CHEBI:43433 - L-alloisoleucine

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ChEBI Name L-alloisoleucine
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
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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
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).
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
(via L-alpha-amino acid )
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)
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
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Registry Numbers Types Sources
1509-34-8 CAS Registry Number ChemIDplus
1721791 Beilstein Registry Number ChemIDplus
1721791 Reaxys Registry Number Reaxys
Citations Waiting for 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