RefMet Compound Details

MW structure37129 (View MW Metabolite Database details)
RefMet nameAnserine
Systematic name(2S)-2-(3-aminopropanamido)-3-(1-methyl-1H-imidazol-5-yl)propanoic acid
SMILESCn1cncc1C[C@@H](C(=O)O)NC(=O)CCN   Run Tanimoto similarity search (with similarity coefficient >=0.6)
Exact mass240.122241 (neutral)
Calculate m/z:   
View other RefMet entries with this exact (neutral) mass:   +/- 0.05 amu   +/- 0.1 amu   +/- 0.2 amu   +/- 0.5 amu
FormulaC10H16N4O3View other entries in RefMet with this formula
InChIKeyMYYIAHXIVFADCU-QMMMGPOBSA-NView other enantiomers/diastereomers of this metabolite in RefMet
Super ClassOrganic acids
Main ClassAmino acids and peptides
Sub ClassDipeptides
Pubchem CID112072
Annotation level1   (1:Known structure; 2:Known regiochemistry; 3:Partial structure; 4:Sum-composition)

Table of KEGG reactions in human pathways involving Anserine

Rxn IDKEGG ReactionEnzyme
R02144 S-Adenosyl-L-methionine + Carnosine <=> S-Adenosyl-L-homocysteine + beta-Alanyl-N(pi)-methyl-L-histidineS-adenosyl-L-methionine:carnosine N-methyltransferase
R03288 beta-Alanyl-N(pi)-methyl-L-histidine + H2O <=> beta-Alanine + N(pi)-Methyl-L-histidinebeta-alanyl-N(pi)-methyl-L-histidine hydrolase
R03286 ATP + N(pi)-Methyl-L-histidine + beta-Alanine <=> ADP + Orthophosphate + beta-Alanyl-N(pi)-methyl-L-histidineN(pi)-methyl-L-histidine:beta-alanine ligase (ADP-forming)

Table of KEGG human pathways containing Anserine

Pathway IDHuman Pathway# of reactions
hsa00340 Histidine metabolism 2
hsa00410 beta-Alanine metabolism 2