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Details

Stereochemistry ACHIRAL
Molecular Formula C20H25ClN4OS.2ClH
Molecular Weight 477.879
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CLOXYPENDYL DIHYDROCHLORIDE

SMILES

Cl.Cl.OCCN1CCN(CCCN2C3=CC=CC=C3SC4=CC(Cl)=CN=C24)CC1

InChI

InChIKey=WVSXGJGMBMQHLN-UHFFFAOYSA-N
InChI=1S/C20H25ClN4OS.2ClH/c21-16-14-19-20(22-15-16)25(17-4-1-2-5-18(17)27-19)7-3-6-23-8-10-24(11-9-23)12-13-26;;/h1-2,4-5,14-15,26H,3,6-13H2;2*1H

HIDE SMILES / InChI
Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula C20H25ClN4OS
Molecular Weight 404.957
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

Cloxypendyl is an antipsychotic drug, invented in the 1960s by the Deutsche Gold und Silber-Scheideanstalt vormals Roessler. The compound was 3.5 times more effective than chlorpromazine in the mouse catalepsy test. No clinical and commercial development was reported.

Originator

Approval Year

Unknown
149124
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:25:45 GMT 2025
Edited
by admin
on Mon Mar 31 23:25:45 GMT 2025
Record UNII
JL21P191Z6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1-PIPERAZINEETHANOL, 4-(3-(3-CHLORO-10H-PYRIDO(3,2-B)(1,4)BENZOTHIAZIN-10-YL)PROPYL)-, DIHYDROCHLORIDE
Preferred Name English
CLOXYPENDYL DIHYDROCHLORIDE
Common Name English
1-PIPERAZINEETHANOL, 4-(3-(3-CHLORO-10H-PYRIDO(3,2-B)(1,4)BENZOTHIAZIN-10-YL)PROPYL)-, HYDROCHLORIDE (1:2)
Systematic Name English
Code System Code Type Description
PUBCHEM
209399
Created by admin on Mon Mar 31 23:25:45 GMT 2025 , Edited by admin on Mon Mar 31 23:25:45 GMT 2025
PRIMARY
FDA UNII
JL21P191Z6
Created by admin on Mon Mar 31 23:25:45 GMT 2025 , Edited by admin on Mon Mar 31 23:25:45 GMT 2025
PRIMARY
CAS
19824-89-6
Created by admin on Mon Mar 31 23:25:45 GMT 2025 , Edited by admin on Mon Mar 31 23:25:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID20173548
Created by admin on Mon Mar 31 23:25:45 GMT 2025 , Edited by admin on Mon Mar 31 23:25:45 GMT 2025
PRIMARY
NIH
NCATS
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