CHEBI:50599 - N^τ-methyl-L-histidine

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ChEBI Name Nτ-methyl-L-histidine ChEBI ID CHEBI:50599 ChEBI ASCII Name N(tele)-methyl-L-histidine Definition A L-histidine derivative in which the methyl group is at Nτ-position. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:18846, CHEBI:50597 Supplier Information ChemicalBook:CB2251044, eMolecules:1934847, ZINC000002015152 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/c1-10-3-5(9-4-10)2-6(8)7(11)12/h3-4,6H,2,8H2,1H3,(H,11,12)/t6-/m0/s1 InChIKey BRMWTNUJHUMWMS-LURJTMIESA-N SMILES Cn1cnc(C[C@H](N)C(O)=O)c1 Metabolite of Species Details 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): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing Nτ-methyl-L-histidine (CHEBI:50599) has role human metabolite (CHEBI:77746) Nτ-methyl-L-histidine (CHEBI:50599) is a L-histidine derivative (CHEBI:84076) Nτ-methyl-L-histidine (CHEBI:50599) is a non-proteinogenic L-α-amino acid (CHEBI:83822) Nτ-methyl-L-histidine (CHEBI:50599) is tautomer of Nτ-methyl-L-histidine zwitterion (CHEBI:192560) Incoming Nτ-methyl-L-histidine residue (CHEBI:16367) is substituent group from Nτ-methyl-L-histidine (CHEBI:50599) Nτ-methyl-L-histidine zwitterion (CHEBI:192560) is tautomer of Nτ-methyl-L-histidine (CHEBI:50599) IUPAC Name 1-methyl-L-histidine Synonyms Sources (2S)-2-amino-3-(1-methyl-1H-imidazol-4-yl)propanoic acid IUPAC 1-methylhistidine ChemIDplus Pi-methylhistidine HMDB Manual Xref Database HMDB0000001 HMDB View more database links Registry Numbers Types Sources 1320034 Gmelin Registry Number Gmelin 332-80-9 CAS Registry Number ChemIDplus 9727 Beilstein Registry Number Beilstein 9727 Reaxys Registry Number Reaxys Citations Types Sources 14363188 PubMed citation Europe PMC 22777757 PubMed citation Europe PMC 23452466 PubMed citation Europe PMC 23980697 PubMed citation Europe PMC 24164354 PubMed citation Europe PMC 24681531 PubMed citation Europe PMC 24783928 PubMed citation Europe PMC Last Modified 23 October 2015