Exact Mass: 210.0376

Exact Mass Matches: 210.0376

Found 29 metabolites which its exact mass value is equals to given mass value 210.0376, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

Glucaric acid

(2S,3S,4S,5R)-2,3,4,5-tetrahydroxyhexanedioic acid

C6H10O8 (210.0376)


Glucaric acid, also known as glucarate or D-saccharic acid, belongs to the class of organic compounds known as glucuronic acid derivatives. Glucuronic acid derivatives are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid. Glucaric acid is a sugar acid derived from D-glucose in which both the aldehydic carbon atom and the carbon atom bearing the primary hydroxyl group are oxidized to carboxylic acid groups. D-glucaric acid is found in fruits, vegetables, and mammals. The highest concentrations of glucaric acid are found in grapefruits, apples, oranges, and cruciferous vegetables (PMID: 18772850). Glucaric acid is produced through the oxidation of glucose. Cytochrome P450 is thought to be responsible for the production of D-glucaric acid in vivo (PMID: 3779687). In mammals, D-glucaric acid and D-glucaro-l,4-lactone are also known end-products of the D-glucuronic acid pathway (PMID: 18772850). Glucaric is available as a dietary supplement in the form of calcium D-glucarate and has been studied for therapeutic purposes including cholesterol reduction and cancer chemotherapy (PMID: 9101079). D-Glucaric acid has a potential use as a building block for a number of polymers, including new nylons and hyperbranched polyesters. D-glucaric acid produced from D-glucose has been successfully utilized to produce a hydroxylated nylon. A sugar acid derived from D-glucose in which both the aldehydic carbon atom and the carbon atom bearing the primary hydroxyl group are oxidized to carboxylic acid groups. [HMDB] KEIO_ID S025

   

Galactaric acid

(2R,3S,4R,5S)-2,3,4,5-Tetrahydroxyhexanedioic acid

C6H10O8 (210.0376)


Galactaric acid, also known as mucic acid or galactarate, belongs to the class of organic compounds known as glucuronic acid derivatives. Glucuronic acid derivatives are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid. Technically, galactaric acid is an aldaric acid obtained by oxidation of galactose. Galactaric acid exists as a white crystalline powder, which melts at 210 - 230 oC. It is insoluble in alcohol, and nearly insoluble in cold water (1 g/300 mL) but more soluble in hot water (1 g/60 mL).. Galactaric acid exists in all living organisms, ranging from bacteria to plants to humans. In plants, galactaric acid is commonly produced or utilized as an osmorgulator (PMID: 31505987). Galactaric acid has been detected, but not quantified in, several different foods, such as fruits, vegetables and bovine milk. A recent large-scale dietary study found that galactaric acid can serve as a biomarker for long-term dairy intake and for the consumption of carotenoid-rich vegetables (PMID: 33566801). In food production, galactaric acid can be used to replace tartaric acid in self-rising flour or fizzies. Present in ripe fruits of peach and pear. Formed in grapes and grape must by the action of Botrytis cinerea on galacturonic acid Acquisition and generation of the data is financially supported in part by CREST/JST. Mucic acid is an endogenous metabolite.

   

L-altraric acid

L-altraric acid

C6H10O8 (210.0376)


Altraric acid of L-configuration.

   

Mucate

Mucic acid

C6H10O8 (210.0376)


KEIO_ID M065 Mucic acid is an endogenous metabolite.

   

Saccharic acid

D-(+)-Saccharic acid

C6H10O8 (210.0376)


Present in apples and grapefruit. D-Glucaric acid is found in pomes and citrus.

   

Schleimsaure

Saccharic acid

C6H10O8 (210.0376)


   

SCHEMBL7534971

SCHEMBL7534971

C6H10O8 (210.0376)


   

Citrate

Citric acid monohydrate, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., buffer substance, 99.5-102\\%

C6H8O7.H2O (210.0376)


Citric acid monohydrate is an organic molecular entity. Citric Acid Monohydrate is a tricarboxylic acid found in citrus fruits. Citric acid is used as an excipient in pharmaceutical preparations due to its antioxidant properties. It maintains stability of active ingredients and is used as a preservative. It is also used as an acidulant to control pH and acts as an anticoagulant by chelating calcium in blood. A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability. See also: Citric Acid (related); Citric Acid monohydrate; Sodium Bicarbonate (component of); Citric Acid Monohydrate; Potassium Citrate (component of) ... View More ... D064449 - Sequestering Agents > D002614 - Chelating Agents > D065096 - Calcium Chelating Agents D006401 - Hematologic Agents > D000925 - Anticoagulants C26170 - Protective Agent > C275 - Antioxidant Citric acid monohydrate is a natural preservative and food tartness enhancer. Citric acid monohydrate induces apoptosis and cell cycle arrest at G2/M phase and S phase. Citric acid monohydrate cause oxidative damage of the liver by means of the decrease of antioxidative enzyme activities. Citric acid monohydrate causes renal toxicity in mice[1][2][3]. Citric acid monohydrate is a natural preservative and food tartness enhancer. Citric acid monohydrate induces apoptosis and cell cycle arrest at G2/M phase and S phase. Citric acid monohydrate cause oxidative damage of the liver by means of the decrease of antioxidative enzyme activities. Citric acid monohydrate causes renal toxicity in mice[1][2][3].

   

D-Saccharic acid

D-Saccharic acid

C6H10O8 (210.0376)


   

Mucic acid

2R,3S,4R,5S-tetrahydroxy-hexanedioic acid

C6H10O8 (210.0376)


A hexaric acid resulting from formal oxidative ring cleavage of galactose. Mucic acid is an endogenous metabolite.

   

Glucaric acid

2S,3S,4S,5R-tetrahydroxy-hexanedioic acid

C6H10O8 (210.0376)


   

Galactarate

Galactarate

C6H10O8 (210.0376)


   

Saccharate

Saccharate

C6H10O8 (210.0376)


   

Galactaric acid

Galactaric acid

C6H10O8 (210.0376)


   

Citric Acid Monohydrate

Citric Acid Monohydrate

C6H10O8 (210.0376)


D064449 - Sequestering Agents > D002614 - Chelating Agents > D065096 - Calcium Chelating Agents D006401 - Hematologic Agents > D000925 - Anticoagulants C26170 - Protective Agent > C275 - Antioxidant Citric acid monohydrate is a natural preservative and food tartness enhancer. Citric acid monohydrate induces apoptosis and cell cycle arrest at G2/M phase and S phase. Citric acid monohydrate cause oxidative damage of the liver by means of the decrease of antioxidative enzyme activities. Citric acid monohydrate causes renal toxicity in mice[1][2][3]. Citric acid monohydrate is a natural preservative and food tartness enhancer. Citric acid monohydrate induces apoptosis and cell cycle arrest at G2/M phase and S phase. Citric acid monohydrate cause oxidative damage of the liver by means of the decrease of antioxidative enzyme activities. Citric acid monohydrate causes renal toxicity in mice[1][2][3].

   

Quinoxalin-6-ylboronic acid hydrochloride

Quinoxalin-6-ylboronic acid hydrochloride

C8H8BClN2O2 (210.0367)


   

GLYOXAL DIHYDRATE

GLYOXAL DIHYDRATE

C6H10O8 (210.0376)


   

D-Saccharic acid 1,4-lactone hydrate

D-Saccharic acid 1,4-lactone hydrate

C6H10O8 (210.0376)


   

D-(tetrahydro-2,3,4-trihydroxy-5-oxofuran-2-yl)glycollic acid

D-(tetrahydro-2,3,4-trihydroxy-5-oxofuran-2-yl)glycollic acid

C6H10O8 (210.0376)


   

D-altraric acid

D-altraric acid

C6H10O8 (210.0376)


   

Allaric acid

Allaric acid

C6H10O8 (210.0376)


   

2-Hydroxy-2-(1,2,3-trihydroxypropyl)propanedioic acid

2-Hydroxy-2-(1,2,3-trihydroxypropyl)propanedioic acid

C6H10O8 (210.0376)


   

L-idaric acid

L-idaric acid

C6H10O8 (210.0376)


   

D-idaric acid

D-idaric acid

C6H10O8 (210.0376)


   

2-hydroxy-2-[(1R,2S)-1,2,3-trihydroxypropyl]propanedioic acid

2-hydroxy-2-[(1R,2S)-1,2,3-trihydroxypropyl]propanedioic acid

C6H10O8 (210.0376)


   

L-glucaric acid

L-glucaric acid

C6H10O8 (210.0376)


The L-enantiomer of glucaric acid.

   

L-mannaric acid

L-mannaric acid

C6H10O8 (210.0376)


The L-enantiomer of mannaric acid.

   

D-mannaric acid

D-mannaric acid

C6H10O8 (210.0376)


The D-enantiomer of mannaric acid.

   

D-Glucaric acid

D-Glucaric acid

C6H10O8 (210.0376)


The D-enantiomer of glucaric acid.