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ChEBI
> Main
CHEBI:50599 -
N
τ
-methyl-
L
-histidine
Main
ChEBI Ontology
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ChEBI Name
N
τ
-methyl-
L
-histidine
ChEBI ID
CHEBI:50599
ChEBI ASCII Name
N(tele)-methyl-L-histidine
Definition
A
L
-histidine derivative in which the methyl group is at
N
τ
-position.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:18846, CHEBI:50597
Supplier Information
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Formula
C7H11N3O2
Net Charge
0
Average Mass
169.18126
Monoisotopic Mass
169.08513
InChI
InChI=1S/C7H11N3O2/c1-10-3-5(9-4-10)2-6(8)7(11)12/h3-4,6H,2,8H2,1H3,(H,11,12)/t6-/m0/s1
InChIKey
BRMWTNUJHUMWMS-LURJTMIESA-N
SMILES
Cn1cnc(C[C@H](N)C(O)=O)c1
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
N
τ
-methyl-
L
-histidine (
CHEBI:50599
)
has role
human metabolite (
CHEBI:77746
)
N
τ
-methyl-
L
-histidine (
CHEBI:50599
)
is a
L
-histidine derivative (
CHEBI:84076
)
N
τ
-methyl-
L
-histidine (
CHEBI:50599
)
is a
non-proteinogenic
L
-α-amino acid (
CHEBI:83822
)
N
τ
-methyl-
L
-histidine (
CHEBI:50599
)
is tautomer of
N
τ
-methyl-
L
-histidine zwitterion (
CHEBI:192560
)
Incoming
N
τ
-methyl-
L
-histidine residue (
CHEBI:16367
)
is substituent group from
N
τ
-methyl-
L
-histidine (
CHEBI:50599
)
N
τ
-methyl-
L
-histidine zwitterion (
CHEBI:192560
)
is tautomer of
N
τ
-methyl-
L
-histidine (
CHEBI:50599
)
IUPAC Name
1-methyl-
L
-histidine
Synonyms
Sources
(2
S
)-2-amino-3-(1-methyl-1
H
-imidazol-4-yl)propanoic acid
IUPAC
1-methylhistidine
ChemIDplus
Pi-methylhistidine
HMDB
Manual Xref
Database
HMDB0000001
HMDB
View more database links
Registry Numbers
Types
Sources
1320034
Gmelin Registry Number
Gmelin
332-80-9
CAS Registry Number
ChemIDplus
9727
Beilstein Registry Number
Beilstein
9727
Reaxys Registry Number
Reaxys
Citations
Types
Sources
14363188
PubMed citation
Europe PMC
22777757
PubMed citation
Europe PMC
23452466
PubMed citation
Europe PMC
23980697
PubMed citation
Europe PMC
24164354
PubMed citation
Europe PMC
24681531
PubMed citation
Europe PMC
24783928
PubMed citation
Europe PMC
Last Modified
23 October 2015