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

ChEBI IDCHEBI:90721
ChEBI NameN-[3-(aminomethyl)benzyl]acetamidine
Stars
ASCII NameN-[3-(aminomethyl)benzyl]acetamidine
DefinitionAn aralkylamine that is Nbenzylacetamidine substituted at position 3 on the benzene ring by an aminomethyl group. An inhibitor of nitric oxide synthase.
Last Modified23 September 2021
SubmitterSteve
DownloadsMolfile
FormulaC10H15N3
Net Charge0
Average Mass177.251
Monoisotopic Mass177.12660
SMILESCC(=N)NCc1cccc(CN)c1
InChIInChI=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)
InChIKeyRODUKNYOEVZQPR-UHFFFAOYSA-N
Roles Classification
Chemical Role:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Role:
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).
Applications:
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.
ChEBI Ontology
Outgoing Relation(s)
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  Source
1400WChEBI
W1400ChEBI
1400 WChEBI
W 1400ChemIDplus
Manual XrefsDatabases
DB02044DrugBank
14WPDBeChem
1389ChemSpider
Registry NumbersSources
Reaxys:8054187Reaxys
CAS:180001-34-7ChemIDplus
Citations