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ChEBI
> Main
CHEBI:133686 - 5-bromotryptophan
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ChEBI Name
5-bromotryptophan
ChEBI ID
CHEBI:133686
Definition
A non-proteinogenic α-amino acid that is tryptophan in which the hydrogen at position 5 on the indole ring is replaced by a bromo group.
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This entity has been manually annotated by the ChEBI Team.
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Formula
C11H11BrN2O2
Net Charge
0
Average Mass
283.121
Monoisotopic Mass
282.00039
InChI
InChI=1S/C11H11BrN2O2/c12-7-1-2-10-8(4-7)6(5-14-10)3-9(13)11(15)16/h1-2,4-5,9,14H,3,13H2,(H,15,16)
InChIKey
KZDNJQUJBMDHJW-UHFFFAOYSA-N
SMILES
C1(=CNC2=C1C=C(C=C2)Br)CC(C(O)=O)N
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
)
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
5-bromotryptophan (
CHEBI:133686
)
is a
bromoamino acid (
CHEBI:22930
)
5-bromotryptophan (
CHEBI:133686
)
is a
bromoindole (
CHEBI:52514
)
5-bromotryptophan (
CHEBI:133686
)
is a
non-proteinogenic α-amino acid (
CHEBI:83925
)
5-bromotryptophan (
CHEBI:133686
)
is a
tryptophan derivative (
CHEBI:27164
)
5-bromotryptophan (
CHEBI:133686
)
is tautomer of
5-bromotryptophan zwitterion (
CHEBI:133688
)
Incoming
5-bromotryptophan zwitterion (
CHEBI:133688
)
is tautomer of
5-bromotryptophan (
CHEBI:133686
)
IUPAC Name
5-bromotryptophan
Synonym
Source
2-amino-3-(5-bromo-1
H
-indol-3-yl)propanoic acid
IUPAC
Registry Numbers
Types
Sources
5280904
Reaxys Registry Number
Reaxys
6548-09-0
CAS Registry Number
ChemIDplus
Last Modified
07 October 2016