and other organisms with data available. Genistin (Genistine), an isoflavone belonging to the phytoestrogen family, is a potent anti-adipogenic and anti-lipogenic agent. Genistin attenuates cellular growth and promotes apoptotic cell death breast cancer cells through modulation of ERalpha signaling pathway[1][2][3]. Genistin (Genistine), an isoflavone belonging to the phytoestrogen family, is a potent anti-adipogenic and anti-lipogenic agent. Genistin attenuates cellular growth and promotes apoptotic cell death breast cancer cells through modulation of ERalpha signaling pathway[1][2][3].

   

3?,4?-dihydroxyisoflavone-7-O-beta-D-glucopyranoside|calycosin 7-O-beta-D-glucopyranoside

3?,4?-dihydroxyisoflavone-7-O-beta-D-glucopyranoside|calycosin 7-O-beta-D-glucopyranoside

C21H20O10 (432.1056)


   
   

sulfuretin 6-glucoside

sulfuretin 6-glucoside

C21H20O10 (432.1056)


   

O-Glucoside-9,10-Dihydro-4,5-dihydroxy-10-oxo-2-anthracenecarboxylic acid

O-Glucoside-9,10-Dihydro-4,5-dihydroxy-10-oxo-2-anthracenecarboxylic acid

C21H20O10 (432.1056)


   

1,8-dihydroxy-2-methylanthraquinone-3-O-beta-D-galactopyranoside

1,8-dihydroxy-2-methylanthraquinone-3-O-beta-D-galactopyranoside

C21H20O10 (432.1056)


   

Emodin-1-O-glucoside

Emodin-1-O-glucoside

C21H20O10 (432.1056)


   

3-Glucopyranosyl-4,5,7-trihydroxyflavone

3-Glucopyranosyl-4,5,7-trihydroxyflavone

C21H20O10 (432.1056)


   

8-C-alpha-glucofuranosyl-7,4-dihydroxyisoflavone|neopuerarin A

8-C-alpha-glucofuranosyl-7,4-dihydroxyisoflavone|neopuerarin A

C21H20O10 (432.1056)


   
   

Baicalein 6-O-glucoside

Baicalein 6-O-glucoside

C21H20O10 (432.1056)


   
   

Luteolin 7-glucoside

Luteolin 7-glucoside

C21H20O10 (432.1056)


   

8-(C-beta-D-glucopyranosyl)-7,3,4-trihydroxyflavone|vijayoside

8-(C-beta-D-glucopyranosyl)-7,3,4-trihydroxyflavone|vijayoside

C21H20O10 (432.1056)


   
   

5-Hydroxy-3,3,6,7,8-pentamethoxy-4,5-methylenedioxyflavone

5-Hydroxy-3,3,6,7,8-pentamethoxy-4,5-methylenedioxyflavone

C21H20O10 (432.1056)


   

3,5,7,3-tetrahydroxyflavone-3-O-alpha-L-rhamnopyranoside

3,5,7,3-tetrahydroxyflavone-3-O-alpha-L-rhamnopyranoside

C21H20O10 (432.1056)


   

genistein 6-C-beta-D-glucoside|isovitexin

genistein 6-C-beta-D-glucoside|isovitexin

C21H20O10 (432.1056)


   

basidifferquinone|Basidifferquinone A|Bassidifferquinone

basidifferquinone|Basidifferquinone A|Bassidifferquinone

C24H16O8 (432.0845)


   

1-Hydroxy-2-methyl-3-beta-D-glucopyranosyloxy-6-hydroxy-9,10-anthraquinone

1-Hydroxy-2-methyl-3-beta-D-glucopyranosyloxy-6-hydroxy-9,10-anthraquinone

C21H20O10 (432.1056)


   

7,3,4-trihydroxy-5-O-alpha-L-rhamnopyranosyl-isoflavone

7,3,4-trihydroxy-5-O-alpha-L-rhamnopyranosyl-isoflavone

C21H20O10 (432.1056)


   

1,3-dihydroxy-2-(hydroxymethyl)-9,10-anthraquinone 3-O-beta-D-glucopyranoside

1,3-dihydroxy-2-(hydroxymethyl)-9,10-anthraquinone 3-O-beta-D-glucopyranoside

C21H20O10 (432.1056)


   

thunberginol F 7-O-beta-d-glucopyranoside

thunberginol F 7-O-beta-d-glucopyranoside

C21H20O10 (432.1056)


An isobenzofuranone that is thunberginol F attached to a beta-D-glucopyranosyl group at position 4 via a glycosidic linkage. It has been isolated from the roots of Scorzonera judaica .

   

sulphuretin 3-O-beta-glucopyranoside

sulphuretin 3-O-beta-glucopyranoside

C21H20O10 (432.1056)


   

isoscutellarein 7-trans p-coumarate

isoscutellarein 7-trans p-coumarate

C24H16O8 (432.0845)


   

11-O-p-hydroxybenzoylnorbergenin

11-O-p-hydroxybenzoylnorbergenin

C21H20O10 (432.1056)


   

4-methylsulfanyl-6-(1-O-alpha-L-rhamanopyranosyl)-phenazine-1-carboxylic acid|izuminoside B

4-methylsulfanyl-6-(1-O-alpha-L-rhamanopyranosyl)-phenazine-1-carboxylic acid|izuminoside B

C20H20N2O7S (432.0991)


   

diosmetin 7-O-beta-D-apiofuranoside

diosmetin 7-O-beta-D-apiofuranoside

C21H20O10 (432.1056)


   
   
   
   
   

datiscetin 3-O-beta-D-rhamnpyranoside

datiscetin 3-O-beta-D-rhamnpyranoside

C21H20O10 (432.1056)


   
   

kaempferol 7-O-alpha-L-rhamnopyranoside

kaempferol 7-O-alpha-L-rhamnopyranoside

C21H20O10 (432.1056)


   

Bis(4-hydroxyphenyl)(2-(phenoxysulfonyl)phenyl)methane

Bis(4-hydroxyphenyl)(2-(phenoxysulfonyl)phenyl)methane

C25H20O5S (432.1031)


   

6,7,4-Hydroxyisoflavon-4-glycosid

6,7,4-Hydroxyisoflavon-4-glycosid

C21H20O10 (432.1056)


   

4-O-alpha-l-Rhamnopyranoside-1,2,4,5-Tetrahydroxy-7-methylanthraquinone

4-O-alpha-l-Rhamnopyranoside-1,2,4,5-Tetrahydroxy-7-methylanthraquinone

C21H20O10 (432.1056)


   
   

2-O-beta-D-glucopyranosyl-1,2,8-trihydroxy-6-methylanthraquinone

2-O-beta-D-glucopyranosyl-1,2,8-trihydroxy-6-methylanthraquinone

C21H20O10 (432.1056)


   

5,5,6,6-Tetrahydro-4,4-dimethoxy-6,6-cyclo-5,5-bi[7H-furo[3,2-g][1]benzopyran]-7,7-dione

5,5,6,6-Tetrahydro-4,4-dimethoxy-6,6-cyclo-5,5-bi[7H-furo[3,2-g][1]benzopyran]-7,7-dione

C24H16O8 (432.0845)


   
   
   
   
   

3-kaempferyl p-coumarate|3-O-(p-Hydroxycinnamoyl)-3,4,5,7-Tetrahydroxyflavone

3-kaempferyl p-coumarate|3-O-(p-Hydroxycinnamoyl)-3,4,5,7-Tetrahydroxyflavone

C24H16O8 (432.0845)


   

1,8-dihydroxy-2-O-beta-glucopyranoside-3-methylanthraquinone|2-(beta-D-glucopyranosyloxy)-1,8-dihydroxy-3-methylanthraquinone|kwanzoquinone C

1,8-dihydroxy-2-O-beta-glucopyranoside-3-methylanthraquinone|2-(beta-D-glucopyranosyloxy)-1,8-dihydroxy-3-methylanthraquinone|kwanzoquinone C

C21H20O10 (432.1056)


   
   

2-(4-hydroxyphenyl)-6,7-dihydroxy-3-C-beta-glucopyranosyl-4H-1-benzopyran-4-one|pakistoside A

2-(4-hydroxyphenyl)-6,7-dihydroxy-3-C-beta-glucopyranosyl-4H-1-benzopyran-4-one|pakistoside A

C21H20O10 (432.1056)


   

Rivulobirin B

Rivulobirin B

C23H12O9 (432.0481)


   

CAY10608

N-[4-[(2S)-3-[[2-(3,4-dichlorophenyl)ethyl]amino]-2-hydroxypropoxy]phenyl]-methanesulfonamide

C18H22Cl2N2O4S (432.0677)


   

Naphthofluorescein

3,11-dihydroxy-spiro[7H-dibenzo[c,h]xanthene-7,1(3H)-isobenzofuran]-3-one

C28H16O5 (432.0998)


D004396 - Coloring Agents > D005456 - Fluorescent Dyes > D005452 - Fluoresceins Naphthofluorescein inhibits the interaction between HIF-1 and Mint3. Naphthofluorescein suppresses Mint3-dependent HIF-1 activity and glycolysis in cancer cells and macrophages without cytotoxicity in vitro and adverse effect in vivo[1]. Naphthofluorescein is also a fluorescent pH-sensitive probe that can be used for functional Cerenkov imaging[2].

   

Luteolinidin 5-glucoside

Luteolinidin 5-glucoside

C21H20O10 (432.1056)


   

Luteolinidin 7-glucoside

Luteolinidin 7-glucoside

C21H20O10 (432.1056)


   

Pelargonidin 5-galactoside

Pelargonidin 5-galactoside

C21H20O10 (432.1056)


   

Pelargonidin 7-glucoside

Pelargonidin 7-glucoside

C21H20O10 (432.1056)


   

6-hydroxy-2-(4-glucosyl-phenoxymethylene)-benzofuran-3-one

6-hydroxy-2-(4-glucosyl-phenoxymethylene)-benzofuran-3-one

C21H20O10 (432.1056)


   

79YJI9GIF1

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

C21H20O10 (432.1056)


Kaempferol-7-rhamnoside is a natural product found in Cleome amblyocarpa, Equisetum palustre, and other organisms with data available. Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1]. Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1].

   

Aloe-emodin-glucoside

1,8-Dihydroxy-3-((((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)anthracene-9,10-dione

C21H20O10 (432.1056)


Aloe-emodin-glucoside is a natural product found in Senna alexandrina with data available.

   

Lucidin3-O-glucoside

1-Hydroxy-2-(hydroxymethyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)anthracene-9,10-dione

C21H20O10 (432.1056)


Lucidin 3-O-glucoside is a natural product found in Rubia tinctorum, Plocama calabrica, and other organisms with data available.

   

3-(β-D-Glucopyranosyloxy)-1,6-dihydroxy-2-methyl-9,10-anthracenedione

1,6-Dihydroxy-2-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione

C21H20O10 (432.1056)


   

Clicoemodin

1,8-dihydroxy-3-methyl-6-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyanthracene-9,10-dione

C21H20O10 (432.1056)


Clicoemodin is a natural product found in Rumex patientia with data available. Emodin-6-O-β-D-glucoside (Glucoemodin) is an active compound from Reynoutria japonica. Emodin-6-O-β-D-glucoside shows potent anti-inflammatory and barrier protective effects. Emodin-6-O-β-D-glucoside can be used for the research of diabetic complications and atherosclerosis[1].

   

kaempferol-7-o-alpha-l-rhamnoside

kaempferol-7-o-alpha-l-rhamnoside

C21H20O10 (432.1056)


Acquisition and generation of the data is financially supported in part by CREST/JST. Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1]. Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1].

   

Aloe-Emodin-8-O-glycoside

Aloe-Emodin-8-O-glycoside

C21H20O10 (432.1056)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.706 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.705

   

Isovitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O10 (432.1056)


Isovitexin is a C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. It has a role as an EC 3.2.1.20 (alpha-glucosidase) inhibitor and a metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of an isovitexin-7-olate. Isovitexin is a natural product found in Carex fraseriana, Rauhiella, and other organisms with data available. See also: Fenugreek seed (part of); Acai (part of); Crataegus monogyna flowering top (part of). A C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. Isovitexin is a member of the class of compounds known as flavonoid c-glycosides. Flavonoid c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Isovitexin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Isovitexin can be found in a number of food items such as common salsify, winged bean, flaxseed, and common buckwheat, which makes isovitexin a potential biomarker for the consumption of these food products. Isovitexin (or homovitexin, saponaretin) is a flavone. the apigenin-6-C-glucoside. It can be found in the passion flower, Cannabis, and the açaí palm . Constituent of Cucumis sativus (cucumber). Isovitexin 2-(6-p-coumaroylglucoside) 4-glucoside is found in cucumber and fruits. Constituent of young green barley leaves (Hordeum vulgare variety nudum). Isovitexin 7-(6-sinapoylglucoside) is found in barley and cereals and cereal products. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB.

   

Apigenin 7-glucoside

Apigenin-7-O-glucoside

C21H20O10 (432.1056)


Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2]. Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2].

   

Apigetrin

Apigenin-7-O-glucoside

C21H20O10 (432.1056)


Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2]. Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2].

   

5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

NCGC00178486-02!5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

NCGC00180834-02!5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

NCGC00163559-03!5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

NCGC00180782-02!5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one

NCGC00180619-02!5,7-dihydroxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one

C21H20O10 (432.1056)


   

Kaempferol 7-O-rhamnoside

Kaempferol 7-O-rhamnoside

C21H20O10 (432.1056)


Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1]. Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1].

   

kaempferol-7-O-deoxyhexoside

kaempferol-7-O-deoxyhexoside

C21H20O10 (432.1056)


   

Emodin-8-beta-D-glucoside

Emodin-8-beta-D-glucoside

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

3-Genistein-8-C-glucoside

3-Genistein-8-C-glucoside

C21H20O10 (432.1056)


   

Emodin 8-O-(beta)-D-glucoside

Emodin 8-O-(beta)-D-glucoside

C21H20O10 (432.1056)


   

Apigenin-7-O-glucoside

Apigenin-7-O-glucoside

C21H20O10 (432.1056)


   

KAEMPFEROL-3-O-RHAMNOSIDE

KAEMPFEROL-3-O-RHAMNOSIDE

C21H20O10 (432.1056)


   

Kaempferol-7-O-rhamnoside

Kaempferol-7-O-rhamnoside

C21H20O10 (432.1056)


Annotation level-1

   

Apigenin-8-C-glucoside

Apigenin-8-C-glucoside

C21H20O10 (432.1056)


   

Isovitexin(4)

Isovitexin(4)

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O10 (432.1056)


Annotation level-1

   

Anthraquinone base + 2O, MeOH, O-Hex

Anthraquinone base + 2O, MeOH, O-Hex

C21H20O10 (432.1056)


Annotation level-3

   

Flavone base + 3O, O-Hex

Flavone base + 3O, O-Hex

C21H20O10 (432.1056)


Annotation level-3

   

3-Genistein-8-C-glucoside_major

3-Genistein-8-C-glucoside_major

C21H20O10 (432.1056)


   

fucosyltransferase V_major

fucosyltransferase V_major

C21H20O10 (432.1056)


   

1-Methyl-4-nitro-5-(S-Gluctathionyl) Imidazole

1-Methyl-4-nitro-5-(S-Gluctathionyl) Imidazole

C14H20N6O8S (432.1063)


   

peonidin pentose

peonidin pentose

C21H20O10 (432.1056)


   

pelargonidin-3-O-glucoside

pelargonidin-3-O-glucoside

C21H20O10 (432.1056)


   

1-(2,4-Dichlorophenyl)-2-(1-imidazolyl)ethanol glucuronide

1-(2,4-Dichlorophenyl)-2-(1-imidazolyl)ethanol glucuronide

C17H18Cl2N2O7 (432.0491)


   

Estradiol disulfate

Estradiol disulfate

C18H24O8S2 (432.0913)


   
   

Pueraria glycoside 1

Pueraria glycoside 1

C21H20O10 (432.1056)


   

Apigenin 7-O-glucoside

Apigenin 7-O-glucoside

C21H20O10 (432.1056)


   

Apigenin 5-glucoside

Apigenin 5-glucoside

C21H20O10 (432.1056)


   

Apigenin 5-galactoside

Apigenin 5-galactoside

C21H20O10 (432.1056)


   

callistephin

3-(Glucosyloxy)-4,5,7-trihydroxyflavylium

C21H20O10 (432.1056)


   

TyrMe-Asp-OH

(S)-2-(3-((4-methoxybenzyl)oxy)-4-nitrobenzamido)pentanedioic acid

C20H20N2O9 (432.1169)


   

a-Rhamnorobin

7-{[3,4-dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


   

6-Hydroxydaidzein 4'-glucoside

6,7-dihydroxy-3-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


   

mollicellin F

6-chloro-5,12-dihydroxy-7,15,15,19-tetramethyl-9,17-dioxo-2,10,14-trioxatetracyclo[9.8.0.0^{3,8}.0^{13,18}]nonadeca-1(19),3(8),4,6,11,13(18)-hexaene-4-carbaldehyde

C21H17ClO8 (432.0612)


A member of the class of depsidones that is 3,4-dihydro-H,11H-chromeno[6,7-b][1,4]benzodioxepine substituted by a chloro group at position 9, hydroxy groups at positions 8 and 13, methyl groups at positions 2, 2, 5 and 10, oxo groups at positions 4 and 11 and a formyl group at position 7. Isolated from Chaetomium brasiliense, it exhibits cytotoxic activity.

   

Isogenistein 7-glucoside

5-hydroxy-3-(2-hydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

C21H20O10 (432.1056)


   

W-O-b-D-Glucopyranosylaloeemodin

1,8-dihydroxy-3-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


   

1-O-b-D-Glucopyranosylaloeemodin

8-hydroxy-3-(hydroxymethyl)-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


   

e3-Prop

7-hydroxy-3-(4-hydroxyphenyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one

C21H20O10 (432.1056)


   

Glucoemodin

1,8-dihydroxy-3-methyl-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-9,10-dihydroanthracene-9,10-dione

C21H20O10 (432.1056)


Emodin-6-O-β-D-glucoside (Glucoemodin) is an active compound from Reynoutria japonica. Emodin-6-O-β-D-glucoside shows potent anti-inflammatory and barrier protective effects. Emodin-6-O-β-D-glucoside can be used for the research of diabetic complications and atherosclerosis[1].

   

6-C-Fucosylluteolin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)-4H-chromen-4-one

C21H20O10 (432.1056)


   

Kaempferol 3-O-a-L-rhamnofuranoside

3-{[3,4-dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy}-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


   

Apigenin 4'-O-glucoside

5,7-dihydroxy-2-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


   

Dihydrodaidzein 7-O-glucuronide

(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-{[3-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}oxane-2-carboxylic acid

C21H20O10 (432.1056)


   

17-Beta-Estradiol-3,17-beta-sulfate

estra-1,3,5(10)-triene-3,17beta-diol 3,17-disulfate

C18H24O8S2 (432.0913)


D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones

   

sodium 5-ethoxy-2-[[4-(phenylazo)phenyl]azo]benzenesulphonate

sodium 5-ethoxy-2-[[4-(phenylazo)phenyl]azo]benzenesulphonate

C20H17N4NaO4S (432.0868)


   

Triphenyl(propyl)phosphonium iodide

Triphenyl(propyl)phosphonium iodide

C21H22IP (432.0504)


   

1,3-Bis(2,4-diaminophenoxy)propane tetrahydrochloride

1,3-Bis(2,4-diaminophenoxy)propane tetrahydrochloride

C15H24Cl4N4O2 (432.0653)


   

N-[[5-(1H-pyrazol-5-yl)-1,3,4-thiadiazol-2-yl]methyl]-4-(2,4,6-trifluorobenzoyl)-1H-pyrrole-2-carboxamide

N-[[5-(1H-pyrazol-5-yl)-1,3,4-thiadiazol-2-yl]methyl]-4-(2,4,6-trifluorobenzoyl)-1H-pyrrole-2-carboxamide

C18H11F3N6O2S (432.0616)


   

3-((3-((tert-Butyldimethylsilyloxy)methyl)-pyrrolidin-1-yl)methyl)-5-iodopyridine

3-((3-((tert-Butyldimethylsilyloxy)methyl)-pyrrolidin-1-yl)methyl)-5-iodopyridine

C17H29IN2OSi (432.1094)


   

Isopropyltriphenylphosphonium iodide

Isopropyltriphenylphosphonium iodide

C21H22IP (432.0504)


   

bis(4-(4-aminophenoxy)phenyl)sulfone

bis(4-(4-aminophenoxy)phenyl)sulfone

C24H20N2O4S (432.1144)


   

Benzyltriphenylphosphonium bromide

Benzyltriphenylphosphonium bromide

C25H22BrP (432.0642)


   

Brovincamine

Brovincamine

C21H25BrN2O3 (432.1048)


C78274 - Agent Affecting Cardiovascular System > C29707 - Vasodilating Agent D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents D000970 - Antineoplastic Agents > D014748 - Vinca Alkaloids

   

5-CHLORO-3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1-TOSYL-1H-PYRROLO[2,3-B]PYRIDINE

5-CHLORO-3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1-TOSYL-1H-PYRROLO[2,3-B]PYRIDINE

C20H22BClN2O4S (432.1082)


   

2-(11-Hydroxy-3-oxo-3H-dibenzo[c,h]xanthen-7-yl)benzoic acid

2-(11-Hydroxy-3-oxo-3H-dibenzo[c,h]xanthen-7-yl)benzoic acid

C28H16O5 (432.0998)


   

9-Bromo-10-(9-phenanthryl)anthracene

9-Bromo-10-(9-phenanthryl)anthracene

C28H17Br (432.0514)


   

Ulixertinib

Ulixertinib (BVD-523)

C21H22Cl2N4O2 (432.112)


C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor > C129824 - Antineoplastic Protein Inhibitor C471 - Enzyme Inhibitor > C1404 - Protein Kinase Inhibitor > C61074 - Serine/Threonine Kinase Inhibitor C471 - Enzyme Inhibitor > C129825 - Antineoplastic Enzyme Inhibitor Ulixertinib (BVD-523; VRT752271) is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC50 of <0.3 nM against ERK2. Ulixertinib (BVD-523; VRT752271) inhibits the phosphorylated ERK2 (pERK) and downstream kinase RSK (pRSK) in an A375 melanoma cell line[1][2].

   

5-cyano-6-(4-fluorophenyl)sulfanyl-N-[[(2R,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]carbamoyl]pyridine-3-carboxamide

5-cyano-6-(4-fluorophenyl)sulfanyl-N-[[(2R,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]carbamoyl]pyridine-3-carboxamide

C19H17FN4O5S (432.0904)


   

3-(biphenyl-4-yl)-3h-benzo[f]chromylium perchlorate

3-(biphenyl-4-yl)-3h-benzo[f]chromylium perchlorate

C25H17ClO5 (432.0764)


   

prop-2-enyl N-[5-[5-(2-chloropyrimidin-4-yl)-2-propan-2-yl-1,3-thiazol-4-yl]-2-fluorophenyl]carbamate

prop-2-enyl N-[5-[5-(2-chloropyrimidin-4-yl)-2-propan-2-yl-1,3-thiazol-4-yl]-2-fluorophenyl]carbamate

C20H18ClFN4O2S (432.0823)


   

xylenol blue sodium salt indicator

xylenol blue sodium salt indicator

C23H21NaO5S (432.1007)


   

2-((tert-butyldiphenylsilyl)oxy)ethyl trifluoromethanesulfonate

2-((tert-butyldiphenylsilyl)oxy)ethyl trifluoromethanesulfonate

C19H23F3O4SSi (432.1038)


   

2,2-(4-Isobutoxy-1,3-phenylene)bis(4-methyl-1,3-thiazole-5-carboxylic acid)

2,2-(4-Isobutoxy-1,3-phenylene)bis(4-methyl-1,3-thiazole-5-carboxylic acid)

C20H20N2O5S2 (432.0814)


   

Baicalein 7-b-D-glucopyranoside

Baicalein 7-b-D-glucopyranoside

C21H20O10 (432.1056)


   

(S)-N-{2-[1-(3-hydroxy-4-methoxy-phenyl)-2-methanesulfonyl-ethyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}-acetamide

(S)-N-{2-[1-(3-hydroxy-4-methoxy-phenyl)-2-methanesulfonyl-ethyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl}-acetamide

C20H20N2O7S (432.0991)


   

MAGNESIUM D-GLUCONATE HYDRATE

MAGNESIUM D-GLUCONATE HYDRATE

C12H24MgO15 (432.0966)


   

Pamoic acid disodium

Pamoic acid disodium

C23H14Na2O6 (432.0586)


Pamoic acid disodium is a potent GPR35 agonist with an EC50 value of 79 nM. Pamoic acid disodium induces GPR35 internalization and activates ERK1/2 with EC50 values of 22 nM and 65 nM, respectively. Pamoic acid disodium potently recruits β-arrestin2 to GPR35 and has an antinociceptive effect[1].

   

3,3-[Sulfonylbis(4,1-phenyleneoxy)]dianiline

3,3-[Sulfonylbis(4,1-phenyleneoxy)]dianiline

C24H20N2O4S (432.1144)


   

4-Fluoro-3-[(4-hydroxy-1-piperidinyl)sulfonyl]-N-(3,4,5-trifluorophenyl)benzamide

4-Fluoro-3-[(4-hydroxy-1-piperidinyl)sulfonyl]-N-(3,4,5-trifluorophenyl)benzamide

C18H16F4N2O4S (432.0767)


   

Purpurquinone B

Purpurquinone B

C21H20O10 (432.1056)


An azaphilone that is 1H-isochromene-6,8(7H,8aH)-dione substituted by a prop-1-en-1-yl group at position 3, hydroxy groups at positions 1 and 8a, a methyl group at position 7 and a (3,4,6-trihydroxy-2-methylbenzoyl)oxy group at position 7. It has been isolated from Penicillium purpurogenum.

   

2-O-[1-Ethyl-1H-imidazol)] thymidine-5-monophosphate

2-O-[1-Ethyl-1H-imidazol)] thymidine-5-monophosphate

C15H21N4O9P (432.1046)


   

cosmetin

5-hydroxy-2-(4-hydroxyphenyl)-7-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone

C21H20O10 (432.1056)


Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2]. Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2].

   

Glucofrangulin

1,6-dihydroxy-3-methyl-8-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]anthracene-9,10-dione

C21H20O10 (432.1056)


Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1]. Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1].

   

66026-80-0

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

Kaempferol-7-rhamnoside

Kaempferol-7-O-\u03b1-L-rhamnoside

C21H20O10 (432.1056)


Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1]. Kaempferol-7-O-rhamnoside, isolated from Chimonanthus nitens Oliv. Leaves, is a potent α-glucosidase activity inhibitor. Kaempferol-7-O-rhamnoside has the potential for diabetes[1].

   

Oroxin A

5,6-dihydroxy-2-phenyl-7-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone

C21H20O10 (432.1056)


Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2]. Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2]. Oroxin A is the major component of an ethanol-water Oroxylum indicum (L.) Kurz (Bignoniaceae) seed extract (OISE). Oroxin A acts as a partial PPARγ agonist that can activate PPARγ transcriptional activation. Oroxin A activates PPARγ by docking into the PPARγ protein ligand-binding domain. Oroxin A also exhibits an inhibitory activity against α-glucosidase and an antioxidant capacity[1]. Oroxin A exerts anti-breast cancer effects by inducing ER stress-mediated senescence[2].

   

pelargonidin-3-O-beta-D-glucoside

5-hydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-7H-chromen-7-one

C21H20O10 (432.1056)


Pelargonidin-3-o-beta-d-glucoside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Pelargonidin-3-o-beta-d-glucoside can be found in a number of food items such as tea leaf willow, carob, sour cherry, and black cabbage, which makes pelargonidin-3-o-beta-d-glucoside a potential biomarker for the consumption of these food products. Pelargonidin-3-o-β-d-glucoside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Pelargonidin-3-o-β-d-glucoside can be found in a number of food items such as tea leaf willow, carob, sour cherry, and black cabbage, which makes pelargonidin-3-o-β-d-glucoside a potential biomarker for the consumption of these food products.

   

3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy]-4H-1-benzopyran-4-one

3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy]-4H-1-benzopyran-4-one

C21H20O10 (432.1056)


   

2-(3,4-Dihydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

2-(3,4-Dihydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

C21H20O10 (432.1056)


   

Demethyltexasin 4'-O-glucoside

6,7-dihydroxy-3-(4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-4-one

C21H20O10 (432.1056)


Demethyltexasin 4-o-glucoside is a member of the class of compounds known as isoflavonoid o-glycosides. Isoflavonoid o-glycosides are o-glycosylated derivatives of isoflavonoids, which are natural products derived from 3-phenylchromen-4-one. Demethyltexasin 4-o-glucoside is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Demethyltexasin 4-o-glucoside can be found in soy bean, which makes demethyltexasin 4-o-glucoside a potential biomarker for the consumption of this food product.

   

luteolin-7-O-alpha-L-rhamnoside

luteolin-7-O-alpha-L-rhamnoside

C21H20O10 (432.1056)


A glycosyloxyflavone that is luteolin substituted by a alpha-L-rhamnosyl residue at position 7 via a glycosidic linkage. It has been isolated from Crotalaria lachnophora.

   

luteolinidin 5-O-glucoside

luteolinidin 5-O-glucoside

C21H20O10 (432.1056)


   

Guanosine 5-(morpholinophosphonic acid)

Guanosine 5-(morpholinophosphonic acid)

C14H21N6O8P (432.1158)


   

Cyclamate calcium dihydrate

Cyclamate calcium dihydrate

C12H28CaN2O8S2 (432.0913)


   

Genistein 4-O-glucoside

Genistein 4-O-glucoside

C21H20O10 (432.1056)


   

2-{[(5-{4-Chloro-3-nitrophenyl}-2-furyl)methylene]amino}-3-(2-furyl)imidazo[1,2-a]pyridine

2-{[(5-{4-Chloro-3-nitrophenyl}-2-furyl)methylene]amino}-3-(2-furyl)imidazo[1,2-a]pyridine

C22H13ClN4O4 (432.0625)


   

N-[2-[(3-nitrophenyl)methylthio]-4-oxo-3-quinazolinyl]benzamide

N-[2-[(3-nitrophenyl)methylthio]-4-oxo-3-quinazolinyl]benzamide

C22H16N4O4S (432.0892)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]-1-benzopyran-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]-1-benzopyran-4-one

C21H20O10 (432.1056)


   

N-(3-chlorophenyl)-3-[ethyl(phenyl)sulfamoyl]-4-fluorobenzamide

N-(3-chlorophenyl)-3-[ethyl(phenyl)sulfamoyl]-4-fluorobenzamide

C21H18ClFN2O3S (432.0711)


   

3-[[[4-(Phenylmethyl)-5-thiophen-2-yl-1,2,4-triazol-3-yl]thio]methyl]-1,2,3-benzotriazin-4-one

3-[[[4-(Phenylmethyl)-5-thiophen-2-yl-1,2,4-triazol-3-yl]thio]methyl]-1,2,3-benzotriazin-4-one

C21H16N6OS2 (432.0827)


   

1-[[4-(6-Chloro-3-pyridinyl)phenyl]methyl]-5-(trifluoromethoxy)indole-2,3-dione

1-[[4-(6-Chloro-3-pyridinyl)phenyl]methyl]-5-(trifluoromethoxy)indole-2,3-dione

C21H12ClF3N2O3 (432.0489)


   

N-[3-oxo-3-(4-pyridin-2-ylpiperazin-1-yl)propyl]-2,1,3-benzothiadiazole-4-sulfonamide

N-[3-oxo-3-(4-pyridin-2-ylpiperazin-1-yl)propyl]-2,1,3-benzothiadiazole-4-sulfonamide

C18H20N6O3S2 (432.1038)


   

2-[(4,6-dioxo-5-phenyl-1,4,5,6-tetrahydropyrimidin-2-yl)sulfanyl]-N-(4-sulfamoylphenyl)acetamide

2-[(4,6-dioxo-5-phenyl-1,4,5,6-tetrahydropyrimidin-2-yl)sulfanyl]-N-(4-sulfamoylphenyl)acetamide

C18H16N4O5S2 (432.0562)


   

2-[2-[[2-[[1-(2,4-Dimethylphenyl)-5-tetrazolyl]thio]-1-oxoethyl]amino]-4-thiazolyl]acetic acid ethyl ester

2-[2-[[2-[[1-(2,4-Dimethylphenyl)-5-tetrazolyl]thio]-1-oxoethyl]amino]-4-thiazolyl]acetic acid ethyl ester

C18H20N6O3S2 (432.1038)


   

2-(1,3-Benzothiazol-2-ylmethylthio)-1-butyl-5-benzimidazolesulfonamide

2-(1,3-Benzothiazol-2-ylmethylthio)-1-butyl-5-benzimidazolesulfonamide

C19H20N4O2S3 (432.0748)


   

Ethyl 2-[(4-fluorobenzoyl)carbamothioylamino]-4-(5-methylfuran-2-yl)thiophene-3-carboxylate

Ethyl 2-[(4-fluorobenzoyl)carbamothioylamino]-4-(5-methylfuran-2-yl)thiophene-3-carboxylate

C20H17FN2O4S2 (432.0614)


   

4-[[1-(2-Furanylmethyl)-2,4,6-trioxo-3-propan-2-yl-1,3-diazinan-5-ylidene]methylamino]benzenesulfonamide

4-[[1-(2-Furanylmethyl)-2,4,6-trioxo-3-propan-2-yl-1,3-diazinan-5-ylidene]methylamino]benzenesulfonamide

C19H20N4O6S (432.1104)


   

8-{(2E)-2-[(2Z)-2-bromo-3-phenylprop-2-en-1-ylidene]hydrazinyl}-6-hydroxy-7-(2-hydroxyethyl)-3-methyl-3,7-dihydro-2H-purin-2-one

8-{(2E)-2-[(2Z)-2-bromo-3-phenylprop-2-en-1-ylidene]hydrazinyl}-6-hydroxy-7-(2-hydroxyethyl)-3-methyl-3,7-dihydro-2H-purin-2-one

C17H17BrN6O3 (432.0545)


   

4-(2,3-Dihydro-1,4-benzodioxin-6-ylsulfonylamino)benzoic acid [2-(cyclopropylamino)-2-oxoethyl] ester

4-(2,3-Dihydro-1,4-benzodioxin-6-ylsulfonylamino)benzoic acid [2-(cyclopropylamino)-2-oxoethyl] ester

C20H20N2O7S (432.0991)


   

5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl beta-L-glucopyranoside

5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl beta-L-glucopyranoside

C21H20O10 (432.1056)


   

(1E,6E)-1-[2,4-dihydroxy-3-(trihydroxymethoxy)phenyl]-7-(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione

(1E,6E)-1-[2,4-dihydroxy-3-(trihydroxymethoxy)phenyl]-7-(4-hydroxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione

C21H20O10 (432.1056)


   

2-[(3S,6aR,8R,10aR)-1-(2-chlorophenyl)sulfonyl-3-hydroxy-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocin-8-yl]-N-methylacetamide

2-[(3S,6aR,8R,10aR)-1-(2-chlorophenyl)sulfonyl-3-hydroxy-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocin-8-yl]-N-methylacetamide

C18H25ClN2O6S (432.1122)


   

anthocyanidin 3-O-beta-D-galactoside

anthocyanidin 3-O-beta-D-galactoside

C21H20O10 (432.1056)


   

[2-ethoxy-4-[(Z)-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)methyl]phenyl] thiophene-2-carboxylate

[2-ethoxy-4-[(Z)-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)methyl]phenyl] thiophene-2-carboxylate

C24H20N2O4S (432.1144)


   

2-(4-Methoxyphenyl)-4,5-dioxo-1-(4-sulfamoylphenyl)-3-pyrrolidinecarboxylic acid ethyl ester

2-(4-Methoxyphenyl)-4,5-dioxo-1-(4-sulfamoylphenyl)-3-pyrrolidinecarboxylic acid ethyl ester

C20H20N2O7S (432.0991)


   

3-(3,4-Dihydroxy-5-methoxyphenyl)-4-hydroxy-7-(4-hydroxyphenyl)-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-one

3-(3,4-Dihydroxy-5-methoxyphenyl)-4-hydroxy-7-(4-hydroxyphenyl)-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-one

C24H16O8 (432.0845)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one

C21H20O10 (432.1056)


   

[1-Acetyloxy-3-[hydroxy-(2,3,4,5,6-pentahydroxycyclohexyl)oxyphosphoryl]oxypropan-2-yl] propanoate

[1-Acetyloxy-3-[hydroxy-(2,3,4,5,6-pentahydroxycyclohexyl)oxyphosphoryl]oxypropan-2-yl] propanoate

C14H25O13P (432.1033)


   

CID 131674916

CID 131674916

C24H24Sn (432.09)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(3R,4S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(3R,4S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

Se-Adenosylselenohomocysteine

Se-Adenosylselenohomocysteine

C14H20N6O5Se (432.066)


   

pelargonidin-3-O-beta-D-glucoside

pelargonidin-3-O-beta-D-glucoside

C21H20O10 (432.1056)


   

5-hydroxy-3-(4-hydroxyphenyl)-7-[[3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]oxy]-1-benzopyran-4-one

5-hydroxy-3-(4-hydroxyphenyl)-7-[[3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]oxy]-1-benzopyran-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

1,8-Dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside

1,8-Dihydroxy-3-hydroxymethylanthraquinone 8-O-b-D-glucoside

C21H20O10 (432.1056)


   

w-O-beta-D-Glucopyranosylaloeemodin

w-O-beta-D-Glucopyranosylaloeemodin

C21H20O10 (432.1056)


   

Kaempferol 3-O-alpha-L-rhamnofuranoside

Kaempferol 3-O-alpha-L-rhamnofuranoside

C21H20O10 (432.1056)


   

alpha-Rhamnorobin

alpha-Rhamnorobin

C21H20O10 (432.1056)


   

1-O-beta-D-Glucopyranosylaloeemodin

1-O-beta-D-Glucopyranosylaloeemodin

C21H20O10 (432.1056)


   

Genistein 5-glucoside

Genistein 5-glucoside

C21H20O10 (432.1056)


   

6-Hydroxydaidzein 4-glucoside

6-Hydroxydaidzein 4-glucoside

C21H20O10 (432.1056)


   

pelargonidin 3-O-beta-D-glucoside betaine

pelargonidin 3-O-beta-D-glucoside betaine

C21H20O10 (432.1056)


An organic betaine obtained by deprotonation of the hydroxy group at the 5 position of pelargonidin 3-O-beta-D-glucoside. It is the major microspecies at pH 7.3.

   

Apigenin 7-O-beta-D-glucoside

Apigenin 7-O-beta-D-glucoside

C21H20O10 (432.1056)


A glycosyloxyflavone that is apigenin substituted by a beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage.

   

L-adenosylselenohomocysteine

L-adenosylselenohomocysteine

C14H20N6O5Se (432.066)


A selenoamino acid that is L-selenomethionine in which the methyl group attached to the selenium is replaced by a 5-adenosyl group.

   
   
   

Plazinemdor

Plazinemdor

C21H19ClF2N4O2 (432.1165)


Plazinemdor is a N-methyl-D-aspartate(NMDA) receptor positive allosteric modulator. Plazinemdor can be uses in the research of psychiatric, neurological, and neurodevelopmental disorders, as well as diseases of the nervous system[1]..

   

TD52 (dihydrochloride)

TD52 (dihydrochloride)

C24H18Cl2N4 (432.0908)


TD52 dihydrochloride, an Erlotinib (HY-50896) derivative, is an orally active, potent cancerous inhibitor of protein phosphatase 2A (CIP2A) inhibitor. TD52 dihydrochloride mediates the apoptotic effect in triple-negative breast cancer (TNBC) cells via regulating the CIP2A/PP2A/p-Akt signalling pathway. TD52 dihydrochloride indirectly reduced CIP2A by disturbing Elk1 binding to the CIP2A promoter. TD52 dihydrochloride has less p-EGFR inhibition and has potent anti-cancer activity[1]. TD52 (dihydrochloride) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

   

3,7-dihydroxy-2-(4-hydroxyphenyl)-5-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

3,7-dihydroxy-2-(4-hydroxyphenyl)-5-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

6-chloro-5,12-dihydroxy-7,15,15,19-tetramethyl-9,17-dioxo-2,10,14-trioxatetracyclo[9.8.0.0³,⁸.0¹³,¹⁸]nonadeca-1(19),3,5,7,11,13(18)-hexaene-4-carbaldehyde

6-chloro-5,12-dihydroxy-7,15,15,19-tetramethyl-9,17-dioxo-2,10,14-trioxatetracyclo[9.8.0.0³,⁸.0¹³,¹⁸]nonadeca-1(19),3,5,7,11,13(18)-hexaene-4-carbaldehyde

C21H17ClO8 (432.0612)


   

5-hydroxy-3-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-3-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-{[(2s,3r,4r,5s)-3,4-dihydroxy-5-[(1s)-1-hydroxyethyl]oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

7-{[(2s,3r,4r,5s)-3,4-dihydroxy-5-[(1s)-1-hydroxyethyl]oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,8-dihydroxy-2-phenyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,8-dihydroxy-2-phenyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

3-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

3-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

7-{[(2s,3r,4s,5r)-3,4-dihydroxy-5-[(1s)-1-hydroxyethyl]oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

7-{[(2s,3r,4s,5r)-3,4-dihydroxy-5-[(1s)-1-hydroxyethyl]oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

methyl 2-{3',4,9-trihydroxy-6'-methyl-4',5,10-trioxo-3,4-dihydrospiro[naphtho[2,3-c]pyran-1,2'-oxan]-3-yl}acetate

methyl 2-{3',4,9-trihydroxy-6'-methyl-4',5,10-trioxo-3,4-dihydrospiro[naphtho[2,3-c]pyran-1,2'-oxan]-3-yl}acetate

C21H20O10 (432.1056)


   

(1r)-4,7,9-trihydroxy-10-methoxy-8-methyl-1-phenyl-1h-anthra[1,2-c]furan-3,6,11-trione

(1r)-4,7,9-trihydroxy-10-methoxy-8-methyl-1-phenyl-1h-anthra[1,2-c]furan-3,6,11-trione

C24H16O8 (432.0845)


   

5,7-dihydroxy-2-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-2-(2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

3-{[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-8-hydroxy-6-(hydroxymethyl)-1-methoxyanthracene-9,10-dione

3-{[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-8-hydroxy-6-(hydroxymethyl)-1-methoxyanthracene-9,10-dione

C21H20O10 (432.1056)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-3-(4-hydroxyphenyl)-7-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-3-(4-hydroxyphenyl)-7-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3s,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3s,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

4-(methylsulfanyl)-6-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenazine-1-carboxylic acid

4-(methylsulfanyl)-6-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenazine-1-carboxylic acid

C20H20N2O7S (432.0991)


   

5,7-dihydroxy-2-(4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-2-(4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

4-(methylsulfanyl)-6-{[(2s,3s,5r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenazine-1-carboxylic acid

4-(methylsulfanyl)-6-{[(2s,3s,5r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenazine-1-carboxylic acid

C20H20N2O7S (432.0991)


   

5,8-dihydroxy-2-phenyl-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,8-dihydroxy-2-phenyl-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

4,7,9-trihydroxy-10-methoxy-8-methyl-1-phenyl-1h-anthra[1,2-c]furan-3,6,11-trione

4,7,9-trihydroxy-10-methoxy-8-methyl-1-phenyl-1h-anthra[1,2-c]furan-3,6,11-trione

C24H16O8 (432.0845)


   

5,7-dihydroxy-2-(3-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(3-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

(4as,5r,8r,8as)-n-(7,8-dimethoxy-2-oxochromen-3-yl)-4a,5,8-trihydroxy-4,5,8,8a-tetrahydro-1,2-benzoxazine-3-carboxamide

(4as,5r,8r,8as)-n-(7,8-dimethoxy-2-oxochromen-3-yl)-4a,5,8-trihydroxy-4,5,8,8a-tetrahydro-1,2-benzoxazine-3-carboxamide

C20H20N2O9 (432.1169)


   

5,7,2'-trihydroxyflavone2'-o-β-d-glucopyranoside

NA

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN011174","Ingredient_name": "5,7,2'-trihydroxyflavone2'-o-\u03b2-d-glucopyranoside","Alias": "NA","Ingredient_formula": "C21H20O10","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "21720","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

5,7-dihydroxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

5,7-dihydroxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-chromone; 5,7-dihydroxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-chromen-4-one; 5,7-dihydroxy-2-phenyl-6-[[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone; 5,7-dihydroxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN011270","Ingredient_name": "5,7-dihydroxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one","Alias": "5,7-dihydroxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-methylol-tetrahydropyran-2-yl]oxy-chromone; 5,7-dihydroxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-chromen-4-one; 5,7-dihydroxy-2-phenyl-6-[[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]oxy]-4-chromenone; 5,7-dihydroxy-2-phenyl-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one","Ingredient_formula": "C21H20O10","Ingredient_Smile": "NA","Ingredient_weight": "432.38","OB_score": "4.905609791","CAS_id": "529-43-1","SymMap_id": "SMIT13770","TCMID_id": "NA","TCMSP_id": "MOL013072","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

aloe-emodin-8-monoglucoside

aloeemodin-8-monoglucoside

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN015287","Ingredient_name": "aloe-emodin-8-monoglucoside","Alias": "aloeemodin-8-monoglucoside","Ingredient_formula": "C21H20O10","Ingredient_Smile": "Not Available","Ingredient_weight": "0","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "25721;971","TCMSP_id": "NA","TCM_ID_id": "6997;21386","PubChem_id": "NA","DrugBank_id": "NA"}

   

aloeemodin-ω-o-β-d-glucopyranoside

NA

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN015294","Ingredient_name": "aloeemodin-\u03c9-o-\u03b2-d-glucopyranoside","Alias": "NA","Ingredient_formula": "C21H20O10","Ingredient_Smile": "C1=CC2=C(C(=C1)O)C(=O)C3=C(C=C(C=C3C2=O)COC4C(C(C(C(O4)CO)O)O)O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "SMIT14254","TCMID_id": "970","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

apigenin-4'-o-β-d-glucopyranoside

NA

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN016413","Ingredient_name": "apigenin-4'-o-\u03b2-d-glucopyranoside","Alias": "NA","Ingredient_formula": "C21H20O10","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "1491","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

Apigenin-5-O-β-D-glucopyranoside

NA

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN016417","Ingredient_name": "Apigenin-5-O-\u03b2-D-glucopyranoside","Alias": "NA","Ingredient_formula": "C21H20O10","Ingredient_Smile": "C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)OC4C(C(C(C(O4)CO)O)O)O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "32677","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

Apigenin-7-O-β-D-glucopyranoside

apigenin-7-o-beta-d-glucopyranoside

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN016453","Ingredient_name": "Apigenin-7-O-\u03b2-D-glucopyranoside","Alias": "apigenin-7-o-beta-d-glucopyranoside","Ingredient_formula": "C21H20O10","Ingredient_Smile": "C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O","Ingredient_weight": "432.4 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "34108","TCMSP_id": "NA","TCM_ID_id": "19548","PubChem_id": "12304094","DrugBank_id": "NA"}

   

apigenin 7-O-beta-D-glucopyranoside

apigenin 7-O-β-D-glucopyranoside

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN016454","Ingredient_name": "apigenin 7-O-beta-D-glucopyranoside","Alias": "apigenin 7-O-\u03b2-D-glucopyranoside","Ingredient_formula": "C21H20O10","Ingredient_Smile": "C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O","Ingredient_weight": "432.4 g/mol","OB_score": "22.48640353","CAS_id": "78-74-5","SymMap_id": "SMIT08244","TCMID_id": "34447","TCMSP_id": "MOL006669","TCM_ID_id": "NA","PubChem_id": "12304094","DrugBank_id": "NA"}

   

apigenin-7-o-glucoside

NA

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN016474","Ingredient_name": "apigenin-7-o-glucoside","Alias": "NA","Ingredient_formula": "C21H20O10","Ingredient_Smile": "C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O","Ingredient_weight": "432.4 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "SMIT14332","TCMID_id": "1492","TCMSP_id": "NA","TCM_ID_id": "19549;19550;21622;21623","PubChem_id": "45933926","DrugBank_id": "NA"}

   

apigetrin

CHEMBL487995; SR-05000002285; Galactosyl-7-apigenin; EINECS 209-430-5; 5-Hydroxy-2-(4-hydroxyphenyl)-7-(4,5,6-trihydroxy-3-(hydroxymethyl)(2-oxanyloxy))-4H-chromen-4-one; Cosemetin; 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one; COSMOSIIN; 4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)- (9CI); Apigenin, 7-beta-D-glucopyranoside; Apigenin 7-O-beta-D-glucopyranoside; 7-(beta-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; Cosmosiine; 7-O-(beta-D-Glucosyl)apigenin; Thalictiin; SR-05000002285-3; A831652; Cosmosioside; 23598-21-2; NSC 407303; Apigetrin; NCGC00163513-01; CCG-208379; 62532-75-6; 5-hydroxy-2-(4-hydroxyphenyl)-7-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]oxy]-1-benzopyran-4-one; UNII-7OF2S66PCH; SR-05000002285-2; 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one; AC1NUZ8G; Apigenin, 7-beta-D-galactopyranoside; 7-[(2S,3R,4S,5R,6R)-6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-2-(4-hydroxyphenyl)-5-oxidanyl-chromen-4-one; 7OF2S66PCH; Cosmosiin (8CI)

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN016480","Ingredient_name": "apigetrin","Alias": "CHEMBL487995; SR-05000002285; Galactosyl-7-apigenin; EINECS 209-430-5; 5-Hydroxy-2-(4-hydroxyphenyl)-7-(4,5,6-trihydroxy-3-(hydroxymethyl)(2-oxanyloxy))-4H-chromen-4-one; Cosemetin; 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one; COSMOSIIN; 4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)- (9CI); Apigenin, 7-beta-D-glucopyranoside; Apigenin 7-O-beta-D-glucopyranoside; 7-(beta-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; Cosmosiine; 7-O-(beta-D-Glucosyl)apigenin; Thalictiin; SR-05000002285-3; A831652; Cosmosioside; 23598-21-2; NSC 407303; Apigetrin; NCGC00163513-01; CCG-208379; 62532-75-6; 5-hydroxy-2-(4-hydroxyphenyl)-7-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]oxy]-1-benzopyran-4-one; UNII-7OF2S66PCH; SR-05000002285-2; 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-chromen-4-one; AC1NUZ8G; Apigenin, 7-beta-D-galactopyranoside; 7-[(2S,3R,4S,5R,6R)-6-(hydroxymethyl)-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-2-(4-hydroxyphenyl)-5-oxidanyl-chromen-4-one; 7OF2S66PCH; Cosmosiin (8CI)","Ingredient_formula": "C21H20O10","Ingredient_Smile": "C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O","Ingredient_weight": "432.4 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "SMIT19095","TCMID_id": "30618","TCMSP_id": "NA","TCM_ID_id": "21625","PubChem_id": "12304093","DrugBank_id": "NA"}

   

baicalein-7-o-β-d-glucopyranoside

NA

C21H20O10 (432.1056)


{"Ingredient_id": "HBIN017513","Ingredient_name": "baicalein-7-o-\u03b2-d-glucopyranoside","Alias": "NA","Ingredient_formula": "C21H20O10","Ingredient_Smile": "C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "SMIT14433","TCMID_id": "2103","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

3-[(3,4-dihydroxyphenyl)methylidene]-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-benzofuran-1-one

3-[(3,4-dihydroxyphenyl)methylidene]-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-benzofuran-1-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-(4-hydroxyphenyl)-6-[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-3-(4-hydroxyphenyl)-6-[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

7-{[(2s,3r,4r,5r)-5-[(1r)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy}-5-hydroxy-3-(4-hydroxyphenyl)chromen-4-one

7-{[(2s,3r,4r,5r)-5-[(1r)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy}-5-hydroxy-3-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

8-[(2s,3r,4r,5r)-5-[(1r)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one

8-[(2s,3r,4r,5r)-5-[(1r)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-2-(4-hydroxyphenyl)-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7-hydroxy-2-(4-hydroxyphenyl)-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}chromen-5-one

7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}chromen-5-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

6,8-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

6,8-dihydroxy-2-(4-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-{4-hydroxy-3-[(2r,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}chromen-4-one

5,7-dihydroxy-2-{4-hydroxy-3-[(2r,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}chromen-4-one

C21H20O10 (432.1056)


   

2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

C21H20O10 (432.1056)


   

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

1-hydroxy-3-(hydroxymethyl)-8-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1-hydroxy-3-(hydroxymethyl)-8-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

2-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2-[(4-hydroxyphenyl)methyl]butanedioic acid

2-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2-[(4-hydroxyphenyl)methyl]butanedioic acid

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-phenyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-phenyl-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

6,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

6,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

7-{[(2r,3s,4r,5s)-3,4-dihydroxy-5-[(1s)-1-hydroxyethyl]oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

7-{[(2r,3s,4r,5s)-3,4-dihydroxy-5-[(1s)-1-hydroxyethyl]oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

4,25-dimethoxy-8,12,17,21-tetraoxaheptacyclo[13.11.0.0²,¹⁴.0³,¹¹.0⁵,⁹.0¹⁸,²⁶.0²⁰,²⁴]hexacosa-3(11),4,6,9,18(26),19,22,24-octaene-13,16-dione

4,25-dimethoxy-8,12,17,21-tetraoxaheptacyclo[13.11.0.0²,¹⁴.0³,¹¹.0⁵,⁹.0¹⁸,²⁶.0²⁰,²⁴]hexacosa-3(11),4,6,9,18(26),19,22,24-octaene-13,16-dione

C24H16O8 (432.0845)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

6,7-dihydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-8-(methylsulfanyl)naphthalene-2-carboxylic acid

6,7-dihydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-8-(methylsulfanyl)naphthalene-2-carboxylic acid

C21H20O8S (432.0879)


   

5,7-dihydroxy-2-(4-hydroxy-3-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-2-(4-hydroxy-3-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2r,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2r,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

1,8-dihydroxy-3-methyl-6-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1,8-dihydroxy-3-methyl-6-{[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2s,3s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2s,3s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-7-{[(2s,3r,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-7-{[(2s,3r,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-{[5-(1,2-dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy}-5,6-dihydroxy-2-phenylchromen-4-one

7-{[5-(1,2-dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy}-5,6-dihydroxy-2-phenylchromen-4-one

C21H20O10 (432.1056)


   

2-hydroxy-3-{[3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy}-2-[(4-hydroxyphenyl)methyl]butanedioic acid

2-hydroxy-3-{[3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy}-2-[(4-hydroxyphenyl)methyl]butanedioic acid

C21H20O10 (432.1056)


   

1-hydroxy-2-(hydroxymethyl)-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1-hydroxy-2-(hydroxymethyl)-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2r,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3r,4s,5r,6s)-2,4,5-trihydroxy-6-methyloxan-3-yl]oxy}chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3r,4s,5r,6s)-2,4,5-trihydroxy-6-methyloxan-3-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-(4-{[(2r,3r,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-3-(4-{[(2r,3r,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-5-one

7-hydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-5-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-3-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

(2z)-2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

(2z)-2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

C21H20O10 (432.1056)


   

emodin 1-o-β-d-glucoside

emodin 1-o-β-d-glucoside

C21H20O10 (432.1056)


   

7-{[5-(1,2-dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy}-5-hydroxy-3-(4-hydroxyphenyl)chromen-4-one

7-{[5-(1,2-dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy}-5-hydroxy-3-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl (2e)-3-(4-hydroxyphenyl)prop-2-enoate

C24H16O8 (432.0845)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-{4-hydroxy-2-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}chromen-4-one

5,7-dihydroxy-2-{4-hydroxy-2-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}chromen-4-one

C21H20O10 (432.1056)


   

(1r,2s,14s,15r)-4,25-dimethoxy-8,12,17,21-tetraoxaheptacyclo[13.11.0.0²,¹⁴.0³,¹¹.0⁵,⁹.0¹⁸,²⁶.0²⁰,²⁴]hexacosa-3(11),4,6,9,18(26),19,22,24-octaene-13,16-dione

(1r,2s,14s,15r)-4,25-dimethoxy-8,12,17,21-tetraoxaheptacyclo[13.11.0.0²,¹⁴.0³,¹¹.0⁵,⁹.0¹⁸,²⁶.0²⁰,²⁴]hexacosa-3(11),4,6,9,18(26),19,22,24-octaene-13,16-dione

C24H16O8 (432.0845)


   

5,6-dihydroxy-2-phenyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,6-dihydroxy-2-phenyl-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-3-(2-hydroxy-4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

7-hydroxy-3-(2-hydroxy-4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-3,6,7,8-tetramethoxy-2-(7-methoxy-2h-1,3-benzodioxol-5-yl)chromen-4-one

5-hydroxy-3,6,7,8-tetramethoxy-2-(7-methoxy-2h-1,3-benzodioxol-5-yl)chromen-4-one

C21H20O10 (432.1056)


   

1,8-dihydroxy-6-methyl-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1,8-dihydroxy-6-methyl-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

7-hydroxy-3-(4-hydroxyphenyl)-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7-hydroxy-3-(4-hydroxyphenyl)-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

(2e)-2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

(2e)-2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

C21H20O10 (432.1056)


   

2-hydroxy-1-methoxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

2-hydroxy-1-methoxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

3,7-dihydroxy-2-(4-hydroxyphenyl)-5-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

3,7-dihydroxy-2-(4-hydroxyphenyl)-5-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7-hydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(3-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

5,7-dihydroxy-2-(3-hydroxyphenyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(3-hydroxy-4-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-2-(3-hydroxy-4-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-3-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-3-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2s,3s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2s,3s,5s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

6-(3-hydroxy-4,5-dimethoxyphenyl)-4,7,9-trimethoxy-2h-[1,3]dioxolo[4,5-g]chromen-8-one

6-(3-hydroxy-4,5-dimethoxyphenyl)-4,7,9-trimethoxy-2h-[1,3]dioxolo[4,5-g]chromen-8-one

C21H20O10 (432.1056)


   

3,5,7-trihydroxy-2-(4-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)chromen-4-one

3,5,7-trihydroxy-2-(4-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

(3z)-3-[(3,4-dihydroxyphenyl)methylidene]-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-benzofuran-1-one

(3z)-3-[(3,4-dihydroxyphenyl)methylidene]-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2-benzofuran-1-one

C21H20O10 (432.1056)


   

3-(3,4-dihydroxyphenyl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

3-(3,4-dihydroxyphenyl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

1,8-dihydroxy-6-methyl-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1,8-dihydroxy-6-methyl-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

3-(3,4-dihydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

3-(3,4-dihydroxyphenyl)-7-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-{[(2s,3r,4s,5s)-3,4-dihydroxy-5-[(1s)-1-hydroxyethyl]oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

7-{[(2s,3r,4s,5s)-3,4-dihydroxy-5-[(1s)-1-hydroxyethyl]oxolan-2-yl]oxy}-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

3,7-dihydroxy-2-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

3,7-dihydroxy-2-(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

6,8-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

6,8-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

8-[(2r,3r,4r,5r)-5-[(1r)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one

8-[(2r,3r,4r,5r)-5-[(1r)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2r,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2r,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

3-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-8-hydroxy-6-(hydroxymethyl)-1-methoxyanthracene-9,10-dione

3-{[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-8-hydroxy-6-(hydroxymethyl)-1-methoxyanthracene-9,10-dione

C21H20O10 (432.1056)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3s,4s,5s,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3s,4s,5s,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4r,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

C21H20O10 (432.1056)


   

1,8-dihydroxy-3-methyl-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1,8-dihydroxy-3-methyl-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-7-hydroxy-8-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-7-hydroxy-8-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,6-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

5,6-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

7-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one

7-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-(4-hydroxyphenyl)-6-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-3-(4-hydroxyphenyl)-6-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

8-hydroxy-3-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

8-hydroxy-3-(hydroxymethyl)-1-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

1,8a-dihydroxy-7-methyl-6,8-dioxo-3-(prop-1-en-1-yl)-1h-isochromen-7-yl 3,4,6-trihydroxy-2-methylbenzoate

1,8a-dihydroxy-7-methyl-6,8-dioxo-3-(prop-1-en-1-yl)-1h-isochromen-7-yl 3,4,6-trihydroxy-2-methylbenzoate

C21H20O10 (432.1056)


   

5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl 3-(4-hydroxyphenyl)prop-2-enoate

5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl 3-(4-hydroxyphenyl)prop-2-enoate

C24H16O8 (432.0845)


   

1-hydroxy-3-(hydroxymethyl)-8-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1-hydroxy-3-(hydroxymethyl)-8-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

2-hydroxy-1-methoxy-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

2-hydroxy-1-methoxy-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,5,6-trihydroxy-4-methyloxan-2-yl)oxy]chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(3,5,6-trihydroxy-4-methyloxan-2-yl)oxy]chromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3r,4r,5r,6r)-3,5,6-trihydroxy-4-methyloxan-2-yl]oxy}chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3r,4r,5r,6r)-3,5,6-trihydroxy-4-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   
   

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-2-(4-hydroxyphenyl)-5-{[(2s,3r,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7-hydroxy-2-(4-hydroxyphenyl)-5-{[(2s,3r,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

(2z)-2-[(3,4-dihydroxyphenyl)methylidene]-4-hydroxy-6-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-1-benzofuran-3-one

(2z)-2-[(3,4-dihydroxyphenyl)methylidene]-4-hydroxy-6-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-1-benzofuran-3-one

C21H20O10 (432.1056)


   

(2z)-6-hydroxy-2-[(4-hydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methylidene]-1-benzofuran-3-one

(2z)-6-hydroxy-2-[(4-hydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methylidene]-1-benzofuran-3-one

C21H20O10 (432.1056)


   

1-hydroxy-2-(hydroxymethyl)-3-{[(2r,3r,4r,5r,6s)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}anthracene-9,10-dione

1-hydroxy-2-(hydroxymethyl)-3-{[(2r,3r,4r,5r,6s)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

2-[(3,4-dihydroxyphenyl)methylidene]-4-hydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-1-benzofuran-3-one

2-[(3,4-dihydroxyphenyl)methylidene]-4-hydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-1-benzofuran-3-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-{4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}chromen-4-one

5,7-dihydroxy-2-{4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-{3-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}chromen-4-one

5,7-dihydroxy-2-{3-hydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}chromen-4-one

C21H20O10 (432.1056)


   

7,8-dihydroxy-2-phenyl-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7,8-dihydroxy-2-phenyl-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

4-(methylsulfanyl)-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenazine-1-carboxylic acid

4-(methylsulfanyl)-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenazine-1-carboxylic acid

C20H20N2O7S (432.0991)


   

(2z)-2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

(2z)-2-[(3,4-dihydroxyphenyl)methylidene]-6-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

C21H20O10 (432.1056)


   

7-hydroxy-2-(4-hydroxyphenyl)-5-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7-hydroxy-2-(4-hydroxyphenyl)-5-{[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-{4-hydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}chromen-4-one

5,7-dihydroxy-3-{4-hydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}chromen-4-one

C21H20O10 (432.1056)


   

5,6-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,6-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,6-dihydroxy-2-phenyl-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,6-dihydroxy-2-phenyl-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

1,8-dihydroxy-3-methyl-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1,8-dihydroxy-3-methyl-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2,4,5-trihydroxy-6-methyloxan-3-yl)oxy]chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2,4,5-trihydroxy-6-methyloxan-3-yl)oxy]chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-7-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-7-hydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

3,5-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3r,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-3-(4-hydroxyphenyl)-8-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7-hydroxy-3-(4-hydroxyphenyl)-8-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-2-(4-hydroxyphenyl)-3-{[(3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-5-one

7-hydroxy-2-(4-hydroxyphenyl)-3-{[(3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-5-one

C21H20O10 (432.1056)


   

octacyclo[15.13.1.1²²,²⁶.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²¹,³¹.0³⁰,³²]dotriaconta-1,3,5(14),6(11),9,12,15,17(31),18,20,22(32),23,25,27,29-pentadecaene-7,8-dione

octacyclo[15.13.1.1²²,²⁶.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹.0²¹,³¹.0³⁰,³²]dotriaconta-1,3,5(14),6(11),9,12,15,17(31),18,20,22(32),23,25,27,29-pentadecaene-7,8-dione

C32H16O2 (432.115)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3s,4s,5s,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3s,4s,5s,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-{4-hydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}chromen-4-one

5,7-dihydroxy-2-{4-hydroxy-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}chromen-4-one

C21H20O10 (432.1056)


   

3,7-dihydroxy-2-(4-hydroxyphenyl)-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

3,7-dihydroxy-2-(4-hydroxyphenyl)-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

C21H20O10 (432.1056)


   

7-hydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-5-one

7-hydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-5-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7,8-dihydroxy-2-phenyl-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7,8-dihydroxy-2-phenyl-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

methyl 2-[(1s,3s,3'r,4s,6's)-3',4,9-trihydroxy-6'-methyl-4',5,10-trioxo-3,4-dihydrospiro[naphtho[2,3-c]pyran-1,2'-oxan]-3-yl]acetate

methyl 2-[(1s,3s,3'r,4s,6's)-3',4,9-trihydroxy-6'-methyl-4',5,10-trioxo-3,4-dihydrospiro[naphtho[2,3-c]pyran-1,2'-oxan]-3-yl]acetate

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,6-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3s,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,6-dihydroxy-2-(4-hydroxyphenyl)-7-{[(2s,3s,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-{4-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}chromen-4-one

5,7-dihydroxy-2-{4-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}chromen-4-one

C21H20O10 (432.1056)


   

5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[(2r,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,8-dihydroxy-2-(4-hydroxyphenyl)-7-[(2r,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

6,7-dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

6,7-dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

(2s,3s,4r,4ar,10br)-3,8,9,10-tetrahydroxy-2-(hydroxymethyl)-6-oxo-1h,2h,3h,4h,4ah,10bh-benzo[c]chromen-4-yl 4-hydroxybenzoate

(2s,3s,4r,4ar,10br)-3,8,9,10-tetrahydroxy-2-(hydroxymethyl)-6-oxo-1h,2h,3h,4h,4ah,10bh-benzo[c]chromen-4-yl 4-hydroxybenzoate

C21H20O10 (432.1056)


   

8-[5-(1,2-dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one

8-[5-(1,2-dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3r,4s,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

7-{[(2s,3r,4r,5r)-5-[(1r)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy}-5,6-dihydroxy-2-phenylchromen-4-one

7-{[(2s,3r,4r,5r)-5-[(1r)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy}-5,6-dihydroxy-2-phenylchromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-2-(3-hydroxyphenyl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(3-hydroxyphenyl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

6-hydroxy-2-[(4-hydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methylidene]-1-benzofuran-3-one

6-hydroxy-2-[(4-hydroxy-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methylidene]-1-benzofuran-3-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-2-(4-hydroxyphenyl)-7-{[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-{[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-2-(4-{[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxy-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-2-(4-hydroxy-3-{[(2s,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2s,3s,4r,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2s,3s,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2s,3s,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

3,5,7-trihydroxy-2-{4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}chromen-4-one

3,5,7-trihydroxy-2-{4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}chromen-4-one

C21H20O10 (432.1056)


   

5-hydroxy-3-(4-hydroxyphenyl)-7-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5-hydroxy-3-(4-hydroxyphenyl)-7-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-7-hydroxy-6-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-7-hydroxy-6-[(2s,3r,4r,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2r,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

n-(7,8-dimethoxy-2-oxochromen-3-yl)-4a,5,8-trihydroxy-4,5,8,8a-tetrahydro-1,2-benzoxazine-3-carboxamide

n-(7,8-dimethoxy-2-oxochromen-3-yl)-4a,5,8-trihydroxy-4,5,8,8a-tetrahydro-1,2-benzoxazine-3-carboxamide

C20H20N2O9 (432.1169)


   

1,8-dihydroxy-3-methyl-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1,8-dihydroxy-3-methyl-2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

2-(3,4-dihydroxyphenyl)-7-hydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

2-(3,4-dihydroxyphenyl)-7-hydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

9-({9-hydroxy-7-oxofuro[3,2-g]chromen-4-yl}oxy)-4-methoxyfuro[3,2-g]chromen-7-one

9-({9-hydroxy-7-oxofuro[3,2-g]chromen-4-yl}oxy)-4-methoxyfuro[3,2-g]chromen-7-one

C23H12O9 (432.0481)


   

7-hydroxy-3-(4-hydroxyphenyl)-8-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

7-hydroxy-3-(4-hydroxyphenyl)-8-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)


   

2-[(3,4-dihydroxyphenyl)methylidene]-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

2-[(3,4-dihydroxyphenyl)methylidene]-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1-benzofuran-3-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-3-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-3-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-(2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

5,7-dihydroxy-2-(2-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one

C21H20O10 (432.1056)


   

1-hydroxy-2-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

1-hydroxy-2-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}anthracene-9,10-dione

C21H20O10 (432.1056)


   

5,7-dihydroxy-2-phenyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

5,7-dihydroxy-2-phenyl-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}chromen-4-one

C21H20O10 (432.1056)