Chlorproethazine

General

Type : Phenothiazine,Sulfur Compound,Not A\/B H target

Chemical_Nomenclature : 3-(2-chlorophenothiazin-10-yl)-N,N-diethylpropan-1-amine

Canonical SMILES : CCN(CC)CCCN1C2=CC=CC=C2SC3=C1C=C(C=C3)Cl

InChI : InChI=1S\/C19H23ClN2S\/c1-3-21(4-2)12-7-13-22-16-8-5-6-9-18(16)23-19-11-10-15(20)14-17(19)22\/h5-6,8-11,14H,3-4,7,12-13H2,1-2H3

InChIKey : DBOUGBAQLIXZLV-UHFFFAOYSA-N

Other name(s) : UNII-960NX27Z07,960NX27Z07,CHEMBL52125,SCHEMBL149201,ZINC1135,CHEBI:135464


MW : 346.9

Formula : C19H23ClN2S

CAS_number : 84-01-5

PubChem : 65750

UniChem : DBOUGBAQLIXZLV-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : Chlorproethazine ligand of proteins in family: BCHE

Stucture :

Protein :

References (3)

Title : Comparative effects of cationic triarylmethane, phenoxazine and phenothiazine dyes on horse serum butyrylcholinesterase - Yucel_2008_Arch.Biochem.Biophys_478_201
Author(s) : Yucel YY , Tacal O , Ozer I
Ref : Archives of Biochemistry & Biophysics , 478 :201 , 2008
Abstract : Yucel_2008_Arch.Biochem.Biophys_478_201
ESTHER : Yucel_2008_Arch.Biochem.Biophys_478_201
PubMedSearch : Yucel_2008_Arch.Biochem.Biophys_478_201
PubMedID: 18656440

Title : Toxic effects of chlorpromazine on Carassius auratus and its oxidative stress - Li_2008_J.Environ.Sci.Health.B_43_638
Author(s) : Li T , Zhou Q , Zhang N , Luo Y
Ref : J Environ Sci Health B , 43 :638 , 2008
Abstract : Li_2008_J.Environ.Sci.Health.B_43_638
ESTHER : Li_2008_J.Environ.Sci.Health.B_43_638
PubMedSearch : Li_2008_J.Environ.Sci.Health.B_43_638
PubMedID: 18941986

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 : Debord_2002_J.Enzyme.Inhib.Med.Chem_17_197
ESTHER : Debord_2002_J.Enzyme.Inhib.Med.Chem_17_197
PubMedSearch : Debord_2002_J.Enzyme.Inhib.Med.Chem_17_197
PubMedID: 12443046