CHEBI:90721 - N-[3-(aminomethyl)benzyl]acetamidine

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ChEBI Name N-[3-(aminomethyl)benzyl]acetamidine
ChEBI ID CHEBI:90721
ChEBI ASCII Name N-[3-(aminomethyl)benzyl]acetamidine
Definition An aralkylamine that is Nbenzylacetamidine substituted at position 3 on the benzene ring by an aminomethyl group. An inhibitor of nitric oxide synthase.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C10H15N3
Net Charge 0
Average Mass 177.251
Monoisotopic Mass 177.12660
InChI InChI=1S/C10H15N3/c1-8(12)13-7-10-4-2-3-9(5-10)6-11/h2-5H,6-7,11H2,1H3,(H2,12,13)
InChIKey RODUKNYOEVZQPR-UHFFFAOYSA-N
SMILES CC(=N)NCC1=CC(CN)=CC=C1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
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).
Application(s): geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
angiogenesis inhibitor
An agent and endogenous substances that antagonize or inhibit the development of new blood vessels.
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ChEBI Ontology
Outgoing N-[3-(aminomethyl)benzyl]acetamidine (CHEBI:90721) has role angiogenesis inhibitor (CHEBI:48422)
N-[3-(aminomethyl)benzyl]acetamidine (CHEBI:90721) has role EC 1.14.13.39 (nitric oxide synthase) inhibitor (CHEBI:61908)
N-[3-(aminomethyl)benzyl]acetamidine (CHEBI:90721) has role geroprotector (CHEBI:176497)
N-[3-(aminomethyl)benzyl]acetamidine (CHEBI:90721) is a aralkylamine (CHEBI:18000)
N-[3-(aminomethyl)benzyl]acetamidine (CHEBI:90721) is a carboxamidine (CHEBI:35359)
N-[3-(aminomethyl)benzyl]acetamidine (CHEBI:90721) is a primary amino compound (CHEBI:50994)
IUPAC Name
N-{[3-(aminomethyl)phenyl]methyl}ethanimidamide
Synonyms Sources
1400 W ChEBI
1400W ChEBI
W 1400 ChemIDplus
W1400 ChEBI
Manual Xrefs Databases
1389 ChemSpider
14W PDBeChem
DB02044 DrugBank
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Registry Numbers Types Sources
180001-34-7 CAS Registry Number ChemIDplus
8054187 Reaxys Registry Number Reaxys
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Last Modified
23 September 2021