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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:43433 -
L
-alloisoleucine
Main
ChEBI Ontology
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ChEBI Name
L
-alloisoleucine
ChEBI ID
CHEBI:43433
ChEBI ASCII Name
L-alloisoleucine
Definition
An optically active form of alloisoleucine having
L
-(2
S
,3
R
)-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
InChIKey
AGPKZVBTJJNPAG-UHNVWZDZSA-N
SMILES
CC[C@@H](C)[C@H](N)C(O)=O
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 (Br
o
nsted acid).
(via
organic amino compound
)
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted base).
(via
oxoacid
)
Biological Role
(s):
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
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
)
IUPAC Name
L
-alloisoleucine
Synonyms
Sources
(2
S
,3
R
)-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
IIL
PDBeChem
View more database links
Registry Numbers
Types
Sources
1509-34-8
CAS Registry Number
ChemIDplus
1721791
Beilstein Registry Number
ChemIDplus
1721791
Reaxys Registry Number
Reaxys
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