CHEBI:43433 - L-alloisoleucine

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ChEBI Name L-alloisoleucine ChEBI ID CHEBI:43433 ChEBI ASCII Name L-alloisoleucine Definition An optically active form of alloisoleucine having L-(2S,3R)-configuration. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:21220, CHEBI:43430, CHEBI:43443 Supplier Information ZINC000001530031 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C6H13NO2 Net Charge 0 Average Mass 131.17296 Monoisotopic Mass 131.09463 InChI InChI=1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5+/m1/s1 InChIKey AGPKZVBTJJNPAG-UHNVWZDZSA-N SMILES CC[C@@H](C)[C@H](N)C(O)=O Metabolite of Species Details Homo sapiens (NCBI:txid9606) See: PubMed 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): human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). View more via ChEBI Ontology ChEBI Ontology Outgoing L-alloisoleucine (CHEBI:43433) has role human metabolite (CHEBI:77746) L-alloisoleucine (CHEBI:43433) is a alloisoleucine (CHEBI:22359) L-alloisoleucine (CHEBI:43433) is a non-proteinogenic L-α-amino acid (CHEBI:83822) L-alloisoleucine (CHEBI:43433) is enantiomer of D-alloisoleucine (CHEBI:20899) L-alloisoleucine (CHEBI:43433) is tautomer of L-alloisoleucine zwitterion (CHEBI:85338) Incoming D-alloisoleucine (CHEBI:20899) is enantiomer of L-alloisoleucine (CHEBI:43433) L-alloisoleucine residue (CHEBI:30008) is substituent group from L-alloisoleucine (CHEBI:43433) L-alloisoleucine zwitterion (CHEBI:85338) is tautomer of L-alloisoleucine (CHEBI:43433) IUPAC Name L-alloisoleucine Synonyms Sources (2S,3R)-2-amino-3-methylpentanoic acid IUPAC alle ChEBI allo-L-isoleucine ChemIDplus L(+)-Alloisoleucine HMDB threo-3-methyl-L-Norvaline HMDB threo-L-Isoleucine HMDB Manual Xrefs Databases HMDB0000557 HMDB IIL PDBeChem View more database links Registry Numbers Types Sources 1509-34-8 CAS Registry Number ChemIDplus 1721791 Beilstein Registry Number ChemIDplus 1721791 Reaxys Registry Number Reaxys Citations Types Sources 10508118 PubMed citation Europe PMC 10674358 PubMed citation Europe PMC 11196106 PubMed citation Europe PMC 1429566 PubMed citation Europe PMC 1638756 PubMed citation Europe PMC 1754297 PubMed citation Europe PMC 2116545 PubMed citation Europe PMC 21680261 PubMed citation Europe PMC 2568853 PubMed citation Europe PMC 7413299 PubMed citation Europe PMC 8844412 PubMed citation Europe PMC 8990521 PubMed citation Europe PMC Last Modified 23 October 2015