CHEBI:17604 - N⁶-methyl-L-lysine

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ChEBI Name N6-methyl-L-lysine ChEBI ID CHEBI:17604 ChEBI ASCII Name N(6)-methyl-L-lysine Definition An L-lysine derivative that is L-lysine in which one of the hydrogens attached to N6 is substituted by a methyl group. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:12671, CHEBI:7418, CHEBI:21888 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 C7H16N2O2 Net Charge 0 Average Mass 160.21422 Monoisotopic Mass 160.12118 InChI InChI=1S/C7H16N2O2/c1-9-5-3-2-4-6(8)7(10)11/h6,9H,2-5,8H2,1H3,(H,10,11)/t6-/m0/s1 InChIKey PQNASZJZHFPQLE-LURJTMIESA-N SMILES CNCCCC[C@H](N)C(O)=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 ) Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) View more via ChEBI Ontology ChEBI Ontology Outgoing N6-methyl-L-lysine (CHEBI:17604) is a L-lysine derivative (CHEBI:25095) N6-methyl-L-lysine (CHEBI:17604) is a non-proteinogenic L-α-amino acid (CHEBI:83822) N6-methyl-L-lysine (CHEBI:17604) is conjugate base of N6-methyl-L-lysinium(1+) (CHEBI:58202) Incoming N6-acetyl-N6-methyl-L-lysine (CHEBI:197458) has functional parent N6-methyl-L-lysine (CHEBI:17604) N6-methyl-L-lysinium(1+) (CHEBI:58202) is conjugate acid of N6-methyl-L-lysine (CHEBI:17604) N6-methyl-L-lysine residue (CHEBI:61928) is substituent group from N6-methyl-L-lysine (CHEBI:17604) IUPAC Names (2S)-2-amino-6-(methylamino)hexanoic acid N6-methyl-L-lysine Synonyms Sources (S)-2-amino-6-methylaminohexanoic acid ChEBI epsilon-methyllysine ChEBI Epsilon-N-methyllysine ChemIDplus MeLys ChEBI N(6)-Methyllysine ChemIDplus N(zeta)-methyllysine ChEBI N-Epsilon-methyllysine ChemIDplus N-methyl-L-lysine ChEBI N6-Methyl-L-lysine KEGG COMPOUND Nε-methyl-L-lysine ChEBI Manual Xrefs Databases C02728 KEGG COMPOUND HMDB0002038 HMDB MLZ PDBeChem View more database links Registry Numbers Types Sources 1188-07-4 CAS Registry Number ChemIDplus 1931417 Reaxys Registry Number Reaxys 1931417 Beilstein Registry Number Beilstein Citations Types Sources 14032673 PubMed citation Europe PMC 1730244 PubMed citation Europe PMC 17636967 PubMed citation Europe PMC 19772323 PubMed citation Europe PMC 20711534 PubMed citation Europe PMC 413481 PubMed citation Europe PMC 426794 PubMed citation Europe PMC 518920 PubMed citation Europe PMC 5222990 PubMed citation Europe PMC 5332039 PubMed citation Europe PMC 5347964 PubMed citation Europe PMC 5356590 PubMed citation Europe PMC 5368259 PubMed citation Europe PMC 5846984 PubMed citation Europe PMC 6770375 PubMed citation Europe PMC 6790681 PubMed citation Europe PMC Last Modified 25 October 2023