Chemical Formula: C7H16N2O2
Chemical Formula C7H16N2O2
Found 45 metabolite its formula value is C7H16N2O2
N(6)-Methyllysine
C7H16N2O2 (160.12117160000003)
N(6)-Methyllysine is a naturally occurring amino acid found in human biofluids. N-monomethyl-lysine is generated by metabolic transmethylation of endogenous lysine. Lysine methylation displays the highest degree of complexity among known covalent histone modifications, with each site of methylation regulating the association of different effector molecules. The versatility of lysine methylation marks is perhaps best exemplified by modifications implicated in transcriptional regulation as well as being required for double-strand break repair in several organisms. Identification of the numerous biological functions encoded by histone lysine methylation is a major area of research interest, as these mechanisms are intimately associated with cellular senescence, genomic instability, and leukemogenesis. While multiple sites of lysine methylation have been linked with gene activation, each modification is distributed to unique positions across the active gene. (PMID: 17030614, 1122639, 15756599, 3111294). N(6)-Methyllysine is a naturally occurring amino acid found in human biofluids. N-monomethyl-lysine is generated by metabolic transmethylation of endogenous lysine.
Isoputreanine
C7H16N2O2 (160.12117160000003)
Isoputreanine is urinary metabolite of spermidine, which is predominantly excreted as the monoacetyl conjugate of N-(3-aminopropyl)pyrrolidin-2-one, the acetylated γ-lactam form of isoputreanine. A human metabolite taken as a putative food compound of mammalian origin [HMDB]
N2-Methyl-L-lysine
C7H16N2O2 (160.12117160000003)
N2-Methyl-L-lysine, also known as N(a)-methyl-L-lysine, belongs to the class of organic compounds known as l-alpha-amino acids. Lysine methylation displays the highest degree of complexity among known covalent histone modifications, with each site of methylation regulating the association of different effector molecules. The versatility of lysine methylation marks is perhaps best exemplified by modifications implicated in transcriptional regulation as well as being required for double-strand break repair in several organisms. Identification of the numerous biological functions encoded by histone lysine methylation is a major area of research interest. (PMID: 32119527)
Emeriamine
C7H16N2O2 (160.12117160000003)
D007004 - Hypoglycemic Agents D004791 - Enzyme Inhibitors
1-tert-butyl-3-(2-hydroxyethyl)urea
C7H16N2O2 (160.12117160000003)
D-2,3,4,6,7-Pentadeoxy-2,6-diamino-ribo-hexose
C7H16N2O2 (160.12117160000003)
L-beta-Homolysine
C7H16N2O2 (160.12117160000003)
Acquisition and generation of the data is financially supported in part by CREST/JST.
N6-Methyl-lysine; AIF; CE0; CorrDec
C7H16N2O2 (160.12117160000003)
N6-Methyl-lysine; AIF; CE10; CorrDec
C7H16N2O2 (160.12117160000003)
N6-Methyl-lysine; AIF; CE30; CorrDec
C7H16N2O2 (160.12117160000003)
N6-Methyl-lysine; AIF; CE0; MS2Dec
C7H16N2O2 (160.12117160000003)
N6-Methyl-lysine; AIF; CE10; MS2Dec
C7H16N2O2 (160.12117160000003)
N6-Methyl-lysine; AIF; CE30; MS2Dec
C7H16N2O2 (160.12117160000003)
N-Amino-N-methylglycine tert-butyl ester
C7H16N2O2 (160.12117160000003)
3-(3-Methoxypropyl)-1,1-dimethylure
C7H16N2O2 (160.12117160000003)
(4s,5s)-4,5-di(aminomethyl)-2,2-dimethyldioxolane
C7H16N2O2 (160.12117160000003)
N-MeLys
C7H16N2O2 (160.12117160000003)
A N-methyl-L-amino acid that is the N(alpha)-methyl derivative of L-lysine.
(R)-3-tert-Butoxy-2-aminopropanamide
C7H16N2O2 (160.12117160000003)
(R)-2-Amino-3-(diethylamino)propanoic acid
C7H16N2O2 (160.12117160000003)
1-amino-3-morpholin-4-yl-propan-2-ol
C7H16N2O2 (160.12117160000003)
(S)-1-AMINO-3-MORPHOLINOPROPAN-2-OL
C7H16N2O2 (160.12117160000003)
N-(5-aminopentyl)-N-hydroxyacetamide
C7H16N2O2 (160.12117160000003)
N(6)-Methyllysine
C7H16N2O2 (160.12117160000003)
A lysine derivative that is lysine in which one of the hydrogens attached to N(6) is substituted by a methyl group.
N(6)-Methyl-L-lysine
C7H16N2O2 (160.12117160000003)
An L-lysine derivative that is L-lysine in which one of the hydrogens attached to N(6) is substituted by a methyl group.