Chemical Formula: C13H8O3

Chemical Formula C13H8O3

Found 23 metabolite its formula value is C13H8O3

Urolithin B

3-hydroxy-6H-benzo[c]chromen-6-one

C13H8O3 (212.0473418)


Urolithin B is a secondary metabolite of ellagic acid which may be glucuronidated by liver enzymes during phase II metabolism. A polyphenol metabolite detected in biological fluids [PhenolExplorer] Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4]. Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects. Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK. Urolithin B is also a regulator of skeletal muscle mass[1][2]. Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4]. Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects. Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK. Urolithin B is also a regulator of skeletal muscle mass[1][2].

   

2-Hydroxyxanthone

2-Hydroxy-9H-xanthen-9-one, 9ci

C13H8O3 (212.0473418)


2-Hydroxyxanthone belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. 2-Hydroxyxanthone exists as a solid and is considered to be practically insoluble (in water) and relatively neutral. Within the cell, 2-hydroxyxanthone is primarily located in the membrane (predicted from logP). Outside of the human body, 2-hydroxyxanthone can be found in fruits, herbs and spices, and mammee apple. This makes 2-hydroxyxanthone a potential biomarker for the consumption of these food products. Constituent of Hypericum subspecies, Mammea americana (mamey). 2-Hydroxyxanthone is found in herbs and spices, fruits, and mammee apple.

   

4-Hydroxyxanthone

4-Hydroxy-9H-xanthen-9-one, 9ci

C13H8O3 (212.0473418)


4-Hydroxyxanthone is found in fruits. 4-Hydroxyxanthone is from seeds of Mammea americana (mamey). From seeds of Mammea americana (mamey). 4-Hydroxyxanthone is found in fruits.

   

5-(Phenylethynyl)furan-2-carboxylic acid

5-(2-phenylethynyl)furan-2-carboxylic acid

C13H8O3 (212.0473418)


   

1-Hydroxyxanthone

1-Hydroxyxanthone

C13H8O3 (212.0473418)


   
   
   

1H-Naphtho[2,3-c]pyran-5,10-dione

1H-Naphtho[2,3-c]pyran-5,10-dione

C13H8O3 (212.0473418)


   

urolithin B

3-hydroxy-6H-benzo[c]chromen-6-one

C13H8O3 (212.0473418)


Coumarins Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4]. Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects. Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK. Urolithin B is also a regulator of skeletal muscle mass[1][2]. Urolithin B is one of Ellagitannins' slow microbial products, and has anti-inflammatory and anti-inflammatory effects. Urolithin B suppresses NF-κB activity. Urolithin B suppresses JNK, ERK and Akt's oxidation, and increases AMPK's oxidation. Urolithin B is also a quantitative change factor for bone and skin quality[1][2][3][4]. Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects. Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK. Urolithin B is also a regulator of skeletal muscle mass[1][2].

   

2-Hydroxyxanthone

2-Hydroxyxanthone

C13H8O3 (212.0473418)


   

4-Hydroxyxanthone

4-Hydroxy-9H-xanthen-9-one, 9ci

C13H8O3 (212.0473418)


   

2,7-Dihydroxy-9-fluorenone

2,7-Dihydroxy-9-fluorenone

C13H8O3 (212.0473418)


   

Dibenzo[b,d]furan-4-carboxylic acid

Dibenzo[b,d]furan-4-carboxylic acid

C13H8O3 (212.0473418)


   

5-(Phenylethynyl)furan-2-carboxylic acid

5-(Phenylethynyl)furan-2-carboxylic acid

C13H8O3 (212.0473418)


   

Dibenzofuran-3-carboxylic acid

Dibenzofuran-3-carboxylic acid

C13H8O3 (212.0473418)


   

2-dibenzofurancarboxylic acid

2-dibenzofurancarboxylic acid

C13H8O3 (212.0473418)


   

3-hydroxy-9H-9-xanthenone

3-hydroxy-9H-9-xanthenone

C13H8O3 (212.0473418)


   
   

Depsidone

Depsidone

C13H8O3 (212.0473418)


The simplest member of the class of depsidones comprising of a heterotricyclic system that is 11H-dibenzo[b,e][1,4]dioxepine substituted by an oxo group at position 11.

   

2-hydroxy-9-xanthenone

2-hydroxy-9-xanthenone

C13H8O3 (212.0473418)


   

1-hydroxyxanthen-9-one

1-hydroxyxanthen-9-one

C13H8O3 (212.0473418)


   

1h-benzo[g]isochromene-5,10-dione

1h-benzo[g]isochromene-5,10-dione

C13H8O3 (212.0473418)


   

3-hydroxyxanthen-9-one

3-hydroxyxanthen-9-one

C13H8O3 (212.0473418)