Chemical Formula: C6H12O4

Chemical Formula C6H12O4

Found 87 metabolite its formula value is C6H12O4

Mevalonic acid

beta,delta-Dihydroxy-beta-methylvaleric acid

C6H12O4 (148.0735552)


Mevalonic acid, also known as MVA, mevalonate, or hiochic acid, belongs to the class of organic compounds known as hydroxy fatty acids. These are fatty acids in which the chain bears a hydroxyl group. Mevalonic acid is a key organic compound in biochemistry. It is found in most higher organisms ranging from plants to animals. Mevalonic acid is a precursor in the biosynthetic pathway known as the mevalonate pathway that produces terpenes (in plants) and steroids (in animals). Mevalonic acid is the primary precursor of isopentenyl pyrophosphate (IPP), that is in turn the basis for all terpenoids. The production of mevalonic acid by the enzyme 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, is the rate-limiting step in the biosynthesis of cholesterol (PMID: 12872277). The cholesterol biosynthetic pathway has three major steps: (1) acetate to mevalonate, (2) mevalonate to squalene, and (3) squalene to cholesterol. In the first step, which catalyzed by thiolase, two acetyl-CoA molecules form acetoacetyl-CoA and one CoA molecule is released, then the acetoacetyl-CoA reacts with another molecule of acetyl-CoA and generates 3-hydroxy-3-methylglutaryl-CoA (HMGCoA). The enzyme responsible for this reaction is 3-hydroxy-3-methylglutaryl-CoA synthase (HMG-CoA synthase): In the pathway to synthesize cholesterol, one of the HMG-CoA carboxyl groups undergoes reduction to an alcohol, releasing CoA, leading to the formation of mevalonate, a six carbon compound. This reaction is catalyzed by hydroxy-methylglutaryl-CoA reductase, In the second step (mevalonate to squalene) mevalonate receives a phosphoryl group from ATP to form 5-phosphomevalonate. This compound accepts another phosphate to generate mevalonate-5-pyrophosphate. After a third phosphorylation, the compound is decarboxylated, loses water, and generates isopentenyl pyrophosphate (IPP). Then through successive condensations, IPP forms squalene, a terpene hydrocarbon that contains 30 carbon atoms. By cyclization and other changes, this compound will finally result in cholesterol. Mevalonic acid is found, on average, in the highest concentration within a few different foods, such as apples, corns, and wild carrots and in a lower concentration in garden tomato (var.), pepper (C. frutescens), and cucumbers. Mevalonic acid has also been detected, but not quantified in, several different foods, such as sweet oranges, potato, milk (cow), cabbages, and white cabbages. This could make mevalonic acid a potential biomarker for the consumption of these foods. Plasma concentrations and urinary excretion of MVA are decreased by HMG-CoA reductase inhibitor drugs such as pravastatin, simvastatin, and atorvastatin (PMID: 8808497). Mevalonic acid (MVA) is a key organic compound in biochemistry. The anion of mevalonic acid, the predominant form in biological media, is known as mevalonate. This compound is of major pharmaceutical importance. Drugs, such as the statins, stop the production of mevalonate by inhibiting HMG-CoA reductase. [Wikipedia]. Mevalonic acid is found in many foods, some of which are pepper (c. frutescens), cabbage, wild carrot, and white cabbage.

   

Pantoate

(2R)-2,4-dihydroxy-3,3-dimethylbutanoic acid

C6H12O4 (148.0735552)


Pantoic acid (along with beta-alanine) is used to synthesize pantothenic acid (vitamin B5) in most microorganisms and plants. Pantothenic acid is a structural component of coenzyme A (CoA) which is involved in essential biological processes such as the citric acid cycle (TCA cycle) and the synthesis of carbohydrates, proteins, and fat. Pantothenic acid is found widespread in foods but especially in egg yolk, offal, fish, whole-grains, legumes, mushrooms, avocados, broccoli, and royal jelly (from bees).

   

colitose

(2R,3S,5S,6S)-6-methyloxane-2,3,5-triol

C6H12O4 (148.0735552)


   

2,3-dihydroxy-3-methylvalerate

2,3-Dihydroxy-3-methylpentanoic acid

C6H12O4 (148.0735552)


2,3-dihydroxy-3-methylvalerate is a member of the class of compounds known as hydroxy fatty acids. Hydroxy fatty acids are fatty acids in which the chain bears a hydroxyl group. Thus, 2,3-dihydroxy-3-methylvalerate is considered to be a fatty acid lipid molecule. 2,3-dihydroxy-3-methylvalerate is soluble (in water) and a weakly acidic compound (based on its pKa). 2,3-dihydroxy-3-methylvalerate can be found in a number of food items such as jostaberry, spelt, roman camomile, and common pea, which makes 2,3-dihydroxy-3-methylvalerate a potential biomarker for the consumption of these food products.

   

D-Digitoxose

Di-deoxyhexose

C6H12O4 (148.0735552)


   

(R)-2,3-Dihydroxy-3-methylvalerate

alpha,beta-Dihydroxy-beta-methylvaleric acid

C6H12O4 (148.0735552)


(R) 2,3-Dihydroxy-methylvalerate is an intermediate in valine, leucine and isoleucine biosynthesis. The pathway of valine biosynthesis is a four-step pathway that shares all of its steps with the parallel pathway of isoleucine biosynthesis. These entwined pathways are part of the superpathway of leucine, valine, and isoleucine biosynthesis, that generates not only isoleucine and valine, but also leucine. (R) 2,3-Dihydroxy-methylvalerate is generated from 3-Hydroxy-3-methyl-2-oxopentanoic acid via the enzyme ketol-acid reductoisomerase (EC 1.1.1.86) then it is converted to (S)-3-methyl-2-oxopentanoic via the dihydroxy-acid dehydratase (EC:4.2.1.9). [HMDB] (R)-2,3-Dihydroxy-methylvalerate is an intermediate in valine, leucine, and isoleucine biosynthesis. The pathway of valine biosynthesis is a four-step pathway that shares all of its steps with the parallel pathway of isoleucine biosynthesis. These entwined pathways are part of the superpathway of leucine, valine, and isoleucine biosynthesis, which generates not only isoleucine and valine but also leucine. (R)-2,3-Dihydroxy-methylvalerate is generated from 3-hydroxy-3-methyl-2-oxopentanoic acid via the enzyme ketol-acid reductoisomerase (EC 1.1.1.86). It is converted into (S)-3-methyl-2-oxopentanoic via the dihydroxy-acid dehydratase (EC 4.2.1.9).

   
   
   

Mevalonic acid

3R-methyl-3,5-dihydroxy-pentanoic acid

C6H12O4 (148.0735552)


A dihydroxy monocarboxylic acid comprising valeric acid having two hydroxy groups at the 3- and 5-positions together with a methyl group at the 3-position.

   
   
   

Ascarylopyranose

Ascarylopyranose

C6H12O4 (148.0735552)


   

3-(2-Methoxyethoxy)propanoic acid

3-(2-Methoxyethoxy)propanoic acid

C6H12O4 (148.0735552)


A monocarboxylic acid that is propanoic acid substituted at C-3 by a 2-methoxyethoxy group.

   

Glycerol 1-propanoate

2,3-Dihydroxypropyl propanoic acid

C6H12O4 (148.0735552)


Glycerol 1-propanoate is classified as a Natural Food Constituent (code WA) in the DF

   

(2-Methoxyethoxy)propanoic acid

2-(2-methoxyethoxy)propanoic acid

C6H12O4 (148.0735552)


(2-Methoxyethoxy)propanoic acid is a monocarboxylic acid that is propanoic acid substituted at C-2 by a 2-methoxyethoxy group.

   

4,5-dihydroxyhexanoic acid

4,5-dihydroxyhexanoic acid

C6H12O4 (148.0735552)


4,5-dihydroxyhexanoic acid or DHHA is a water-soluble organic acid. It probably arises from the reaction of succinic semialdehyde with an intermediate in the pyruvate dehydrogenase pathway. DHHA is found in the urine and appears to be a marker for Succinic semialdehyde dehydrogenase (SSADH) deficiency (PMID: 3126356 ). SSADH is a disorder that arises from a defect in gamma-aminobutyric acid catabolism, resulting in the accumulation of gamma-hydroxybutyric acid (GHB), 2,4-dihydroxybutyric acid, adipic acid as well as elevated levels of 4,5-dihydroxyhexanoic acid, and 4,5-dihydroxyhexanoic acid lactone. SSADH causes neurological and cognitive disorders of varying severity (PMID: 3126356 ). Children with SSADH deficiency usually manifest with developmental delay, behavioral symptoms, language dysfunction, seizures, hypotonia, extrapyramidal symptoms, and ataxia (PMID: 32055132).

   

Aldehydo-ascarylose

2,4,5-trihydroxyhexanal

C6H12O4 (148.0735552)


   

beta-tyvelose

3,6-dideoxy-D-xylo-hexose

C6H12O4 (148.0735552)


   

(2R,3R,4R,5S)-2-Methyl-tetrahydro-pyran-3,4,5-triol

(2R,3R,4R,5S)-2-Methyl-tetrahydro-pyran-3,4,5-triol

C6H12O4 (148.0735552)


   

D-Digitoxose

6-methyloxane-2,4,5-triol

C6H12O4 (148.0735552)


   

2,3-Dihydroxy-3-methylpentanoic acid

2,3-Dihydroxy-3-methylpentanoic acid

C6H12O4 (148.0735552)


   

Digitoxose, D-

D-ribo-Hexose,2,6-dideoxy-

C6H12O4 (148.0735552)


   

2,2-diethoxyacetic Acid

2,2-diethoxyacetic Acid

C6H12O4 (148.0735552)


   

1,2,3,4-Cyclohexanetetrol

1,2,3,4-Cyclohexanetetrol

C6H12O4 (148.0735552)


   
   

3,6-dideoxyhexose

3,6-dideoxyhexose

C6H12O4 (148.0735552)


   

Deoxy-erythro-pentose,9CI,8CI-beta-D-Pyranose-form-Me glycoside

Deoxy-erythro-pentose,9CI,8CI-beta-D-Pyranose-form-Me glycoside

C6H12O4 (148.0735552)


   

SCHEMBL18023809

SCHEMBL18023809

C6H12O4 (148.0735552)


   
   
   

digitoxose

D-ribo-Hexose,2,6-dideoxy-

C6H12O4 (148.0735552)


   

Propionin

1,2,3-Propanetriol 1-propanoate

C6H12O4 (148.0735552)


   

(2-Methoxyethoxy)propanoic acid

2-(2-methoxyethoxy)propanoic acid

C6H12O4 (148.0735552)


   

FA 6:0;O2

(2R,3R)-2,3-dihydroxy-3-methylpentanoic acid

C6H12O4 (148.0735552)


   

Ethyl acetate-PEG1

Ethyl acetate-PEG1

C6H12O4 (148.0735552)


   

Methyl 2-deoxy-L-erythro-pentofuranoside

Methyl 2-deoxy-L-erythro-pentofuranoside

C6H12O4 (148.0735552)


   

Methyl 2,2-dimethoxypropanoate

2,2-DIMETHOXYPROPIONIC ACID METHYL ESTER

C6H12O4 (148.0735552)


   

Methyl 2-deoxypentofuranoside

Methyl 2-deoxypentofuranoside

C6H12O4 (148.0735552)


   

Methyl-2-deoxy-L-erythro-pentofuranose

Methyl-2-deoxy-L-erythro-pentofuranose

C6H12O4 (148.0735552)


   

1,3-DIOXANE-5,5-DIMETHANOL

1,3-DIOXANE-5,5-DIMETHANOL

C6H12O4 (148.0735552)


   

Kethoxal

1,1-dihydroxy-3-ethoxy-2-butanone

C6H12O4 (148.0735552)


D000890 - Anti-Infective Agents > D000998 - Antiviral Agents C784 - Protein Synthesis Inhibitor

   

2,2-Bis(hydroxymethyl)butyric acid

2,2-Bis(hydroxymethyl)butyric acid

C6H12O4 (148.0735552)


   

Methyl 2-deoxy-α-D-erythro-pentofuranoside

Methyl 2-deoxy-α-D-erythro-pentofuranoside

C6H12O4 (148.0735552)


   

Methyl 3,3-dimethoxypropionate

Methyl 3,3-dimethoxypropionate

C6H12O4 (148.0735552)


   

ethyl 2-(methoxymethoxy)acetate

ethyl 2-(methoxymethoxy)acetate

C6H12O4 (148.0735552)


   

1,2,3-Propanetriol, glycidyl ethers

1,2,3-Propanetriol, glycidyl ethers

C6H12O4 (148.0735552)


   

3,6-dideoxy-alpha-D-xylo-hexopyranose

3,6-dideoxy-alpha-D-xylo-hexopyranose

C6H12O4 (148.0735552)


   

3,6-Dideoxy-D-ribo-hexose

3,6-Dideoxy-D-ribo-hexose

C6H12O4 (148.0735552)


   

beta-D-Digitoxopyranose

beta-D-Digitoxopyranose

C6H12O4 (148.0735552)


   

alpha-D-Digitoxopyranose

alpha-D-Digitoxopyranose

C6H12O4 (148.0735552)


   
   

2-(2-Hydroxyethyl)-4-hydroxy-1,3-dioxane

2-(2-Hydroxyethyl)-4-hydroxy-1,3-dioxane

C6H12O4 (148.0735552)


   

2,6-Dideoxy-L-arabino-hexopyranose

2,6-Dideoxy-L-arabino-hexopyranose

C6H12O4 (148.0735552)


   

(2-Ethoxyethoxy)acetic acid

(2-Ethoxyethoxy)acetic acid

C6H12O4 (148.0735552)


A monocarboxylic acid that is acetic acid in which one of the methyl hydrogens has been replaced by a 2-ethoxyethoxy group.

   

1,2,3,5-Cyclohexanetetrol

1,2,3,5-Cyclohexanetetrol

C6H12O4 (148.0735552)


   

1,2,4,5-Cyclohexanetetrol

1,2,4,5-Cyclohexanetetrol

C6H12O4 (148.0735552)


   

alpha-Tyvelopyranose

alpha-Tyvelopyranose

C6H12O4 (148.0735552)


   

4,6-Dideoxyglucose

4,6-Dideoxyglucose

C6H12O4 (148.0735552)


   

alpha-D-paratopyranose

alpha-D-paratopyranose

C6H12O4 (148.0735552)


   
   
   

Aldehydo-ascarylose

Aldehydo-ascarylose

C6H12O4 (148.0735552)


   

aldehydo-L-colitose

aldehydo-L-colitose

C6H12O4 (148.0735552)


   

(2R,4R,5R)-2,4,5-trihydroxyhexanal

(2R,4R,5R)-2,4,5-trihydroxyhexanal

C6H12O4 (148.0735552)


   

2-deoxy-beta-L-fucose

2-deoxy-beta-L-fucose

C6H12O4 (148.0735552)


   
   

L-digitoxopyranose

L-digitoxopyranose

C6H12O4 (148.0735552)


   

beta-Ascarylopyranose

beta-Ascarylopyranose

C6H12O4 (148.0735552)


   

3,6-dideoxy-beta-L-xylo-hexopyranose

3,6-dideoxy-beta-L-xylo-hexopyranose

C6H12O4 (148.0735552)


   

alpha-L-digitoxopyranose

alpha-L-digitoxopyranose

C6H12O4 (148.0735552)


   

beta-L-digitoxopyranose

beta-L-digitoxopyranose

C6H12O4 (148.0735552)


   
   

alpha-Ascarylopyranose

alpha-Ascarylopyranose

C6H12O4 (148.0735552)


   

(2R,3R)-2,3-dihydroxy-3-methylpentanoic acid

(2R,3R)-2,3-dihydroxy-3-methylpentanoic acid

C6H12O4 (148.0735552)


   

Pantoic acid

D-pantoic acid

C6H12O4 (148.0735552)


   

2,3-dihydroxy-3-methylpentanoate

2,3-Dihydroxy-3-methylpentanoic acid

C6H12O4 (148.0735552)


   

(S)-Mevalonic acid

(S)-Mevalonic acid

C6H12O4 (148.0735552)


The (S)-enantiomer of mevalonic acid.

   

(2R,3S,5S,6S)-6-methyloxane-2,3,5-triol

(2R,3S,5S,6S)-6-methyloxane-2,3,5-triol

C6H12O4 (148.0735552)


   

2-(2-methoxyethoxy)propanoic acid

2-(2-methoxyethoxy)propanoic acid

C6H12O4 (148.0735552)


A monocarboxylic acid that is propanoic acid substituted at C-2 by a 2-methoxyethoxy group.

   

glycerol propionate

2,3-Dihydroxypropyl propionate

C6H12O4 (148.0735552)


   
   

2,4-dihydroxy-3,3-dimethylbutanoic acid

2,4-dihydroxy-3,3-dimethylbutanoic acid

C6H12O4 (148.0735552)


   

3,5-dihydroxy-3-methylpentanoic acid

3,5-dihydroxy-3-methylpentanoic acid

C6H12O4 (148.0735552)


   

(R)-Mevalonic acid

(R)-Mevalonic acid

C6H12O4 (148.0735552)


The (R)-enantiomer of mevalonic acid.

   

(R)-Pantoic acid

(R)-Pantoic acid

C6H12O4 (148.0735552)


   

Dihydroxymethylvaleric acid

Dihydroxymethylvaleric acid

C6H12O4 (148.0735552)


   

Methoxyethoxy-propanoic acid

Methoxyethoxy-propanoic acid

C6H12O4 (148.0735552)