Exact Mass: 190.0517954

Exact Mass Matches: 190.0517954

Found 213 metabolites which its exact mass value is equals to given mass value 190.0517954, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Carglumic acid

(2S)-2-(Carbamoylamino)pentanedioic acid

C6H10N2O5 (190.058969)

Carglumic acid is an orphan drug used for the treatment of hyperammonaemia in patients with N-acetylglutamate synthase deficiency. This rare genetic disorder results in elevated blood levels of ammonia, which can eventually cross the blood-brain barrier and cause neurologic problems, cerebral edema, coma, and death. Carglumic acid was approved by the U.S. Food and Drug Administration (FDA) on 18 March 2010. A - Alimentary tract and metabolism > A16 - Other alimentary tract and metabolism products > A16A - Other alimentary tract and metabolism products > A16AA - Amino acids and derivatives C78275 - Agent Affecting Blood or Body Fluid KEIO_ID C078

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

C7H10O6 (190.04773600000001)

2,4-dihydroxy-2-heptenedioc acid

2,4-Dihydroxyhept-2-enedioic acid

C7H10O6 (190.04773600000001)

L-alpha-Amino-gamma-oxalylaminobutyric acid

2-Amino-4-((carboxycarbonyl)amino)butanoic acid, (2S)-

C6H10N2O5 (190.058969)

A monocarboxylic acid amide obtained by the formal condensation of the amino group at position 4 of L-2,4-diaminobutyric acid with the carboxy group of oxalic acid.

2-Keto-5-epi-valiolone

C7H10O6 (190.04773600000001)

L-beta-aspartyl-L-glycine

2-Amino-3-[(carboxymethyl)-C-hydroxycarbonimidoyl]propanoate

C6H10N2O5 (190.058969)

L-beta-aspartyl-l-glycine is a proteolytic breakdown product of larger proteins. It belongs to the family of Acyl Glycines. These are organic compounds containing a glycine residue with the N-atom attached to another moiety through an N-ester bond. It is found in urine (PMID: 3782411). A dipeptide found in urine (PMID: 3782411). This is a proteolytic breakdown product of larger proteins. [HMDB]

Aspartyl-Glycine

3-Amino-3-[(carboxymethyl)-C-hydroxycarbonimidoyl]propanoate

C6H10N2O5 (190.058969)

Aspartyl-Glycine is a dipeptide composed of aspartate and glycine. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite.

Glycyl-Aspartate

2-[(2-Amino-1-hydroxyethylidene)amino]butanedioate

C6H10N2O5 (190.058969)

Glycyl-Aspartate is a dipeptide composed of glycine and aspartate. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an Expected metabolite.

5-(Methylthio)-2-[(methylthio)methyl]-2-pentenal

(2E)-5-(Methylsulphanyl)-2-[(methylsulphanyl)methyl]pent-2-enal

C8H14OS2 (190.04860340000002)

5-(Methylthio)-2-[(methylthio)methyl]-2-pentenal is found in garden tomato. 5-(Methylthio)-2-[(methylthio)methyl]-2-pentenal is a flavouring ingredient and antioxidant. 5-(Methylthio)-2-[(methylthio)methyl]-2-pentenal is present in tomato juice and hydrolysed vegetable protein. 5-(Methylthio)-2-[(methylthio)methyl]-2-pentenal is a flavouring ingredient and antioxidant. It is found in tomato juice and hydrolysed vegetable protein.

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.

N-carbamoylglutamic Acid

2-[(C-hydroxycarbonimidoyl)amino]pentanedioic acid

C6H10N2O5 (190.058969)

N-carbamoylglutamic Acid, also known as N-Carbamoylglutamate, is classified as a glutamic acid or a Glutamic acid derivative. Glutamic acids are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. N-carbamoylglutamic Acid is considered to be soluble (in water) and acidic

2-O-Methylascorbic acid

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

C7H10O6 (190.047736)

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).

1,1'-Oxalyldiimidazole

bis(1H-imidazol-1-yl)ethane-1,2-dione

C8H6N4O2 (190.0490736)

4-Methyl-1-homopiperazinedithiocarboxylic acid

C7H14N2S2 (190.0598364)

1-Nitro-3,5-dinitroso-1,3,5-triazinane

Hexahydro-1,3-dinitroso-5-nitro-1,3,5-triazine

C3H6N6O4 (190.0450516)

L-alpha-Amino-beta-oxalylaminopropionic acid

C6H10N2O5 (190.058969)

ACMC-20n6bh

C6H10N2O5 (190.058969)

L-Glutamic acid-??-methylamide