Chemical Formula: C20H20O4

Chemical Formula C20H20O4

Found 156 metabolite its formula value is C20H20O4

Corylifolinin

2-PROPEN-1-ONE, 1-(2,4-DIHYDROXY-3-(3-METHYL-2-BUTEN-1-YL)PHENYL)-3-(4-HYDROXYPHENYL)-, (2E)-

C20H20O4 (324.13615200000004)


Isobavachalcone is a member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 4, 2 and 4 and a prenyl group at position 3. It has a role as an antibacterial agent, a platelet aggregation inhibitor and a metabolite. It is a polyphenol and a member of chalcones. It is functionally related to a trans-chalcone. Isobavachalcone is a natural product found in Broussonetia papyrifera, Anthyllis hermanniae, and other organisms with data available. See also: Angelica keiskei top (part of). A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 4, 2 and 4 and a prenyl group at position 3. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1].

   

Glabranin

4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-8-(3-methyl-2-butenyl)-2-phenyl-, (2S)-

C20H20O4 (324.13615200000004)


Glabranin is a dihydroxyflavanone that is pinocembrin substituted by a prenyl group at position 8. It has a role as a plant metabolite. It is a dihydroxyflavanone and a (2S)-flavan-4-one. It is functionally related to a pinocembrin. Glabranin is a natural product found in Sophora tomentosa, Annona squamosa, and other organisms with data available. A dihydroxyflavanone that is pinocembrin substituted by a prenyl group at position 8. Saponin from licorice (Glycyrrhiza glabra). Glabranin B is found in tea and herbs and spices. Origin: Plant, Pyrans Glabranin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=41983-91-9 (retrieved 2024-07-09) (CAS RN: 41983-91-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

(R)-Glabridin

4-{8,8-dimethyl-2H,3H,4H,8H-pyrano[2,3-f]chromen-3-yl}benzene-1,3-diol

C20H20O4 (324.13615200000004)


(R)-Glabridin is found in herbs and spices. (R)-Glabridin is isolated from Glycyrrhiza glabra (licorice). Isolated from Glycyrrhiza glabra (licorice). (R)-Glabridin is found in tea and herbs and spices. C26170 - Protective Agent > C275 - Antioxidant > C306 - Bioflavonoid Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2]. Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2]. Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2].

   

Phaseollidin

15-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,14-diol

C20H20O4 (324.13615200000004)


Phaseollidin is found in common bean. Phaseollidin is isolated from kidney bean Phaseolus vulgaris, mung bean Phaseolus aureus, rice bean Phaseolus calcaratus, papadi Dolichos biflorus, and hyacinth bean Lablab niger.

   

Spathelia bischromene

2,2,6,6,10-Pentamethyl-2H,6H,12H-benzo[1,2-b:3,4-b:5,6-b]tripyran-12-one

C20H20O4 (324.13615200000004)


   

Phaseollinisoflavan

6-(7-hydroxy-3,4-dihydro-2H-1-benzopyran-3-yl)-2,2-dimethyl-2H-chromen-5-ol

C20H20O4 (324.13615200000004)


Phytoalexin from Phaseolus vulgaris (kidney bean), other Phaseolus subspecies and Glycyrrhiza glabra (licorice). Phaseollinisoflavan is found in many foods, some of which are green bean, yellow wax bean, herbs and spices, and common bean. Phaseollinisoflavan is found in common bean. Phytoalexin from Phaseolus vulgaris (kidney bean), other Phaseolus species and Glycyrrhiza glabra (licorice

   
   
   

(S)-5,7-Dihydroxy-6-prenylflavanone

5,7-dihydroxy-6-(3-methylbut-2-en-1-yl)-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one

C20H20O4 (324.13615200000004)


(S)-5,7-Dihydroxy-6-prenylflavanone is found in herbs and spices. (S)-5,7-Dihydroxy-6-prenylflavanone is a constituent of Glycyrrhiza glabra (licorice). Constituent of Glycyrrhiza glabra (licorice). (S)-5,7-Dihydroxy-6-prenylflavanone is found in tea and herbs and spices.

   

(E)-2',4,4'-Trihydroxy-3-prenylchalcone

(2E)-1-(2,4-dihydroxyphenyl)-3-[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]prop-2-en-1-one

C20H20O4 (324.13615200000004)


(E)-2,4,4-Trihydroxy-3-prenylchalcone is found in herbs and spices. (E)-2,4,4-Trihydroxy-3-prenylchalcone is a constituent of hairy root cultures of Glycyrrhiza glabra (licorice)

   

Moracin I

2-[5-hydroxy-3-methoxy-2-(3-methylbut-2-en-1-yl)phenyl]-1-benzofuran-6-ol

C20H20O4 (324.13615200000004)


Isolated from Morus alba (white mulberry) infected with Fusarium solani. Moracin I is found in mulberry and fruits. Moracin I is found in fruits. Moracin I is isolated from Morus alba (white mulberry) infected with Fusarium solani.

   

6-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0(2),.0(1)(1),(1)]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,14-diol

6-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0(2),.0(1)(1),(1)]heptadeca-2(7),3,5,11(16),12,14-hexaene-5,14-diol

C20H20O4 (324.13615200000004)


   

2,4,6-trihydroxy-3-c-prenylchalcone

2,4,6-trihydroxy-3-c-prenylchalcone

C20H20O4 (324.13615200000004)


   

Bavachalcone

1-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one

C20H20O4 (324.13615200000004)


Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1].

   

7-Hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

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

C20H20O4 (324.13615200000004)


   

Bavachin

(2S)-7-hydroxy-2-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

C20H20O4 (324.136152)


Bavachin is a natural product found in Broussonetia papyrifera, Cullen corylifolium, and other organisms with data available. Bavachin, a flavonoid first isolated from seeds of P. corylifolia, acts as a phytoestrogen that activates the estrogen receptors ERα and ERβ with EC50s of 320 and 680 nM, respectively. Bavachin, a flavonoid first isolated from seeds of P. corylifolia, acts as a phytoestrogen that activates the estrogen receptors ERα and ERβ with EC50s of 320 and 680 nM, respectively.

   

Glabridin

1,3-Benzenediol, 4-[(3R)-3,4-dihydro-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b]dipyran-3-yl]-; 1,3-Benzenediol, 4-(3,4-dihydro-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b]dipyran-3-yl)-, (R)-; 2H,8H-Benzo[1,2-b:3,4-b]dipyran, 1,3-benzenediol deriv.; 4-[(3R)-3,4-Dihydro-8,8-dimethyl-2H,8H-benzo[1,2-b:3,4-b]dipyran-3-yl]-1,3-benzenediol; Glabridin

C20H20O4 (324.13615200000004)


Glabridin is a member of the class of hydroxyisoflavans that is (R)-isoflavan substituted by hydroxy groups at positions 2 and 4 and a 2,2-dimethyl-2H-pyran group across positions 7 and 8 respectively. It has a role as an antiplasmodial drug. It derives from a hydride of a (R)-isoflavan. Glabridin is a natural product found in Ornithopus sativus, Glycyrrhiza glabra, and other organisms with data available. See also: Glycyrrhiza Glabra (part of). C26170 - Protective Agent > C275 - Antioxidant > C306 - Bioflavonoid Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2]. Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2]. Glabridin is a natural isoflavan from Glycyrrhiza uralensis, binds to and activates PPARγ, with an EC50 of 6115 nM. Glabridin exhibits antioxidant, anti-bacterial, anti-nephritic, anti-diabetic, anti-fungal, antitumor, anti-inflammatory, antiosteoporotic, cardiovascular protective, neuroprotective and radical scavenging activities[1][2].

   

Bavachalcone

(E) -1- [ 2,4-Dihydroxy-5- (3-methyl-2-butenyl) phenyl ] -3- (4-hydroxyphenyl) -2-propen-1-one

C20H20O4 (324.13615200000004)


Bavachalcone is a member of chalcones. Bavachalcone is a natural product found in Broussonetia papyrifera, Cullen corylifolium, and Sophora prostrata with data available. Bavachalcone is a compound isolated from psoralen. It is widely used in traditional Chinese medicine and has antibiotic and anti-cancer activities. Bavachalcone is a compound isolated from psoralen. It is widely used in traditional Chinese medicine and has antibiotic and anti-cancer activities.

   

Isobavachin

(2S)-7-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

C20H20O4 (324.136152)


Isobavachin is a member of flavanones. Isobavachin is a natural product found in Brosimum acutifolium, Erythrina sigmoidea, and other organisms with data available. Isobavachin, an antioxidant isaolated from Psoralea corylifolia with a prenyl group at position 8 of ring A, promotes neuronal differentiation and the potential role of its protein prenylation[1][2]. Isobavachin, an antioxidant isaolated from Psoralea corylifolia with a prenyl group at position 8 of ring A, promotes neuronal differentiation and the potential role of its protein prenylation[1][2].

   

Calocarpin

(6aR,11aR)-6a,11a-Dihydro-2-(3-methyl-2-buten-1-yl)-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol

C20H20O4 (324.13615200000004)


   

Eryvarin C

(3R)-2,4-Dihydroxy-6,6-dimethylpyrano[2,3:7,6]isoflavan

C20H20O4 (324.13615200000004)


   
   
   
   

7-O-Prenylpinocembrin

(S) -2,3-Dihydro-5-hydroxy-7- (prenyloxy) -2-phenyl-4H-1-benzopyran-4-one

C20H20O4 (324.13615200000004)


   

Lespedezol D2

(6aR,11aR)-3,9-Dihydroxy-6a-prenylpterocarpan

C20H20O4 (324.13615200000004)


   
   
   
   
   

Flemistrictin E

(E) -1- [ 2,3-Dihydro-4-hydroxy-2- (1-hydroxy-1-methylethyl) benzofuran-7-yl ] -3-phenyl-2-propen-1-one

C20H20O4 (324.13615200000004)


   
   
   

Flemistrictin F

(E) -1- (3,4-Dihydro-3,5-dihydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl) -3-phenyl-2-propen-1-one

C20H20O4 (324.13615200000004)


   
   

6-Carboxy-5-hydroxy-2,2-dimethyl-7-(2-phenylethyl)chromene

6-Carboxy-5-hydroxy-2,2-dimethyl-7-(2-phenylethyl)chromene

C20H20O4 (324.13615200000004)


   

Erythbidin A

(3R)-7,4-Dihydroxy-6,6-dimethylpyrano[2,3:2,3]isoflavan

C20H20O4 (324.13615200000004)


   
   
   

Artoindonesianin O

6,3-Dihydroxy-5-methoxy-4-prenyl-2-arylbenzofuran

C20H20O4 (324.13615200000004)


   

1-(1,3-Benzodioxole-5-yl)-2,3-dimethyl-6,7-(methylenedioxy)-1,2,3,4-tetrahydronaphthalene

1-(1,3-Benzodioxole-5-yl)-2,3-dimethyl-6,7-(methylenedioxy)-1,2,3,4-tetrahydronaphthalene

C20H20O4 (324.13615200000004)


   
   
   

Burttinol D

6,4-Dihydroxy-2-methoxy-6-(1,1-dimethyl-2-propenyl)-2-arylbenzofuran

C20H20O4 (324.13615200000004)


   

3,3-Dimethyl-5,6-pyrano-2,4-dihydroxychalcone

3,3-Dimethyl-5,6-pyrano-2,4-dihydroxychalcone

C20H20O4 (324.13615200000004)


   
   

Homoedudiol

3,9-Dihydroxy-8-prenylpterocarpan

C20H20O4 (324.13615200000004)


   
   

Crotaramosmin

8-(2,3-Dihydroxy-3-methylbutyl)-2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one

C20H20O4 (324.13615200000004)


   

Bidwillol B

6,4-Dihydroxy-2-methoxy-3-prenyl-2-arylbenzofuran

C20H20O4 (324.13615200000004)


   
   

Desmethylisoxanthohumol

2,4,6-Trihydroxy-3-prenylchalcone

C20H20O4 (324.13615200000004)


   

1-(2,5-dihydro-6,8-dihydroxy-3-methyl-1-benzoxepin-7-yl)-3-phenyl-1-propanone

1-(2,5-dihydro-6,8-dihydroxy-3-methyl-1-benzoxepin-7-yl)-3-phenyl-1-propanone

C20H20O4 (324.13615200000004)


   

2,6-Dihydroxy-4-prenyloxychalcone

2,6-Dihydroxy-4-prenyloxychalcone

C20H20O4 (324.13615200000004)


   

Dorsmanin A

5-Prenyl-6",6"-Dimethyl-4",5"-dihydropyrano [ 2",3":4,3 ] -4,2-dihydroxychalcone

C20H20O4 (324.13615200000004)


   

4-Hydroxycordoin

4,2-Dihydroxy-4-prenyloxychalcone

C20H20O4 (324.13615200000004)


A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at position 4 and 2 and a (3-methylbut-2-en-1-yl)oxy group at position 4. It has been isolated from Lonchocarpus neuroscapha.

   
   

crotmadine

4",5"-Dihydro-4,4-dihydroxy-6",6"-dimethylpyrano [ 2",3":3,2 ] chalcone

C20H20O4 (324.13615200000004)


   

Licoagrochalcone A

3-Prenyl-4,2,4-trihydroxychalcone

C20H20O4 (324.13615200000004)


   

Isoglabranin

5,7-Dihydroxy-6-C-prenylflavanone

C20H20O4 (324.13615200000004)


   
   

1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one

1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one

C20H20O4 (324.13615200000004)


   
   

dimethyl 2,4-diphenylcyclobutane-1,3-dicarboxylate

dimethyl 2,4-diphenylcyclobutane-1,3-dicarboxylate

C20H20O4 (324.13615200000004)


   
   
   
   
   
   

(E)-cinnamyl (E)-3,4-dimethoxycinnamate|(E)-cinnamyl (E)-O,O-dimethyl-caffeate|(E)-cinnamyl-(E)-O,O-dimethyl caffeate|cinnamyl 3,4-dimethoxycinnamate

(E)-cinnamyl (E)-3,4-dimethoxycinnamate|(E)-cinnamyl (E)-O,O-dimethyl-caffeate|(E)-cinnamyl-(E)-O,O-dimethyl caffeate|cinnamyl 3,4-dimethoxycinnamate

C20H20O4 (324.13615200000004)


   
   

5-(E)-propenyl-2-(2,4,5-trimethoxyphenyl)benzofuran|6-Demethoxy,5-methoxy-5-(1-Propenyl)-2-(2,4,6-trimethoxyphenyl)benzofuran

5-(E)-propenyl-2-(2,4,5-trimethoxyphenyl)benzofuran|6-Demethoxy,5-methoxy-5-(1-Propenyl)-2-(2,4,6-trimethoxyphenyl)benzofuran

C20H20O4 (324.13615200000004)


   
   

1,1,10-Trimethyl-3-hydroxy-7-isopropylanthracene-2,5,6(1H)-trione

1,1,10-Trimethyl-3-hydroxy-7-isopropylanthracene-2,5,6(1H)-trione

C20H20O4 (324.13615200000004)


   
   
   

(+)-teretifolione B|teretifolione B

(+)-teretifolione B|teretifolione B

C20H20O4 (324.13615200000004)


   

1-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one

1-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one

C20H20O4 (324.13615200000004)


   
   

2-(3,4-methylenedioxyphenyl)-5-(1,2-dihydroxypropyl)-3-methylbenzofuran

2-(3,4-methylenedioxyphenyl)-5-(1,2-dihydroxypropyl)-3-methylbenzofuran

C20H20O4 (324.13615200000004)


   

2,3-dihydro-3,7-dihydroxy-6-(3-methyl-2-butenyl)-2-phenyl-4h -1-benzopyran-4-one

2,3-dihydro-3,7-dihydroxy-6-(3-methyl-2-butenyl)-2-phenyl-4h -1-benzopyran-4-one

C20H20O4 (324.13615200000004)


   

2-(3,4-Dimethoxyphenyl)-3-methyl-7-(2-propenyl)benzofuran-5-ol

2-(3,4-Dimethoxyphenyl)-3-methyl-7-(2-propenyl)benzofuran-5-ol

C20H20O4 (324.13615200000004)


   
   
   
   

Cneorum-chromom-G|Cneorum-Chromon-G|Neochamelin

Cneorum-chromom-G|Cneorum-Chromon-G|Neochamelin

C20H20O4 (324.13615200000004)


   

2,2-Dimethyl-5-hydroxy-7-(2-phenylethyl)-2H-1-benzopyran-6-carboxylic acid

2,2-Dimethyl-5-hydroxy-7-(2-phenylethyl)-2H-1-benzopyran-6-carboxylic acid

C20H20O4 (324.13615200000004)


   
   

Sanggenofuran B

5-(6-methoxy-1-benzofuran-2-yl)-2-(3-methylbut-2-enyl)benzene-1,3-diol

C20H20O4 (324.13615200000004)


Sanggenofuran B is a natural product found in Morus cathayana with data available.

   

1-(4-hydroxy-3-methoxyphenyl)-7-phenyl-5-hydroxy-4,6-heptadiene-3-one

1-(4-hydroxy-3-methoxyphenyl)-7-phenyl-5-hydroxy-4,6-heptadiene-3-one

C20H20O4 (324.13615200000004)


   

(E)-1-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one

(E)-1-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one

C20H20O4 (324.13615200000004)


   
   

O(C)c1c(C/C=C(\C)/C)c(O)cc(-c2oc3c(c2)ccc(O)c3)c1

O(C)c1c(C/C=C(\C)/C)c(O)cc(-c2oc3c(c2)ccc(O)c3)c1

C20H20O4 (324.13615200000004)


   
   
   
   
   

3alpha-hydroxy-9(10->20)abeo-abieta-1,5,8,10(20),13-pentaene-7,11,12-trione

3alpha-hydroxy-9(10->20)abeo-abieta-1,5,8,10(20),13-pentaene-7,11,12-trione

C20H20O4 (324.13615200000004)


   
   
   
   

4-O-(3-Methyl-2-butenyl)-2,4,6-Trihydroxychalcone

4-O-(3-Methyl-2-butenyl)-2,4,6-Trihydroxychalcone

C20H20O4 (324.13615200000004)


   
   
   
   

1-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dimethylnaphthalen-6-ol

1-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dimethylnaphthalen-6-ol

C20H20O4 (324.13615200000004)


   
   

(+-)-alpha-truxillic acid monoethyl ester|(+-)-alpha-Truxillsaeure-monoaethylester

(+-)-alpha-truxillic acid monoethyl ester|(+-)-alpha-Truxillsaeure-monoaethylester

C20H20O4 (324.13615200000004)


   

(2RS,3RS)-3,7-Dihydroxy-8-prenylflavanone

(2RS,3RS)-3,7-Dihydroxy-8-prenylflavanone

C20H20O4 (324.13615200000004)


   

licarinB

5-((2R,3R)-7-methoxy-3-methyl-5-((E)-prop-1-en-1-yl)-2,3-dihydrobenzofuran-2-yl)benzo[d][1,3]dioxole

C20H20O4 (324.13615200000004)


Licarin B is a natural product found in Magnolia kachirachirai, Licaria guianensis, and other organisms with data available. Licarin B, a nitric oxide production inhibitor extracted from the component of the seeds of Myristica fragrans, improves insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway[1][2][3]. Licarin B, a nitric oxide production inhibitor extracted from the component of the seeds of Myristica fragrans, improves insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway[1][2][3]. Licarin B, a nitric oxide production inhibitor extracted from the component of the seeds of Myristica fragrans, improves insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway[1][2][3]. Licarin B, a nitric oxide production inhibitor extracted from the component of the seeds of Myristica fragrans, improves insulin sensitivity via PPARγ and activation of GLUT4 in the IRS-1/PI3K/AKT pathway[1][2][3].

   

5,7-dihydroxy-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one

NCGC00169676-02!5,7-dihydroxy-8-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one

C20H20O4 (324.13615200000004)


   

7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one

NCGC00385490-01!7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one

C20H20O4 (324.13615200000004)


   

(E)-1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one

NCGC00384540-01!(E)-1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one

C20H20O4 (324.13615200000004)


   

Isobavachalcone

(E)-1-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one

C20H20O4 (324.136152)


Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1]. Isobavachalcone (Corylifolinin) is derived from Psoralea corylifolia Linn. and is a potent inhibitor of Akt signaling pathway, which induces apoptosis in human cancer cells (Inhibits OVCAR-8 cell growth with an IC50 value of 7.92 μM). Isobavachalcone also induces Reactive Oxyen Species (ROS) generation in OVCAR-8 cells and has exhibit cancer anti-promotive and anti-proliferative activity[1].

   

C20H20O4_6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2-(3-methyl-2-buten-1-yl)-, (6aR,11aR)

NCGC00347827-02_C20H20O4_6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-2-(3-methyl-2-buten-1-yl)-, (6aR,11aR)-

C20H20O4 (324.13615200000004)


   

C20H20O4_1,3-Benzenediol, 4-[3,4,8,9-tetrahydro-8-(1-methylethenyl)-2H-furo[2,3-h]-1-benzopyran-3-yl]

NCGC00347653-02_C20H20O4_1,3-Benzenediol, 4-[3,4,8,9-tetrahydro-8-(1-methylethenyl)-2H-furo[2,3-h]-1-benzopyran-3-yl]-

C20H20O4 (324.13615200000004)


   

(E)-1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one

(E)-1-(2,4-dihydroxyphenyl)-3-[4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-one

C20H20O4 (324.13615200000004)


   

4-(8-prop-1-en-2-yl-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-3-yl)benzene-1,3-diol

4-(8-prop-1-en-2-yl-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-3-yl)benzene-1,3-diol

C20H20O4 (324.13615200000004)


   
   

Flavanone base + 2O, 1Prenyl

Flavanone base + 2O, 1Prenyl

C20H20O4 (324.13615200000004)


Annotation level-3 Annotation level-2

   

Chalcone base + 3O, 1Prenyl

Chalcone base + 3O, 1Prenyl

C20H20O4 (324.13615200000004)


Annotation level-3

   

4-(8-prop-1-en-2-yl-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-3-yl)benzene-1,3-diol_major

4-(8-prop-1-en-2-yl-3,4,8,9-tetrahydro-2H-furo[2,3-h]chromen-3-yl)benzene-1,3-diol_major

C20H20O4 (324.13615200000004)


   
   

5,7-Dihydroxy-6-C-prenylflavanone

5,7-Dihydroxy-6-C-prenylflavanone

C20H20O4 (324.13615200000004)


   

moracin I

2-[5-hydroxy-3-methoxy-2-(3-methylbut-2-en-1-yl)phenyl]-1-benzofuran-6-ol

C20H20O4 (324.13615200000004)


   
   

1,1,3-TRIMETHYL-3-PHENYLINDAN-4,5-DICARBOXYLIC ACID

1,1,3-TRIMETHYL-3-PHENYLINDAN-4,5-DICARBOXYLIC ACID

C20H20O4 (324.13615200000004)


   

Des(diethylaMinoethyl)-didesiodo-1-Methoxy AMiodarone

Des(diethylaMinoethyl)-didesiodo-1-Methoxy AMiodarone

C20H20O4 (324.13615200000004)


   

6-Hydroxy-3-methyl-8-(2-phenylethyl)-2,5-dihydro-1-benzoxepine-7-carboxylic acid

6-Hydroxy-3-methyl-8-(2-phenylethyl)-2,5-dihydro-1-benzoxepine-7-carboxylic acid

C20H20O4 (324.13615200000004)


   

7-(4-Hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)hepta-4,6-dien-3-one

7-(4-Hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)hepta-4,6-dien-3-one

C20H20O4 (324.13615200000004)


   

7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

7-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one

C20H20O4 (324.13615200000004)


   

2,4-Dihydroxy-4-prenyloxychalcone

2,4-Dihydroxy-4-prenyloxychalcone

C20H20O4 (324.13615200000004)


   

phaseollidin

6H-Benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-10-(3-methyl-2-butenyl)-, (6aR,11aR)-

C20H20O4 (324.13615200000004)


Phaseollidin is a member of the class of compounds known as pterocarpans. Pterocarpans are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. Phaseollidin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Phaseollidin can be found in a number of food items such as hyacinth bean, lima bean, yellow wax bean, and scarlet bean, which makes phaseollidin a potential biomarker for the consumption of these food products.

   

(-)-Phaseolin

(-)-Phaseolin

C20H20O4 (324.13615200000004)


A prenylated member of the class of pterocarpans and an organic heteropentacyclic compound that is 2,3,6b,12b-tetrahydro-1H,7H-chromeno[6,5:4,5]furo[3,2-c]chromen-10-ol in which both of the hydrogens at position 3 have been replaced by methyl groups (the R,R stereoisomer). It is found in found in the seeds of Phaseolus vulgaris (French bean) and in the stems of Erythrina subumbrans.

   

3-(5-Hydroxy-2,2-dimethylchromen-6-yl)-1-(4-hydroxyphenyl)propan-1-one

3-(5-Hydroxy-2,2-dimethylchromen-6-yl)-1-(4-hydroxyphenyl)propan-1-one

C20H20O4 (324.13615200000004)


   

Phaseollinisoflavan

(-)-Phaseollinisoflavan

C20H20O4 (324.13615200000004)


   

(-)-Phaseollinisoflavan

(-)-Phaseollinisoflavan

C20H20O4 (324.13615200000004)


A member of the class of hydroxyisoflavans that is (3R)-3,4-dihydro-2H,2H-3,6-bichromene substituted by two methyl groups at positions 2 and 2 and hydroxy groups at positions 5 and 7 respectively.

   

(2s)-5-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]-2-phenyl-2,3-dihydro-1-benzopyran-4-one

(2s)-5-hydroxy-7-[(3-methylbut-2-en-1-yl)oxy]-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C20H20O4 (324.13615200000004)


   

5-methoxy-2,2-dimethyl-6-(3-methylbuta-1,3-dien-1-yl)pyrano[2,3-h]chromen-8-one

5-methoxy-2,2-dimethyl-6-(3-methylbuta-1,3-dien-1-yl)pyrano[2,3-h]chromen-8-one

C20H20O4 (324.13615200000004)


   

2-(4-hydroxy-2-methoxyphenyl)-5-(3-methylbut-2-en-1-yl)-1-benzofuran-6-ol

2-(4-hydroxy-2-methoxyphenyl)-5-(3-methylbut-2-en-1-yl)-1-benzofuran-6-ol

C20H20O4 (324.13615200000004)


   

8-(7-hydroxy-3,4-dihydro-2h-1-benzopyran-3-yl)-2,2-dimethylchromen-5-ol

8-(7-hydroxy-3,4-dihydro-2h-1-benzopyran-3-yl)-2,2-dimethylchromen-5-ol

C20H20O4 (324.13615200000004)


   

5,7-dihydroxy-8-(3-methylbut-1-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

5,7-dihydroxy-8-(3-methylbut-1-en-1-yl)-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C20H20O4 (324.13615200000004)


   

(2e)-1-{2,6-dihydroxy-4-[(3-methylbut-2-en-1-yl)oxy]phenyl}-3-phenylprop-2-en-1-one

(2e)-1-{2,6-dihydroxy-4-[(3-methylbut-2-en-1-yl)oxy]phenyl}-3-phenylprop-2-en-1-one

C20H20O4 (324.13615200000004)


   

(1r,10r)-15-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaene-5,14-diol

(1r,10r)-15-(3-methylbut-2-en-1-yl)-8,17-dioxatetracyclo[8.7.0.0²,⁷.0¹¹,¹⁶]heptadeca-2,4,6,11(16),12,14-hexaene-5,14-diol

C20H20O4 (324.13615200000004)


   

(2s,4r)-11-hydroxy-4-methyl-9-(2-phenylethyl)-6-oxatricyclo[5.4.0.0²,⁴]undeca-1(11),7,9-triene-10-carboxylic acid

(2s,4r)-11-hydroxy-4-methyl-9-(2-phenylethyl)-6-oxatricyclo[5.4.0.0²,⁴]undeca-1(11),7,9-triene-10-carboxylic acid

C20H20O4 (324.13615200000004)


   

4b,9-dihydroxy-7-methoxy-11,11-dimethyl-10h,10ah-benzo[b]fluoren-5-one

4b,9-dihydroxy-7-methoxy-11,11-dimethyl-10h,10ah-benzo[b]fluoren-5-one

C20H20O4 (324.13615200000004)


   

(4e,6e)-7-(4-hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)hepta-4,6-dien-3-one

(4e,6e)-7-(4-hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)hepta-4,6-dien-3-one

C20H20O4 (324.13615200000004)


   

5-{6,7-dimethyl-2h,5h,6h,7h,8h-naphtho[2,3-d][1,3]dioxol-5-yl}-2h-1,3-benzodioxole

5-{6,7-dimethyl-2h,5h,6h,7h,8h-naphtho[2,3-d][1,3]dioxol-5-yl}-2h-1,3-benzodioxole

C20H20O4 (324.13615200000004)


   

7-hydroxy-3-isopropyl-5,5,9-trimethylanthracene-1,2,6-trione

7-hydroxy-3-isopropyl-5,5,9-trimethylanthracene-1,2,6-trione

C20H20O4 (324.13615200000004)


   

6-[9-(furan-2-yl)nona-2,4,6,8-tetraen-2-yl]-4-methoxy-3-methylpyran-2-one

6-[9-(furan-2-yl)nona-2,4,6,8-tetraen-2-yl]-4-methoxy-3-methylpyran-2-one

C20H20O4 (324.13615200000004)


   

2-[3-hydroxy-5-methoxy-4-(3-methylbut-2-en-1-yl)phenyl]-1-benzofuran-6-ol

2-[3-hydroxy-5-methoxy-4-(3-methylbut-2-en-1-yl)phenyl]-1-benzofuran-6-ol

C20H20O4 (324.13615200000004)


   

(2s)-7-hydroxy-8-[(1z)-3-hydroxy-3-methylbut-1-en-1-yl]-2-phenyl-2,3-dihydro-1-benzopyran-4-one

(2s)-7-hydroxy-8-[(1z)-3-hydroxy-3-methylbut-1-en-1-yl]-2-phenyl-2,3-dihydro-1-benzopyran-4-one

C20H20O4 (324.13615200000004)


   

5-[(1e)-prop-1-en-1-yl]-2-(2,4,6-trimethoxyphenyl)-1-benzofuran

5-[(1e)-prop-1-en-1-yl]-2-(2,4,6-trimethoxyphenyl)-1-benzofuran

C20H20O4 (324.13615200000004)