Exact Mass: 286.0376

Exact Mass Matches: 286.0376

Found 500 metabolites which its exact mass value is equals to given mass value 286.0376, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Luteolin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one

C15H10O6 (286.0477)


Luteolin is a naturally occurring flavonoid. (PMID:17168665). The flavonoids are polyphenolic compounds found as integral components of the human diet. They are universally present as constituents of flowering plants, particularly of food plants. The flavonoids are phenyl substituted chromones (benzopyran derivatives) consisting of a 15-carbon basic skeleton (C6-C3-C6), composed of a chroman (C6-C3) nucleus (the benzo ring A and the heterocyclic ring C), also shared by the tocopherols, with a phenyl (the aromatic ring B) substitution usually at the 2-position. Different substitutions can typically occur in the rings, A and B. Several plants and spices containing flavonoid derivatives have found application as disease preventive and therapeutic agents in traditional medicine in Asia for thousands of years. The selection of a particular food plant, plant tissue or herb for its potential health benefits appears to mirror its flavonoid composition. The much lower risk of colon, prostate and breast cancers in Asians, who consume more vegetables, fruits and tea than populations in the Western hemisphere do, raises the question of whether flavonoid components mediate the protective effects of diets rich in these foodstuffs by acting as natural chemopreventive and anticancer agents. An impressive body of information exists on the antitumoral action of plant flavonoids. In vitro work has concentrated on the direct and indirect actions of flavonoids on tumor cells, and has found a variety of anticancer effects such as cell growth and kinase activity inhibition, apoptosis induction, suppression of the secretion of matrix metalloproteinases and of tumor invasive behavior. Furthermore, some studies have reported the impairment of in vivo angiogenesis by dietary flavonoids. Experimental animal studies indicate that certain dietary flavonoids possess antitumoral activity. The hydroxylation pattern of the B ring of the flavones and flavonols, such as luteolin seems to critically influence their activities, especially the inhibition of protein kinase activity and antiproliferation. The different mechanisms underlying the potential anticancer action of plant flavonoids await further elucidation. Certain dietary flavonols and flavones targeting cell surface signal transduction enzymes, such as protein tyrosine and focal adhesion kinases, and the processes of angiogenesis appear to be promising candidates as anticancer agents. Further in vivo studies of these bioactive constituents is deemed necessary in order to develop flavonoid-based anticancer strategies. In view of the increasing interest in the association between dietary flavonoids and cancer initiation and progression, this important field is likely to witness expanded effort and to attract and stimulate further vigorous investigations (PMID:16097445). Luteolin is a tetrahydroxyflavone in which the four hydroxy groups are located at positions 3, 4, 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers. It has a role as an EC 2.3.1.85 (fatty acid synthase) inhibitor, an antineoplastic agent, a vascular endothelial growth factor receptor antagonist, a plant metabolite, a nephroprotective agent, an angiogenesis inhibitor, a c-Jun N-terminal kinase inhibitor, an anti-inflammatory agent, an apoptosis inducer, a radical scavenger and an immunomodulator. It is a 3-hydroxyflavonoid and a tetrahydroxyflavone. It is a conjugate acid of a luteolin-7-olate. Luteolin is a natural product found in Verbascum lychnitis, Carex fraseriana, and other organisms with data available. Luteolin is a naturally-occurring flavonoid, with potential anti-oxidant, anti-inflammatory, apoptosis-inducing and chemopreventive activities. Upon administration, luteolin scavenges free radicals, protects cells from reactive oxygen species (ROS)-induced damage and induces direct cell cycle arrest and apoptosis in tumor cells. This inhibits tumor cell proliferation and suppresses metastasis. 5,7,3,4-tetrahydroxy-flavone, one of the FLAVONES. See also: Chamomile (part of); Cannabis sativa subsp. indica top (part of); Fenugreek seed (part of). A tetrahydroxyflavone in which the four hydroxy groups are located at positions 3, 4, 5 and 7. It is thought to play an important role in the human body as an antioxidant, a free radical scavenger, an anti-inflammatory agent and an immune system modulator as well as being active against several cancers. Flavone v. widespread in plant world; found especies in celery, peppermint, rosemary, thyme and Queen Annes Lace leaves (wild carrot). Potential nutriceutical. Luteolin is found in many foods, some of which are soy bean, ginger, abalone, and swiss chard. Acquisition and generation of the data is financially supported in part by CREST/JST. IPB_RECORD: 361; CONFIDENCE confident structure CONFIDENCE standard compound; INTERNAL_ID 48 Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. Luteolin has anti-inflammatory, anti-cancer properties, including the induction of apoptosis and cell cycle arrest, and the inhibition of metastasis and angiogenesis, in several cancer cell lines, including human non-small lung cancer cells[1][2][3]. Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. Luteolin has anti-inflammatory, anti-cancer properties, including the induction of apoptosis and cell cycle arrest, and the inhibition of metastasis and angiogenesis, in several cancer cell lines, including human non-small lung cancer cells[1][2][3].

   

Fisetin

2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4H-chromen-4-one

C15H10O6 (286.0477)


Fisetin is a 7-hydroxyflavonol with additional hydroxy groups at positions 3, 3 and 4. It has a role as an EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor, an antioxidant, an anti-inflammatory agent, a metabolite, a plant metabolite and a geroprotector. It is a 3-hydroxyflavonoid, a 7-hydroxyflavonol and a tetrahydroxyflavone. It is a conjugate acid of a fisetin(1-). Fisetin is a natural product found in Acacia carneorum, Acacia buxifolia, and other organisms with data available. Fisetin is an orally bioavailable naturally occurring polyphenol found in many fruits and vegetables, with potential antioxidant, neuroprotective, anti-inflammatory, antineoplastic, senolytic, and longevity promoting activities. Upon administration, fisetin, as an antioxidant, scavenges free radicals, protect cells from oxidative stress, and is able to upregulate glutathione. It inhibits pro-inflammatory mediators, such as tumor necrosis factor alpha (TNF-a), interleukin-6 (IL-6), and nuclear factor kappa B (NF-kB). Fisetin promotes cellular metabolism, reduces senescence, regulates sirtuin function and may promote longevity. Fisetin also exerts anti-cancer activity by inhibiting certain signaling pathways. It also inhibits certain anti-apoptotic proteins and induces apoptosis in susceptible cells. COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials A 7-hydroxyflavonol with additional hydroxy groups at positions 3, 3 and 4. C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor C26170 - Protective Agent > C1509 - Neuroprotective Agent C26170 - Protective Agent > C275 - Antioxidant Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS 3,7,3,4-tetrahydroxyflavone, also known as 5-desoxyquercetin or fisetinidin, is a member of the class of compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position. Thus, 3,7,3,4-tetrahydroxyflavone is considered to be a flavonoid lipid molecule. 3,7,3,4-tetrahydroxyflavone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 3,7,3,4-tetrahydroxyflavone is a bitter tasting compound found in soy bean, which makes 3,7,3,4-tetrahydroxyflavone a potential biomarker for the consumption of this food product. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.847 [Raw Data] CB035_Fisetin_pos_20eV_CB000018.txt [Raw Data] CB035_Fisetin_pos_30eV_CB000018.txt [Raw Data] CB035_Fisetin_pos_40eV_CB000018.txt [Raw Data] CB035_Fisetin_pos_10eV_CB000018.txt [Raw Data] CB035_Fisetin_pos_50eV_CB000018.txt [Raw Data] CB035_Fisetin_neg_10eV_000011.txt [Raw Data] CB035_Fisetin_neg_30eV_000011.txt [Raw Data] CB035_Fisetin_neg_40eV_000011.txt [Raw Data] CB035_Fisetin_neg_20eV_000011.txt [Raw Data] CB035_Fisetin_neg_50eV_000011.txt Fisetin is a natural flavonol found in many fruits and vegetables with various benefits, such as antioxidant, anticancer, neuroprotection effects. Fisetin is a natural flavonol found in many fruits and vegetables with various benefits, such as antioxidant, anticancer, neuroprotection effects. Fisetin is a natural flavonol found in many fruits and vegetables with various benefits, such as antioxidant, anticancer, neuroprotection effects.

   

Kaempferol

3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

C15H10O6 (286.0477)


Kaempferol is a tetrahydroxyflavone in which the four hydroxy groups are located at positions 3, 5, 7 and 4. Acting as an antioxidant by reducing oxidative stress, it is currently under consideration as a possible cancer treatment. It has a role as an antibacterial agent, a plant metabolite, a human xenobiotic metabolite, a human urinary metabolite, a human blood serum metabolite and a geroprotector. It is a member of flavonols, a 7-hydroxyflavonol and a tetrahydroxyflavone. It is a conjugate acid of a kaempferol oxoanion. Kaempferol is a natural product found in Lotus ucrainicus, Visnea mocanera, and other organisms with data available. Kaempferol is a natural flavonoid which has been isolated from Delphinium, Witch-hazel, grapefruit, and other plant sources. Kaempferol is a yellow crystalline solid with a melting point of 276-278 degree centigrade. It is slightly soluble in water, and well soluble in hot ethanol and diethyl ether. Kaempferol is a metabolite found in or produced by Saccharomyces cerevisiae. See also: Cannabis sativa subsp. indica top (part of); Tussilago farfara flower (part of). Kaempferol, also known as rhamnolutein or c.i. 75640, belongs to the class of organic compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position. Thus, kaempferol is considered to be a flavonoid molecule. A tetrahydroxyflavone in which the four hydroxy groups are located at positions 3, 5, 7 and 4. Kaempferol is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. Kaempferol exists in all eukaryotes, ranging from yeast to humans. Kaempferol is a bitter tasting compound. Kaempferol is found, on average, in the highest concentration within a few different foods, such as saffrons, capers, and cumins and in a lower concentration in lovages, endives, and cloves. Kaempferol has also been detected, but not quantified, in several different foods, such as shallots, pine nuts, feijoa, kombus, and chicory leaves. This could make kaempferol a potential biomarker for the consumption of these foods. Kaempferol is a potentially toxic compound. Very widespread in the plant world, e.g. in Brassicaceae, Apocynaceae, Dilleniaceae, Ranunculaceae, Leguminosae, etc. Found especies in broccoli, capers, chives, kale, garden cress, fennel, lovage, dill weed and tarragon [CCD] A tetrahydroxyflavone in which the four hydroxy groups are located at positions 3, 5, 7 and 4. Acting as an antioxidant by reducing oxidative stress, it is currently under consideration as a possible cancer treatment. CONFIDENCE standard compound; INTERNAL_ID 898; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3906; ORIGINAL_PRECURSOR_SCAN_NO 3905 CONFIDENCE standard compound; INTERNAL_ID 898; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3916; ORIGINAL_PRECURSOR_SCAN_NO 3915 CONFIDENCE standard compound; INTERNAL_ID 898; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3928; ORIGINAL_PRECURSOR_SCAN_NO 3927 CONFIDENCE standard compound; INTERNAL_ID 898; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4291; ORIGINAL_PRECURSOR_SCAN_NO 4290 CONFIDENCE standard compound; INTERNAL_ID 898; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3918; ORIGINAL_PRECURSOR_SCAN_NO 3917 CONFIDENCE standard compound; INTERNAL_ID 898; DATASET 20200303_ENTACT_RP_MIX500; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3915; ORIGINAL_PRECURSOR_SCAN_NO 3914 Acquisition and generation of the data is financially supported in part by CREST/JST. INTERNAL_ID 2358; CONFIDENCE Reference Standard (Level 1) CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 2358 CONFIDENCE standard compound; INTERNAL_ID 47 CONFIDENCE standard compound; ML_ID 45 Kaempferol (Kempferol), a flavonoid found in many edible plants, inhibits estrogen receptor α expression in breast cancer cells and induces apoptosis in glioblastoma cells and lung cancer cells by activation of MEK-MAPK. Kaempferol can be uesd for the research of breast cancer[1][2][3][4]. Kaempferol (Kempferol), a flavonoid found in many edible plants, inhibits estrogen receptor α expression in breast cancer cells and induces apoptosis in glioblastoma cells and lung cancer cells by activation of MEK-MAPK. Kaempferol can be uesd for the research of breast cancer[1][2][3][4].

   

Brazilin

(1R,10S)-8-oxatetracyclo[8.7.0.0?,?.0??,??]heptadeca-2(7),3,5,12,14,16-hexaene-5,10,14,15-tetrol

C16H14O5 (286.0841)


Brazilin is a organic heterotetracyclic compound that is a red pigment obtained from the wood of Caesalpinia echinata (Brazil-wood) or Caesalpinia sappan (sappan-wood). It has a role as a plant metabolite, a histological dye, an antineoplastic agent, a biological pigment, an anti-inflammatory agent, an apoptosis inducer, an antioxidant, an antibacterial agent, a NF-kappaB inhibitor and a hepatoprotective agent. It is an organic heterotetracyclic compound, a member of catechols and a tertiary alcohol. Brazilin is a natural product found in Guilandina bonduc, Biancaea decapetala, and other organisms with data available. A organic heterotetracyclic compound that is a red pigment obtained from the wood of Caesalpinia echinata (Brazil-wood) or Caesalpinia sappan (sappan-wood). Brazilin is a red dye precursor obtained from the heartwood of several species of tropical hardwoods. Brazilin inhibits the cells proliferation, promotes apoptosis, and induces autophagy through the AMPK/mTOR pathway. Brazilin shows chondroprotective and anti-inflammatory activities[1][2][3]. Brazilin is a red dye precursor obtained from the heartwood of several species of tropical hardwoods. Brazilin inhibits the cells proliferation, promotes apoptosis, and induces autophagy through the AMPK/mTOR pathway. Brazilin shows chondroprotective and anti-inflammatory activities[1][2][3].

   

Isosakuranetin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-methoxyphenyl)-, (2S)-

C16H14O5 (286.0841)


4-methoxy-5,7-dihydroxyflavanone is a dihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5 and 7 and a methoxy group at position 4 (the 2S stereoisomer). It has a role as a plant metabolite. It is a dihydroxyflavanone, a monomethoxyflavanone, a member of 4-methoxyflavanones and a (2S)-flavan-4-one. It is functionally related to a (S)-naringenin. Isosakuranetin is a natural product found in Ageratina altissima, Chromolaena odorata, and other organisms with data available. Isosakuranetin is a flavanone flavonoid which can be found in the fruit of Citrus bergamia. Isosakuranetin is a flavanone flavonoid which can be found in the fruit of Citrus bergamia.

   

Sakuranetin

4H-1-Benzopyran-4-one, 2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-, (2S)-

C16H14O5 (286.0841)


Sakuranetin is a flavonoid phytoalexin that is (S)-naringenin in which the hydroxy group at position 7 is replaced by a methoxy group. It has a role as an antimycobacterial drug and a plant metabolite. It is a dihydroxyflavanone, a monomethoxyflavanone, a flavonoid phytoalexin, a member of 4-hydroxyflavanones and a (2S)-flavan-4-one. It is functionally related to a (S)-naringenin. Sakuranetin is a natural product found in Ageratina altissima, Chromolaena odorata, and other organisms with data available. Sakuranetin is found in black walnut. Sakuranetin is a flavanone, a type of flavonoid. It can be found in Polymnia fruticosa and rice, where it acts as a phytoalexin against spore germination of Pyricularia oryzae Sakuranetin is a flavanone, a type of flavonoid. It can be found in Polymnia fruticosa and rice, where it acts as a phytoalexin against spore germination of Pyricularia oryzae. A flavonoid phytoalexin that is (S)-naringenin in which the hydroxy group at position 7 is replaced by a methoxy group. Sakuranetin is a cherry flavonoid phytoalexin, shows strong antifungal activity[1]. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury[2]. Sakuranetin is a cherry flavonoid phytoalexin, shows strong antifungal activity[1]. Sakuranetin has anti-inflammatory and antioxidative activities. Sakuranetin ameliorates LPS-induced acute lung injury[2].

   

Maritimetin

(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-6,7-dihydroxy-2,3-dihydro-1-benzofuran-3-one

C15H10O6 (286.0477)


Maritimetin is a hydroxyaurone that is aurone substituted by hydroxy groups at positions 6, 7, 3 and 4 respectively. It has a role as a radical scavenger and a plant metabolite. It is functionally related to an aurone. Maritimetin is a natural product found in Lasthenia californica, Coreopsis tinctoria, and Bidens aurea with data available. A hydroxyaurone that is aurone substituted by hydroxy groups at positions 6, 7, 3 and 4 respectively. Maritimetin is used in flavourin

   

Cernuine

(2E)-2-[(3,4-dihydroxyphenyl)methylidene]-4,6-dihydroxy-2,3-dihydro-1-benzofuran-3-one

C15H10O6 (286.0477)


Aureusidin is a hydroxyaurone that is aurone substituted by hydroxy groups at positions 4, 6, 3 and 4 respectively. It has a role as a plant metabolite. It is functionally related to an aurone. It is a conjugate acid of an aureusidin-6-olate. Aureusidin is a natural product found in Eleocharis dulcis, Eleocharis pallens, and other organisms with data available. Cernuine is found in citrus. Cernuine is isolated from Citrus medica (citron). Isolated from Citrus medica (citron). Cernuine is found in lemon and citrus. Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1]. Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1]. Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1].

   

oxazepam

oxazepam

C15H11ClN2O2 (286.0509)


D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D006993 - Hypnotics and Sedatives D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014151 - Anti-Anxiety Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents N - Nervous system > N05 - Psycholeptics > N05B - Anxiolytics > N05BA - Benzodiazepine derivatives C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic > C1012 - Benzodiazepine D018377 - Neurotransmitter Agents > D018682 - GABA Agents > D018757 - GABA Modulators C78272 - Agent Affecting Nervous System > C28197 - Antianxiety Agent CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8781; ORIGINAL_PRECURSOR_SCAN_NO 8778 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8746; ORIGINAL_PRECURSOR_SCAN_NO 8744 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4409; ORIGINAL_PRECURSOR_SCAN_NO 4408 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8712; ORIGINAL_PRECURSOR_SCAN_NO 8710 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4423; ORIGINAL_PRECURSOR_SCAN_NO 4421 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8742; ORIGINAL_PRECURSOR_SCAN_NO 8740 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8757; ORIGINAL_PRECURSOR_SCAN_NO 8755 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4422; ORIGINAL_PRECURSOR_SCAN_NO 4421 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4393; ORIGINAL_PRECURSOR_SCAN_NO 4390 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 8709; ORIGINAL_PRECURSOR_SCAN_NO 8708 CONFIDENCE standard compound; INTERNAL_ID 799; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4374; ORIGINAL_PRECURSOR_SCAN_NO 4372 CONFIDENCE Reference Standard (Level 1); INTERNAL_ID 1083 CONFIDENCE standard compound; EAWAG_UCHEM_ID 2743 CONFIDENCE standard compound; INTERNAL_ID 8604 CONFIDENCE standard compound; INTERNAL_ID 2680

   

Vestitone

7-hydroxy-3-(2-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C16H14O5 (286.0841)


Isolated from Trifolium repens (white clover). Vestitone is found in many foods, some of which are climbing bean, lichee, sesbania flower, and grass pea. Vestitone is found in green vegetables. Vestitone is isolated from Trifolium repens (white clover

   

Scutellarein

6-hydroxyapigenin

C15H10O6 (286.0477)


Scutellarein is a natural flavonoid compound with anti-inflammatory effects. Scutellarein is a natural flavonoid compound with anti-inflammatory effects.

   

2'-Hydroxygenistein

3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one, 9CI

C15H10O6 (286.0477)


Isolated from Cajanus cajan (pigeon pea), Dolichos biflorus (papadi), Lablab niger (hyacinth bean), Phaseolus vulgaris (kidney bean) and Phaseolus coccineus (scarlet runner bean). 2-Hydroxygenistein is found in many foods, some of which are pulses, walnut, saskatoon berry, and garden tomato (variety). 2-Hydroxygenistein is found in adzuki bean. 2-Hydroxygenistein is isolated from Cajanus cajan (pigeon pea), Dolichos biflorus (papadi), Lablab niger (hyacinth bean), Phaseolus vulgaris (kidney bean) and Phaseolus coccineus (scarlet runner bean).

   

3'-Hydroxygenistein

4H-1-Benzopyran-4-one, 3-(3,4-dihydroxyphenyl)-5,7-dihydroxy-

C15H10O6 (286.0477)


Orobol is a member of the class of 7-hydroxyisoflavones which consists of isoflavone substituted by hydroxy groups at positions 5, 7, 3 and 4. It has been isolated from the mycelia of Cordyceps sinensis. It has a role as an anti-inflammatory agent, a radical scavenger, a plant metabolite and a fungal metabolite. It is functionally related to an isoflavone. Orobol is a natural product found in Tritirachium, Ammopiptanthus mongolicus, and other organisms with data available. A member of the class of 7-hydroxyisoflavones which consists of isoflavone substituted by hydroxy groups at positions 5, 7, 3 and 4. It has been isolated from the mycelia of Cordyceps sinensis. 3-Hydroxygenistein is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

Dihydrobiochanin A

Dihydrobiochanin A

C16H14O5 (286.0841)


   

2-O-Methyllicodione

Licodione 2-methyl ether

C16H14O5 (286.0841)


   

Glycineamideribotide

{[(2R,3S,4R,5R)-5-(2-aminoacetamido)-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

C7H15N2O8P (286.0566)


Glycinamidoribotide conversion to N-formylglycinamide ribonucleotide is the third reaction of the de novo purine biosynthesis, a reaction catalyzed by the enzyme Glycinamide ribonucleotide transformylase (EC 2.1.2.2), with concomitant conversion of 10-formyltetrahydrofolate to tetrahydrofolate. (PMID: 9143358). Glycineamideribotide formation is stimulated by Luteinizing hormone (LH) and Chorionic gonadotropin (HCG) via activation of Glc-6-P-dehydrogenase (EC 1.1.1.49). (PMID: 4366083) [HMDB] Glycinamidoribotide conversion to N-formylglycinamide ribonucleotide is the third reaction of the de novo purine biosynthesis, a reaction catalyzed by the enzyme Glycinamide ribonucleotide transformylase (EC 2.1.2.2), with concomitant conversion of 10-formyltetrahydrofolate to tetrahydrofolate. (PMID: 9143358). Glycineamideribotide formation is stimulated by Luteinizing hormone (LH) and Chorionic gonadotropin (HCG) via activation of Glc-6-P-dehydrogenase (EC 1.1.1.49). (PMID: 4366083).

   

Moracin A

5-(4,6-dimethoxy-1-benzofuran-2-yl)benzene-1,3-diol

C16H14O5 (286.0841)


   

Sainfuran

2- (2-Hydroxy-4-methoxyphenyl) -5-hydroxy-6-methoxybenzofuran

C16H14O5 (286.0841)


   

Quinquangulin

Quinquangulin

C16H14O5 (286.0841)


   

3-Formyl-2,4,6-trihydroxydihydrochalcone

3-Formyl-2,4,6-trihydroxydihydrochalcone

C16H14O5 (286.0841)


   

Datiscetin

3,5,7-Trihydroxy-2- (2-hydroxyphenyl) -4H-1-benzopyran-4-one

C15H10O6 (286.0477)


   

(R)-Oxypeucedanin

7H-Furo[3,2-g][1]benzopyran-7-one, 4-((3,3-dimethyloxiranyl)methoxy)-, (S-)-

C16H14O5 (286.0841)


(r)-oxypeucedanin, also known as hishigado or phosphine, is a member of the class of compounds known as psoralens. Psoralens are organic compounds containing a psoralen moiety, which consists of a furan fused to a chromenone to for 7H-furo[3,2-g]chromen-7-one (r)-oxypeucedanin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). (r)-oxypeucedanin can be found in carrot, lemon, parsley, and wild carrot, which makes (r)-oxypeucedanin a potential biomarker for the consumption of these food products. (R)-Oxypeucedanin is a member of psoralens. 4-[(3,3-Dimethyloxiran-2-yl)methoxy]furo[3,2-g]chromen-7-one is a natural product found in Prangos latiloba, Citrus medica, and other organisms with data available. D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins (R)-Oxypeucedanin is found in herbs and spices. (R)-Oxypeucedanin is isolated from Angelica glauc Oxypeucedanin is a furocoumarin derivative isolated from Angelica dahurica. Oxypeucedanin is a selective open-channel blocker, inhibits the hKv1.5 current with an IC50 value of 76 nM.?Oxypeucedanin prolongs cardiac action potential duration (APD), is a potential antiarrhythmic agent for atrial fibrillation[1]. Oxypeucedanin induces cell?apoptosis through inhibition of cancer cell migration[2]. Oxypeucedanin is a furocoumarin derivative isolated from Angelica dahurica. Oxypeucedanin is a selective open-channel blocker, inhibits the hKv1.5 current with an IC50 value of 76 nM.?Oxypeucedanin prolongs cardiac action potential duration (APD), is a potential antiarrhythmic agent for atrial fibrillation[1]. Oxypeucedanin induces cell?apoptosis through inhibition of cancer cell migration[2].

   

Isoscutellarein

5,7,8-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


   

3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-1H-2-benzopyran-1-one

3,4-Dihydro-8-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-1H-2-benzopyran-1-one

C16H14O5 (286.0841)


Natural sweetener approximately 600-800 times sweeter than sucros Natural sweetener approx. 600-800 times sweeter than sucrose

   

(-)-Nissolin

(-)-Nissolin

C16H14O5 (286.0841)


   

(S)-Dnpa

SCHEMBL17866715

C16H14O5 (286.0841)


   

Phenyl-P

2-Methacryloyloxyethyl phenyl phosphate

C12H15O6P (286.0606)


   

2,7-dihydroxy-4'-methoxyisoflavanone

2,7-dihydroxy-3-(4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one

C16H14O5 (286.0841)


2,7-dihydroxy-4-methoxyisoflavanone is a member of the class of compounds known as 4-o-methylated isoflavonoids. 4-o-methylated isoflavonoids are isoflavonoids with methoxy groups attached to the C4 atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one. 2,7-dihydroxy-4-methoxyisoflavanone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 2,7-dihydroxy-4-methoxyisoflavanone can be found in a number of food items such as rice, mango, wild rice, and purslane, which makes 2,7-dihydroxy-4-methoxyisoflavanone a potential biomarker for the consumption of these food products.

   

Demethoxycapillarisin

6-Demethoxycapillarisin

C15H10O6 (286.0477)


   

Citreorosein

1,3,8-trihydroxy-6-(hydroxymethyl)-9,10-dihydroanthracene-9,10-dione

C15H10O6 (286.0477)


Citreorosein is found in green vegetables. Citreorosein is found in roots of Polygonum cuspidatum (Japanese knotweed Found in roots of Polygonum cuspidatum (Japanese knotweed)

   
   

ITE

Methyl 2-(1H-indole-3-carbonyl)thiazole-4-carboxylate

C14H10N2O3S (286.0412)


   

Licochalcone B

2-PROPEN-1-ONE, 3-(3,4-DIHYDROXY-2-METHOXYPHENYL)-1-(4-HYDROXYPHENYL)-, (2E)-

C16H14O5 (286.0841)


Licochalcone B is a member of chalcones. Licochalcone B is a natural product found in Euphorbia helioscopia, Glycyrrhiza glabra, and other organisms with data available. See also: Glycyrrhiza inflata root (part of). Licochalcone B is found in herbs and spices. Licochalcone B is a constituent of the roots of Glycyrrhiza glabra (licorice). Constituent of the roots of Glycyrrhiza glabra (licorice). Licochalcone B is found in tea and herbs and spices. Licochalcone B is an extract from the root of Glycyrrhiza uralensis. Licochalcone B inhibits amyloid β (42) self-aggregation (IC50=2.16 μM) and disaggregate pre-formed Aβ42 fibrils, reduce metal-induced Aβ42 aggregation through chelating metal ionsLicochalcone B inhibits phosphorylation of NF-κB p65 in LPS signaling pathway. Licochalcone B inhibits growth and induces apoptosis of NSCLC cells. Licochalcone B specifically inhibits the NLRP3 inflammasome by disrupting NEK7‐NLRP3 interaction[1][2][3][4]. Licochalcone B is an extract from the root of Glycyrrhiza uralensis. Licochalcone B inhibits amyloid β (42) self-aggregation (IC50=2.16 μM) and disaggregate pre-formed Aβ42 fibrils, reduce metal-induced Aβ42 aggregation through chelating metal ionsLicochalcone B inhibits phosphorylation of NF-κB p65 in LPS signaling pathway. Licochalcone B inhibits growth and induces apoptosis of NSCLC cells. Licochalcone B specifically inhibits the NLRP3 inflammasome by disrupting NEK7‐NLRP3 interaction[1][2][3][4].

   

Norartocarpetin

2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one, 9CI

C15H10O6 (286.0477)


Norartocarpetin is a member of flavones. Norartocarpetin is a natural product found in Dalbergia sissoo, Ficus formosana, and other organisms with data available. Norartocarpetin is found in fruits. Norartocarpetin is a constituent of the heartwood of Artocarpus heterophyllus (jackfruit) Constituent of the heartwood of Artocarpus heterophyllus (jackfruit). Norartocarpetin is found in jackfruit and fruits. Norartocarpetin is a tyrosinase inhibitor. Norartocarpetin has strong tyrosinase inhibitory activity with an IC50 value of 0.47 μM. Norartocarpetin as an antibrowning agent can be used for the research of food systems. Norartocarpetin also has a significant anticancer activity in lung carcinoma cells (NCI-H460) with an IC50 value of 22 μM. Norartocarpetin has antiproliferative effects are mediated via targeting Ras/Raf/MAPK signalling pathway, mitochondrial mediated apoptosis, S-phase cell cycle arrest and suppression of cell migration and invasion in human lung carcinoma cells[1][2]. Norartocarpetin is a tyrosinase inhibitor. Norartocarpetin has strong tyrosinase inhibitory activity with an IC50 value of 0.47 μM. Norartocarpetin as an antibrowning agent can be used for the research of food systems. Norartocarpetin also has a significant anticancer activity in lung carcinoma cells (NCI-H460) with an IC50 value of 22 μM. Norartocarpetin has antiproliferative effects are mediated via targeting Ras/Raf/MAPK signalling pathway, mitochondrial mediated apoptosis, S-phase cell cycle arrest and suppression of cell migration and invasion in human lung carcinoma cells[1][2].

   

Helichysetin

2-Propen-1-one, 1-(2,4-dihydroxy-6-methoxyphenyl)-3-(4-hydroxyphenyl)-, (2E)-

C16H14O5 (286.0841)


Helichrysetin, also known as 2,​4,​4-​trihydroxy-​6-​methoxychalcone, belongs to the class of organic compounds known as 2-hydroxychalcones. These are organic compounds containing a chalcone skeleton that carries a hydroxyl group at the 2-position. Thus, helichrysetin is considered to be a flavonoid lipid molecule. Helichrysetin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. BioTransformer predicts that helichysetin is a product of 2-O-methylisoliquiritigenin metabolism via a hydroxylation-of-benzene-ortho-to-edg reaction catalyzed by CYP2C9 and CYP2C19 enzymes (PMID: 30612223). Helichrysetin is a member of chalcones. Helichrysetin is a natural product found in Alpinia blepharocalyx, Alpinia hainanensis, and other organisms with data available. Helichrysetin, isolated from the flowers of Helichrysum odoratissimum, is an ID2 (inhibitor of DNA binding 2) inhibitor, and suppresses DCIS (ductal carcinoma in situ) formation. Helichrysetin possess strong inhibitory effects on cell growth and is capable of inducing apoptosis in A549 cells[1][2]. Helichrysetin, isolated from the flowers of Helichrysum odoratissimum, is an ID2 (inhibitor of DNA binding 2) inhibitor, and suppresses DCIS (ductal carcinoma in situ) formation. Helichrysetin possess strong inhibitory effects on cell growth and is capable of inducing apoptosis in A549 cells[1][2].

   

Dihydrooroxylin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-6-methoxy-2-phenyl-, (S)-

C16H14O5 (286.0841)


Dihydrooroxylin A is a dihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5 and 7 and a methoxy group at position 6. Isolated from Pisonia aculeata, it exhibits antitubercular activity. It has a role as an antitubercular agent and a plant metabolite. It is a dihydroxyflavanone and a monomethoxyflavanone. Dihydrooroxylin A is a natural product found in Scutellaria scandens, Scutellaria caerulea, and other organisms with data available. A dihydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5 and 7 and a methoxy group at position 6. Isolated from Pisonia aculeata, it exhibits antitubercular activity. Dihydrooroxylin is found in fruits. Dihydrooroxylin is isolated from Prunus avium (wild cherry) and Piper sp. Isolated from Prunus avium (wild cherry) and Piper species Dihydrooroxylin is found in fruits.

   

(R)-Pabulenol

InChI=1/C16H14O5/c1-9(2)12(17)8-20-16-10-3-4-15(18)21-14(10)7-13-11(16)5-6-19-13/h3-7,12,17H,1,8H2,2H3

C16H14O5 (286.0841)


(R)-Pabulenol is a member of psoralens. (R)-Pabulenol is a natural product found in Prangos latiloba, Prangos lophoptera, and other organisms with data available. (R)-Pabulenol is found in herbs and spices. (R)-Pabulenol is a constituent of Ruta graveolens (rue) Constituent of Ruta graveolens (rue). (R)-Pabulenol is found in herbs and spices. Pangelin is a coumarin that can be found in Ducrosia anethifolia. Pangelin exhibits anti-mycobacterial and anti-tumor activities[1][2].

   

Oxazepam

7-chloro-3-hydroxy-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepin-2-one

C15H11ClN2O2 (286.0509)


Oxazepam is only found in individuals that have used or taken this drug. It is an intermediate-acting benzodiazepine used to treat alcohol withdrawal and anxiety disorders. It is a metabolite of diazepam, prazepam, temazepam, and clorazepate, and has moderate amnesic, anxiolytic, anticonvulsant, hypnotic, sedative, and skeletal muscle relaxant properties compared to other benzodiazepines (Wikipedia). Like other benzodiazepines, oxazepam exerts its anxiolytic effects by potentiating the effect of gamma-aminobutyric acid (GABA) on GABA-A receptors through a cooperative mechanism of action. GABA receptors are ionotropic chloride-linked channel receptors that produce inhibitory postsynaptic potentials. When activated by GABA, the GABA receptor/chloride ionophore complex undergoes a conformational change that allows the passage of chloride ions through the channel. Benzodiazepines are believed to exert their effect by increasing the effect of GABA at its receptor. Benzodiazepine binding increases chloride conductance in the presence of GABA by increasing the frequency at which the channel opens. In contrast, barbiturates increase chloride conductance in the presence of GABA by prolonging the time in which the channel remains open. There are 18 subtypes of the GABA receptor subunits. The α2 subunit of the α2β3γ2 receptor complex is thought to mediate anxiolytic effects while the α1 subunit of the α1β2γ2 receptor complex is thought to mediate sedative, anticonvulsant, and anterograde amnesia effects. D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D006993 - Hypnotics and Sedatives D002492 - Central Nervous System Depressants > D014149 - Tranquilizing Agents > D014151 - Anti-Anxiety Agents D002491 - Central Nervous System Agents > D011619 - Psychotropic Drugs > D014149 - Tranquilizing Agents N - Nervous system > N05 - Psycholeptics > N05B - Anxiolytics > N05BA - Benzodiazepine derivatives C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic > C1012 - Benzodiazepine D018377 - Neurotransmitter Agents > D018682 - GABA Agents > D018757 - GABA Modulators C78272 - Agent Affecting Nervous System > C28197 - Antianxiety Agent

   

norclobazam

8-chloro-4-hydroxy-1-phenyl-2,3-dihydro-1H-1,5-benzodiazepin-2-one

C15H11ClN2O2 (286.0509)


norclobazam is a metabolite of clobazam. Clobazam (marketed under the brand names Frisium, Urbanol and Onfi), is a drug which is a benzodiazepine derivative. It has been marketed as an anxiolytic since 1975 and an anticonvulsant since 1984. (Wikipedia) D002491 - Central Nervous System Agents > D000927 - Anticonvulsants

   

p-Hydroxynordiazepam

7-chloro-5-(4-hydroxyphenyl)-2,3-dihydro-1H-1,4-benzodiazepin-2-one

C15H11ClN2O2 (286.0509)


p-Hydroxynordiazepam is a metabolite of clorazepate. Clorazepate (marketed under the brand names Tranxene and Novo-Clopate), also known as clorazepate dipotassium, is a drug that is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative, hypnotic and skeletal muscle relaxant properties. Clorazepate is a prodrug for desmethyldiazepam, which is rapidly produced as an active metabolite. Desmethyldiazepam is responsible for most of the therapeutic effects of clorazepate. (Wikipedia)

   

7,3,4,5-Tetrahydroxyflavone

7,3,4,5-Tetrahydroxyflavone

C15H10O6 (286.0477)


   

3,8-Dihydroxy-9-methoxypterocarpan

14-methoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,13-diol

C16H14O5 (286.0841)


3,8-Dihydroxy-9-methoxypterocarpan is found in green vegetables. 3,8-Dihydroxy-9-methoxypterocarpan is a constituent of Pterocarpus soyauxii. Constituent of Pterocarpus soyauxii. 3,8-Dihydroxy-9-methoxypterocarpan is found in green vegetables.

   

Uralenneoside

3,4,5-Trihydroxyoxan-2-yl 3,4-dihydroxybenzoic acid

C12H14O8 (286.0689)


Uralenneoside is found in herbs and spices. Uralenneoside is a constituent of the leaves of Glycyrrhiza uralensis (Chinese licorice). Constituent of the leaves of Glycyrrhiza uralensis (Chinese licorice). Uralenneoside is found in herbs and spices.

   

3,5,6,7-tetrahydroxy-2-(4-hydroxyphenyl)-1λ⁴-chromen-1-ylium

3,5,6,7-tetrahydroxy-2-(4-hydroxyphenyl)-1λ⁴-chromen-1-ylium

C15H10O6 (286.0477)


   

(-)-5,7-Dihydroxy-3-(4-hydroxybenzyl)-4-chromanone

5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-1-benzopyran-4-one

C16H14O5 (286.0841)


(-)-5,7-Dihydroxy-3-(4-hydroxybenzyl)-4-chromanone is found in herbs and spices. (-)-5,7-Dihydroxy-3-(4-hydroxybenzyl)-4-chromanone is a constituent of Muscari comosum (tassel hyacinth). Constituent of Muscari comosum (tassel hyacinth). (-)-5,7-Dihydroxy-3-(4-hydroxybenzyl)-4-chromanone is found in herbs and spices.

   

6,7,3,4-TETRAHYDROXYFLAVONE

6,7,3,4-TETRAHYDROXYFLAVONE

C15H10O6 (286.0477)


   

4,6,7,8-Tetrahydroxyisoflavone

4,6,7,8-Tetrahydroxyisoflavone

C15H10O6 (286.0477)


   

Desmocarpin

1,9-Dihydroxy-3-methoxypterocarpan

C16H14O5 (286.0841)


   

5,6,7,4'-Tetrahydroxyisoflavone

5,6,7-trihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one

C15H10O6 (286.0477)


5,6,7,4-Tetrahydroxyisoflavone is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

Dihydrowogonin

5,7-dihydroxy-8-methoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

C16H14O5 (286.0841)


Isolated from Prunus avium (wild cherry). Dihydrowogonin is found in fruits, sweet cherry, and sour cherry. Dihydrowogonin is found in fruits. Dihydrowogonin is isolated from Prunus avium (wild cherry).

   

3,3,5,7-Tetrahydroxyflavone

3,3,5,7-Tetrahydroxyflavone

C15H10O6 (286.0477)


   

(2E)-1-(2,6-dihydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one

(2E)-1-(2,6-dihydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one

C16H14O5 (286.0841)


   

(2E)-1-(2,4-dihydroxy-3-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one

(2E)-1-(2,4-dihydroxy-3-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one

C16H14O5 (286.0841)


   

5,7-Dihydroxy-3-methoxyflavanone

5,7-Dihydroxy-3-methoxyflavanone

C16H14O5 (286.0841)


   

7,8,2,4-Tetrahydroxyisoflavone

7,8,2,4-Tetrahydroxyisoflavone

C15H10O6 (286.0477)


   

5,7,3,5-Tetrahydroxyflavone

5,7,3,5-Tetrahydroxyflavone

C15H10O6 (286.0477)


   

Dihydroglycitein

7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-3,4-dihydro-2H-1-benzopyran-4-one

C16H14O5 (286.0841)


Dihydroglycitein is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

3'-Methoxyfukiic acid

2,3-dihydroxy-2-[(4-hydroxy-3-methoxyphenyl)methyl]butanedioic acid

C12H14O8 (286.0689)


3-Methoxyfukiic acid is found in green vegetables. 3-Methoxyfukiic acid is isolated from Petasites japonicus (sweet coltsfoot

   

6-Hydroxygalangin

6-Hydroxygalangin

C15H10O6 (286.0477)


   

6alpha-Hydroxymedicarpin

14-methoxy-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,10-diol

C16H14O5 (286.0841)


6alpha-Hydroxymedicarpin is found in fruits. 6alpha-Hydroxymedicarpin is isolated from fungus-infected leaves of Melilotus alba (white melilot).

   

7,8,3',4'-Tetrahydroxyisoflavone

3-(3,4-dihydroxyphenyl)-7,8-dihydroxy-4H-chromen-4-one

C15H10O6 (286.0477)


7,8,3,4-Tetrahydroxyisoflavone is a polyphenol metabolite detected in biological fluids (PMID: 20428313). A polyphenol metabolite detected in biological fluids [PhenolExplorer]

   

Demoxepam

7-chloro-2-hydroxy-5-phenyl-3H-1,4λ⁵-benzodiazepin-4-one

C15H11ClN2O2 (286.0509)


Demoxepam belongs to the family of Benzodiazepines. These are organic compounds containing a benzene ring fused to either isomers of diazepine(unsaturated seven-member heterocycle with two nitrogen atoms replacing two carbon atoms).

   

Diphenol glucuronide

(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(2-hydroxyphenoxy)oxane-2-carboxylic acid

C12H14O8 (286.0689)


Diphenol glucuronide belongs to the family of Glucuronides. These are compounds comprising the glucuronic acid linked to another substance via a glycosidic bond.

   

Catechol glucuronide

(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(2-hydroxyphenoxy)oxane-2-carboxylic acid

C12H14O8 (286.0689)


   

Methyl 2-(1H-indole-3-carbonyl)thiazole-4-carboxylate

methyl 2-(1H-indole-3-carbonyl)-1,3-thiazole-4-carboxylate

C14H10N2O3S (286.0412)


   

Azvudine

4-Amino-1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)-5-((imino-L,5-azanylidene)amino)tetrahydrofuran-2-yl)pyrimidin-2-one

C9H11FN6O4 (286.0826)


COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

Fenclorac

alpha-m-Dichloro-p-cyclohexylphenylacetic acid diethylammonium salt

C14H16Cl2O2 (286.0527)


C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic C471 - Enzyme Inhibitor > C1323 - Cyclooxygenase Inhibitor

   

Imirestat

Spiro(2,7-difluoro-9H-fluoren-9,4-imidazolidine)-2,5-dione

C15H8F2N2O2 (286.0554)


C471 - Enzyme Inhibitor > C72880 - Aldose Reductase Inhibitor

   

Protoapigenone

5,7-dihydroxy-2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)-4H-chromen-4-one

C15H10O6 (286.0477)


   

9-(6-Oxo-1H-purin-9-yl)-3H-purine-2,6-dione

3,6-dihydro-1H,1H,2H,6H-[9,9-bipurine]-2,6,6-trione

C10H6N8O3 (286.0563)


   

Sulfametrole

4-amino-N-(4-methoxy-2,3-dihydro-1,2,5-thiadiazol-3-ylidene)benzene-1-sulfonamide

C9H10N4O3S2 (286.0194)


   

Tauromustine

N-(2-Chloroethyl)-2-(dimethylsulphamoyl)-N-nitrosoethane-1-carbamimidic acid

C7H15ClN4O4S (286.0502)


   

Quinol glucuronide

3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxane-2-carboxylic acid

C12H14O8 (286.0689)


   

8-Hydroxygenistein

5,7,8-trihydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one

C15H10O6 (286.0477)


8-hydroxygenistein is a member of the class of compounds known as isoflavones. Isoflavones are polycyclic compounds containing a 2-isoflavene skeleton which bears a ketone group at the C4 carbon atom. 8-hydroxygenistein is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 8-hydroxygenistein can be found in a number of food items such as scarlet bean, mung bean, lima bean, and adzuki bean, which makes 8-hydroxygenistein a potential biomarker for the consumption of these food products.

   

Scutellarein

(2S)-2,3-dihydro-5,6,7-trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


Scutellarein is flavone substituted with hydroxy groups at C-4, -5, -6 and -7. It has a role as a metabolite. It is functionally related to an apigenin. It is a conjugate acid of a scutellarein(1-). Scutellarein is a natural product found in Scoparia dulcis, Artemisia douglasiana, and other organisms with data available. Flavone substituted with hydroxy groups at C-4, -5, -6 and -7. Scutellarein, also known as 6-hydroxyapigenin or 4,5,6,7-tetrahydroxyflavanone, is a member of the class of compounds known as flavones. Flavones are flavonoids with a structure based on the backbone of 2-phenylchromen-4-one (2-phenyl-1-benzopyran-4-one). Thus, scutellarein is considered to be a flavonoid lipid molecule. Scutellarein is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Scutellarein can be synthesized from apigenin. Scutellarein is also a parent compound for other transformation products, including but not limited to, scutellarin, 4,6-dihydroxy-5,7-dimethoxyflavone, and 6-hydroxy-4,5,7-trimethoxyflavone. Scutellarein is a bitter tasting compound found in mexican oregano and sweet orange, which makes scutellarein a potential biomarker for the consumption of these food products. Scutellarein is a flavone that can be found in Scutellaria lateriflora and other members of the genus Scutellaria, as well as the fern Asplenium belangeri . Scutellarein is a natural flavonoid compound with anti-inflammatory effects. Scutellarein is a natural flavonoid compound with anti-inflammatory effects.

   

Aplidioxin A

Aplidioxin A

C15H10O6 (286.0477)


   

L-Malic acid 2-O-gallate

L-Malic acid 2-O-gallate

C11H10O9 (286.0325)


   
   

Thunberginol B

Thunberginol B

C15H10O6 (286.0477)


   

7-Hydroxyemodin

7-Hydroxyemodin

C15H10O6 (286.0477)


   

Cynodontin

1,4,5,8-Tetrahydroxy-2-methylanthraquinone

C15H10O6 (286.0477)


   
   
   

1,3,8-trihydroxy-2-methoxyanthraquinone

1,3,8-trihydroxy-2-methoxyanthraquinone

C15H10O6 (286.0477)


   

Melacacinidin

Melacacinidin

C15H10O6 (286.0477)


   

Tournefolal

Tournefolal

C15H10O6 (286.0477)


   

6-Hydroxygalangin

3,5,6,7-Tetrahydroxy-2-phenyl-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


   

5,7,2,5-Tetrahydroxyflavone

2-(2,5-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


   

5,7,2,6-Tetrahydroxyflavone

2- (2,6-Dihydroxyphenyl) -5,7-dihydroxy-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


   

5,7,2,3-Tetrahydroxyflavone

2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


   

7,3,4,5-Tetrahydroxyflavone

7,3,4,5-Tetrahydroxyflavone

C15H10O6 (286.0477)


   

3,7,8,4-Tetrahydroxyflavone

3,7,8,4-Tetrahydroxyflavone

C15H10O6 (286.0477)


   

7,8,2,4-Tetrahydroxyisoflavone

7,8,2,4-Tetrahydroxyisoflavone

C15H10O6 (286.0477)


   

8-Hydroxygalangin

2-Phenyl-3,5,6,7-tetrahydroxy-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


   

Helmon

4,7,4,6-Tetrahydroxyaurone

C15H10O6 (286.0477)


   

2-hydroxy-1H-naphtho[2,1,8-mna]xanthen-1-one

2-hydroxy-1H-naphtho[2,1,8-mna]xanthen-1-one

C19H10O3 (286.063)


   

5-Hydroxy-1H-naphtho[2,1,8-mna]xanthen-1-one

5-Hydroxy-1H-naphtho[2,1,8-mna]xanthen-1-one

C19H10O3 (286.063)


   

Baptigenin

7,3,4,5-Tetrahydroxyisoflavone

C15H10O6 (286.0477)


   

Luteolin

4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy- (9CI)

C15H10O6 (286.0477)


Annotation level-1 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.976 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.975 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.968 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.971 Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. Luteolin has anti-inflammatory, anti-cancer properties, including the induction of apoptosis and cell cycle arrest, and the inhibition of metastasis and angiogenesis, in several cancer cell lines, including human non-small lung cancer cells[1][2][3]. Luteolin (Luteoline), a flavanoid compound, is a potent Nrf2 inhibitor. Luteolin has anti-inflammatory, anti-cancer properties, including the induction of apoptosis and cell cycle arrest, and the inhibition of metastasis and angiogenesis, in several cancer cell lines, including human non-small lung cancer cells[1][2][3].

   

Isoscutellarein

5,7,8-Trihydroxy-2- (4-hydroxyphenyl) -4H-1-benzopyran-4-one

C15H10O6 (286.0477)


A tetrahydroxyflavone that is apigenin with an extra hydroxy group at position 8.

   

2-Hydroxygenistein

3- [ 2,4-Dihydroxyphenyl ] -5,7-dihydroxy-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


   

Maritimetin

6,7-Dihydroxy-2- [ (Z) -3,4-dihydroxyphenylmethylene ] benzofuran-3 (2H) -one

C15H10O6 (286.0477)


   

Swartziol

4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4-Trihydroxyflavonol

C15H10O6 (286.0477)


Kaempferol (Kempferol), a flavonoid found in many edible plants, inhibits estrogen receptor α expression in breast cancer cells and induces apoptosis in glioblastoma cells and lung cancer cells by activation of MEK-MAPK. Kaempferol can be uesd for the research of breast cancer[1][2][3][4]. Kaempferol (Kempferol), a flavonoid found in many edible plants, inhibits estrogen receptor α expression in breast cancer cells and induces apoptosis in glioblastoma cells and lung cancer cells by activation of MEK-MAPK. Kaempferol can be uesd for the research of breast cancer[1][2][3][4].

   

Norartocarpetin

2- (2,4-Dihydroxyphenyl) -5,7-dihydroxy-4H-1-benzopyran-4-one

C15H10O6 (286.0477)


Norartocarpetin is a tyrosinase inhibitor. Norartocarpetin has strong tyrosinase inhibitory activity with an IC50 value of 0.47 μM. Norartocarpetin as an antibrowning agent can be used for the research of food systems. Norartocarpetin also has a significant anticancer activity in lung carcinoma cells (NCI-H460) with an IC50 value of 22 μM. Norartocarpetin has antiproliferative effects are mediated via targeting Ras/Raf/MAPK signalling pathway, mitochondrial mediated apoptosis, S-phase cell cycle arrest and suppression of cell migration and invasion in human lung carcinoma cells[1][2]. Norartocarpetin is a tyrosinase inhibitor. Norartocarpetin has strong tyrosinase inhibitory activity with an IC50 value of 0.47 μM. Norartocarpetin as an antibrowning agent can be used for the research of food systems. Norartocarpetin also has a significant anticancer activity in lung carcinoma cells (NCI-H460) with an IC50 value of 22 μM. Norartocarpetin has antiproliferative effects are mediated via targeting Ras/Raf/MAPK signalling pathway, mitochondrial mediated apoptosis, S-phase cell cycle arrest and suppression of cell migration and invasion in human lung carcinoma cells[1][2].

   

Orobol

4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(3,4-dihydroxyphenyl)-

C15H10O6 (286.0477)


   

6-Hydroxygenistein

5,6,7,4-Tetrahydroxyisoflavone

C15H10O6 (286.0477)


   

Demoxepam

Demoxepam

C15H11ClN2O2 (286.0509)


C78272 - Agent Affecting Nervous System > C264 - Anticonvulsant Agent

   

Maybridge1_006093

Maybridge1_006093

C14H11FN4S (286.0688)


   

5-(4-chlorophenyl)-3-phenyl-1H-imidazole-2-thione

5-(4-chlorophenyl)-3-phenyl-1H-imidazole-2-thione

C15H11ClN2S (286.0331)


   
   

3,6,3,4-TETRAHYDROXYFLAVONE

3,6,3,4-TETRAHYDROXYFLAVONE

C15H10O6 (286.0477)


   

3,6,2,3-Tetrahydroxyflavone

3,6,2,3-Tetrahydroxyflavone

C15H10O6 (286.0477)


   

3,6,2,4-TETRAHYDROXYFLAVONE

3,6,2,4-TETRAHYDROXYFLAVONE

C15H10O6 (286.0477)


   

SCHEMBL14281489

SCHEMBL14281489

C15H10O6 (286.0477)


   

SCHEMBL17867307

SCHEMBL17867307

C9H18S5 (286.0012)


   

7-Hydroxy-1-methoxy-2,3-methylenedioxy xanthone

7-Hydroxy-1-methoxy-2,3-methylenedioxy xanthone

C15H10O6 (286.0477)


   

Ac-3-[5-(2-Thienylethynyl)-2-thienyl]-2-propyn-1-ol

Ac-3-[5-(2-Thienylethynyl)-2-thienyl]-2-propyn-1-ol

C15H10O2S2 (286.0122)


   

2-Hydroxygerustein

2-Hydroxygerustein

C15H10O6 (286.0477)


   

2,5,6,6-Tetrahydroxyflavone

2,5,6,6-Tetrahydroxyflavone

C15H10O6 (286.0477)


   

Kaempferol

Kaempferol

C15H10O6 (286.0477)


Annotation level-3 Annotation level-1 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.010 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.011 Acquisition and generation of the data is financially supported by the Max-Planck-Society IPB_RECORD: 2141; CONFIDENCE confident structure IPB_RECORD: 3341; CONFIDENCE confident structure IPB_RECORD: 3321; CONFIDENCE confident structure CONFIDENCE confident structure; IPB_RECORD: 3321 IPB_RECORD: 141; CONFIDENCE confident structure Kaempferol (Kempferol), a flavonoid found in many edible plants, inhibits estrogen receptor α expression in breast cancer cells and induces apoptosis in glioblastoma cells and lung cancer cells by activation of MEK-MAPK. Kaempferol can be uesd for the research of breast cancer[1][2][3][4]. Kaempferol (Kempferol), a flavonoid found in many edible plants, inhibits estrogen receptor α expression in breast cancer cells and induces apoptosis in glioblastoma cells and lung cancer cells by activation of MEK-MAPK. Kaempferol can be uesd for the research of breast cancer[1][2][3][4].

   

1,3,5,8-tetrahydroxy-2-methylanthracene-9,10-dione

1,3,5,8-tetrahydroxy-2-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   

CHEMBL519331

CHEMBL519331

C15H10O6 (286.0477)


   

Protoapigenone

Protoapigenone

C15H10O6 (286.0477)


   

5-O-beta-xylopyranosyl gentisic acid

5-O-beta-xylopyranosyl gentisic acid

C12H14O8 (286.0689)


   

5,6,7-trihydroxy-2-(2-hydroxyphenyl)chromen-4-one

5,6,7-trihydroxy-2-(2-hydroxyphenyl)chromen-4-one

C15H10O6 (286.0477)


   

Pinselic acid

Pinselic acid

C15H10O6 (286.0477)


   
   

Djenkolic acid disulfoxide

Djenkolic acid disulfoxide

C7H14N2O6S2 (286.0293)


   

7,8,3,4-tetrahydroxyflavone

7,8,3,4-tetrahydroxyflavone

C15H10O6 (286.0477)


   
   

2-methoxy-6-[5-(prop-1-yn-1-yl)-2-thienyl]-hexa-3,5-diyn-1-yl acetate

2-methoxy-6-[5-(prop-1-yn-1-yl)-2-thienyl]-hexa-3,5-diyn-1-yl acetate

C16H14O3S (286.0664)


   

1,2,5,7- Tetrahydroxy-3-methylanthrachinon

1,2,5,7- Tetrahydroxy-3-methylanthrachinon

C15H10O6 (286.0477)


   

6-Hydroxy-1-methoxy-2,3-methylenedioxyxanthone

6-Hydroxy-1-methoxy-2,3-methylenedioxyxanthone

C15H10O6 (286.0477)


   

3-alpha-L-arabinopyranosyloxy-4-hydroxybenzoic acid

3-alpha-L-arabinopyranosyloxy-4-hydroxybenzoic acid

C12H14O8 (286.0689)


   

6,8-dihydroxy-3-methyl-9-oxo-9h-xanthene-1-carboxylic acid

6,8-dihydroxy-3-methyl-9-oxo-9h-xanthene-1-carboxylic acid

C15H10O6 (286.0477)


   

1,2,4,5-Tetrahydroxy-3-methylanthracene-9,10-dione

1,2,4,5-Tetrahydroxy-3-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   
   
   

CHEMBL1079734

CHEMBL1079734

C15H10O6 (286.0477)


   
   
   

1,2,8-Trihydroxy-6-(hydroxymethyl)anthraquinone

1,2,8-Trihydroxy-6-(hydroxymethyl)anthraquinone

C15H10O6 (286.0477)


   

ASPHODELIN A

ASPHODELIN A

C15H10O6 (286.0477)


A hydroxycoumarin that is 4,7-dihydroxy-2H-chromen-2-one substituted by a 2,4-dihydroxyphenyl group at position 3. It is isolated from the roots of Asphodelus microcarpus and exhibits antimicrobial activity against bacteria like Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa and fungal microorganisms like Candida albicans and Botrytis cinerea.

   

5,7,8,2-tetrahydroxyflavone

5,7,8,2-tetrahydroxyflavone

C15H10O6 (286.0477)


   

3-(3,4-Dihydroxyphenyl)-5,7-dihydroxycoumarin

3-(3,4-Dihydroxyphenyl)-5,7-dihydroxycoumarin

C15H10O6 (286.0477)


   

2-(2,4-dihydroxyphenyl)-3,7-dihydroxychromen-4-one

2-(2,4-dihydroxyphenyl)-3,7-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

3,4,5,8-tetrahydroxyflavone

3,4,5,8-tetrahydroxyflavone

C15H10O6 (286.0477)


   

SCHEMBL13090739

SCHEMBL13090739

C15H10O6 (286.0477)


   

5-Hydroxyemodin

5-Hydroxyemodin

C15H10O6 (286.0477)


   

Erythrolaccin

Erythrolaccin

C15H10O6 (286.0477)


   

1-Acetoxymethyl-8-hydroxynaphtho[2,3-c]furan-4,9-dione

1-Acetoxymethyl-8-hydroxynaphtho[2,3-c]furan-4,9-dione

C15H10O6 (286.0477)


   

SCHEMBL20798544

SCHEMBL20798544

C15H10O6 (286.0477)


   

2-Me ether-1,2,3,5-Tetrahydroxyanthraquinone

2-Me ether-1,2,3,5-Tetrahydroxyanthraquinone

C15H10O6 (286.0477)


   

1,3,4,5-Tetrahydroxy-2-methylanthracene-9,10-dione

1,3,4,5-Tetrahydroxy-2-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   

3-Hydroxymorindone

1,3,5,6-Tetrahydroxy-2-methylanthracene-9,10-dione

C15H10O6 (286.0477)


3-Hydroxymorindone is a natural product found in Pentas suswaensis and Morinda citrifolia with data available.

   

8-Hydroxygenistein

4,5,7,8-Tetrahydroxyisoflavone

C15H10O6 (286.0477)


   

Calyxanthone

Calyxanthone

C15H10O6 (286.0477)


   

SCHEMBL22394347

SCHEMBL22394347

C15H10O6 (286.0477)


   

1-methoxy-2,4,5-trihydroxyanthraquinone

1-methoxy-2,4,5-trihydroxyanthraquinone

C15H10O6 (286.0477)


   

Kwanzoquinone E

Kwanzoquinone E

C15H10O6 (286.0477)


   

gentisate 5-O-beta-D-xylopyranoside

gentisate 5-O-beta-D-xylopyranoside

C12H14O8 (286.0689)


   

1,2,3,6-Tetrahydroxy-8-methylanthraquinone

1,2,3,6-Tetrahydroxy-8-methylanthraquinone

C15H10O6 (286.0477)


   

UNII-87C66SE4CP

UNII-87C66SE4CP

C15H10O6 (286.0477)


   

copareolatin

copareolatin

C15H10O6 (286.0477)


   

Hypostrepsilalic acid

Hypostrepsilalic acid

C15H10O6 (286.0477)


   

2-Chloro-1,3,5-benzenetriol triacetate

2-Chloro-1,3,5-benzenetriol triacetate

C12H11ClO6 (286.0244)


   

CHEMBL251908

CHEMBL251908

C15H10O6 (286.0477)


   
   

CHEMBL83759

CHEMBL83759

C15H10O6 (286.0477)


   

2-hydroxyvertixanthone

2-hydroxyvertixanthone

C15H10O6 (286.0477)


A member of the class of xanthones that is methyl 9H-xanthene-1-carboxylate substituted by hydroxy groups at positions 2 and 8 and an oxo group at position 9. It has been isolated from Chaetomium globosum.

   

1,3,8-Trihydroxy-2-(hydroxymethyl)-9,10-dihydroanthracene-9,10-dione

1,3,8-Trihydroxy-2-(hydroxymethyl)-9,10-dihydroanthracene-9,10-dione

C15H10O6 (286.0477)


   

6-Dimethoxycapillarisin

6-Dimethoxycapillarisin

C15H10O6 (286.0477)


   
   

1,6,7,8-tetrahydroxy-2-methylanthraquinone

1,6,7,8-tetrahydroxy-2-methylanthraquinone

C15H10O6 (286.0477)


   

indol-3-yl-acetothiohydroxamate-O-sulfonate

indol-3-yl-acetothiohydroxamate-O-sulfonate

C10H10N2O4S2 (286.0082)


   

alaternin

9,10-Anthracenedione, 1,2,6,8-tetrahydroxy-3-methyl-(9CI)

C15H10O6 (286.0477)


   

2'-Hydroxygenistein

3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one, 9CI

C15H10O6 (286.0477)


2-hydroxygenistein is a hydroxyisoflavone that is genistein substituted by an additional hydroxy group at position 2. It has been isolated from Crotalaria lachnophora. It has a role as a plant metabolite. It is functionally related to a genistein. It is a conjugate acid of a 2-hydroxygenistein(1-). 2-Hydroxygenistein is a natural product found in Crotalaria lachnophora, Vigna radiata, and other organisms with data available. Isolated from Cajanus cajan (pigeon pea), Dolichos biflorus (papadi), Lablab niger (hyacinth bean), Phaseolus vulgaris (kidney bean) and Phaseolus coccineus (scarlet runner bean). 2-Hydroxygenistein is found in many foods, some of which are pulses, walnut, saskatoon berry, and garden tomato (variety). 2-Hydroxygenistein is found in adzuki bean. 2-Hydroxygenistein is isolated from Cajanus cajan (pigeon pea), Dolichos biflorus (papadi), Lablab niger (hyacinth bean), Phaseolus vulgaris (kidney bean) and Phaseolus coccineus (scarlet runner bean). A hydroxyisoflavone that is genistein substituted by an additional hydroxy group at position 2. It has been isolated from Crotalaria lachnophora.

   

2,5,6,7-tetrahydroxyflavone

4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-5,7-dihydroxy-

C15H10O6 (286.0477)


5,7,2,6-Tetrahydroxyflavone is a natural product found in Scutellaria amoena, Andrographis macrobotrys, and other organisms with data available.

   

6-CHLOROPURINE RIBOSIDE

6-Chloro-9-(beta-D-arabinofuranosyl)purine

C10H11ClN4O4 (286.0469)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.348 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.349 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.343

   

2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

NCGC00016467-11!2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one

NCGC00016480-11!3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C15H10O6 (286.0477)


   

3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylic acid

NCGC00180266-02!3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylic acid

C15H10O6 (286.0477)


   

3,4,5,7-Tetrahydroxyflavone

3,4,5,7-Tetrahydroxyflavone

C15H10O6 (286.0477)


   

Norclobazam

N-Desmethyl Clobazam

C15H11ClN2O2 (286.0509)


D002491 - Central Nervous System Agents > D000927 - Anticonvulsants

   

Citreorosein

9,10-Anthracenedione, 1,3,8-trihydroxy-6-(hydroxymethyl)-

C15H10O6 (286.0477)


   

Dihydrobenzoic acid pentose

Dihydrobenzoic acid pentose

C12H14O8 (286.0689)


Annotation level-3

   

Benzoic acid + 2O, O-Pen

Benzoic acid + 2O, O-Pen

C12H14O8 (286.0689)


Annotation level-3

   

Flavonol base + 3O

Flavonol base + 3O

C15H10O6 (286.0477)


Annotation level-3

   

3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylic acid [IIN-based on: CCMSLIB00000847899]

NCGC00180266-02!3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylic acid [IIN-based on: CCMSLIB00000847899]

C15H10O6 (286.0477)


   

3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylic acid [IIN-based: Match]

NCGC00180266-02!3,8-dihydroxy-6-methyl-9-oxoxanthene-1-carboxylic acid [IIN-based: Match]

C15H10O6 (286.0477)


   

2,2-dimethyl-8-(phenylthio)-4H-benzo[d][1,3]dioxin-4-one

2,2-dimethyl-8-(phenylthio)-4H-benzo[d][1,3]dioxin-4-one

C16H14O3S (286.0664)


   

ethyl phenothiazine-2-carbamate

ethyl phenothiazine-2-carbamate

C15H14N2O2S (286.0776)


   

Pyrocatechol glucuronide

Pyrocatechol glucuronide

C12H14O8 (286.0689)


   

Quinol glucuronide

Quinol glucuronide

C12H14O8 (286.0689)


   

N-Desmethylclobazam

N-Desmethyl Clobazam

C15H11ClN2O2 (286.0509)


   

cyanidin

3,3,4,5,7-Pentahydroxyflavylium

C15H10O6 (286.0477)


   

Phosphoribosylglycinamide

Phosphoribosylglycinamide

C7H15N2O8P (286.0566)


   

Aurantinidin

6-Hydroxypelargonidin

C15H10O6 (286.0477)


   

Tricetinidin

Tricetinidin

C15H10O6 (286.0477)


   

3'-Methoxyfukiic acid

2,3-dihydroxy-2-[(4-hydroxy-3-methoxyphenyl)methyl]butanedioic acid

C12H14O8 (286.0689)


   

Uralenneoside

3,4,5-trihydroxyoxan-2-yl 3,4-dihydroxybenzoate

C12H14O8 (286.0689)


   

7,8,3',4'-Tetrahydroxyisoflavone

3-(3,4-dihydroxyphenyl)-7,8-dihydroxy-4H-chromen-4-one

C15H10O6 (286.0477)


   

Aureusidin

(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-4,6-dihydroxy-2,3-dihydro-1-benzofuran-3-one

C15H10O6 (286.0477)


Aureusidin is a hydroxyaurone that is aurone substituted by hydroxy groups at positions 4, 6, 3 and 4 respectively. It has a role as a plant metabolite. It is functionally related to an aurone. It is a conjugate acid of an aureusidin-6-olate. Aureusidin is a natural product found in Eleocharis dulcis, Eleocharis pallens, and other organisms with data available. A hydroxyaurone that is aurone substituted by hydroxy groups at positions 4, 6, 3 and 4 respectively. Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1]. Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1]. Aureusidin is an aurone with high antioxidant and lipoxygenase inhibitory activity. Aureusidin also shows anti-inflammatory effects[1].

   

6-(3-chloropropoxy)-4-chloro-7-Methoxyquinazoline

6-(3-chloropropoxy)-4-chloro-7-Methoxyquinazoline

C12H12Cl2N2O2 (286.0276)


   

3,4-diphenylthiophene-2,5-dicarbonitrile

3,4-diphenylthiophene-2,5-dicarbonitrile

C18H10N2S (286.0565)


   

N-(4-AMINO-2-METHYLPHENYL)-4-CHLOROPHTHALIMIDE

N-(4-AMINO-2-METHYLPHENYL)-4-CHLOROPHTHALIMIDE

C15H11ClN2O2 (286.0509)


   

Sulfametrole

Sulfametrole

C9H10N4O3S2 (286.0194)


C254 - Anti-Infective Agent > C29739 - Sulfonamide Anti-Infective Agent D000890 - Anti-Infective Agents > D013424 - Sulfanilamides

   

ethyl 2-(4-bromophenoxy)-2-methylpropanoate

ethyl 2-(4-bromophenoxy)-2-methylpropanoate

C12H15BrO3 (286.0204)


   

Germane, [5-(diethoxymethyl)-2-furanyl]trimethyl

Germane, [5-(diethoxymethyl)-2-furanyl]trimethyl

C12H22GeO3 (286.079)


   

6-chloro-4-phenyl-1,4-dihydroquinazoline-2-carboxylic acid

6-chloro-4-phenyl-1,4-dihydroquinazoline-2-carboxylic acid

C15H11ClN2O2 (286.0509)


   

3-(PHENYLAMINOCARBONYL)-5-NITROPHENYLBORONIC ACID

3-(PHENYLAMINOCARBONYL)-5-NITROPHENYLBORONIC ACID

C13H11BN2O5 (286.0761)


   

tert-Butyl (5-bromopyridin-2-yl)(methyl)carbamate

tert-Butyl (5-bromopyridin-2-yl)(methyl)carbamate

C11H15BrN2O2 (286.0317)


   

4-CHLORO-6-(THIAZOL-2-YLCARBAMOYL)-CYCLOHEX-3-ENECARBOXYLIC ACID

4-CHLORO-6-(THIAZOL-2-YLCARBAMOYL)-CYCLOHEX-3-ENECARBOXYLIC ACID

C11H11ClN2O3S (286.0179)


   

Tauromustine

Tauromustine

C7H15ClN4O4S (286.0502)


C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C2842 - DNA Binding Agent D000970 - Antineoplastic Agents

   

Olprinone hydrochloride

Olprinone (Hydrochloride)

C14H11ClN4O (286.0621)


D004791 - Enzyme Inhibitors > D010726 - Phosphodiesterase Inhibitors > D058987 - Phosphodiesterase 3 Inhibitors D020011 - Protective Agents > D002316 - Cardiotonic Agents D002317 - Cardiovascular Agents

   

2-FLUORO-2-METHANESULFONYLOXYMETHYL-MALONIC ACID DIETHYL ESTER

2-FLUORO-2-METHANESULFONYLOXYMETHYL-MALONIC ACID DIETHYL ESTER

C9H15FO7S (286.0522)


   

4-Bromo-1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

4-Bromo-1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

C10H16BBrN2O2 (286.0488)


   

1-methyl-5-phenoxy-3-(trifluoromethyl)pyrazole-4-carboxylic acid

1-methyl-5-phenoxy-3-(trifluoromethyl)pyrazole-4-carboxylic acid

C12H9F3N2O3 (286.0565)


   

carbon monoxide,chromium,ethyl benzoate

carbon monoxide,chromium,ethyl benzoate

C12H10CrO5 (285.9933)


   

(E)-3-(4-Bromophenyl)-1-phenyl-prop-2-en-1-one

(E)-3-(4-Bromophenyl)-1-phenyl-prop-2-en-1-one

C15H11BrO (285.9993)


   

2-Propen-1-one,1-(4-bromophenyl)-3-phenyl-

2-Propen-1-one,1-(4-bromophenyl)-3-phenyl-

C15H11BrO (285.9993)


   

1-(5-Bromo-3-nitropyridin-2-yl)piperazine

1-(5-Bromo-3-nitropyridin-2-yl)piperazine

C9H11BrN4O2 (286.0065)


   

3-Bromo-2-isopropoxy-5-formylphenylboronic acid

3-Bromo-2-isopropoxy-5-formylphenylboronic acid

C10H12BBrO4 (286.0012)


   

METHYL 3-BROMO-5-ISOBUTOXYBENZOATE

METHYL 3-BROMO-5-ISOBUTOXYBENZOATE

C12H15BrO3 (286.0204)


   

2-BROMO-5-METHOXY-BENZENEPROPANOIC ACID ETHYL ESTER

2-BROMO-5-METHOXY-BENZENEPROPANOIC ACID ETHYL ESTER

C12H15BrO3 (286.0204)


   

2-(4-amino-3-nitrobenzoyl)benzoic acid

2-(4-amino-3-nitrobenzoyl)benzoic acid

C14H10N2O5 (286.059)


   

(4-METHOXY-BENZYL)-PYRIDIN-3-YL-AMINE DIHYDROCHLORIDE

(4-METHOXY-BENZYL)-PYRIDIN-3-YL-AMINE DIHYDROCHLORIDE

C13H16Cl2N2O (286.064)


   

3-(N-Boc-aminomethyl)-5-bromopyridine

3-(N-Boc-aminomethyl)-5-bromopyridine

C11H15BrN2O2 (286.0317)


   

5-(N-Boc-aminomethyl)-2-bromopyridine

5-(N-Boc-aminomethyl)-2-bromopyridine

C11H15BrN2O2 (286.0317)


   

3-chloro-9,10-dihydro-9,10-dioxoanthracene-2-carboxylic acid

3-chloro-9,10-dihydro-9,10-dioxoanthracene-2-carboxylic acid

C15H7ClO4 (286.0033)


   

5-METHYL-2-(4-TRIFLUOROMETHOXYPHENYL)-3H-IMIDAZOLE-4-CARBOXYLIC ACID

5-METHYL-2-(4-TRIFLUOROMETHOXYPHENYL)-3H-IMIDAZOLE-4-CARBOXYLIC ACID

C12H9F3N2O3 (286.0565)


   

prop-2-enyl N-(2-nitrophenyl)sulfonylcarbamate

prop-2-enyl N-(2-nitrophenyl)sulfonylcarbamate

C10H10N2O6S (286.026)


   

1,3-bis-(Chloropropyl)tetramethyldisiloxane

1,3-bis-(Chloropropyl)tetramethyldisiloxane

C10H24Cl2OSi2 (286.0743)


   

3 5-dimethoxyphenyl trifluoromethanesul&

3 5-dimethoxyphenyl trifluoromethanesul&

C9H9F3O5S (286.0123)


   

(2,5-dioxopyrrolidin-1-yl) 6-hydrazinylpyridine-3-carboxylate,hydrochloride

(2,5-dioxopyrrolidin-1-yl) 6-hydrazinylpyridine-3-carboxylate,hydrochloride

C10H11ClN4O4 (286.0469)


   

2-[4-(5-bromopyrimidin-2-yl)piperazin-1-yl]ethanol

2-[4-(5-bromopyrimidin-2-yl)piperazin-1-yl]ethanol

C10H15BrN4O (286.0429)


   

5-Bromo-2-(4-morpholinyl)-3-pyridinecarboxylic acid

5-Bromo-2-(4-morpholinyl)-3-pyridinecarboxylic acid

C10H11BrN2O3 (285.9953)


   

N-(2-bromo-5-methoxypyridin-3-yl)pivalamide

N-(2-bromo-5-methoxypyridin-3-yl)pivalamide

C11H15BrN2O2 (286.0317)


   

3-bromo-5-nitro-N-propylbenzamide

3-bromo-5-nitro-N-propylbenzamide

C10H11BrN2O3 (285.9953)


   

3-Bromo-N-isopropyl-5-nitrobenzamide

3-Bromo-N-isopropyl-5-nitrobenzamide

C10H11BrN2O3 (285.9953)


   

2-(4-bromophenyl)-6-methylimidazo(1,2-a&

2-(4-bromophenyl)-6-methylimidazo(1,2-a&

C14H11BrN2 (286.0106)


   

Ethyl 3-bromo-4-isopropoxybenzoate

Ethyl 3-bromo-4-isopropoxybenzoate

C12H15BrO3 (286.0204)


   

5-(4-carboxyphenyl)benzene-1,3-dicarboxylic acid

5-(4-carboxyphenyl)benzene-1,3-dicarboxylic acid

C15H10O6 (286.0477)


   

METHYL 2-(5-OXAZOLYL)BENZOATE

METHYL 2-(5-OXAZOLYL)BENZOATE

C13H12Cl2O3 (286.0163)


   

Phosphoric acid, octyl ester, potassium salt

Phosphoric acid, octyl ester, potassium salt

C8H17K2O4P (286.0139)


   

2-CHLOROMETHYL-5-METHYL-4-OXO-3,4-DIHYDRO-THIENO[2,3-D]PYRIMIDINE-6-CARBOXYLIC ACID ETHYL ESTER

2-CHLOROMETHYL-5-METHYL-4-OXO-3,4-DIHYDRO-THIENO[2,3-D]PYRIMIDINE-6-CARBOXYLIC ACID ETHYL ESTER

C11H11ClN2O3S (286.0179)


   

5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRO-2-NAPHTHALENESULFONYL CHLORIDE

5,5,8,8-TETRAMETHYL-5,6,7,8-TETRAHYDRO-2-NAPHTHALENESULFONYL CHLORIDE

C14H19ClO2S (286.0794)


   

1-(4-BENZYLOXYPHENYL)PIPERAZINE-HYDROCHLORIDE

1-(4-BENZYLOXYPHENYL)PIPERAZINE-HYDROCHLORIDE

C12H16BrFN2 (286.0481)


   

3-[3,5-bis(trifluoromethyl)phenyl]propanoic acid

3-[3,5-bis(trifluoromethyl)phenyl]propanoic acid

C11H8F6O2 (286.0428)


   

3-[2,5-bis(trifluoromethyl)phenyl]propanoic acid

3-[2,5-bis(trifluoromethyl)phenyl]propanoic acid

C11H8F6O2 (286.0428)


   

6-Chloropurineriboside

6-Chloropurineriboside

C10H11ClN4O4 (286.0469)


   

2-[[2-(benzylsulfonylamino)acetyl]amino]acetate

2-[[2-(benzylsulfonylamino)acetyl]amino]acetate

C11H14N2O5S (286.0623)


   

3-[(4-acetamidophenyl)sulfonylamino]propanoic acid

3-[(4-acetamidophenyl)sulfonylamino]propanoic acid

C11H14N2O5S (286.0623)


   

4-[(1-phenyl-1H-tetrazol-5-yl)thio]pyrocatechol

4-[(1-phenyl-1H-tetrazol-5-yl)thio]pyrocatechol

C13H10N4O2S (286.0524)


   

1-(3,4-DICHLOROPHENYL)-4-OXOCYCLOHEXANECARBOXYLIC ACID

1-(3,4-DICHLOROPHENYL)-4-OXOCYCLOHEXANECARBOXYLIC ACID

C13H12Cl2O3 (286.0163)


   

2-(Butylthio)-4,5-dihydro-1H-imidazole

2-(Butylthio)-4,5-dihydro-1H-imidazole

C7H15IN2S (286.0001)


   

tert-Butyl [(6-bromopyridin-2-yl)methyl]carbamate

tert-Butyl [(6-bromopyridin-2-yl)methyl]carbamate

C11H15BrN2O2 (286.0317)


   

4-(BENZYLOXY)BENZENE-1,2-DIAMINE DIHYDROCHLORIDE

4-(BENZYLOXY)BENZENE-1,2-DIAMINE DIHYDROCHLORIDE

C13H16Cl2N2O (286.064)


   

2,3-O-(Methoxymethylene)uridine

2,3-O-(Methoxymethylene)uridine

C11H14N2O7 (286.0801)


   

[5,5-Bipyrimidine]-2,2,4,4,6,6(1H,1H,3H,3H,5H,5H)-hexone,5,5-dihydroxy-

[5,5-Bipyrimidine]-2,2,4,4,6,6(1H,1H,3H,3H,5H,5H)-hexone,5,5-dihydroxy-

C8H6N4O8 (286.0186)


   

4-(2-Bromo-4-nitrophenyl)morpholine

4-(2-Bromo-4-nitrophenyl)morpholine

C10H11BrN2O3 (285.9953)


   

1-BENZYL-3-BROMO-7-AZAINDOLE

1-BENZYL-3-BROMO-7-AZAINDOLE

C14H11BrN2 (286.0106)


   

6-methoxy-2-(4-nitrophenyl)-1,3-benzothiazole

6-methoxy-2-(4-nitrophenyl)-1,3-benzothiazole

C14H10N2O3S (286.0412)


   

Sodium carbonate decahydrate

Sodium carbonate decahydrate

CH20Na2O13 (286.0699)


C78275 - Agent Affecting Blood or Body Fluid > C29730 - Electrolyte Replacement Agent

   

1-naphthyl phosphate disodium salt monohydrate

1-naphthyl phosphate disodium salt monohydrate

C10H9Na2O5P (285.9983)


   

CARBAMIC ACID, (5-BROMO-4-METHYL-2-PYRIDINYL)-,1,1-DIMETHYLETHYL ESTER

CARBAMIC ACID, (5-BROMO-4-METHYL-2-PYRIDINYL)-,1,1-DIMETHYLETHYL ESTER

C11H15BrN2O2 (286.0317)


   

1-(PHENYLSULFONYL)-1H-PYRROLO[3,2-C]PYRIDINE-2-CARBALDEHYDE

1-(PHENYLSULFONYL)-1H-PYRROLO[3,2-C]PYRIDINE-2-CARBALDEHYDE

C14H10N2O3S (286.0412)


   

4-Bromophenoxy t-Butyl-Dimethylsilane

4-Bromophenoxy t-Butyl-Dimethylsilane

C12H19BrOSi (286.0388)


   

tert-butyl 2-(4-chlorophenyl)sulfanyl-2-methylpropanoate

tert-butyl 2-(4-chlorophenyl)sulfanyl-2-methylpropanoate

C14H19ClO2S (286.0794)


   

4-BROMO-10,11-DIHYDRO-DIBENZO[A,D]CYCLOHEPTEN-5-ONE

4-BROMO-10,11-DIHYDRO-DIBENZO[A,D]CYCLOHEPTEN-5-ONE

C15H11BrO (285.9993)


   

tert-butyl 4-bromo-3-methoxybenzoate

tert-butyl 4-bromo-3-methoxybenzoate

C12H15BrO3 (286.0204)


   

5-ethyl-5-[[methoxy(methyl)phosphoryl]oxymethyl]-2-methyl-1,3,2λ5-dioxaphosphinane 2-oxide

5-ethyl-5-[[methoxy(methyl)phosphoryl]oxymethyl]-2-methyl-1,3,2λ5-dioxaphosphinane 2-oxide

C9H20O6P2 (286.0735)


   

4-(N-Boc-aminomethyl)-2-Bromopyridine

4-(N-Boc-aminomethyl)-2-Bromopyridine

C11H15BrN2O2 (286.0317)


   

1H-PYRROLO[2,3-B]PYRIDINE, 3-METHYL-1-[(4-METHYLPHENYL)SULFONYL]-

1H-PYRROLO[2,3-B]PYRIDINE, 3-METHYL-1-[(4-METHYLPHENYL)SULFONYL]-

C15H14N2O2S (286.0776)


   

1-(PHENYLSULFONYL)-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBALDEHYDE

1-(PHENYLSULFONYL)-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBALDEHYDE

C14H10N2O3S (286.0412)


   

3-Cyano-N,N-dimethyl-6-nitro-4-oxo-1,4-dihydro-8-quinolinecarboxa mide

3-Cyano-N,N-dimethyl-6-nitro-4-oxo-1,4-dihydro-8-quinolinecarboxa mide

C13H10N4O4 (286.0702)


   

4-Oxo-1-[3-(trifluoromethyl)phenyl]cyclohexanecarboxylic acid

4-Oxo-1-[3-(trifluoromethyl)phenyl]cyclohexanecarboxylic acid

C14H13F3O3 (286.0817)


   

Methyl 4-oxo-1-(2,4,5-trifluorophenyl)cyclohexanecarboxylate

Methyl 4-oxo-1-(2,4,5-trifluorophenyl)cyclohexanecarboxylate

C14H13F3O3 (286.0817)


   

methyl 2-(3,5-bis(trifluoromethyl)phenyl)acetate

methyl 2-(3,5-bis(trifluoromethyl)phenyl)acetate

C11H8F6O2 (286.0428)


   

4-chloro-1-[(4-chlorophenoxy)methyl]pyrazole-3-carboxylic acid

4-chloro-1-[(4-chlorophenoxy)methyl]pyrazole-3-carboxylic acid

C11H8Cl2N2O3 (285.9912)


   

Thieno[3,4-b]-1,4-dioxin-5,7-dicarboxylic acid, 2,3-dihydro-, diethyl ester

Thieno[3,4-b]-1,4-dioxin-5,7-dicarboxylic acid, 2,3-dihydro-, diethyl ester

C12H14O6S (286.0511)


   

1-cyclohexyl-2-iodobenzene

1-cyclohexyl-2-iodobenzene

C12H15I (286.0218)


   

5-bromo-3-tert-butyl-2-hydroxy-6-methylbenzoic acid

5-bromo-3-tert-butyl-2-hydroxy-6-methylbenzoic acid

C12H15BrO3 (286.0204)


   

(5ALPHA,17BETA)-N-(2-HYDROXY-1,1-DIMETHYLETHYL)-3-OXO-4-AZAANDROST-1-ENE-17-CARBOXAMIDE

(5ALPHA,17BETA)-N-(2-HYDROXY-1,1-DIMETHYLETHYL)-3-OXO-4-AZAANDROST-1-ENE-17-CARBOXAMIDE

C11H15BrN2O2 (286.0317)


   

tert-Butyl 2-bromo-5-methoxybenzoate

tert-Butyl 2-bromo-5-methoxybenzoate

C12H15BrO3 (286.0204)


   

4-chloro-6-methoxy-2-(trifluoromethyl)quinoline-3-carbonitrile

4-chloro-6-methoxy-2-(trifluoromethyl)quinoline-3-carbonitrile

C12H6ClF3N2O (286.0121)


   

4-methoxy-6-methyl-5-nitro-2-(trifluoromethyl)quinoline

4-methoxy-6-methyl-5-nitro-2-(trifluoromethyl)quinoline

C12H9F3N2O3 (286.0565)


   

Methyl 3-bromo-5-butoxybenzoate

Methyl 3-bromo-5-butoxybenzoate

C12H15BrO3 (286.0204)


   

6-chloro-4-phenyl-1,2-dihydroquinazoline-2-carboxylic acid

6-chloro-4-phenyl-1,2-dihydroquinazoline-2-carboxylic acid

C15H11ClN2O2 (286.0509)


   

(4,6-DIMETHYL-PYRIMIDIN-2-YLSULFANYL)-PHENYL-ACETICACID

(4,6-DIMETHYL-PYRIMIDIN-2-YLSULFANYL)-PHENYL-ACETICACID

C11H14N2O5S (286.0623)


   

4-Iodo-6-isopropyl-1H-indazole

4-Iodo-6-isopropyl-1H-indazole

C10H11IN2 (285.9967)


   

3-(BENZO[D]THIAZOL-2-YL)-4,5,6,7-TETRAHYDROBENZO[B]THIOPHEN-2-AMINE

3-(BENZO[D]THIAZOL-2-YL)-4,5,6,7-TETRAHYDROBENZO[B]THIOPHEN-2-AMINE

C15H14N2S2 (286.0598)


   

6-bromo-2-(4-methylphenyl)imidazo[1,2-a]pyridine

6-bromo-2-(4-methylphenyl)imidazo[1,2-a]pyridine

C14H11BrN2 (286.0106)


   

2-(5-chloro-2-methoxyphenyl)-4-pyridin-2-yl-1,3-oxazole

2-(5-chloro-2-methoxyphenyl)-4-pyridin-2-yl-1,3-oxazole

C15H11ClN2O2 (286.0509)


   

Tosyl-L-asparagine

Tosyl-L-asparagine

C11H14N2O5S (286.0623)


   

5-CHLORO-5-DEOXYINOSINE

5-CHLORO-5-DEOXYINOSINE

C10H11ClN4O4 (286.0469)


   

4-Bromo[2.2]paracyclophane

4-Bromo[2.2]paracyclophane

C16H15Br (286.0357)


   
   

Benzaldehyde,2-(2,4-dinitrophenyl)hydrazone

Benzaldehyde,2-(2,4-dinitrophenyl)hydrazone

C13H10N4O4 (286.0702)


   

2 6-dimethoxyphenyl trifluoromethanesul&

2 6-dimethoxyphenyl trifluoromethanesul&

C9H9F3O5S (286.0123)


   

strontium 2,4-pentanedionate

strontium 2,4-pentanedionate

C10H14O4Sr (285.9948)


   

2-Boc-amino-4-bromomethylpyridine

2-Boc-amino-4-bromomethylpyridine

C11H15BrN2O2 (286.0317)


   

1-(4-methoxyphenyl)-5-(trifluoromethyl)pyrazole-4-carboxylic acid

1-(4-methoxyphenyl)-5-(trifluoromethyl)pyrazole-4-carboxylic acid

C12H9F3N2O3 (286.0565)


   

(3-BROMOPHENOXY)(TERT-BUTYL)DIMETHYLSILANE

(3-BROMOPHENOXY)(TERT-BUTYL)DIMETHYLSILANE

C12H19BrOSi (286.0388)


   

1-(4-Chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)-2-phenoxyethanone

1-(4-Chloro-1H-pyrrolo[2,3-b]pyridin-5-yl)-2-phenoxyethanone

C15H11ClN2O2 (286.0509)


   

tert-butyl 4-bromo-2-methoxybenzoate

tert-butyl 4-bromo-2-methoxybenzoate

C12H15BrO3 (286.0204)


   

5-(AMINOSULFONYL)-2-MORPHOLIN-4-YLBENZOIC ACID

5-(AMINOSULFONYL)-2-MORPHOLIN-4-YLBENZOIC ACID

C11H14N2O5S (286.0623)


   

1-(4-(3-Bromopropoxy)- 3-methoxyphenyl)ethanone

1-(4-(3-Bromopropoxy)- 3-methoxyphenyl)ethanone

C12H15BrO3 (286.0204)


   

5-(3-fluoro-4-methylsulfonylphenyl)-4-methyl-1,3-thiazol-2-amine

5-(3-fluoro-4-methylsulfonylphenyl)-4-methyl-1,3-thiazol-2-amine

C11H11FN2O2S2 (286.0246)


   

4-(furan-2-ylmethyl)-2,3-dihydro-1H-quinoxaline

4-(furan-2-ylmethyl)-2,3-dihydro-1H-quinoxaline

C13H16Cl2N2O (286.064)


   

2-(4-Bromobenzyl)-1H-benzimidazole

2-(4-Bromobenzyl)-1H-benzimidazole

C14H11BrN2 (286.0106)


   

3-ethyl-5-[(3-methylthiazolidin-2-ylidene)ethylidene]rhodanine

3-ethyl-5-[(3-methylthiazolidin-2-ylidene)ethylidene]rhodanine

C11H14N2OS3 (286.0268)


   

2-(trifluoromethyl)-1H-benzo[d]imidazole

2-(trifluoromethyl)-1H-benzo[d]imidazole

C8H6ClF3N2O4 (285.9968)


   

4-(3-BENZYL-THIOUREIDO)-BENZOIC ACID

4-(3-BENZYL-THIOUREIDO)-BENZOIC ACID

C15H14N2O2S (286.0776)


   

tert-Butyl (5-bromo-3-methylpyridin-2-yl)carbamate

tert-Butyl (5-bromo-3-methylpyridin-2-yl)carbamate

C11H15BrN2O2 (286.0317)


   

2-Chloro-3-(2-chloroethyl)-6-methoxyquinoline

2-Chloro-3-(2-chloroethyl)-6-methoxyquinoline

C11H15BrN2O2 (286.0317)


   

Chalcone, .alpha.-bromo-

Chalcone, .alpha.-bromo-

C15H11BrO (285.9993)


   

Brallobarbital

Brallobarbital

C10H11BrN2O3 (285.9953)


C78272 - Agent Affecting Nervous System > C29756 - Sedative and Hypnotic > C67084 - Barbiturate

   

Benzyl 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylate

Benzyl 4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carboxylate

C15H11ClN2O2 (286.0509)


   

1H-PYRROLO[2,3-B]PYRIDINE, 2-METHYL-1-[(4-METHYLPHENYL)SULFONYL]-

1H-PYRROLO[2,3-B]PYRIDINE, 2-METHYL-1-[(4-METHYLPHENYL)SULFONYL]-

C15H14N2O2S (286.0776)


   

1H-PYRROLO[2,3-B]PYRIDINE, 5-METHYL-1-[(4-METHYLPHENYL)SULFONYL]-

1H-PYRROLO[2,3-B]PYRIDINE, 5-METHYL-1-[(4-METHYLPHENYL)SULFONYL]-

C15H14N2O2S (286.0776)


   

Methyl 3-bromo-4-butoxybenzoate

Methyl 3-bromo-4-butoxybenzoate

C12H15BrO3 (286.0204)


   

methyl 3-bromo-4-[(2-methylpropan-2-yl)oxy]benzoate

methyl 3-bromo-4-[(2-methylpropan-2-yl)oxy]benzoate

C12H15BrO3 (286.0204)


   

3-Cyclopentyl-2-(3,4-dichlorophenyl)propanoic acid

3-Cyclopentyl-2-(3,4-dichlorophenyl)propanoic acid

C14H16Cl2O2 (286.0527)


   

tert-butyl N-[6-(bromomethyl)pyridin-2-yl]carbamate

tert-butyl N-[6-(bromomethyl)pyridin-2-yl]carbamate

C11H15BrN2O2 (286.0317)


   

Tris(2-carboxyethyl)phosphine Hydrochloride

Tris(2-carboxyethyl)phosphine Hydrochloride

C9H16ClO6P (286.0373)


   
   

3-BROMO-2-BUTOXY-5-METHYLPHENYLBORONIC &

3-BROMO-2-BUTOXY-5-METHYLPHENYLBORONIC &

C11H16BBrO3 (286.0376)


   

2-[3,5-bis(trifluoromethyl)phenyl]-N-hydroxyethanimidamide

2-[3,5-bis(trifluoromethyl)phenyl]-N-hydroxyethanimidamide

C10H8F6N2O (286.0541)


   

4-N,N-Dimethylamino-2-(trimethylstannyl)-pyridine

4-N,N-Dimethylamino-2-(trimethylstannyl)-pyridine

C10H18N2Sn (286.0492)


   

2,2,3,3-tetrafluoropropyl 4-toluenesulfonate

2,2,3,3-tetrafluoropropyl 4-toluenesulfonate

C10H10F4O3S (286.0287)


   

1h,1h,5h-octafluoropentyl acrylate

1h,1h,5h-octafluoropentyl acrylate

C8H6F8O2 (286.024)


   

Fisetin hydrate

Fisetin hydrate

C15H10O6 (286.0477)


   

4-(5,6-dichloro-1H-indol-2-yl)benzonitrile

4-(5,6-dichloro-1H-indol-2-yl)benzonitrile

C15H8Cl2N2 (286.0065)


   

Benzoic acid,2-[[(4-nitrophenyl)amino]carbonyl]-

Benzoic acid,2-[[(4-nitrophenyl)amino]carbonyl]-

C14H10N2O5 (286.059)


   

sodium,formaldehyde,2-hydroxybenzenesulfonate,urea

sodium,formaldehyde,2-hydroxybenzenesulfonate,urea

C8H11N2NaO6S (286.0236)


   

tert-butyl (5-(bromomethyl)pyridin-2-yl)carbamate

tert-butyl (5-(bromomethyl)pyridin-2-yl)carbamate

C11H15BrN2O2 (286.0317)


   

5-(4-METHOXYPHENYL)-2-(TRIFLUOROMETHYL)-3-FUROIC ACID

5-(4-METHOXYPHENYL)-2-(TRIFLUOROMETHYL)-3-FUROIC ACID

C13H9F3O4 (286.0453)


   

6-(4-fluorophenyl)-4-methylsulfanylpyrido[3,2-d]pyrimidin-2-amine

6-(4-fluorophenyl)-4-methylsulfanylpyrido[3,2-d]pyrimidin-2-amine

C14H11FN4S (286.0688)


   

Benzoic acid,4,4-(1-oxido-1,2-diazenediyl)bis-

Benzoic acid,4,4-(1-oxido-1,2-diazenediyl)bis-

C14H10N2O5 (286.059)


   

sulfamerazine sodium

sulfamerazine sodium

C11H11N4NaO2S (286.05)


   

Ferrocene,(3-carboxy-1-oxopropyl)-

Ferrocene,(3-carboxy-1-oxopropyl)-

C14H14FeO3 (286.0292)


   

7-(2-Bromoethyl)theophylline

7-(2-Bromoethyl)theophylline

C9H11BrN4O2 (286.0065)


   

1-(3-Bromo-5-fluorobenzyl)-4-methylpiperazine

1-(3-Bromo-5-fluorobenzyl)-4-methylpiperazine

C12H16BrFN2 (286.0481)


   

methyl 4-fluoro-2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)benzoate

methyl 4-fluoro-2-(1H-pyrrolo[2,3-b]pyridin-5-yloxy)benzoate

C15H11FN2O3 (286.0754)


   

DL-GLYCERIC ACID HEMICALCIUM SALT

DL-GLYCERIC ACID HEMICALCIUM SALT

C6H14CaO10 (286.0213)


   

4-C-Azido-3-deoxy-3-fluorocytidine

4-C-Azido-3-deoxy-3-fluorocytidine

C9H11FN6O4 (286.0826)


   

2-Propanesulfinamide, N-[1-(2-fluoro-5-nitrophenyl)ethylidene]-2-methyl-

2-Propanesulfinamide, N-[1-(2-fluoro-5-nitrophenyl)ethylidene]-2-methyl-

C12H15FN2O3S (286.0787)


   

tert-butyl 3-bromo-2-methoxybenzoate

tert-butyl 3-bromo-2-methoxybenzoate

C12H15BrO3 (286.0204)


   

2-Propanesulfinamide, N-[1-(2-fluoro-5-nitrophenyl)ethylidene]-2-methyl-, [N(E),S(R)]-

2-Propanesulfinamide, N-[1-(2-fluoro-5-nitrophenyl)ethylidene]-2-methyl-, [N(E),S(R)]-

C12H15FN2O3S (286.0787)


   

LITHIUM NIOBIUM METHOXIDE

LITHIUM NIOBIUM METHOXIDE

C6H18LiNbO6 (286.0327)


   

2-(perfluoropropyl)-1H-benzo[d]imidazole

1H-Benzimidazole,2-(1,1,2,2,3,3,3-heptafluoropropyl)-

C10H5F7N2 (286.0341)


   

Glycine,N-[(4-methylphenyl)sulfonyl]glycyl-

Glycine,N-[(4-methylphenyl)sulfonyl]glycyl-

C11H14N2O5S (286.0623)


   

4(1H)-Quinazolinone,3-(3-fluoro-4-methylphenyl)-2,3-dihydro-2-thioxo-

4(1H)-Quinazolinone,3-(3-fluoro-4-methylphenyl)-2,3-dihydro-2-thioxo-

C15H11FN2OS (286.0576)


   

2-(3,5-Dichloro-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

2-(3,5-Dichloro-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

C13H17BCl2O2 (286.0699)


   

4-(3-((3-CHLOROPROPANOYL)OXY)PROPOXY)BENZOIC ACID

4-(3-((3-CHLOROPROPANOYL)OXY)PROPOXY)BENZOIC ACID

C13H15ClO5 (286.0608)


   

7-Chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine-2-thione

7-Chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepine-2-thione

C15H11ClN2S (286.0331)


   

TERT-BUTYL (4-BROMOPYRIDIN-2-YL)(METHYL)CARBAMATE

TERT-BUTYL (4-BROMOPYRIDIN-2-YL)(METHYL)CARBAMATE

C11H15BrN2O2 (286.0317)


   

6,7-dimethoxynaphthalene-2-sulfonyl chloride

6,7-dimethoxynaphthalene-2-sulfonyl chloride

C12H11ClO4S (286.0067)


   

TERT-BUTYL ((3-BROMOPYRIDIN-4-YL)METHYL)CARBAMATE

TERT-BUTYL ((3-BROMOPYRIDIN-4-YL)METHYL)CARBAMATE

C11H15BrN2O2 (286.0317)


   

10-Undecenyl Trichlorosilane

10-Undecenyl Trichlorosilane

C11H21Cl3Si (286.0478)


   

ethyl 3,5-bis(trifluoromethyl)benzoate

ethyl 3,5-bis(trifluoromethyl)benzoate

C11H8F6O2 (286.0428)


   

tert-Butyl [(5-bromopyridin-2-yl)methyl]carbamate

tert-Butyl [(5-bromopyridin-2-yl)methyl]carbamate

C11H15BrN2O2 (286.0317)


   

uranium(vi) oxide

uranium(vi) oxide

O3U (286.0355)


   

1,4,5,8-Naphthalenetetracarboxylic acid 1,8-monoanhydride

1,4,5,8-Naphthalenetetracarboxylic acid 1,8-monoanhydride

C14H6O7 (286.0114)


   

Ethyl 3-bromo-4-propoxybenzoate

Ethyl 3-bromo-4-propoxybenzoate

C12H15BrO3 (286.0204)


   

ETHYL4-(2-IODOETHOXY)BUTANOATE

ETHYL4-(2-IODOETHOXY)BUTANOATE

C8H15IO3 (286.0066)


   

methyl (Z)-5-chloro-5-(4-chlorophenyl)-3-hydroxy-2-methylidenepent-4-enoate

methyl (Z)-5-chloro-5-(4-chlorophenyl)-3-hydroxy-2-methylidenepent-4-enoate

C13H12Cl2O3 (286.0163)


   

methyl (Z)-5-chloro-5-(3-chlorophenyl)-3-hydroxy-2-methylidenepent-4-enoate

methyl (Z)-5-chloro-5-(3-chlorophenyl)-3-hydroxy-2-methylidenepent-4-enoate

C13H12Cl2O3 (286.0163)


   

1-(5-Bromo-2-fluorobenzyl)-4-methylpiperazine

1-(5-Bromo-2-fluorobenzyl)-4-methylpiperazine

C12H16BrFN2 (286.0481)


   

2-[2-fluoro-4-[(2-methylpropan-2-yl)oxycarbonyl]phenyl]sulfanylacetic acid

2-[2-fluoro-4-[(2-methylpropan-2-yl)oxycarbonyl]phenyl]sulfanylacetic acid

C13H15FO4S (286.0675)


   

2-Amino-4-Boc-amino-phenylbromide

2-Amino-4-Boc-amino-phenylbromide

C11H15BrN2O2 (286.0317)


   

8-BROMO-7-ETHYL-1,3-DIMETHYL-2,3,6,7-TETRAHYDRO-1H-PURINE-2,6-DIONE

8-BROMO-7-ETHYL-1,3-DIMETHYL-2,3,6,7-TETRAHYDRO-1H-PURINE-2,6-DIONE

C9H11BrN4O2 (286.0065)


   

methyl 4-phenyl-5-(trifluoromethyl)thiophene-2-carboxylate

methyl 4-phenyl-5-(trifluoromethyl)thiophene-2-carboxylate

C13H9F3O2S (286.0275)


   

7-chloro-5-phenyl-2-thioxo-2,3-dihydro-1h-1,4-benzodiazepine

7-chloro-5-phenyl-2-thioxo-2,3-dihydro-1h-1,4-benzodiazepine

C15H11ClN2S (286.0331)


   

4-Oxo-1-[4-(trifluoromethyl)phenyl]cyclohexanecarboxylic acid

4-Oxo-1-[4-(trifluoromethyl)phenyl]cyclohexanecarboxylic acid

C14H13F3O3 (286.0817)


   

4,6-dichloro-2-methyl-5-(1-acetyl-2-imidazolin-2-yl)-aminopyridine

4,6-dichloro-2-methyl-5-(1-acetyl-2-imidazolin-2-yl)-aminopyridine

C11H12Cl2N4O (286.0388)


   

tert-Butyl-(2-iodoethoxy)-dimethylsilane

tert-Butyl-(2-iodoethoxy)-dimethylsilane

C8H19IOSi (286.025)


   

3-bromo-4-pentoxybenzoic acid

3-bromo-4-pentoxybenzoic acid

C12H15BrO3 (286.0204)


   

3-bromo-4-pentan-2-yloxybenzoic acid

3-bromo-4-pentan-2-yloxybenzoic acid

C12H15BrO3 (286.0204)


   

2H-1,4-Benzodiazepin-2-one, 7-chloro-1,3-dihydro-5-(4-hydroxyphenyl)-

2H-1,4-Benzodiazepin-2-one, 7-chloro-1,3-dihydro-5-(4-hydroxyphenyl)-

C15H11ClN2O2 (286.0509)


   

1-p-Chlorobenzyl-1H-indazole-3-carboxylic acid

1-p-Chlorobenzyl-1H-indazole-3-carboxylic acid

C15H11ClN2O2 (286.0509)


   

2-(4-Nitro-benzylsulfanyl)-benzooxazole

2-(4-Nitro-benzylsulfanyl)-benzooxazole

C14H10N2O3S (286.0412)


   

N-[(E)-(4-hydroxy-3-nitrophenyl)methylidene]pyridine-4-carbohydrazide

N-[(E)-(4-hydroxy-3-nitrophenyl)methylidene]pyridine-4-carbohydrazide

C13H10N4O4 (286.0702)


   

5-(4-chlorophenyl)-1-phenyl-1H-imidazole-2-thiol

5-(4-chlorophenyl)-1-phenyl-1H-imidazole-2-thiol

C15H11ClN2S (286.0331)


   

2-(Benzoylamino)-4-nitrobenzoic acid

2-(Benzoylamino)-4-nitrobenzoic acid

C14H10N2O5 (286.059)


   

N-(3-nitrophenyl)-1,3-benzodioxole-5-carboxamide

N-(3-nitrophenyl)-1,3-benzodioxole-5-carboxamide

C14H10N2O5 (286.059)


   

3-[(3-Fluorophenyl)methylthio]-6-(2-furanyl)pyridazine

3-[(3-Fluorophenyl)methylthio]-6-(2-furanyl)pyridazine

C15H11FN2OS (286.0576)


   

Quinclorac-dimethylammonium

Quinclorac-dimethylammonium

C12H12Cl2N2O2 (286.0276)


   
   

3,8-Dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid

3,8-Dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid

C15H10O6 (286.0477)


   

N(1)-(5-phospho-D-Ribosyl)glycinamide

N(1)-(5-phospho-D-Ribosyl)glycinamide

C7H15N2O8P (286.0566)


   

2-Amino-6-(3,5-dimethylphenyl)sulfonylbenzonitrile

2-Amino-6-(3,5-dimethylphenyl)sulfonylbenzonitrile

C15H14N2O2S (286.0776)


   

3-deoxy-3-fluoro-D-erythro-alpha-L-manno-non-2-ulopyranosonic acid

3-deoxy-3-fluoro-D-erythro-alpha-L-manno-non-2-ulopyranosonic acid

C9H15FO9 (286.07)


   

Fenclorac

Fenclorac

C14H16Cl2O2 (286.0527)


C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2198 - Nonnarcotic Analgesic C471 - Enzyme Inhibitor > C1323 - Cyclooxygenase Inhibitor

   

Flavonoid

4H-1-Benzopyran-4-one, 5,6,7-trihydroxy-2-(4-hydroxyphenyl)-

C15H10O6 (286.0477)


Scutellarein is a natural flavonoid compound with anti-inflammatory effects. Scutellarein is a natural flavonoid compound with anti-inflammatory effects.

   

520-30-9

4H-1-Benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-

C15H10O6 (286.0477)


Norartocarpetin is a tyrosinase inhibitor. Norartocarpetin has strong tyrosinase inhibitory activity with an IC50 value of 0.47 μM. Norartocarpetin as an antibrowning agent can be used for the research of food systems. Norartocarpetin also has a significant anticancer activity in lung carcinoma cells (NCI-H460) with an IC50 value of 22 μM. Norartocarpetin has antiproliferative effects are mediated via targeting Ras/Raf/MAPK signalling pathway, mitochondrial mediated apoptosis, S-phase cell cycle arrest and suppression of cell migration and invasion in human lung carcinoma cells[1][2]. Norartocarpetin is a tyrosinase inhibitor. Norartocarpetin has strong tyrosinase inhibitory activity with an IC50 value of 0.47 μM. Norartocarpetin as an antibrowning agent can be used for the research of food systems. Norartocarpetin also has a significant anticancer activity in lung carcinoma cells (NCI-H460) with an IC50 value of 22 μM. Norartocarpetin has antiproliferative effects are mediated via targeting Ras/Raf/MAPK signalling pathway, mitochondrial mediated apoptosis, S-phase cell cycle arrest and suppression of cell migration and invasion in human lung carcinoma cells[1][2].

   

61854-36-2

5,7-dihydroxy-2-(4-hydroxyphenoxy)chromen-4-one

C15H10O6 (286.0477)


   

Viset

InChI=1\C15H10O6\c16-8-2-3-9-12(6-8)21-15(14(20)13(9)19)7-1-4-10(17)11(18)5-7\h1-6,16-18,20

C15H10O6 (286.0477)


COVID info from clinicaltrial, clinicaltrials, clinical trial, clinical trials C274 - Antineoplastic Agent > C2189 - Signal Transduction Inhibitor C26170 - Protective Agent > C1509 - Neuroprotective Agent C26170 - Protective Agent > C275 - Antioxidant Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS Fisetin is a natural flavonol found in many fruits and vegetables with various benefits, such as antioxidant, anticancer, neuroprotection effects. Fisetin is a natural flavonol found in many fruits and vegetables with various benefits, such as antioxidant, anticancer, neuroprotection effects. Fisetin is a natural flavonol found in many fruits and vegetables with various benefits, such as antioxidant, anticancer, neuroprotection effects.

   

4-(3,5,7-Trihydroxy-2H-1-benzopyran-2-ylidene)-2-hydroxy-2,5-cyclohexadiene-1-one

4-(3,5,7-Trihydroxy-2H-1-benzopyran-2-ylidene)-2-hydroxy-2,5-cyclohexadiene-1-one

C15H10O6 (286.0477)


   

3,5,6-Trihydroxy-2-(4-hydroxyphenyl)chromen-7-one

3,5,6-Trihydroxy-2-(4-hydroxyphenyl)chromen-7-one

C15H10O6 (286.0477)


   

1,2,3,8-Tetrahydroxy-7-methylanthracene-9,10-dione

1,2,3,8-Tetrahydroxy-7-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   

[[2-(1H-indol-3-yl)ethanethioyl]amino] hydrogen sulfate

[[2-(1H-indol-3-yl)ethanethioyl]amino] hydrogen sulfate

C10H10N2O4S2 (286.0082)


   

cytosyl-beta-D-glucuronate

cytosyl-beta-D-glucuronate

C10H12N3O7- (286.0675)


   

N-Succinyl-L-2-amino-6-oxoheptanedioate

N-Succinyl-L-2-amino-6-oxoheptanedioate

C11H12NO8-3 (286.0563)


   

3,4,5,6-Tetrahydroxyaurone

3,4,5,6-Tetrahydroxyaurone

C15H10O6 (286.0477)


   

(4S)-2,3-dehydroleucopelargonidin

(4S)-2,3-dehydroleucopelargonidin

C15H10O6-2 (286.0477)


   

2-hydroxy-5-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxybenzoic acid

2-hydroxy-5-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxybenzoic acid

C12H14O8 (286.0689)


   

2-[(2-Nitrophenyl)methylthio]-1,3-benzoxazole

2-[(2-Nitrophenyl)methylthio]-1,3-benzoxazole

C14H10N2O3S (286.0412)


   

(2-Methylbenzimidazol-1-yl)-[(5-nitro-2-thienyl)methylene]amine

(2-Methylbenzimidazol-1-yl)-[(5-nitro-2-thienyl)methylene]amine

C13H10N4O2S (286.0524)


   

2-Bromo-5,6-dihydrodibenzo[3,1-[7]annulen-11-one

2-Bromo-5,6-dihydrodibenzo[3,1-[7]annulen-11-one

C15H11BrO (285.9993)


   

N-[(2-nitrophenyl)-oxomethyl]-2-pyridinecarbohydrazide

N-[(2-nitrophenyl)-oxomethyl]-2-pyridinecarbohydrazide

C13H10N4O4 (286.0702)


   

N-(3-nitrobenzoyl)pyridine-2-carbohydrazide

N-(3-nitrobenzoyl)pyridine-2-carbohydrazide

C13H10N4O4 (286.0702)


   

2-Furancarboxylic acid (2-acetyl-1-benzothiophen-3-yl) ester

2-Furancarboxylic acid (2-acetyl-1-benzothiophen-3-yl) ester

C15H10O4S (286.03)


   

4-Methoxy-1,3-dimethyl-6-thiophen-2-yl-8-cyclohepta[c]furanone

4-Methoxy-1,3-dimethyl-6-thiophen-2-yl-8-cyclohepta[c]furanone

C16H14O3S (286.0664)


   

N-[(2-nitrobenzoyl)oxy]pyridine-2-carboximidamide

N-[(2-nitrobenzoyl)oxy]pyridine-2-carboximidamide

C13H10N4O4 (286.0702)


   

2-cyano-3-oxo-N-[4-(trifluoromethoxy)phenyl]butanamide

2-cyano-3-oxo-N-[4-(trifluoromethoxy)phenyl]butanamide

C12H9F3N2O3 (286.0565)


   

2-Hydroxy-3-(beta-D-xylopyranosyloxy)benzoic acid

2-Hydroxy-3-(beta-D-xylopyranosyloxy)benzoic acid

C12H14O8 (286.0689)


   

3-(4-Chlorophenyl)-3-oxo-2-(2-phenylhydrazono)propanal

3-(4-Chlorophenyl)-3-oxo-2-(2-phenylhydrazono)propanal

C15H11ClN2O2 (286.0509)


   

1-(5-Fluoro-3-methyl-1-benzofuran-2-yl)-3-(2-thienyl)-2-propen-1-one

1-(5-Fluoro-3-methyl-1-benzofuran-2-yl)-3-(2-thienyl)-2-propen-1-one

C16H11FO2S (286.0464)


   

N-(4-carboxy-4-oxobutanoyl)-L-ethylglycylglycine

N-(4-carboxy-4-oxobutanoyl)-L-ethylglycylglycine

C11H14N2O7-2 (286.0801)


   

4-oxo-2-(trifluoromethyl)-1H-quinazoline-6-carboxylic acid ethyl ester

4-oxo-2-(trifluoromethyl)-1H-quinazoline-6-carboxylic acid ethyl ester

C12H9F3N2O3 (286.0565)


   

N-(2-hydroxybenzylidene)-2-(phenylthio)acetohydrazide

N-(2-hydroxybenzylidene)-2-(phenylthio)acetohydrazide

C15H14N2O2S (286.0776)


   

hydrogen ({[(2R)-1-(6-amino-9H-purin-9-yl)propan-2-yl]oxy}methyl)phosphonate

hydrogen ({[(2R)-1-(6-amino-9H-purin-9-yl)propan-2-yl]oxy}methyl)phosphonate

C9H13N5O4P- (286.0705)


   

3,4,5-Trihydroxy-6-(2-hydroxyphenoxy)oxane-2-carboxylic acid

3,4,5-Trihydroxy-6-(2-hydroxyphenoxy)oxane-2-carboxylic acid

C12H14O8 (286.0689)


   

3,5-dihydroxy-2-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]cyclohexa-2,5-diene-1,4-dione

3,5-dihydroxy-2-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]cyclohexa-2,5-diene-1,4-dione

C15H10O6 (286.0477)


   

[(E)-5-(4-methoxyphenyl)-3-oxopent-4-enyl] hydrogen sulate

[(E)-5-(4-methoxyphenyl)-3-oxopent-4-enyl] hydrogen sulate

C12H14O6S (286.0511)


   

4-Acetoxymethyl-6-chloromethyl-2,5-dimethoxy-2,4,6-cycloheptatrien-1-one

4-Acetoxymethyl-6-chloromethyl-2,5-dimethoxy-2,4,6-cycloheptatrien-1-one

C13H15ClO5 (286.0608)


   

cytosylglucuronate

cytosylglucuronate

C10H12N3O7 (286.0675)


A carbohydrate acid derivative anion that is the conjugate base of cytosylglucuronic acid, obtained by deprotonation of the carboxy group.

   

7,8,3,4-Tetrahydroxyisoflavone

7,8,3,4-Tetrahydroxyisoflavone

C15H10O6 (286.0477)


   

2-Hydroxyphenyl-beta-D-glucopyranosiduronic acid

2-Hydroxyphenyl-beta-D-glucopyranosiduronic acid

C12H14O8 (286.0689)


   

Diphenol glucuronide

Diphenol glucuronide

C12H14O8 (286.0689)


   

3-Methoxyfukiic acid

3-Methoxyfukiic acid

C12H14O8 (286.0689)


   

2,3-dihydroxybenzoic acid 3-O-beta-D-xyloside

2,3-dihydroxybenzoic acid 3-O-beta-D-xyloside

C12H14O8 (286.0689)


A monohydroxybenzoic acid that is 2-hydroxybenzoic acid in which the hydrogen at position 3 is replaced by a beta-D-xylosyloxy group.

   

tenofovir(1-)

tenofovir(1-)

C9H13N5O4P (286.0705)


A phosphorus oxoanion resulting from the removal of one proton from the phosphonic acid group of tenofovir. The major microspecies at pH 7.3.

   

catechol beta-D-glucuronide

catechol beta-D-glucuronide

C12H14O8 (286.0689)


A glucosiduronic acid that is beta-D-glucuronic acid in which the anomeric hydroxyl hydrogen has been replaced by a 2-hydroxyphenyl group.

   
   

3'-Azido-3'-deoxy-5-fluorocytidine

3'-Azido-3'-deoxy-5-fluorocytidine

C9H11FN6O4 (286.0826)


3'-Azido-3'-deoxy-5-fluorocytidine (Compound 12) is a cytidine derivative. 3'-Azido-3'-deoxy-5-fluorocytidine is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

   

Azvudine

Azvudine

C9H11FN6O4 (286.0826)


Azvudine (RO-0622) is a potent nucleoside reverse transcriptase inhibitor (NRTI), with antiviral activity on HIV, HBV and HCV. Azvudine exerts highly potent inhibition on HIV-1 (EC50s ranging from 0.03 to 6.92 nM) and HIV-2 (EC50s ranging from 0.018 to 0.025 nM). Azvudine inhibits NRTI-resistant viral strains[1]. Azvudine is a click chemistry reagent, itcontains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

   

2-(3,4-dihydroxyphenyl)-6,7-dihydroxychromen-4-one

2-(3,4-dihydroxyphenyl)-6,7-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

1,2,5,7-tetrahydroxy-4-methylanthracene-9,10-dione

1,2,5,7-tetrahydroxy-4-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   

2-(3,4-dihydroxyphenyl)-7-hydroxy-1-benzofuran-4-carboxylic acid

2-(3,4-dihydroxyphenyl)-7-hydroxy-1-benzofuran-4-carboxylic acid

C15H10O6 (286.0477)


   

(10r)-7,14-dihydroxy-10-methoxy-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

(10r)-7,14-dihydroxy-10-methoxy-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

C15H10O6 (286.0477)


   

1,2,8-trihydroxy-3-(hydroxymethyl)anthracene-9,10-dione

1,2,8-trihydroxy-3-(hydroxymethyl)anthracene-9,10-dione

C15H10O6 (286.0477)


   

2,6,8-trihydroxy-3-(4-hydroxyphenyl)chromen-4-one

2,6,8-trihydroxy-3-(4-hydroxyphenyl)chromen-4-one

C15H10O6 (286.0477)


   

2-(3,4-dihydroxyphenyl)-6,8-dihydroxychromen-4-one

2-(3,4-dihydroxyphenyl)-6,8-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

hexahydroxy-[5,5'-bipyrimidine]-2,2'-dione

hexahydroxy-[5,5'-bipyrimidine]-2,2'-dione

C8H6N4O8 (286.0186)


   

1,2,3,7-tetrahydroxyxanthone; 2,3-methylene,1-me ether

NA

C15H10O6 (286.0477)


{"Ingredient_id": "HBIN000608","Ingredient_name": "1,2,3,7-tetrahydroxyxanthone; 2,3-methylene,1-me ether","Alias": "NA","Ingredient_formula": "C15H10O6","Ingredient_Smile": "NA","Ingredient_weight": "0","OB_score": "NA","CAS_id": "200509-34-8","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "9615","PubChem_id": "NA","DrugBank_id": "NA"}

   

6-hydroxy-1-methoxy-2,3-methylenedioxy-xanthone

NA

C15H10O6 (286.0477)


{"Ingredient_id": "HBIN012383","Ingredient_name": "6-hydroxy-1-methoxy-2,3-methylenedioxy-xanthone","Alias": "NA","Ingredient_formula": "C15H10O6","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "10421","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

7-hydroxy-1-methoxy-2,3-methylenedioxy xanthone

NA

C15H10O6 (286.0477)


{"Ingredient_id": "HBIN013201","Ingredient_name": "7-hydroxy-1-methoxy-2,3-methylenedioxy xanthone","Alias": "NA","Ingredient_formula": "C15H10O6","Ingredient_Smile": "COC1=C2C(=CC3=C1OCO3)OC4=C(C2=O)C=C(C=C4)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "31223","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

8-hydroxy-11-methoxy-[1,3]dioxolo[4,5-b]xanthen-10-one

NA

C15H10O6 (286.0477)


{"Ingredient_id": "HBIN013754","Ingredient_name": "8-hydroxy-11-methoxy-[1,3]dioxolo[4,5-b]xanthen-10-one","Alias": "NA","Ingredient_formula": "C15H10O6","Ingredient_Smile": "COC1=C2C(=CC3=C1OCO3)OC4=C(C2=O)C=C(C=C4)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "10422","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

   

methyl 2-[4,5-dimethoxy-2-(methylsulfanyl)-3,6-dioxocyclohexa-1,4-dien-1-yl]acetate

methyl 2-[4,5-dimethoxy-2-(methylsulfanyl)-3,6-dioxocyclohexa-1,4-dien-1-yl]acetate

C12H14O6S (286.0511)


   

6,7,8-trihydroxy-3-(4-hydroxyphenyl)chromen-4-one

6,7,8-trihydroxy-3-(4-hydroxyphenyl)chromen-4-one

C15H10O6 (286.0477)


   

1,3,5-trihydroxy-7-(hydroxymethyl)anthracene-9,10-dione

1,3,5-trihydroxy-7-(hydroxymethyl)anthracene-9,10-dione

C15H10O6 (286.0477)


   

4-hydroxy-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}benzoic acid

4-hydroxy-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}benzoic acid

C12H14O8 (286.0689)


   

2-amino-n-[(3r,4s,5r)-3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl]ethanimidic acid

2-amino-n-[(3r,4s,5r)-3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl]ethanimidic acid

C7H15N2O8P (286.0566)


   

2-hydroxy-3-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}benzoic acid

2-hydroxy-3-{[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}benzoic acid

C12H14O8 (286.0689)


   

{8-hydroxy-4,9-dioxonaphtho[2,3-c]furan-1-yl}methyl acetate

{8-hydroxy-4,9-dioxonaphtho[2,3-c]furan-1-yl}methyl acetate

C15H10O6 (286.0477)


   

4,9-dihydroxy-6-methoxy-7-methylphenalene-1,2,3-trione

4,9-dihydroxy-6-methoxy-7-methylphenalene-1,2,3-trione

C15H10O6 (286.0477)


   

3,5-bis(acetyloxy)-2-chlorophenyl acetate

3,5-bis(acetyloxy)-2-chlorophenyl acetate

C12H11ClO6 (286.0244)


   

2-(2,3-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

2-(2,3-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

(2e)-3-(methylsulfanyl)-n-[(2r)-1-[(2e)-3-(methylsulfanyl)prop-2-enoyl]pyrrolidin-2-yl]prop-2-enimidic acid

(2e)-3-(methylsulfanyl)-n-[(2r)-1-[(2e)-3-(methylsulfanyl)prop-2-enoyl]pyrrolidin-2-yl]prop-2-enimidic acid

C12H18N2O2S2 (286.081)


   

3-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-2-one

3-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-2-one

C15H10O6 (286.0477)


   

2-(2,5-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

2-(2,5-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

2,4,8-trihydroxy-1-methoxyanthracene-9,10-dione

2,4,8-trihydroxy-1-methoxyanthracene-9,10-dione

C15H10O6 (286.0477)


   

1,2,3,5-tetrahydroxy-6-methylanthracene-9,10-dione

1,2,3,5-tetrahydroxy-6-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   

4-hydroxy-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]benzoic acid

4-hydroxy-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]benzoic acid

C12H14O8 (286.0689)


   

3,7,13-trihydroxy-15-methyl-4,10-dioxatetracyclo[7.7.0.0²,⁶.0¹¹,¹⁶]hexadeca-1(9),2(6),7,11(16),12,14-hexaen-5-one

3,7,13-trihydroxy-15-methyl-4,10-dioxatetracyclo[7.7.0.0²,⁶.0¹¹,¹⁶]hexadeca-1(9),2(6),7,11(16),12,14-hexaen-5-one

C15H10O6 (286.0477)


   

1,4,5,7-tetrahydroxy-2-methylanthracene-9,10-dione

1,4,5,7-tetrahydroxy-2-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   

3-(3,5-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

3-(3,5-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

3-(methylsulfanyl)-n-{1-[3-(methylsulfanyl)prop-2-enoyl]pyrrolidin-2-yl}prop-2-enimidic acid

3-(methylsulfanyl)-n-{1-[3-(methylsulfanyl)prop-2-enoyl]pyrrolidin-2-yl}prop-2-enimidic acid

C12H18N2O2S2 (286.081)


   

(2r,3s)-2,3-dihydroxy-2-[(4-hydroxy-3-methoxyphenyl)methyl]butanedioic acid

(2r,3s)-2,3-dihydroxy-2-[(4-hydroxy-3-methoxyphenyl)methyl]butanedioic acid

C12H14O8 (286.0689)


   

(2s)-2-methoxy-6-[5-(prop-1-yn-1-yl)thiophen-2-yl]hexa-3,5-diyn-1-yl acetate

(2s)-2-methoxy-6-[5-(prop-1-yn-1-yl)thiophen-2-yl]hexa-3,5-diyn-1-yl acetate

C16H14O3S (286.0664)


   

3-(2,4-dihydroxyphenyl)-7,8-dihydroxychromen-4-one

3-(2,4-dihydroxyphenyl)-7,8-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

(2s)-2-(3,4,5-trihydroxybenzoyloxy)butanedioic acid

(2s)-2-(3,4,5-trihydroxybenzoyloxy)butanedioic acid

C11H10O9 (286.0325)


   

3,4,5-trihydroxyoxan-2-yl 2,5-dihydroxybenzoate

3,4,5-trihydroxyoxan-2-yl 2,5-dihydroxybenzoate

C12H14O8 (286.0689)


   

13-formyl-5,11-dihydroxy-3-methyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylic acid

13-formyl-5,11-dihydroxy-3-methyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-4-carboxylic acid

C15H10O6 (286.0477)


   

(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl 2,5-dihydroxybenzoate

(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl 2,5-dihydroxybenzoate

C12H14O8 (286.0689)


   

2-(3,4-dihydroxyphenyl)-7,8-dihydroxychromen-4-one

2-(3,4-dihydroxyphenyl)-7,8-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

(2e)-3-(methylsulfanyl)-n-{1-[(2e)-3-(methylsulfanyl)prop-2-enoyl]pyrrolidin-2-yl}prop-2-enimidic acid

(2e)-3-(methylsulfanyl)-n-{1-[(2e)-3-(methylsulfanyl)prop-2-enoyl]pyrrolidin-2-yl}prop-2-enimidic acid

C12H18N2O2S2 (286.081)


   

2-hydroxy-5-{[(2r,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}benzoic acid

2-hydroxy-5-{[(2r,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}benzoic acid

C12H14O8 (286.0689)


   

1,3,6-trihydroxy-2-methoxyanthracene-9,10-dione

1,3,6-trihydroxy-2-methoxyanthracene-9,10-dione

C15H10O6 (286.0477)


   

3,5,7-trihydroxy-2-(3-hydroxyphenyl)chromen-4-one

3,5,7-trihydroxy-2-(3-hydroxyphenyl)chromen-4-one

C15H10O6 (286.0477)


   

1,3,8-trihydroxy-2-methoxyanthracene-9,10-dione

1,3,8-trihydroxy-2-methoxyanthracene-9,10-dione

C15H10O6 (286.0477)


   

1,4,5,8-tetrahydroxy-2-methylanthracene-9,10-dione

1,4,5,8-tetrahydroxy-2-methylanthracene-9,10-dione

C15H10O6 (286.0477)


   

7,14-dihydroxy-10-methoxy-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

7,14-dihydroxy-10-methoxy-2,9-dioxatetracyclo[6.6.2.0⁴,¹⁶.0¹¹,¹⁵]hexadeca-1(15),4(16),5,7,11,13-hexaen-3-one

C15H10O6 (286.0477)


   

5,7-dihydroxy-2-(3-hydroxyphenoxy)chromen-4-one

5,7-dihydroxy-2-(3-hydroxyphenoxy)chromen-4-one

C15H10O6 (286.0477)


   

3,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one

3,7,8-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one

C15H10O6 (286.0477)


   

2-methoxy-6-[5-(prop-1-yn-1-yl)thiophen-2-yl]hexa-3,5-diyn-1-yl acetate

2-methoxy-6-[5-(prop-1-yn-1-yl)thiophen-2-yl]hexa-3,5-diyn-1-yl acetate

C16H14O3S (286.0664)


   

n'-[2-(3-bromo-4-hydroxyphenyl)ethyl]ethanediamide

n'-[2-(3-bromo-4-hydroxyphenyl)ethyl]ethanediamide

C10H11BrN2O3 (285.9953)


   

2-(3,4,5-trihydroxybenzoyloxy)butanedioic acid

2-(3,4,5-trihydroxybenzoyloxy)butanedioic acid

C11H10O9 (286.0325)


   

2,4,5-trihydroxy-1-methoxyanthracene-9,10-dione

2,4,5-trihydroxy-1-methoxyanthracene-9,10-dione

C15H10O6 (286.0477)


   

5,6,8-trihydroxy-3-(4-hydroxyphenyl)chromen-4-one

5,6,8-trihydroxy-3-(4-hydroxyphenyl)chromen-4-one

C15H10O6 (286.0477)


   

2-(3,5-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

2-(3,5-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

C15H10O6 (286.0477)


   

2-(3,5-dihydroxy-4-oxidophenyl)-5,7-dihydroxy-1λ⁴-chromen-1-ylium

2-(3,5-dihydroxy-4-oxidophenyl)-5,7-dihydroxy-1λ⁴-chromen-1-ylium

C15H10O6 (286.0477)


   

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1λ⁴-chromen-1-ylium-3-olate

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1λ⁴-chromen-1-ylium-3-olate

C15H10O6 (286.0477)


   

4-isopropyl-7-(2-methylpropyl)-1,2,3,5,6-pentathiepane

4-isopropyl-7-(2-methylpropyl)-1,2,3,5,6-pentathiepane

C9H18S5 (286.0012)