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ChEBI
> Main
CHEBI:16628 - methylguanidine
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ChEBI Ontology
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ChEBI Name
methylguanidine
ChEBI ID
CHEBI:16628
Definition
A guanidine in which one of the amino hydrogens of guanidine itself is substituted by a methyl group.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:43998, CHEBI:6876, CHEBI:14600, CHEBI:25304
Supplier Information
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Formula
C2H7N3
Net Charge
0
Average Mass
73.09720
Monoisotopic Mass
73.06400
InChI
InChI=1S/C2H7N3/c1-5-2(3)4/h1H3,(H4,3,4,5)
InChIKey
CHJJGSNFBQVOTG-UHFFFAOYSA-N
SMILES
CNC(N)=N
Roles Classification
Biological Role
(s):
EC 1.14.13.39 (nitric oxide synthase) inhibitor
An EC 1.14.13.* (oxidoreductase acting on paired donors, incorporating 1 atom of oxygen, with NADH or NADPH as one donor) inhibitor that interferes with the action of nitric oxide synthase (EC 1.14.13.39).
uremic toxin
A toxin that accumulates in patients with chronic kidney disease.
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
methylguanidine (
CHEBI:16628
)
has role
EC 1.14.13.39 (nitric oxide synthase) inhibitor (
CHEBI:61908
)
methylguanidine (
CHEBI:16628
)
has role
metabolite (
CHEBI:25212
)
methylguanidine (
CHEBI:16628
)
has role
uremic toxin (
CHEBI:64584
)
methylguanidine (
CHEBI:16628
)
is a
guanidines (
CHEBI:24436
)
methylguanidine (
CHEBI:16628
)
is conjugate base of
methylguanidinium (
CHEBI:57840
)
Incoming
methylguanidinium (
CHEBI:57840
)
is conjugate acid of
methylguanidine (
CHEBI:16628
)
IUPAC Name
1-methylguanidine
Synonyms
Sources
1-METHYLGUANIDINE
PDBeChem
Methylguanidin
ChemIDplus
Methylguanidine
KEGG COMPOUND
MGX
HMDB
Monomethyl guanidin
HMDB
monomethylguanidine
NIST Chemistry WebBook
N
-methylguanidine
NIST Chemistry WebBook
N1-Methylguanidine
HMDB
Manual Xrefs
Databases
C02294
KEGG COMPOUND
CPD-593
MetaCyc
HMDB0001522
HMDB
MGX
PDBeChem
PL391702
Patent
View more database links
Registry Numbers
Types
Sources
1738993
Reaxys Registry Number
Reaxys
323399
Gmelin Registry Number
Gmelin
471-29-4
CAS Registry Number
ChemIDplus
471-29-4
CAS Registry Number
NIST Chemistry WebBook
Citations
Types
Sources
14744621
PubMed citation
Europe PMC
17190852
PubMed citation
Europe PMC
17409514
PubMed citation
Europe PMC
19286340
PubMed citation
Europe PMC
21090628
PubMed citation
Europe PMC
22342614
PubMed citation
Europe PMC
Last Modified
25 September 2017