CHEBI:27596 - N^π-methyl-L-histidine

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name Nπ-methyl-L-histidine ChEBI ID CHEBI:27596 ChEBI ASCII Name N(pros)-methyl-L-histidine Definition A L-histidine derivative that is L-histidine substituted by a methyl group at position 3 on the imidazole ring. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:7067, CHEBI:21445, CHEBI:19854 Supplier Information No supplier information found for this compound. Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C7H11N3O2 Net Charge 0 Average Mass 169.18126 Monoisotopic Mass 169.08513 InChI InChI=1S/C7H11N3O2/c1-10-4-9-3-5(10)2-6(8)7(11)12/h3-4,6H,2,8H2,1H3,(H,11,12)/t6-/m0/s1 InChIKey JDHILDINMRGULE-LURJTMIESA-N SMILES Cn1cncc1C[C@H](N)C(O)=O Metabolite of Species Details Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net See: PubMed Homo sapiens (NCBI:txid9606) See: PubMed Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) Biological Role(s): Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing Nπ-methyl-L-histidine (CHEBI:27596) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) Nπ-methyl-L-histidine (CHEBI:27596) has role human metabolite (CHEBI:77746) Nπ-methyl-L-histidine (CHEBI:27596) is a L-histidine derivative (CHEBI:84076) Nπ-methyl-L-histidine (CHEBI:27596) is a non-proteinogenic L-α-amino acid (CHEBI:83822) Nπ-methyl-L-histidine (CHEBI:27596) is tautomer of Nπ-methyl-L-histidine zwitterion (CHEBI:143076) Incoming Nπ-methyl-L-histidine residue (CHEBI:43903) is substituent group from Nπ-methyl-L-histidine (CHEBI:27596) Nπ-methyl-L-histidine zwitterion (CHEBI:143076) is tautomer of Nπ-methyl-L-histidine (CHEBI:27596) IUPAC Name Nπ-methyl-L-histidine Synonyms Sources (2S)-2-amino-3-(1-methyl-1H-imidazol-5-yl)propanoic acid IUPAC 1-Methylhistidine Note: (2014-08-28) A misnomer. KEGG COMPOUND 3-Methyl-L-histidine HMDB 3-methylhistidine ChemIDplus 3-Methylhistidine KEGG COMPOUND N(pai)-Methyl-L-histidine KEGG COMPOUND N-pros-Methyl-L-histidine KEGG COMPOUND Tau-methylhistidine HMDB Manual Xrefs Databases C01152 KEGG COMPOUND HMDB0000479 HMDB MHS PDBeChem View more database links Registry Numbers Types Sources 1568650 Gmelin Registry Number Gmelin 368-16-1 CAS Registry Number ChemIDplus 83651 Reaxys Registry Number Reaxys Citations Types Sources 22612948 PubMed citation Europe PMC 24009031 PubMed citation Europe PMC 24681531 PubMed citation Europe PMC Last Modified 21 January 2016