CHEBI:27730 - D-isoleucine

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ChEBI Name D-isoleucine ChEBI ID CHEBI:27730 ChEBI ASCII Name D-isoleucine Definition The D-enantiomer of isoleucine. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:21044, CHEBI:42091, CHEBI:4201 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 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-RFZPGFLSSA-N SMILES CC[C@@H](C)[C@@H](N)C(O)=O Metabolite of Species Details Saccharomyces cerevisiae (NCBI:txid4932) 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): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. Saccharomyces cerevisiae metabolite Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ). Daphnia magna metabolite A Daphnia metabolite produced by the species Daphnia magna. (via isoleucine ) View more via ChEBI Ontology ChEBI Ontology Outgoing D-isoleucine (CHEBI:27730) has role Saccharomyces cerevisiae metabolite (CHEBI:75772) D-isoleucine (CHEBI:27730) has role bacterial metabolite (CHEBI:76969) D-isoleucine (CHEBI:27730) is a D-α-amino acid (CHEBI:16733) D-isoleucine (CHEBI:27730) is a isoleucine (CHEBI:24898) D-isoleucine (CHEBI:27730) is conjugate acid of D-isoleucinate (CHEBI:32608) D-isoleucine (CHEBI:27730) is conjugate base of D-isoleucinium (CHEBI:32609) D-isoleucine (CHEBI:27730) is enantiomer of L-isoleucine (CHEBI:17191) D-isoleucine (CHEBI:27730) is tautomer of D-isoleucine zwitterion (CHEBI:193151) Incoming D-isoleucine derivative (CHEBI:84113) has functional parent D-isoleucine (CHEBI:27730) D-isoleucinium (CHEBI:32609) is conjugate acid of D-isoleucine (CHEBI:27730) D-isoleucinate (CHEBI:32608) is conjugate base of D-isoleucine (CHEBI:27730) L-isoleucine (CHEBI:17191) is enantiomer of D-isoleucine (CHEBI:27730) D-isoleucine residue (CHEBI:30010) is substituent group from D-isoleucine (CHEBI:27730) D-isoleucino group (CHEBI:32611) is substituent group from D-isoleucine (CHEBI:27730) D-isoleucyl group (CHEBI:32610) is substituent group from D-isoleucine (CHEBI:27730) D-isoleucine zwitterion (CHEBI:193151) is tautomer of D-isoleucine (CHEBI:27730) IUPAC Name D-isoleucine Synonyms Sources (2R,3R)-2-amino-3-methylpentanoic acid IUPAC (2R,3R)-2-Amino-3-methylvaleric acid KEGG COMPOUND (R)-2-Amino-(S)-3-methylvaleric acid KEGG COMPOUND D-Isoleucine KEGG COMPOUND D-ISOLEUCINE PDBeChem DIL PDBeChem Manual Xrefs Databases C06418 KEGG COMPOUND DIL PDBeChem US2011059503 Patent US7741540 Patent YMDB00853 YMDB View more database links Registry Numbers Types Sources 1721793 Beilstein Registry Number Beilstein 1721793 Reaxys Registry Number Reaxys 278733 Gmelin Registry Number Gmelin 319-78-8 CAS Registry Number ChemIDplus Citations Types Sources 24312553 PubMed citation Europe PMC 24966047 PubMed citation Europe PMC 3289762 PubMed citation Europe PMC 4150713 PubMed citation Europe PMC 57739 PubMed citation Europe PMC Last Modified 14 September 2015