CHEBI:27730 - D-isoleucine

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
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
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)
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)
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 Waiting for 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