CHEBI:136987 - N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid

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ChEBI Name N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid ChEBI ID CHEBI:136987 ChEBI ASCII Name N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid Definition An L-glutamic acid derivative obtained by replacement of one of the amino hydrogens of L-glutamic acid has been replaced by a (2S)-2-amino-2-carboxyethyl group. 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 C8H14N2O6 Net Charge 0 Average Mass 234.207 Monoisotopic Mass 234.08519 InChI InChI=1S/C8H14N2O6/c9-4(7(13)14)3-10-5(8(15)16)1-2-6(11)12/h4-5,10H,1-3,9H2,(H,11,12)(H,13,14)(H,15,16)/t4-,5-/m0/s1 InChIKey XYQHCOGLGSNTNV-WHFBIAKZSA-N SMILES O=C(O)[C@@H](NC[C@@H](C(O)=O)N)CCC(=O)O Metabolite of Species Details Staphylococcus aureus (NCBI:txid1280) See: PubMed Roles Classification Chemical Role(s): Bronsted acid A molecular entity capable of donating a hydron to an acceptor (Bronsted base). (via oxoacid ) Biological Role(s): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. View more via ChEBI Ontology ChEBI Ontology Outgoing N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid (CHEBI:136987) has role bacterial metabolite (CHEBI:76969) N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid (CHEBI:136987) is a L-glutamic acid derivative (CHEBI:83982) N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid (CHEBI:136987) is a tricarboxylic acid (CHEBI:27093) N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid (CHEBI:136987) is conjugate acid of N-[(2S)-2-amino-2-carboxyethyl]-L-glutamate(2−) (CHEBI:134610) Incoming N-[(2S)-2-amino-2-carboxyethyl]-L-glutamate(2−) (CHEBI:134610) is conjugate base of N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid (CHEBI:136987) IUPAC Name N-[(2S)-2-amino-2-carboxyethyl]-L-glutamic acid Synonym Source N-[(2S)-2-amino-2-carboxyethyl]glutamic acid ChEBI Manual Xrefs Databases AE5 PDBeChem CPD-19754 MetaCyc View more database links Registry Number Type Source 26884893 Reaxys Registry Number Reaxys Citations Types Sources 21906287 PubMed citation Europe PMC 24485762 PubMed citation Europe PMC Last Modified 09 May 2017