CHEBI:145225 - promazine sulfoxide

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ChEBI Name promazine sulfoxide ChEBI ID CHEBI:145225 Definition A member of the class of phenothiazines that is promazine carrying an oxo group at position 5. It is a metabolite of the anti-psychotic medication, chlorpromazine. Stars This entity has been manually annotated by the ChEBI Team. Submitter Mark Williams Supplier Information ZINC000015149528 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C17H20N2OS Net Charge 0 Average Mass 300.420 Monoisotopic Mass 300.12963 InChI InChI=1S/C17H20N2OS/c1-18(2)12-7-13-19-14-8-3-5-10-16(14)21(20)17-11-6-4-9-15(17)19/h3-6,8-11H,7,12-13H2,1-2H3 InChIKey KSHDHDWHIWBNHA-UHFFFAOYSA-N SMILES S1(C=2C(N(CCCN(C)C)C=3C1=CC=CC3)=CC=CC2)=O 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): drug metabolite View more via ChEBI Ontology ChEBI Ontology Outgoing promazine sulfoxide (CHEBI:145225) has functional parent promazine (CHEBI:8459) promazine sulfoxide (CHEBI:145225) has role drug metabolite (CHEBI:49103) promazine sulfoxide (CHEBI:145225) is a phenothiazines (CHEBI:38093) promazine sulfoxide (CHEBI:145225) is a sulfoxide (CHEBI:22063) promazine sulfoxide (CHEBI:145225) is a tertiary amino compound (CHEBI:50996) IUPAC Name N,N-dimethyl-3-(5-oxido-10H-phenothiazin-10-yl)propan-1-amine Synonyms Sources 10-[3-(dimethylamino)propyl]-10H-phenothiazine 5-oxide ChEBI 10-[3-(dimethylamino)propyl]-5λ4-phenothiazin-5(10H)-one IUPAC 10-[3-(dimethylamino)propyl]phenothiazine 5-oxide ChEBI 3-(10H-phenothiazin-10-yl)-N,N-dimethylpropan-1-amine S-oxide ChEBI N,N-dimethyl-10H-phenothiazine-10-propanamine 5-oxide ChEBI promazine 5-oxide ChEBI promazine 5-sulfoxide ChEBI promazine S-oxide ChEBI promazine sulphoxide ChEBI propazin sulfoxide ChEBI propazine sulfoxide ChEBI SKF 5418A NIST Chemistry WebBook Manual Xref Database HMDB0013938 HMDB View more database links Registry Number Type Source 146-21-4 CAS Registry Number NIST Chemistry WebBook Citations Last Modified 07 November 2019