CHEBI:64859 - N^α-acetyl-L-lysine methyl ester

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ChEBI Name Nα-acetyl-L-lysine methyl ester ChEBI ID CHEBI:64859 ChEBI ASCII Name N(alpha)-acetyl-L-lysine methyl ester Definition An α-amino acid ester obtained by formal condensation of the carboxy group of Nα-acetyl-L-lysine with the hydroxy group of methanol. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C9H18N2O3 Net Charge 0 Average Mass 202.25080 Monoisotopic Mass 202.13174 InChI InChI=1S/C9H18N2O3/c1-7(12)11-8(9(13)14-2)5-3-4-6-10/h8H,3-6,10H2,1-2H3,(H,11,12)/t8-/m0/s1 InChIKey HHOLXTXLQMKUGJ-QMMMGPOBSA-N SMILES COC(=O)[C@H](CCCCN)NC(C)=O Roles Classification Chemical Role(s): Bronsted base A molecular entity capable of accepting a hydron from a donor (Bronsted acid). (via organic amino compound ) View more via ChEBI Ontology ChEBI Ontology Outgoing Nα-acetyl-L-lysine methyl ester (CHEBI:64859) is a α-amino acid ester (CHEBI:46874) Nα-acetyl-L-lysine methyl ester (CHEBI:64859) is a L-lysine derivative (CHEBI:25095) Nα-acetyl-L-lysine methyl ester (CHEBI:64859) is a acetamides (CHEBI:22160) Nα-acetyl-L-lysine methyl ester (CHEBI:64859) is a methyl ester (CHEBI:25248) Nα-acetyl-L-lysine methyl ester (CHEBI:64859) is a primary amino compound (CHEBI:50994) Nα-acetyl-L-lysine methyl ester (CHEBI:64859) is conjugate base of Nα-acetyl-L-lysine methyl ester(1+) (CHEBI:64854) Incoming Nα-acetyl-L-lysine methyl ester(1+) (CHEBI:64854) is conjugate acid of Nα-acetyl-L-lysine methyl ester (CHEBI:64859) IUPAC Name methyl N2-acetyl-L-lysinate Synonyms Sources alpha-Acetyl-L-lysine methyl ester ChemIDplus alpha-Acetyllysine methyl ester ChemIDplus methyl N-acetyl-6-amino-L-norleucinate ChEBI methyl N-acetyl-L-lysinate ChEBI methyl N2-acetyllysinate ChEBI Manual Xref Database CPD0-1442 MetaCyc View more database links Registry Numbers Types Sources 2255115 Reaxys Registry Number Reaxys 6072-02-2 CAS Registry Number ChemIDplus Citations Types Sources 19199600 PubMed citation Europe PMC 5429516 PubMed citation Europe PMC Last Modified 03 March 2015