Chemical Formula: C7H10O6

Chemical Formula C7H10O6

Found 29 metabolite its formula value is C7H10O6

3-Dehydroquinic acid

(1R,3R,4S)-1,3,4-trihydroxy-5-oxocyclohexane-1-carboxylic acid

C7H10O6 (190.04773600000001)


3-Dehydroquinic acid belongs to the class of organic compounds known as alpha-hydroxy acids and derivatives. These are organic compounds containing a carboxylic acid substituted with a hydroxyl group on the adjacent carbon. 3-Dehydroquinic acid is an extremely weak basic (essentially neutral) compound (based on its pKa). In most organisms, 3-dehydroquinic acid is synthesized from D-erythrose-4-phosphate in two steps. However, archaea genomes contain no orthologs for the genes that encode these first two steps. Instead, archaeabacteria appear to utilize an alternative pathway in which 3-dehydroquinic acid is synthesized from 6-deoxy-5-ketofructose-1-phosphate and L-aspartate-semialdehyde. These two compounds are first condensed to form 2-amino-3,7-dideoxy-D-threo-hept-6-ulosonate, which cyclizes to 3-dehydroquinic acid. From 3-dehydroquinic acid and on to chorismate, the archaeal pathway appears to be identical to the bacterial pathway. In most organisms, 3-dehydroquinate is synthesized from D-erythrose-4-phosphate in two steps . However, the genomes of the archaea contain no orthologs for the genes that encode these first two steps. Instead, archaeabacteria appear to utilize an alternative pathway in which 3-dehydroquinate is synthesized from 6-deoxy-5-ketofructose-1-phosphate and L-aspartate-semialdehyde . These two compounds are first condensed to form 2-amino-3,7-dideoxy-D-threo-hept-6-ulosonate , which cyclizes to 3-dehydroquinate . From 3-dehydroquinate and on to chorismate , the archaeal pathway appears to be identical to the bacterial pathway [HMDB]. 3-Dehydroquinate is found in many foods, some of which are allium (onion), cashew nut, american cranberry, and common wheat.

   

4-Hydroxy-4-methyl-2-oxoadipate

4-Hydroxy-4-methyl-2-oxohexanedioic acid

C7H10O6 (190.04773600000001)


   

4-Hydroxy-2-oxoheptanedioic acid

4-Hydroxy-2-oxoheptanedioic acid

C7H10O6 (190.04773600000001)


   

2,4-dihydroxy-2-heptenedioc acid

2,4-Dihydroxyhept-2-enedioic acid

C7H10O6 (190.04773600000001)


   
   

2-Hydroxy-2-(2-oxopropyl)butanedioic acid

2-Hydroxy-2-(2-oxopropyl)butanedioic acid

C7H10O6 (190.04773600000001)


2-Hydroxy-2-(2-oxopropyl)butanedioic acid belongs to the family of Medium-chain Keto Acids and Derivatives. These are keto acids with a 6 to 12 carbon atoms long side chain.

   

2-O-Methylascorbic acid

(5R)-5-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-3-methoxy-2,5-dihydrofuran-2-one

C7H10O6 (190.04773600000001)


2-O-Methylascorbic acid (2-O-MA) is a derivative of vitamin C (ascorbic acid). The enzyme catechol-O-methyltransferase catalyzes the methylation of L-ascorbic acid into 2-O-methylascorbic acid (PMID: 7129800). 2-O-Methylascorbic acid belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom. 2-O-Methylascorbic acid has been identified in urine and was found to be higher in older women than in younger women (PMID: 28813537).

   

4-hydroxy-2-oxo-Heptanedioic acid

4-hydroxy-2-oxo-Heptanedioic acid

C7H10O6 (190.04773600000001)


   

FA 7:2;O4

(4R,5S)-4,5-dihydroxy-2,6-dioxoheptanoic acid;3,7-dideoxy-D-threo-hepto-2,6-diuolosonic acid

C7H10O6 (190.04773600000001)


   

1,2,4-Butanetricarboxylic acid

1,2,4-Butanetricarboxylic acid

C7H10O6 (190.04773600000001)


   
   

1,3,5-O-METHYLIDYNE-MYO-INOSITOL

1,3,5-O-METHYLIDYNE-MYO-INOSITOL

C7H10O6 (190.04773600000001)


   

1,3-DIOXOLANE-2,2-DIACETIC ACID

1,3-DIOXOLANE-2,2-DIACETIC ACID

C7H10O6 (190.04773600000001)


   

trimethylmethane tricarboxylate

trimethylmethane tricarboxylate

C7H10O6 (190.04773600000001)


   

Methyl 4-deoxy-alpha-L-threo-hex-4-enopyranosiduronic acid

Methyl 4-deoxy-alpha-L-threo-hex-4-enopyranosiduronic acid

C7H10O6 (190.04773600000001)


   

2-Hydroxy-2-methylpropane-1,2,3-tricarboxylic acid

2-Hydroxy-2-methylpropane-1,2,3-tricarboxylic acid

C7H10O6 (190.04773600000001)


   

4-deoxy-6-O-methyl-L-threo-hex-4-enopyranuronate

4-deoxy-6-O-methyl-L-threo-hex-4-enopyranuronate

C7H10O6 (190.04773600000001)


   

(S)-4-hydroxy-2-oxoheptanedioic acid

(S)-4-hydroxy-2-oxoheptanedioic acid

C7H10O6 (190.04773600000001)


   

1,4,5-Trihydroxy-5-hydroxymethyl-cyclohex-1-en-3-one

1,4,5-Trihydroxy-5-hydroxymethyl-cyclohex-1-en-3-one

C7H10O6 (190.04773600000001)


   

3-Dehydroquinic acid

3-Dehydroquinic acid

C7H10O6 (190.04773600000001)


A 4-oxo monocarboxylic acid derived from quinic acid by oxidation of the hydroxy group at position 3 to the corresponding keto group.

   

2,4-Dihydroxyhept-2-enedioic acid

2,4-Dihydroxyhept-2-enedioic acid

C7H10O6 (190.04773600000001)


   

2-Hydroxy-2-(2-oxopropyl)butanedioic acid

2-Hydroxy-2-(2-oxopropyl)butanedioic acid

C7H10O6 (190.04773600000001)


   

1,3,4-Trihydroxy-5-oxocyclohexane-1-carboxylic acid

1,3,4-Trihydroxy-5-oxocyclohexane-1-carboxylic acid

C7H10O6 (190.04773600000001)


   

3,7-dideoxy-D-threo-hepto-2,6-diuolosonic acid

3,7-dideoxy-D-threo-hepto-2,6-diuolosonic acid

C7H10O6 (190.04773600000001)


   
   

2,4-Dihydroxy-2-heptenedioic acid

2,4-Dihydroxy-2-heptenedioic acid

C7H10O6 (190.04773600000001)


   
   

Hydroxy-oxo-heptanedioic acid

Hydroxy-oxo-heptanedioic acid

C7H10O6 (190.04773600000001)