Exact Mass: 212.0473

Exact Mass Matches: 212.0473

Found 24 metabolites which its exact mass value is equals to given mass value 212.0473, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

Urolithin B

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

C13H8O3 (212.0473)


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 (212.0473)


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 (212.0473)


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 (212.0473)


   

1-Hydroxyxanthone

1-Hydroxyxanthone

C13H8O3 (212.0473)


   

Peniophorin B

Peniophorin B

C13H8O3 (212.0473)


   

SIEBER LINKER

SIEBER LINKER

C13H8O3 (212.0473)


   

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

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

C13H8O3 (212.0473)


   

urolithin B

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

C13H8O3 (212.0473)


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 (212.0473)


   

4-Hydroxyxanthone

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

C13H8O3 (212.0473)


   

2,7-Dihydroxy-9-fluorenone

2,7-Dihydroxy-9-fluorenone

C13H8O3 (212.0473)


   

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

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

C13H8O3 (212.0473)


   

5-(Phenylethynyl)furan-2-carboxylic acid

5-(Phenylethynyl)furan-2-carboxylic acid

C13H8O3 (212.0473)


   

Dibenzofuran-3-carboxylic acid

Dibenzofuran-3-carboxylic acid

C13H8O3 (212.0473)


   

2-dibenzofurancarboxylic acid

2-dibenzofurancarboxylic acid

C13H8O3 (212.0473)


   

3-hydroxy-9H-9-xanthenone

3-hydroxy-9H-9-xanthenone

C13H8O3 (212.0473)


   

(R)-1-(6-chloro-9H-purin-9-yl)propan-2-ol

(R)-1-(6-chloro-9H-purin-9-yl)propan-2-ol

C8H9ClN4O (212.0465)


   

Isourolithin B

Isourolithin B

C13H8O3 (212.0473)


   

Depsidone

Depsidone

C13H8O3 (212.0473)


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 (212.0473)


   

1-hydroxyxanthen-9-one

1-hydroxyxanthen-9-one

C13H8O3 (212.0473)


   

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

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

C13H8O3 (212.0473)


   

3-hydroxyxanthen-9-one

3-hydroxyxanthen-9-one

C13H8O3 (212.0473)