CHEBI:3649 - chlorpromazine hydrochloride

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ChEBI Name chlorpromazine hydrochloride ChEBI ID CHEBI:3649 Definition The hydrochloride salt of chlorpromazine. 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 C17H19ClN2S.HCl Net Charge 0 Average Mass 355.32558 Monoisotopic Mass 354.07243 InChI InChI=1S/C17H19ClN2S.ClH/c1-19(2)10-5-11-20-14-6-3-4-7-16(14)21-17-9-8-13(18)12-15(17)20;/h3-4,6-9,12H,5,10-11H2,1-2H3;1H InChIKey FBSMERQALIEGJT-UHFFFAOYSA-N SMILES [H+].[Cl-].CN(C)CCCN1c2ccccc2Sc2ccc(Cl)cc12 Roles Classification Biological Role(s): anticoronaviral agent Any antiviral agent which inhibits the activity of coronaviruses. Application(s): phenothiazine antipsychotic drug View more via ChEBI Ontology ChEBI Ontology Outgoing chlorpromazine hydrochloride (CHEBI:3649) has part chlorpromazine (CHEBI:3647) chlorpromazine hydrochloride (CHEBI:3649) has role anticoronaviral agent (CHEBI:149553) chlorpromazine hydrochloride (CHEBI:3649) has role phenothiazine antipsychotic drug (CHEBI:37930) chlorpromazine hydrochloride (CHEBI:3649) is a hydrochloride (CHEBI:36807) chlorpromazine hydrochloride (CHEBI:3649) is a phenothiazines (CHEBI:38093) IUPAC Name 3-(2-chloro-10H-phenothiazin-10-yl)-N,N-dimethylpropan-1-amine hydrochloride Synonyms Sources 2-chloro-10-(3-(dimethylamino)propyl)phenothiazine monohydrochloride ChemIDplus 2-chloro-N,N-dimethyl-10H-phenothiazine-10-propanamine monohydrochloride ChemIDplus Chloropromazine monohydrochloride KEGG COMPOUND Chlorpromazine hydrochloride KEGG COMPOUND chlorpromazinium chloride ChemIDplus Brand Names Sources Aminazin DrugBank Ampliactil DrugBank Chlorazin ChemIDplus Hibernal ChemIDplus Largactil DrugBank Plegomazin DrugBank Propaphenin DrugBank Thorazine ChemIDplus Manual Xrefs Databases C07952 KEGG COMPOUND D00789 KEGG DRUG DB00477 DrugBank View more database links Registry Numbers Types Sources 3779989 Reaxys Registry Number Reaxys 3779989 Beilstein Registry Number Beilstein 69-09-0 CAS Registry Number ChemIDplus Citations Types Sources 18968700 PubMed citation Europe PMC 18969944 PubMed citation Europe PMC 20541454 PubMed citation Europe PMC 22527301 PubMed citation Europe PMC 24521912 PubMed citation Europe PMC 6196640 PubMed citation Europe PMC Last Modified 23 April 2020