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    The database and ontology of Chemical Entities of Biological Interest

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isoleucine (CHEBI:24898)

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ChEBI Name isoleucine
ChEBI ID CHEBI:24898
Definition A 2-amino-3-methylpentanoic acid having either (2R,3R)- or (2S,3S)-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
View more on the ChEBI Ontology
ChEBI Ontology
Outgoing isoleucine (CHEBI:24898) has part sec-butyl group (CHEBI:45557)
isoleucine (CHEBI:24898) has role metabolite (CHEBI:25212)
isoleucine (CHEBI:24898) is a 2-amino-3-methylpentanoic acid (CHEBI:38264)
isoleucine (CHEBI:24898) is conjugate acid of isoleucinate (CHEBI:32612)
isoleucine (CHEBI:24898) is conjugate base of isoleucinium (CHEBI:32613)
Incoming β-Asp-Ile (CHEBI:68601) has functional parent isoleucine (CHEBI:24898)
D-isoleucine (CHEBI:27730) is a isoleucine (CHEBI:24898)
L-isoleucine (CHEBI:17191) is a isoleucine (CHEBI:24898)
isoleucinium (CHEBI:32613) is conjugate acid of isoleucine (CHEBI:24898)
isoleucinate (CHEBI:32612) is conjugate base of isoleucine (CHEBI:24898)
isoleucine residue (CHEBI:32615) is substituent group from isoleucine (CHEBI:24898)
isoleucino group (CHEBI:32614) is substituent group from isoleucine (CHEBI:24898)
isoleucyl group (CHEBI:37905) is substituent group from isoleucine (CHEBI:24898)
IUPAC Name
isoleucine
Synonyms Sources
Hile IUPAC
rel-(2R,3R)-2-amino-3-methylpentanoic acid IUPAC
Registry Numbers Types Sources
1721790 Reaxys Registry Number Reaxys
1721790 Beilstein Registry Number Beilstein
443-79-8 CAS Registry Number NIST Chemistry WebBook
443-79-8 CAS Registry Number ChemIDplus
Citation Waiting for Citations Type Source
17190852 PubMed citation CiteXplore
Last Modified
15 October 2012

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