CHEBI:20899 - D-alloisoleucine

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ChEBI Name D-alloisoleucine
ChEBI ID CHEBI:20899
ChEBI ASCII Name D-alloisoleucine
Stars This entity has been manually annotated by the ChEBI Team.
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+/m0/s1
InChIKey AGPKZVBTJJNPAG-CRCLSJGQSA-N
SMILES CC[C@H](C)[C@@H](N)C(O)=O
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 )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing D-alloisoleucine (CHEBI:20899) is a D-α-amino acid (CHEBI:16733)
D-alloisoleucine (CHEBI:20899) is a alloisoleucine (CHEBI:22359)
D-alloisoleucine (CHEBI:20899) is enantiomer of L-alloisoleucine (CHEBI:43433)
D-alloisoleucine (CHEBI:20899) is tautomer of D-alloisoleucine zwitterion (CHEBI:85306)
Incoming L-alloisoleucine (CHEBI:43433) is enantiomer of D-alloisoleucine (CHEBI:20899)
D-alloisoleucine residue (CHEBI:30007) is substituent group from D-alloisoleucine (CHEBI:20899)
D-alloisoleucine zwitterion (CHEBI:85306) is tautomer of D-alloisoleucine (CHEBI:20899)
IUPAC Name
D-alloisoleucine
Synonyms Sources
(2R,3S)-2-amino-3-methylpentanoic acid IUPAC
allo-D-isoleucine ChemIDplus
Registry Numbers Types Sources
1317451 Gmelin Registry Number Gmelin
1509-35-9 CAS Registry Number ChemIDplus
1721794 Beilstein Registry Number ChemIDplus
Last Modified
01 June 2006