Promazine

Chlorpromazine was the first antipsychotic drug to be discovered. It is one of the most sedating of the typical antipsychotics and also causes antimuscarinic effects. It has a role as a dopaminergic antagonist, a H1-receptor antagonist, a muscarinic antagonist, a serotonergic antagonist, a phenothiazine antipsychotic drug, an antiemetic and an EC 3.4.21.26 (prolyl oligopeptidase) inhibitor. Tricyclic amine-containing compound. Promazine is a phenothiazine with actions similar to Chlorpromazine but with less antipsychotic activity. It is primarily used in short-term treatment of disturbed behavior and as an antiemetic. eqBChE Ki 3.31 microM Debord et al.

General

Type : Phenothiazine, Drug, Sulfur Compound, Not AlphaBeta Hydrolase target

Chemical_Nomenclature : 10-[3-(dimethylamino)propyl]phenothiazine

Canonical SMILES : CN(C)CCCN1C2=CC=CC=C2SC3=CC=CC=C31

InChI : InChI=1S\/C17H20N2S\/c1-18(2)12-7-13-19-14-8-3-5-10-16(14)20-17-11-6-4-9-15(17)19\/h3-6,8-11H,7,12-13H2,1-2H3

InChIKey : ZGUGWUXLJSTTMA-UHFFFAOYSA-N

Other name(s) :


MW : 320.9

Formula : C17H20N2S

CAS_number : 53-60-1

PubChem : 4926

UniChem : ZGUGWUXLJSTTMA-UHFFFAOYSA-N

IUPHAR : 7281

Wikipedia : Promazine

Target

Families : Promazine ligand of proteins in family
ACHE BCHE

References (2)

Title : Inhibition of butyrylcholinesterase by phenothiazine derivatives - Debord_2002_J.Enzyme.Inhib.Med.Chem_17_197
Author(s) : Debord J , Merle L , Bollinger JC , Dantoine T
Ref : J Enzyme Inhib Med Chem , 17 :197 , 2002
Abstract :
PubMedSearch : Debord_2002_J.Enzyme.Inhib.Med.Chem_17_197
PubMedID: 12443046

Title : Three distinct domains in the cholinesterase molecule confer selectivity for acetyl- and butyrylcholinesterase inhibitors - Radic_1993_Biochemistry_32_12074
Author(s) : Radic Z , Pickering NA , Vellom DC , Camp S , Taylor P
Ref : Biochemistry , 32 :12074 , 1993
Abstract :
PubMedSearch : Radic_1993_Biochemistry_32_12074
PubMedID: 8218285