Metabolite List
metabolites which its exact mass nearly 158.0732 with tolerance error 0.01 da.
4-Methylene-L-glutamine (BioCAD00000004458)
Formula: C6H10N2O3 (Exact Mass: 158.0691)
A non-proteinogenic L-alpha-amino acid that is L-glutamine in which the hydrogens attached to the carbon gamma to the carboxy group are replaced by a methylene group." []
5-Hydroxyectoine (BioCAD00000004837)
Formula: C6H10N2O3 (Exact Mass: 158.0691)
A carboxamidine heterocycle which is obtained by formal condensation of 4-amino-L-allothreonine with acetic acid." []
1-(Hydroxymethyl)-5,5-dimethyl-2,4-imidazolidinedione (BioCAD00000028976)
Formula: C6H10N2O3 (Exact Mass: 158.0691)
1-(Hydroxymethyl)-5,5-dimethyl-2,4-imidazolidinedione is a fda approved for use as an adjuvant in the bleaching of food-contact recycled paper and board used in food packagin
N-Nitrosobis(2-oxopropyl)amine (BioCAD00000183243)
Formula: C6H10N2O3 (Exact Mass: 158.0691)
Nitrosobis(2-oxopropyl)amine is a nitrosamine that is iminodiacetone that is substituted by a nitroso group at the N-atom. It induces pancreatic ductal adenocarcinomas in Syrian golden hamsters (other rodents are not susceptible). It has a role as a carcinogenic agent. It is a nitrosamine and a ketone.
Oxiracetam (BioCAD00000183876)
Formula: C6H10N2O3 (Exact Mass: 158.0691)
Oxiracetam is an organooxygen compound and an organonitrogen compound. It is functionally related to an alpha-amino acid.
5-hydroxyectoine zwitterion (BioCAD00000480215)
Formula: C6H10N2O3 (Exact Mass: 158.0691)
An iminium betaine resulting from a transfer of a proton from the carboxy group to the imino group of 5-hydroxyectoine. It is the major microspecies at pH 7.3 (according to Marvin v 6.2.0.)." []
4-methylene-L-glutamine zwitterion (BioCAD00000560271)
Formula: C6H10N2O3 (Exact Mass: 158.0691)
Zwitterionic form of 4-methylene-L-glutamine having an anionic carboxy group and a cationic amino group; major species at pH 7.3." []
nitrosobis(2-oxopropyl)amine (BioCAD00000597905)
Formula: C6H10N2O3 (Exact Mass: 158.0691)
A nitrosamine that is iminodiacetone that is substituted by a nitroso group at the N-atom. It induces pancreatic ductal adenocarcinomas in Syrian golden hamsters (other rodents are not susceptible)." []