CHEBI:25094 - lysine

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ChEBI Name lysine ChEBI ID CHEBI:25094 Definition A diamino acid that is caproic (hexanoic) acid bearing two amino substituents at positions 2 and 6. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information ChemicalBook:CB5309777 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Wikipedia License L-α-Glycerophosphorylcholine (alpha-GPC, choline alfoscerate, sn-glycero-3-phosphocholine) is a natural choline compound found in the brain. It is also a parasympathomimetic acetylcholine precursor which has been investigated for its potential for the treatment of Alzheimer's disease and other dementias. Alpha-GPC rapidly delivers choline to the brain across the blood–brain barrier and is a biosynthetic precursor of acetylcholine. It is a non-prescription drug in most countries. The FDA determined that intake of no more than 196.2 mg/person/day is considered generally recognized as safe (GRAS). Read full article at Wikipedia Formula C6H14N2O2 Net Charge 0 Average Mass 146.18764 Monoisotopic Mass 146.10553 InChI InChI=1S/C6H14N2O2/c7-4-2-1-3-5(8)6(9)10/h5H,1-4,7-8H2,(H,9,10) InChIKey KDXKERNSBIXSRK-UHFFFAOYSA-N SMILES NCCCCC(N)C(O)=O Metabolite of Species Details Daphnia magna (NCBI:txid35525) See: Mixtures of similarly acting compounds in Daphnia magna: From gene to metabolite and beyondTine Vandenbrouck, Oliver A.H. Jones, Nathalie Dom, Julian L. Griffin, Wim De CoenEnvironment International 36 (2010) 254-268 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): Daphnia magna metabolite A Daphnia metabolite produced by the species Daphnia magna. View more via ChEBI Ontology ChEBI Ontology Outgoing lysine (CHEBI:25094) has functional parent hexanoic acid (CHEBI:30776) lysine (CHEBI:25094) has part 4-aminobutyl group (CHEBI:50339) lysine (CHEBI:25094) has role Daphnia magna metabolite (CHEBI:83056) lysine (CHEBI:25094) is a α-amino acid (CHEBI:33704) lysine (CHEBI:25094) is a diamino acid (CHEBI:35987) lysine (CHEBI:25094) is a polar amino acid (CHEBI:26167) lysine (CHEBI:25094) is conjugate acid of lysinate (CHEBI:32563) lysine (CHEBI:25094) is conjugate base of lysinium(1+) (CHEBI:32564) Incoming 2-(difluoromethyl)lysine (CHEBI:74111) has functional parent lysine (CHEBI:25094) N6-(2,4-dinitrophenyl)lysine (CHEBI:53078) has functional parent lysine (CHEBI:25094) lysine derivative (CHEBI:53079) has functional parent lysine (CHEBI:25094) D-lysine (CHEBI:16855) is a lysine (CHEBI:25094) L-lysine (CHEBI:18019) is a lysine (CHEBI:25094) lysinium(1+) (CHEBI:32564) is conjugate acid of lysine (CHEBI:25094) lysinate (CHEBI:32563) is conjugate base of lysine (CHEBI:25094) N2-lysino group (CHEBI:32566) is substituent group from lysine (CHEBI:25094) N6-lysino group (CHEBI:32567) is substituent group from lysine (CHEBI:25094) lysine residue (CHEBI:32568) is substituent group from lysine (CHEBI:25094) lysyl group (CHEBI:37903) is substituent group from lysine (CHEBI:25094) IUPAC Names 2,6-diaminohexanoic acid lysine Synonyms Sources α,ε-diaminocaproic acid ChEBI K ChEBI LYS ChEBI Lysin ChEBI Manual Xrefs Databases C16440 KEGG COMPOUND Lysine Wikipedia View more database links Registry Numbers Types Sources 1616991 Reaxys Registry Number Reaxys 279284 Gmelin Registry Number Gmelin 70-54-2 CAS Registry Number NIST Chemistry WebBook 70-54-2 CAS Registry Number ChemIDplus Citations Types Sources 17439666 PubMed citation Europe PMC 22264337 PubMed citation Europe PMC Last Modified 29 July 2019