NCBI Taxonomy: 864330

Cedrelopsis (ncbi_taxid: 864330)

found 293 associated metabolites at genus taxonomy rank level.

Ancestor: Cneoroideae

Child Taxonomies: Cedrelopsis grevei, Cedrelopsis gracilis, Cedrelopsis trivalvis, Cedrelopsis rakotozafyi, unclassified Cedrelopsis, Cedrelopsis microfoliolata

Aesculetin

6,7-dihydroxychromen-2-one

C9H6O4 (178.0266076)


Aesculetin, also known as cichorigenin or cichoriin aglucon, belongs to the class of organic compounds known as 6,7-dihydroxycoumarins. These are coumarins bearing two hydroxyl groups at positions 6 and 7 of the coumarin skeleton, respectively. Aesculetin is found, on average, in the highest concentration within sherries. Aesculetin has also been detected, but not quantified, in several different foods, such as horseradish, carrots, dandelions, grape wines, and highbush blueberries. This could make aesculetin a potential biomarker for the consumption of these foods. Esculetin is a hydroxycoumarin that is umbelliferone in which the hydrogen at position 6 is substituted by a hydroxy group. It is used in filters for absorption of ultraviolet light. It has a role as an antioxidant, an ultraviolet filter and a plant metabolite. Esculetin is a natural product found in Artemisia eriopoda, Euphorbia decipiens, and other organisms with data available. A hydroxycoumarin that is umbelliferone in which the hydrogen at position 6 is substituted by a hydroxy group. It is used in filters for absorption of ultraviolet light. Metabolite of infected sweet potato. Aesculetin is found in many foods, some of which are root vegetables, wild carrot, sweet basil, and carrot. D020011 - Protective Agents > D000975 - Antioxidants Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CB031_Aesculetin_pos_20eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_10eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_40eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_50eV_CB000017.txt [Raw Data] CB031_Aesculetin_pos_30eV_CB000017.txt [Raw Data] CB031_Aesculetin_neg_10eV_000010.txt [Raw Data] CB031_Aesculetin_neg_20eV_000010.txt [Raw Data] CB031_Aesculetin_neg_30eV_000010.txt CONFIDENCE standard compound; ML_ID 39 Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1].

   

Scoparone

6,7-dimethoxychromen-2-one

C11H10O4 (206.057906)


Scoparone is a member of the class of coumarins that is esculetin in which the two hydroxy groups at positions 6 and 7 are replaced by methoxy groups. It is a major constituent of the Chinese herbal medicine Yin Chen Hao, and exhibits a variety of pharmacological activities such as anti-inflammatory, anti-allergic, and anti-tumor activities. It has a role as a plant metabolite, an anti-inflammatory agent, an antilipemic drug, an immunosuppressive agent, an antihypertensive agent and an anti-allergic agent. It is a member of coumarins and an aromatic ether. It is functionally related to an esculetin. Scoparone is a natural product found in Haplophyllum ramosissimum, Haplophyllum thesioides, and other organisms with data available. A member of the class of coumarins that is esculetin in which the two hydroxy groups at positions 6 and 7 are replaced by methoxy groups. It is a major constituent of the Chinese herbal medicine Yin Chen Hao, and exhibits a variety of pharmacological activities such as anti-inflammatory, anti-allergic, and anti-tumor activities. D005765 - Gastrointestinal Agents > D002756 - Cholagogues and Choleretics Scoparone is found in anise. Scoparone is found in several citrus oil D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents Found in several citrus oils Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1]. Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1].

   

beta-Sitosterol 3-O-beta-D-galactopyranoside

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.4389659999999)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. beta-Sitosterol 3-O-beta-D-galactopyranoside is found in herbs and spices. beta-Sitosterol 3-O-beta-D-galactopyranoside is a constituent of Hibiscus sabdariffa (roselle) leaves. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

Amyrin

(3S,4aR,5R,6aR,6bR,8S,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol

C30H50O (426.386145)


Beta-amyrin is a pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. It has a role as a plant metabolite and an Aspergillus metabolite. It is a pentacyclic triterpenoid and a secondary alcohol. It derives from a hydride of an oleanane. beta-Amyrin is a natural product found in Ficus pertusa, Ficus septica, and other organisms with data available. See also: Calendula Officinalis Flower (part of); Viburnum opulus bark (part of); Centaurium erythraea whole (part of). A pentacyclic triterpenoid that is oleanane substituted at the 3beta-position by a hydroxy group and containing a double bond between positions 12 and 13. It is one of the most commonly occurring triterpenoids in higher plants. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].

   

Perforatin A

5-O-Methylalloptaeroxylin

C16H16O4 (272.1048536)


   
   
   

2'-Hydroxy-4',6'-dimethoxychalcone

2-Propen-1-one, 1-(2-hydroxy-4,6-dimethoxyphenyl)-3-phenyl-, (2E)-

C17H16O4 (284.1048536)


Flavokawain B is a member of the class of chalcones that consists of trans-chalcone substituted by hydroxy group at positions 2 and methoxy groups at positions 4 and 6. Isolated from Piper methysticum and Piper rusbyi, it exhibits antileishmanial, anti-inflammatory and antineoplastic activities. It has a role as a metabolite, an antileishmanial agent, an anti-inflammatory agent, an apoptosis inducer and an antineoplastic agent. It is a member of chalcones, a dimethoxybenzene and a member of phenols. It is functionally related to a trans-chalcone. Flavokawain b is a natural product found in Alpinia rafflesiana, Bistorta officinalis, and other organisms with data available. See also: Piper methysticum root (part of). A member of the class of chalcones that consists of trans-chalcone substituted by hydroxy group at positions 2 and methoxy groups at positions 4 and 6. Isolated from Piper methysticum and Piper rusbyi, it exhibits antileishmanial, anti-inflammatory and antineoplastic activities. 2-Hydroxy-4,6-dimethoxychalcone is found in beverages. 2-Hydroxy-4,6-dimethoxychalcone is found in kava (Piper methysticum), FDA advises against use of kava in food due to potential risk of severe liver damage (2002). Found in kava (Piper methysticum), FDA advises against use of kava in food due to potential risk of severe liver damage (2002) Flavokawain B (Flavokavain B) is a chalcone isolated from the root extracts of kava-kava plant and a potent apoptosis inducer for inhibiting the growth of various cancer cell lines. Flavokawain B (Flavokavain B) shows strong antiangiogenic activity. Flavokawain B (Flavokavain B) inhibits human brain endothelial cell (HUVEC) migration and tube formation with very low and non-toxic concentrations[1][2]. Flavokawain B (Flavokavain B) is a chalcone isolated from the root extracts of kava-kava plant and a potent apoptosis inducer for inhibiting the growth of various cancer cell lines. Flavokawain B (Flavokavain B) shows strong antiangiogenic activity. Flavokawain B (Flavokavain B) inhibits human brain endothelial cell (HUVEC) migration and tube formation with very low and non-toxic concentrations[1][2].

   

1-(2,4-dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one

1-(2,4-dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one

C16H14O4 (270.0892044)


   
   

beta-Amyrin

4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-ol

C30H50O (426.386145)


Beta-amryin, also known as B-amryin, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Beta-amryin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amryin can be found in pigeon pea, which makes beta-amryin a potential biomarker for the consumption of this food product.

   

Braylin

6-methoxy-8,8-dimethyl-2H,8H-pyrano[2,3-h]chromen-2-one

C15H14O4 (258.0892044)


Braylin is a member of the class of compounds known as angular pyranocoumarins. Angular pyranocoumarins are organic compounds containing a pyran (or a hydrogenated derivative) angularly fused to a coumarin moiety. Braylin is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Braylin can be found in lemon, mandarin orange (clementine, tangerine), and sweet orange, which makes braylin a potential biomarker for the consumption of these food products.

   

Cardamomin

InChI=1/C16H14O4/c1-20-15-10-12(17)9-14(19)16(15)13(18)8-7-11-5-3-2-4-6-11/h2-10,17,19H,1H3/b8-7

C16H14O4 (270.0892044)


Cardamonin is a member of chalcones. Cardamonin (also known as Dihydroxymethoxychalcone), as shown by the increasing number of publications, has received growing attention from the scientific community due to the expectations toward its benefits to human health. Cardamonins name comes from the fact that it can be found in cardamom spice. Cardamonin is a natural product found in Amomum subulatum, Alpinia blepharocalyx, and other organisms with data available. (E)-Cardamonin ((E)-Cardamomin) is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM. (E)-Cardamonin ((E)-Cardamomin) is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM. Cardamonin can be found from cardamom, and target various signaling molecules, transcriptional factors, cytokines and enzymes. Cardamonin can inhibit mTOR, NF-κB, Akt, STAT3, Wnt/β-catenin and COX-2. Cardamonin shows anticancer, anti-inflammatory, antimicrobial and antidiabetic activities[1][2].

   

Cedrediprenone

2,4-Dihydroxy-3-prenyl-5"- (2-hydroxyisopropyl) -4",5"-dihydrofurano [ 2",3":6,5 ] chalcone

C25H28O5 (408.1936638)


   
   
   
   

Norbraylin

Norbraylin

C14H12O4 (244.0735552)


Origin: Plant, Coumarins

   
   

β-Amyrin

beta-amyrin-H2O

C30H50O (426.386145)


Beta-amyrin, also known as amyrin or (3beta)-olean-12-en-3-ol, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Thus, beta-amyrin is considered to be an isoprenoid lipid molecule. Beta-amyrin is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta-amyrin can be synthesized from oleanane. Beta-amyrin is also a parent compound for other transformation products, including but not limited to, erythrodiol, glycyrrhetaldehyde, and 24-hydroxy-beta-amyrin. Beta-amyrin can be found in a number of food items such as thistle, pepper (c. baccatum), wakame, and endive, which makes beta-amyrin a potential biomarker for the consumption of these food products. The amyrins are three closely related natural chemical compounds of the triterpene class. They are designated α-amyrin (ursane skeleton), β-amyrin (oleanane skeleton) and δ-amyrin. Each is a pentacyclic triterpenol with the chemical formula C30H50O. They are widely distributed in nature and have been isolated from a variety of plant sources such as epicuticular wax. In plant biosynthesis, α-amyrin is the precursor of ursolic acid and β-amyrin is the precursor of oleanolic acid. All three amyrins occur in the surface wax of tomato fruit. α-Amyrin is found in dandelion coffee . β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1]. β-Amyrin, an ingredient of Celastrus hindsii, blocks amyloid β (Aβ)-induced long-term potentiation (LTP) impairment. β-amyrin is a promising candidate of treatment for AD[1].

   

cedreprenone

(2E) -1- (5-Hydroxy-7-methoxy-2,2-dimethyl-2H-1-benzopyran-8-yl) -3-phenyl-2-propen-1-one

C21H20O4 (336.13615200000004)


   

agrandol

5,7-Dihydroxy-6-methoxy-8-prenylflavanone

C21H22O5 (354.1467162)


   

Microfolione

(2R) -5,7-Dihydroxy-8-methoxy-6-prenylflavanone

C21H22O5 (354.1467162)


   

2,4-dihydroxy-6-methoxychalcone

1-(2,4-dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one

C16H14O4 (270.0892044)


Cardamonin can be found from cardamom, and target various signaling molecules, transcriptional factors, cytokines and enzymes. Cardamonin can inhibit mTOR, NF-κB, Akt, STAT3, Wnt/β-catenin and COX-2. Cardamonin shows anticancer, anti-inflammatory, antimicrobial and antidiabetic activities[1][2].

   

Cardamonin

(E) -2,4-Dihydroxy-6-methoxychalcone

C16H14O4 (270.0892044)


(E)-Cardamonin ((E)-Cardamomin) is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM. (E)-Cardamonin ((E)-Cardamomin) is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM.

   

Uvangoletin

1-Propanone, 1-(2,4-dihydroxy-6-methoxyphenyl)-3-phenyl-

C16H16O4 (272.1048536)


   
   
   

Daucosterol

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.4389659999999)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. A steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

orbraylin

6-Hydroxy-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b]dipyran-2-one

C14H12O4 (244.0735552)


Norbraylin is a natural product found in Zanthoxylum asiaticum and Cedrelopsis grevei with data available.

   

Scoparone

6,7-dimethoxycoumarin

C11H10O4 (206.057906)


Annotation level-1 D005765 - Gastrointestinal Agents > D002756 - Cholagogues and Choleretics D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1]. Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1].

   

Esculetin

InChI=1\C9H6O4\c10-6-3-5-1-2-9(12)13-8(5)4-7(6)11\h1-4,10-11

C9H6O4 (178.0266076)


D020011 - Protective Agents > D000975 - Antioxidants relative retention time with respect to 9-anthracene Carboxylic Acid is 0.434 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.428 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.430 Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1]. Esculetin is an active ingredient extracted mainly from the bark of Fraxinus rhynchophylla. Esculetin inhibits platelet-derived growth factor (PDGF)-induced airway smooth muscle cells (ASMCs) phenotype switching through inhibition of PI3K/Akt pathway. Esculetin has antioxidant, antiinflammatory, and antitumor activities[1].

   

Pinocembrin 5,7-dimethyl ether

Pinocembrin 5,7-dimethyl ether

C17H16O4 (284.1048536)


   

Dihydroagarofuran. cis-

Dihydroagarofuran. cis-

C15H26O (222.1983546)


   

cardamomin

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

C16H14O4 (270.0892044)


(E)-Cardamonin ((E)-Cardamomin) is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM. (E)-Cardamonin ((E)-Cardamomin) is a novel antagonist of hTRPA1 cation channel with an IC50 of 454 nM. Cardamonin can be found from cardamom, and target various signaling molecules, transcriptional factors, cytokines and enzymes. Cardamonin can inhibit mTOR, NF-κB, Akt, STAT3, Wnt/β-catenin and COX-2. Cardamonin shows anticancer, anti-inflammatory, antimicrobial and antidiabetic activities[1][2].

   

Scoparon

5-18-03-00204 (Beilstein Handbook Reference)

C11H10O4 (206.057906)


D005765 - Gastrointestinal Agents > D002756 - Cholagogues and Choleretics D002317 - Cardiovascular Agents > D000959 - Antihypertensive Agents D002317 - Cardiovascular Agents > D000889 - Anti-Arrhythmia Agents D002317 - Cardiovascular Agents > D014665 - Vasodilator Agents Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1]. Scoparone is isolated from Artemisia capillaris Thunb., has anticoagulant, vasorelaxant antioxidant, anti-inflammatory activities[1].

   

6-methoxy-8,8-dimethyl-9h,10h-pyrano[2,3-h]chromen-2-one

6-methoxy-8,8-dimethyl-9h,10h-pyrano[2,3-h]chromen-2-one

C15H16O4 (260.1048536)


   

2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane

2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane

C15H26O (222.1983546)


   

1-(5-hydroxy-7-methoxy-2,2-dimethylchromen-8-yl)-3-phenylprop-2-en-1-one

1-(5-hydroxy-7-methoxy-2,2-dimethylchromen-8-yl)-3-phenylprop-2-en-1-one

C21H20O4 (336.13615200000004)


   

(2s)-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

(2s)-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C14H12O4 (244.0735552)


   

(2r)-4-hydroxy-7-(hydroxymethyl)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one

(2r)-4-hydroxy-7-(hydroxymethyl)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one

C15H14O5 (274.0841194)


   

5-hydroxy-2,8,8-trimethylpyrano[2,3-h]chromen-4-one

5-hydroxy-2,8,8-trimethylpyrano[2,3-h]chromen-4-one

C15H14O4 (258.0892044)


   

5,7-dihydroxy-2-methyl-8-(3-methylbut-2-en-1-yl)chromen-4-one

5,7-dihydroxy-2-methyl-8-(3-methylbut-2-en-1-yl)chromen-4-one

C15H16O4 (260.1048536)


   

(2e)-1-[(3s)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]-3-phenylprop-2-en-1-one

(2e)-1-[(3s)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]-3-phenylprop-2-en-1-one

C21H22O5 (354.1467162)


   

5-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

5-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C15H14O5 (274.0841194)


   

1-(3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-3-phenylprop-2-en-1-one

1-(3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl)-3-phenylprop-2-en-1-one

C21H22O5 (354.1467162)


   

(1's,2r,2's,4s,6'r,9's,10'r)-10'-(furan-3-yl)-5,5-dimethyl-4-[(2s)-2-methyl-5-oxofuran-2-yl]-5',11'-dioxaspiro[oxolane-2,4'-tetracyclo[7.3.1.0¹,⁹.0²,⁶]tridecan]-12'-one

(1's,2r,2's,4s,6'r,9's,10'r)-10'-(furan-3-yl)-5,5-dimethyl-4-[(2s)-2-methyl-5-oxofuran-2-yl]-5',11'-dioxaspiro[oxolane-2,4'-tetracyclo[7.3.1.0¹,⁹.0²,⁶]tridecan]-12'-one

C25H28O7 (440.1834938)


   

16-(2-hydroxy-5-oxo-2h-furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

16-(2-hydroxy-5-oxo-2h-furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

C24H28O8 (444.1784088)


   

2,4-dihydroxy-5-methoxybenzophenone

2,4-dihydroxy-5-methoxy-benzo-phenone

C14H12O4 (244.0735552)


{"Ingredient_id": "HBIN004321","Ingredient_name": "2,4-dihydroxy-5-methoxybenzophenone","Alias": "2,4-dihydroxy-5-methoxy-benzo-phenone","Ingredient_formula": "C14H12O4","Ingredient_Smile": "COC1=C(C=C(C(=C1)C(=O)C2=CC=CC=C2)O)O","Ingredient_weight": "244.24 g/mol","OB_score": "67.20784963","CAS_id": "NA","SymMap_id": "SMIT05097","TCMID_id": "42071","TCMSP_id": "MOL002948","TCM_ID_id": "NA","PubChem_id": "85777815","DrugBank_id": "NA"}

   

5-hydroxy-2-(hydroxymethyl)-8,8-dimethylpyrano[3,2-g]chromen-4-one

5-hydroxy-2-(hydroxymethyl)-8,8-dimethylpyrano[3,2-g]chromen-4-one

C15H14O5 (274.0841194)


   

(3s,4as,6ar,6br,8ar,12as,12br,14ar,14bs)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,12b,14a-tetradecahydropicen-3-ol

(3s,4as,6ar,6br,8ar,12as,12br,14ar,14bs)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,12b,14a-tetradecahydropicen-3-ol

C30H50O (426.386145)


   

5,6,9-trimethyltetracyclo[7.2.1.0¹,⁶.0⁸,¹⁰]dodecan-4-ol

5,6,9-trimethyltetracyclo[7.2.1.0¹,⁶.0⁸,¹⁰]dodecan-4-ol

C15H24O (220.18270539999997)


   

(2e)-1-[(2r)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one

(2e)-1-[(2r)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one

C25H28O5 (408.1936638)


   

16-(furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

16-(furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

C24H28O6 (412.1885788)


   

5-methoxy-2,8,8-trimethyl-9h,10h-pyrano[2,3-h]chromen-4-one

5-methoxy-2,8,8-trimethyl-9h,10h-pyrano[2,3-h]chromen-4-one

C16H18O4 (274.1205028)


   

(2s)-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

(2s)-5,7-dimethoxy-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C17H16O4 (284.1048536)


   

(5s)-5-(2-hydroxy-5-methylphenyl)-6-methylheptan-2-one

(5s)-5-(2-hydroxy-5-methylphenyl)-6-methylheptan-2-one

C15H22O2 (234.1619712)


   

(1r,2s,3s,4s,6r,7s,9r,14r,16r,17r)-3-hydroxy-4-methoxy-2,6,14,17-tetramethyl-11-oxo-14-[(5-oxo-2h-furan-3-yl)methyl]-10-oxatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadec-12-en-16-yl acetate

(1r,2s,3s,4s,6r,7s,9r,14r,16r,17r)-3-hydroxy-4-methoxy-2,6,14,17-tetramethyl-11-oxo-14-[(5-oxo-2h-furan-3-yl)methyl]-10-oxatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadec-12-en-16-yl acetate

C28H38O8 (502.2566548)


   

5-hydroxy-8-(hydroxymethyl)-2-methyl-6h,9h-oxepino[3,2-g]chromen-4-one

5-hydroxy-8-(hydroxymethyl)-2-methyl-6h,9h-oxepino[3,2-g]chromen-4-one

C15H14O5 (274.0841194)


   

9,10-dihydroxy-5-methoxy-2,8,8-trimethyl-9h,10h-pyrano[2,3-h]chromen-4-one

9,10-dihydroxy-5-methoxy-2,8,8-trimethyl-9h,10h-pyrano[2,3-h]chromen-4-one

C16H18O6 (306.11033280000004)


   

(1r,5r,11r,12s,15r,16s)-16-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

(1r,5r,11r,12s,15r,16s)-16-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

C24H28O8 (444.1784088)


   

(1s,5r,11s,12r,15s,16s)-16-(furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

(1s,5r,11s,12r,15s,16s)-16-(furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

C24H28O6 (412.1885788)


   

2-{[1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

2-{[1-(5-ethyl-6-methylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C35H60O6 (576.4389659999999)


   

4-hydroxy-7-(hydroxymethyl)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one

4-hydroxy-7-(hydroxymethyl)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one

C15H14O5 (274.0841194)


   

(2s)-5-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

(2s)-5-methoxy-2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C15H14O5 (274.0841194)


   

(9s,10r)-9,10-dihydroxy-5-methoxy-2,8,8-trimethyl-9h,10h-pyrano[2,3-h]chromen-4-one

(9s,10r)-9,10-dihydroxy-5-methoxy-2,8,8-trimethyl-9h,10h-pyrano[2,3-h]chromen-4-one

C16H18O6 (306.11033280000004)


   

5,7-dihydroxy-2-methyl-6-(3-methylbut-2-en-1-yl)chromen-4-one

5,7-dihydroxy-2-methyl-6-(3-methylbut-2-en-1-yl)chromen-4-one

C15H16O4 (260.1048536)


   

(1r,5r,11s,12r,15r,16r)-16-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

(1r,5r,11s,12r,15r,16r)-16-[(2s)-2-hydroxy-5-oxo-2h-furan-3-yl]-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

C24H28O8 (444.1784088)


   

6,7-dimethoxy-8-(3-methylbut-2-en-1-yl)chromen-2-one

6,7-dimethoxy-8-(3-methylbut-2-en-1-yl)chromen-2-one

C16H18O4 (274.1205028)


   

5-hydroxy-2,8-dimethyl-6h,9h-oxepino[3,2-g]chromen-4-one

5-hydroxy-2,8-dimethyl-6h,9h-oxepino[3,2-g]chromen-4-one

C15H14O4 (258.0892044)


   

5-methoxy-2,8,8-trimethylpyrano[2,3-f]chromen-4-one

5-methoxy-2,8,8-trimethylpyrano[2,3-f]chromen-4-one

C16H16O4 (272.1048536)


   

(2s)-4-hydroxy-7-(hydroxymethyl)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one

(2s)-4-hydroxy-7-(hydroxymethyl)-2-(prop-1-en-2-yl)-2h,3h-furo[3,2-g]chromen-5-one

C15H14O5 (274.0841194)


   

3-hydroxy-4-methoxy-2,6,14,17-tetramethyl-11-oxo-14-[(5-oxo-2h-furan-3-yl)methyl]-10-oxatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadec-12-en-16-yl acetate

3-hydroxy-4-methoxy-2,6,14,17-tetramethyl-11-oxo-14-[(5-oxo-2h-furan-3-yl)methyl]-10-oxatetracyclo[7.7.1.0²,⁷.0¹³,¹⁷]heptadec-12-en-16-yl acetate

C28H38O8 (502.2566548)


   

2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

2-(prop-1-en-2-yl)-2h,3h-[1,4]dioxino[2,3-g]chromen-7-one

C14H12O4 (244.0735552)


   

2'-methoxyhelikrausichalcone

2'-methoxyhelikrausichalcone

C21H22O5 (354.1467162)


   

(2r,6s)-2,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-en-1-yl)-2-[(2e)-3-phenylprop-2-enoyl]cyclohex-4-ene-1,3-dione

(2r,6s)-2,5-dihydroxy-6-methoxy-4,6-bis(3-methylbut-2-en-1-yl)-2-[(2e)-3-phenylprop-2-enoyl]cyclohex-4-ene-1,3-dione

C26H30O6 (438.204228)


   

(1's,2s,2's,4s,6'r,9's,10'r)-10'-(furan-3-yl)-5,5-dimethyl-4-[(2s)-2-methyl-5-oxofuran-2-yl]-5',11'-dioxaspiro[oxolane-2,4'-tetracyclo[7.3.1.0¹,⁹.0²,⁶]tridecan]-12'-one

(1's,2s,2's,4s,6'r,9's,10'r)-10'-(furan-3-yl)-5,5-dimethyl-4-[(2s)-2-methyl-5-oxofuran-2-yl]-5',11'-dioxaspiro[oxolane-2,4'-tetracyclo[7.3.1.0¹,⁹.0²,⁶]tridecan]-12'-one

C25H28O7 (440.1834938)


   

(9r,10s)-9,10-dihydroxy-5-methoxy-2,8,8-trimethyl-9h,10h-pyrano[2,3-h]chromen-4-one

(9r,10s)-9,10-dihydroxy-5-methoxy-2,8,8-trimethyl-9h,10h-pyrano[2,3-h]chromen-4-one

C16H18O6 (306.11033280000004)


   

7-hydroxy-6-methoxy-8-(3-methylbut-2-en-1-yl)chromen-2-one

7-hydroxy-6-methoxy-8-(3-methylbut-2-en-1-yl)chromen-2-one

C15H16O4 (260.1048536)


   

(2e)-1-[(3r)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]-3-phenylprop-2-en-1-one

(2e)-1-[(3r)-3,5-dihydroxy-7-methoxy-2,2-dimethyl-3,4-dihydro-1-benzopyran-6-yl]-3-phenylprop-2-en-1-one

C21H22O5 (354.1467162)


   

(1r,5r,11s,12r,15r,16r)-16-(furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

(1r,5r,11s,12r,15r,16r)-16-(furan-3-yl)-6,6,11,15-tetramethyl-7,17-dioxatetracyclo[13.2.1.0¹,¹².0⁵,¹¹]octadec-9-ene-3,8,18-trione

C24H28O6 (412.1885788)


   

6,7-dimethoxy-5-(3-methylbut-2-en-1-yl)chromen-2-one

6,7-dimethoxy-5-(3-methylbut-2-en-1-yl)chromen-2-one

C16H18O4 (274.1205028)


   

6-hydroxy-8,8-dimethylpyrano[3,2-f]chromen-3-one

6-hydroxy-8,8-dimethylpyrano[3,2-f]chromen-3-one

C14H12O4 (244.0735552)


   

6-hydroxy-7-methoxy-5-(3-methylbut-2-en-1-yl)chromen-2-one

6-hydroxy-7-methoxy-5-(3-methylbut-2-en-1-yl)chromen-2-one

C15H16O4 (260.1048536)


   

(1r,4r,5r,6s,8s,9r,10r)-5,6,9-trimethyltetracyclo[7.2.1.0¹,⁶.0⁸,¹⁰]dodecan-4-ol

(1r,4r,5r,6s,8s,9r,10r)-5,6,9-trimethyltetracyclo[7.2.1.0¹,⁶.0⁸,¹⁰]dodecan-4-ol

C15H24O (220.18270539999997)


   

(2e)-1-[(2s)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one

(2e)-1-[(2s)-4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one

C25H28O5 (408.1936638)


   

1-[4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one

1-[4,6-dihydroxy-2-(2-hydroxypropan-2-yl)-5-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzofuran-7-yl]-3-phenylprop-2-en-1-one

C25H28O5 (408.1936638)


   

(8s)-5,8-dihydroxy-8-(hydroxymethyl)-2-methyl-9h-oxepino[3,2-g]chromen-4-one

(8s)-5,8-dihydroxy-8-(hydroxymethyl)-2-methyl-9h-oxepino[3,2-g]chromen-4-one

C15H14O6 (290.0790344)