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ChEBI
> Main
CHEBI:74640 -
N
-acetyl-
L
-tryptophan
Main
ChEBI Ontology
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ChEBI Name
N
-acetyl-
L
-tryptophan
ChEBI ID
CHEBI:74640
ChEBI ASCII Name
N-acetyl-L-tryptophan
Definition
A
N
-acetyl-
L
-amino acid that is the
N
-acetyl derivative of
L
-tryptophan.
Stars
This entity has been manually annotated by the ChEBI Team.
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Formula
C13H14N2O3
Net Charge
0
Average Mass
246.26190
Monoisotopic Mass
246.10044
InChI
InChI=1S/C13H14N2O3/c1-
8(16)
15-
12(13(17)
18)
6-
9-
7-
14-
11-
5-
3-
2-
4-
10(9)
11/h2-
5,7,12,14H,6H2,1H3,(H,15,16)
(H,17,18)
/t12-
/m0/s1
InChIKey
DZTHIGRZJZPRDV-LBPRGKRZSA-N
SMILES
CC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(O)=O
Roles Classification
Chemical Role
(s):
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Br
o
nsted 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 via ChEBI Ontology
ChEBI Ontology
Outgoing
N
-acetyl-
L
-tryptophan (
CHEBI:74640
)
has role
metabolite (
CHEBI:25212
)
N
-acetyl-
L
-tryptophan (
CHEBI:74640
)
is a
N
-acetyl-
L
-amino acid (
CHEBI:21545
)
N
-acetyl-
L
-tryptophan (
CHEBI:74640
)
is a
L
-tryptophan derivative (
CHEBI:47994
)
N
-acetyl-
L
-tryptophan (
CHEBI:74640
)
is conjugate acid of
N
-acetyl-
L
-tryptophanate (
CHEBI:143877
)
N
-acetyl-
L
-tryptophan (
CHEBI:74640
)
is enantiomer of
N
-acetyl-
D
-tryptophan (
CHEBI:16734
)
Incoming
N
-acetyl-
L
-tryptophanate (
CHEBI:143877
)
is conjugate base of
N
-acetyl-
L
-tryptophan (
CHEBI:74640
)
N
-acetyl-
D
-tryptophan (
CHEBI:16734
)
is enantiomer of
N
-acetyl-
L
-tryptophan (
CHEBI:74640
)
IUPAC Name
N
-acetyl-
L
-tryptophan
Manual Xrefs
Databases
HMDB0013713
HMDB
LSM-19010
LINCS
View more database links
Registry Numbers
Types
Sources
1218-34-4
CAS Registry Number
ChemIDplus
89476
Reaxys Registry Number
Reaxys
Citations
Types
Sources
3141295
PubMed citation
Europe PMC
6538443
PubMed citation
Europe PMC
7229743
PubMed citation
Europe PMC
Last Modified
25 February 2016