CHEBI:138016 - 5-(N-methyl-N-propyl)amiloride

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ChEBI Name 5-(N-methyl-N-propyl)amiloride ChEBI ID CHEBI:138016 ChEBI ASCII Name 5-(N-methyl-N-propyl)amiloride Definition A member of the class of pyrazines that is amiloride in which the primary amino group adjacent to the chloro substiuent has been substituted by a methyl group and a propyl group. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C10H16ClN7O Net Charge 0 Average Mass 285.734 Monoisotopic Mass 285.11049 InChI InChI=1S/C10H16ClN7O/c1-3-4-18(2)8-6(11)15-5(7(12)16-8)9(19)17-10(13)14/h3-4H2,1-2H3,(H2,12,16)(H4,13,14,17,19) InChIKey HDJJAWCPAZTZIG-UHFFFAOYSA-N SMILES N1=C(C(=NC(=C1Cl)N(C)CCC)N)C(=O)NC(N)=N 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): sodium channel blocker An agent that inhibits sodium influx through cell membranes. View more via ChEBI Ontology ChEBI Ontology Outgoing 5-(N-methyl-N-propyl)amiloride (CHEBI:138016) has functional parent amiloride (CHEBI:2639) 5-(N-methyl-N-propyl)amiloride (CHEBI:138016) has role sodium channel blocker (CHEBI:38633) 5-(N-methyl-N-propyl)amiloride (CHEBI:138016) is a guanidines (CHEBI:24436) 5-(N-methyl-N-propyl)amiloride (CHEBI:138016) is a organochlorine compound (CHEBI:36683) 5-(N-methyl-N-propyl)amiloride (CHEBI:138016) is a primary amino compound (CHEBI:50994) 5-(N-methyl-N-propyl)amiloride (CHEBI:138016) is a pyrazines (CHEBI:38314) 5-(N-methyl-N-propyl)amiloride (CHEBI:138016) is a tertiary amino compound (CHEBI:50996) IUPAC Name 3-amino-N-carbamimidoyl-6-chloro-5-[methyl(propyl)amino]pyrazine-2-carboxamide Synonyms Sources 3-amino-N-(aminoiminomethyl)-6-chloro-5-(methylpropylamino)-pyrazinecarboxamide ChemIDplus 5-N-MPA ChEBI 5-N-Mpa ChemIDplus MPA ChEBI Registry Numbers Types Sources 1151-75-3 CAS Registry Number ChemIDplus 548085 Reaxys Registry Number Reaxys Last Modified 27 July 2017