Chemical Formula: C15H12O7

Chemical Formula C15H12O7

Found 104 metabolite its formula value is C15H12O7

(+)-taxifolin

(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O7 (304.05830019999996)


Taxifolin, also known as dihydroquercetin or (+)-taxifolin, is a member of the class of compounds known as flavanonols. Flavanonols are compounds containing a flavan-3-one moiety, with a structure characterized by a 2-phenyl-3,4-dihydro-2H-1-benzopyran bearing a hydroxyl group and a ketone at the carbon C2 and C3, respectively. Taxifolin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Taxifolin can be found in a number of food items such as sweet rowanberry, arrowroot, evening primrose, and walnut, which makes taxifolin a potential biomarker for the consumption of these food products. Taxifolin is a flavanonol, a type of flavonoid . D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2]. Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2].

   

Dihydrotricetin

5,7,3,4,5-Pentahydroxyflavanone

C15H12O7 (304.05830019999996)


   

Taxifolin

4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, trans-(+/-)-

C15H12O7 (304.05830019999996)


(+)-taxifolin is a taxifolin that has (2R,3R)-configuration. It has a role as a metabolite. It is a conjugate acid of a (+)-taxifolin(1-). It is an enantiomer of a (-)-taxifolin. Taxifolin is a natural product found in Austrocedrus chilensis, Smilax corbularia, and other organisms with data available. See also: Milk Thistle (part of); Maritime Pine (part of). D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics A taxifolin that has (2R,3R)-configuration. D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2]. Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2].

   

Taxifolin

dihydroquercetin

C15H12O7 (304.05830019999996)


D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2]. Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2].

   

3-(3,4-dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propane-1,2-dione

3-(3,4-dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propane-1,2-dione

C15H12O7 (304.05830019999996)


   

Pratenol B

(2E)-3-(7-hydroxy-2H-chromen-3-yl)-4-oxohex-2-enedioic acid

C15H12O7 (304.05830019999996)


Pratenol B is found in herbs and spices. Pratenol B is a constituent of Trifolium pratense (red clover). Constituent of Trifolium pratense (red clover). Pratenol B is found in tea and herbs and spices.

   
   
   

3,4,5,6,7-pentahydroxyflavanone

3,4,5,6,7-pentahydroxyflavanone

C15H12O7 (304.05830019999996)


   

(2R)-2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one

2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-4-one

C15H12O7 (304.05830019999996)


Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2]. Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2].

   

2-(3,4-Dihydroxy-phenyl)-3,5,7-trihydroxy-chroman-4-one

2-(3,4-dihydroxyphenyl)-4,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-3-one

C15H12O7 (304.05830019999996)


   

3,5,7,2,6-Pentahydroxyflavanone

3,5,7,2,6-Pentahydroxyflavanone

C15H12O7 (304.05830019999996)


   

8-Hydroxyfustin

(2R,3R) -3,7,3,4,8-Pentahydroxyflavanone

C15H12O7 (304.05830019999996)


   

3,5,7,2,5-Pentahydroxyflavanone

3,5,7,2,5-Pentahydroxyflavanone

C15H12O7 (304.05830019999996)


   

Dihydrorobinetin

[ 2R,3R, (-) ] -3beta,3,4,5,7-Pentahydroxyflavanone

C15H12O7 (304.05830019999996)


Dihydrorobinetin is a natural product found in Robinia pseudoacacia and Adenanthera pavonina Dihydrorobinetin is a naturally occurring organic compound, classified as a flavanonol, which is a type of flavonoid. It is the dihydro derivative of robinetin, meaning it has two additional hydrogen atoms compared to robinetin. The chemical formula of dihydrorobinetin is C15H14O6. This compound is found in various plants and has been studied for its potential biological activities, including antioxidant and anti-inflammatory properties. Dihydrorobinetin, like other flavonoids, is known for its ability to scavenge free radicals and modulate cellular processes, which may contribute to its health benefits. (+)-Dihydrorobinetin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=4382-33-6 (retrieved 2024-07-12) (CAS RN: 4382-33-6). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

Onjixanthone II

1,3,6-Trihydroxy-2,7-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   

Nigrescin

2- [ (3,4-Dihydroxyphenyl) methyl ] -2,6,7-trihydroxybenzofuran-3 (2H) -one

C15H12O7 (304.05830019999996)


   
   

1,3,7-Trihydroxy-5,6-dimethoxyxanthone

1,3,7-Trihydroxy-5,6-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   

Nectriafurone

5,8-Dihydroxy-4,9-dione-3-(2-hydroxyethyl)-7-methoxynaphtho[2,3-c]furan

C15H12O7 (304.05830019999996)


   
   
   
   
   

(2R,3S)-3,7,8,3,4-Pentahydroxyflavanone

(2R,3S)-3,7,8,3,4-Pentahydroxyflavanone

C15H12O7 (304.05830019999996)


   

Alphitonin

2- [ (3,4-Dihydroxyphenyl) methyl ] -2,4,6-trihydroxy-3 (2H) -benzofuranone

C15H12O7 (304.05830019999996)


A hydroxyaurone that is aurone substituted by hydroxy groups at positions 2, 4, 6, 3 and 4 respectively. It has been isolated from Alphitonia excelsa.

   

Dihydromorin

(2R,3R)-2-(2,4-Dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-4H-1-benzopyran-4-one; (+)-Dihydromorin

C15H12O7 (304.05830019999996)


Dihydromorin is a natural product found in Broussonetia papyrifera, Artocarpus altilis, and other organisms with data available.

   

2,3,5,6,7-Pentahydroxyflavanone

2,3,5,6,7-Pentahydroxyflavanone

C15H12O7 (304.05830019999996)


   

7,8-Dimethoxy-1,3,6-trihyroxyxanthen-9-one

7,8-Dimethoxy-1,3,6-trihyroxyxanthen-9-one

C15H12O7 (304.05830019999996)


   

1,5,7-Trihydroxy-3,6-dimethoxy-9H-xanthene-9-one

1,5,7-Trihydroxy-3,6-dimethoxy-9H-xanthene-9-one

C15H12O7 (304.05830019999996)


   
   
   
   

3,7,8,3,4-pentahydroxy flavanone

3,7,8,3,4-pentahydroxy flavanone

C15H12O7 (304.05830019999996)


   
   
   
   
   

1,3,6-Trihydroxy-5,7-Dimethoxyxanthen-9-one

1,3,6-Trihydroxy-5,7-Dimethoxyxanthen-9-one

C15H12O7 (304.05830019999996)


   
   
   
   

1,5,6-trihydroxy-3,7-dimethoxyxanthone

1,5,6-trihydroxy-3,7-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   

2,6,8-Trihydroxy-1,5-dimethoxyxanthone

2,6,8-Trihydroxy-1,5-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   

1,5,8-trihydroxy-3,4-dimethoxyxanthone

1,5,8-trihydroxy-3,4-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   

1,6,7-Trihydroxy-3,5-Dimethoxyxanthen-9-one

1,6,7-Trihydroxy-3,5-Dimethoxyxanthen-9-one

C15H12O7 (304.05830019999996)


   

1,3,8-trihydroxy-5,7-dimethoxyxanthone

1,3,8-trihydroxy-5,7-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   

1,5,8-Trihydroxy-2,6-dimethoxyxanthone

1,5,8-Trihydroxy-2,6-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   

2-(cis-1,2-dihydroxy-4-oxo-cyclohex-5-enyl)-5,7-dihydroxychromone

2-(cis-1,2-dihydroxy-4-oxo-cyclohex-5-enyl)-5,7-dihydroxychromone

C15H12O7 (304.05830019999996)


   
   
   

1,7-Dimethoxy-2,3,8-trihydroxyxanthon|2,3,8-trihydroxy-1,7-dimethoxy-xanthen-9-one

1,7-Dimethoxy-2,3,8-trihydroxyxanthon|2,3,8-trihydroxy-1,7-dimethoxy-xanthen-9-one

C15H12O7 (304.05830019999996)


   

4,5,7,8-tetra-hydroxyflavanonol

4,5,7,8-tetra-hydroxyflavanonol

C15H12O7 (304.05830019999996)


   

1,6,8-Trihydroxy-2,3-dimethoxyxanthone

1,6,8-Trihydroxy-2,3-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   
   

Corymbiferin

1,3,8-trihydroxy-4,5-dimethoxy-9H-xanthen-9-one

C15H12O7 (304.05830019999996)


Corymbiferin is a natural product found in Gentiana orbicularis, Gentianopsis barbata, and other organisms with data available.

   

2-(3,4-Dihydroxy-phenyl)-2,5,7-trihydroxy-chroman-3-on|2-(3,4-dihydroxy-phenyl)-2,5,7-trihydroxy-chroman-3-one

2-(3,4-Dihydroxy-phenyl)-2,5,7-trihydroxy-chroman-3-on|2-(3,4-dihydroxy-phenyl)-2,5,7-trihydroxy-chroman-3-one

C15H12O7 (304.05830019999996)


   

3-Methyl-5,10-dihydroxy-7-methoxy-3,4-dihydro-1H-naphtho[2,3-c]pyran-1,6,9-trione

3-Methyl-5,10-dihydroxy-7-methoxy-3,4-dihydro-1H-naphtho[2,3-c]pyran-1,6,9-trione

C15H12O7 (304.05830019999996)


   

2-O-(4-hydroxybenzoyl)-2,4,6-trihydroxyphenylacetic acid

2-O-(4-hydroxybenzoyl)-2,4,6-trihydroxyphenylacetic acid

C15H12O7 (304.05830019999996)


   

1,3,6-trihydroxy-2,5-dimethoxyxanthone

1,3,6-trihydroxy-2,5-dimethoxyxanthone

C15H12O7 (304.05830019999996)


   

1,3,8-trihydroxy-2,4-dimethoxy-xanthen-9-one

1,3,8-trihydroxy-2,4-dimethoxy-xanthen-9-one

C15H12O7 (304.05830019999996)


   
   

1,3,5-trihydroxy-6,7-dimethoxy-9h-xanthen-9-one

1,3,5-trihydroxy-6,7-dimethoxy-9h-xanthen-9-one

C15H12O7 (304.05830019999996)


   

1,3,7-trihydroxy-5,6-dimethoxy-9h-xanthen-9-one

1,3,7-trihydroxy-5,6-dimethoxy-9h-xanthen-9-one

C15H12O7 (304.05830019999996)


   

globosuxanthone A

globosuxanthone A

C15H12O7 (304.05830019999996)


A member of the class of xanthones that is methyl 9-oxo-2,9-dihydro-1H-xanthene-1-carboxylate substituted by hydroxy groups at positions 1, 2 and 8 (the 1R,2R stereoisomer). Isolated from Chaetomium globosum, it exhibits cytotoxicity towards human tumour cell lines.

   
   
   
   
   
   

1-(3,4-dihydro xyphenyl)-3-(2,4,6-trihydroxyphenyl)-1,3-propanedione

1-(3,4-dihydro xyphenyl)-3-(2,4,6-trihydroxyphenyl)-1,3-propanedione

C15H12O7 (304.05830019999996)


   

(-)-Taxifolin

4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, (2S-trans)-

C15H12O7 (304.05830019999996)


(-)-taxifolin is the (2S,3S)-stereoisomer of taxifolin. It is an enantiomer of a (+)-taxifolin. (-)-Taxifolin is a natural product found in Acer mandshuricum, Artabotrys hexapetalus, and Bauhinia purpurea with data available. The (2S,3S)-stereoisomer of taxifolin.

   

2,3-Dihydro-2-hydroxyprotoapigenone

2-(cis-1,2-dihydroxy-4-oxo-cyclohex-5-enyl)-5,7-dihydroxychromone

C15H12O7 (304.05830019999996)


   

Taxifolin

(2R,3R)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-4H-1-benzopyran-4-one

C15H12O7 (304.05830019999996)


A pentahydroxyflavanone that is the 2,3-dihydro derivative of quercetin. D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents Origin: Plant; Formula(Parent): C15H12O7; Bottle Name:(+-)-Taxifolin; PRIME Parent Name:Dihydroquercetin; PRIME in-house No.:S0088, Pyrans relative retention time with respect to 9-anthracene Carboxylic Acid is 0.594 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.596 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.590 Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2]. Taxifolin ((+)-Dihydroquercetin) exhibits important anti-tyrosinase activity. Taxifolin exhibits significant inhibitory activity against collagenase with an IC50 value of 193.3 μM[1]. Taxifolin is an important natural compound with antifibrotic activity. Taxifolin is a free radical scavenger with antioxidant capacity[2].

   

(2R,3R)-2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one

NCGC00385208-01!(2R,3R)-2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one

C15H12O7 (304.05830019999996)


   

(2R,3R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one

NCGC00178041-02!(2R,3R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one

C15H12O7 (304.05830019999996)


   

8-hydroxy-7-methoxy-3-methyl-10-oxo-1H-pyrano[4,3-b]chromene-9-carboxylic acid

NCGC00381172-01!8-hydroxy-7-methoxy-3-methyl-10-oxo-1H-pyrano[4,3-b]chromene-9-carboxylic acid

C15H12O7 (304.05830019999996)


   

1,3,8-trihydroxy-4,5-dimethoxyxanthen-9-one

NCGC00385773-01!1,3,8-trihydroxy-4,5-dimethoxyxanthen-9-one

C15H12O7 (304.05830019999996)


   

(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one

NCGC00180750-02!(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one

C15H12O7 (304.05830019999996)


   

(2R,3R)-2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one

(2R,3R)-2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one

C15H12O7 (304.05830019999996)


   
   

Flavanone base + 5O

Flavanone base + 5O

C15H12O7 (304.05830019999996)


Annotation level-3

   

(2R,3R)-2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one_major

(2R,3R)-2-(2,6-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one_major

C15H12O7 (304.05830019999996)


   

5,7,3,4,5-Pentahydroxyflavanone

5,7,3,4,5-Pentahydroxyflavanone

C15H12O7 (304.05830019999996)


   

Pratenol B

(2E)-3-(7-hydroxy-2H-chromen-3-yl)-4-oxohex-2-enedioic acid

C15H12O7 (304.05830019999996)


   

2-(METHACRYLOYLOXY)ETHYL 1,3-DIOXO-1,3-DIHYDROISOBENZOFURAN-5-CARBOXYLATE

2-(METHACRYLOYLOXY)ETHYL 1,3-DIOXO-1,3-DIHYDROISOBENZOFURAN-5-CARBOXYLATE

C15H12O7 (304.05830019999996)


   

(+)-Epitaxifolin

(+)-Epitaxifolin

C15H12O7 (304.05830019999996)


A taxifolin that has (2S,3R)-configuration.

   

(-)-Epitaxifolin

(-)-Epitaxifolin

C15H12O7 (304.05830019999996)


A taxifolin that has (2R,3S)-configuration.

   
   

4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, (2R,3R)-

4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-2,3-dihydro-3,5,7-trihydroxy-, (2R,3R)-

C15H12O7 (304.05830019999996)


   

CHEBI:41963

(2S,3S)-2-(3,4-DIHYDROXYPHENYL)-3,5,7-TRIHYDROXY-2,3-DIHYDRO-4H-CHROMEN-4-ONE

C15H12O7 (304.05830019999996)


   

(3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydro-4H-chromen-4-one

(3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydro-4H-chromen-4-one

C15H12O7 (304.05830019999996)


   

(4S)-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-3,4,5,7-tetrol

(4S)-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-3,4,5,7-tetrol

C15H12O7 (304.05830019999996)


   

1-(2,3-Dihydroxy-5-methylphenyl)-2-(2,4,6-trihydroxyphenyl)ethane-1,2-dione

1-(2,3-Dihydroxy-5-methylphenyl)-2-(2,4,6-trihydroxyphenyl)ethane-1,2-dione

C15H12O7 (304.05830019999996)


   

(2R)-2-(3,4-dihydroxyphenyl)-2,5,7-trihydroxy-2,3-dihydro-4H-chromen-4-one

(2R)-2-(3,4-dihydroxyphenyl)-2,5,7-trihydroxy-2,3-dihydro-4H-chromen-4-one

C15H12O7 (304.05830019999996)


   

5,7-Dihydroxy-2-(2,3,4-trihydroxyphenyl)-2,3-dihydrochromen-4-one

5,7-Dihydroxy-2-(2,3,4-trihydroxyphenyl)-2,3-dihydrochromen-4-one

C15H12O7 (304.05830019999996)


   

3,3,4,5,7-Pentahydroxy-flavanone

(2R,3R)-3,7-Dihydroxy-2-(3,4,5-trihydroxyphenyl)chroman-4-one

C15H12O7 (304.05830019999996)


   

8-hydroxy-7-methoxy-3-methyl-10-oxo-1H-pyrano[4,3-b]chromene-9-carboxylic acid

8-hydroxy-7-methoxy-3-methyl-10-oxo-1H-pyrano[4,3-b]chromene-9-carboxylic acid

C15H12O7 (304.05830019999996)


   

(2S)-dihydrotricetin

(2S)-dihydrotricetin

C15H12O7 (304.05830019999996)


The (2S)-enantiomer of dihydrotricetin.

   

Dihydrotricetin

Dihydrotricetin

C15H12O7 (304.05830019999996)


A pentahydroxyflavanone that is flavanone substituted by hydroxy groups at positions 5, 7, 3, 4 and 5.