CHEBI:53014 - N6-carboxymethyl-L-lysine

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ChEBI Name N6-carboxymethyl-L-lysine
ChEBI ASCII Name N(6)-carboxymethyl-L-lysine
Definition An L-lysine derivative with a carboxymethyl substituent at the N6-position.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C8H16N2O4
Net Charge 0
Average Mass 204.22360
Monoisotopic Mass 204.11101
InChI InChI=1S/C8H16N2O4/c9-6(8(13)14)3-1-2-4-10-5-7(11)12/h6,10H,1-5,9H2,(H,11,12)(H,13,14)/t6-/m0/s1
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): antigen
Any substance that stimulates an immune response in the body, such as through antibody production or by presentation to a T-cell receptor after binding to a major histocompability complex (MHC).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing N6-carboxymethyl-L-lysine (CHEBI:53014) has role antigen (CHEBI:59132)
N6-carboxymethyl-L-lysine (CHEBI:53014) is a L-lysine derivative (CHEBI:25095)
N6-carboxymethyl-L-lysine (CHEBI:53014) is a non-proteinogenic L-α-amino acid (CHEBI:83822)
Incoming N6-carboxymethyl-L-lysine residue (CHEBI:53015) is substituent group from N6-carboxymethyl-L-lysine (CHEBI:53014)
Synonyms Sources
N(6)-Carboxymethyllysine ChemIDplus
N(epsilon)-(Carboxymethyl)lysine ChemIDplus
NECML ChemIDplus
Nε-carboxymethyl-L-lysine ChEBI
Registry Numbers Types Sources
4989963 Reaxys Registry Number Reaxys
4989963 Beilstein Registry Number Beilstein
5746-04-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17939855 PubMed citation Europe PMC
19962413 PubMed citation Europe PMC
20030411 PubMed citation Europe PMC
7662668 PubMed citation Europe PMC
9129235 PubMed citation Europe PMC
9506998 PubMed citation Europe PMC
Last Modified
22 August 2017