Chemical Formula: C13H8O5

Chemical Formula C13H8O5

Found 34 metabolite its formula value is C13H8O5

Gentisein

1,3,7-Trihydroxy-9H-xanthen-9-one, 9CI

C13H8O5 (244.0371718)


Gentisein is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 7. It has a role as a plant metabolite. It is a member of xanthones and a polyphenol. Gentisein is a natural product found in Hypericum scabrum, Cratoxylum formosum, and other organisms with data available. A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 3 and 7. Gentisein is found in alcoholic beverages. Gentisein is isolated from Gentiana lutea (yellow gentian Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].

   

Mesuaxanthone B

1,5,6-Trihydroxyxanthone

C13H8O5 (244.0371718)


A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1, 5 and 6.

   

1,3,5-Trihydroxyxanthone

1,3,5-Trihydroxyxanthone

C13H8O5 (244.0371718)


A member of the class of xanthones that is xanthone substituted by hydroxy groups at positions 1, 3 and 5. It has been isolated from Anaxagorea luzonensis.

   

Urolithin C

3,8,9-trihydroxy-6H-benzo[c]chromen-6-one

C13H8O5 (244.0371718)


Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].

   

urolithin M7

Urolithin M-7

C13H8O5 (244.0371718)


   

Urolithin C

3,8,9-trihydroxy-6H-benzo[c]chromen-6-one

C13H8O5 (244.0371718)


A polyphenol metabolite detected in biological fluids [PhenolExplorer] Urolithin C is a biomarker of nut consumption in urine. Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion. Urolithin C is a L-type Ca2+ channel opener and enhances Ca2+ influx. Urolithin C induces cell apoptosis through a mitochondria-mediated pathway and also stimulates reactive oxygen species (ROS) formation[1][2].

   

1,2,8-Trihydroxyxanthone

1,2,8-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,2,5-Trihydroxyxanthone

1,2,5-Trihydroxyxanthone

C13H8O5 (244.0371718)


A member of the class of xanthones that is 9H-xanthen-9-one substituted bybhydroxy groups at positions 1, 2 and 5. It is isolated from Garcinia subelliptica.

   

1,3,8-Trihydroxyxanthone

1,3,8-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,4,5-Trihydroxyxanthone

1,4,5-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,6,7-Trihydroxyxanthone

1,6,7-Trihydroxy-9H-xanthen-9-one

C13H8O5 (244.0371718)


   

2,4,7-Trihydroxyxanthone

2,4,7-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,3,6-Trihydroxyxanthone

1,3,6-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

Subelliptenone G

Subelliptenone G

C13H8O5 (244.0371718)


   

2,3,4-Trihydroxyxanthone

2,3,4-Trihydroxyxanthone

C13H8O5 (244.0371718)


   
   

7,8-Dihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione

7,8-Dihydroxy-1-methylnaphtho[2,3-c]furan-4,9-dione

C13H8O5 (244.0371718)


   
   

2,4,7-Trihydroxy-9H-xanthene-9-one

2,4,7-Trihydroxy-9H-xanthene-9-one

C13H8O5 (244.0371718)


   

3,4,5-Trihydroxy-9H-xanthen-9-one

3,4,5-Trihydroxy-9H-xanthen-9-one

C13H8O5 (244.0371718)


   
   

5-Hydroxy-7-methoxynaphtho[2,3-b]furan-4,9-dione

5-Hydroxy-7-methoxynaphtho[2,3-b]furan-4,9-dione

C13H8O5 (244.0371718)


   

1,4,8-trihydroxyxanthone

1,4,8-trihydroxyxanthone

C13H8O5 (244.0371718)


   

1,4,7-trihydroxyxanthone

1,4,7-trihydroxyxanthone

C13H8O5 (244.0371718)


   

8-Hydroxy-6-methoxynaphtho[2,3-b]furan-4,9-dione

8-Hydroxy-6-methoxynaphtho[2,3-b]furan-4,9-dione

C13H8O5 (244.0371718)


   

1,7,8-Trihydroxyxanthone

1,7,8-Trihydroxyxanthone

C13H8O5 (244.0371718)


   

Norneolambertellin

Norneolambertellin

C13H8O5 (244.0371718)


   
   

3,9,10-trihydro xydibenzo[b,d]pyran-6-one

3,9,10-trihydro xydibenzo[b,d]pyran-6-one

C13H8O5 (244.0371718)


   

5-hydroxy-6-methoxynaphtho<2,3-b>furan-4,9-quinone

5-hydroxy-6-methoxynaphtho<2,3-b>furan-4,9-quinone

C13H8O5 (244.0371718)


   
   

Gentisein

9H-Xanthen-9-one, 1,3,7-trihydroxy-

C13H8O5 (244.0371718)


Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2]. Gentisein (NSC 329491), the major metabolite of Mangiferin, shows the most potent serotonin uptake inhibition with an IC50 value of 4.7 μM[1][2].

   

AIDS-011160

1,3,5-trihydroxy-9-xanthenone

C13H8O5 (244.0371718)


   

1,5,6-Trihydroxyxanthone

1,5,6-Trihydroxyxanthone

C13H8O5 (244.0371718)