CHEBI:43433 - L-alloisoleucine

ChEBI IDCHEBI:43433
ChEBI NameL-alloisoleucine
Stars
ASCII NameL-alloisoleucine
DefinitionAn optically active form of alloisoleucine having L-(2S,3R)-configuration.
Secondary ChEBI IDsCHEBI:21220, CHEBI:43430, CHEBI:43443
Last Modified23 October 2015
DownloadsMolfile
FormulaC6H13NO2
Net Charge0
Average Mass131.175
Monoisotopic Mass131.09463
SMILESCC[C@@H](C)[C@H](N)C(=O)O
InChIInChI=1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5+/m1/s1
InChIKeyAGPKZVBTJJNPAG-UHNVWZDZSA-N
Species of MetaboliteComponentSourceComments
Homo sapiens (ncbitaxon:9606) - PubMed (10508118)
Roles Classification
Chemical Roles:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
human metabolite  Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
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  Source
(2S,3R)-2-amino-3-methylpentanoic acidIUPAC
alleChEBI
allo-L-isoleucineChemIDplus
L(+)-AlloisoleucineHMDB
threo-3-methyl-L-NorvalineHMDB
threo-L-IsoleucineHMDB
Manual XrefsDatabases
HMDB0000557HMDB
IILPDBeChem
Registry NumbersSources
Reaxys:1721791Reaxys
Beilstein:1721791Beilstein
CAS:1509-34-8ChemIDplus
Citations