U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C20H24N2OS.ClH
Molecular Weight 376.943
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROPIOPROMAZINE HYDROCHLORIDE

SMILES

Cl.CCC(=O)C1=CC2=C(SC3=C(C=CC=C3)N2CCCN(C)C)C=C1

InChI

InChIKey=ZFWVWZODBGTOIL-UHFFFAOYSA-N
InChI=1S/C20H24N2OS.ClH/c1-4-18(23)15-10-11-20-17(14-15)22(13-7-12-21(2)3)16-8-5-6-9-19(16)24-20;/h5-6,8-11,14H,4,7,12-13H2,1-3H3;1H

HIDE SMILES / InChI

Molecular Formula C20H24N2OS
Molecular Weight 340.482
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

Propionylpromazine is used as a neuroleptic to combat stress in pets and farm animals. The main use is to combat stress in the transport of pigs. Propionylpromazine was in common use in veterinary practice in the 1950s and 1960s. Propionylpromazine is of interest to JECFA because of the illicit use at pharmacological dosage (< 1 mg/kg i.m.) in the immediate pre-slaughter period.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Propiopromazine

Approved Use

Indications for use. For oral administration as a tranquilizer. As an aid in handling difficult, excited, and unruly dogs, and in controlling excessive kennel barking, car sickness, and severe dermatitis. It is also indicated for use in minor surgery and prior to routine examinations, laboratory procedures, and diagnostic procedures.
Primary
TRANVET

Approved Use

Propionylpromazine is used as a neuroleptic to combat stress in pets and farm animals. The main use is to combat stress in the transport of pigs.

Launch Date

1960
PubMed

PubMed

TitleDatePubMed
Effects of electroanesthesia and a phenothiazine tranquilizer on thermoregulation in the sheep.
1977 Mar
[Effect of phenothiazine derivative on adrenal cortex response of sheep to repeated emotional stress].
1991
[Hepatic resection in the fetal rabbit. Histologic comparison of tissue regeneration in the fetus versus the adult].
1996 Nov
Retrospective evaluation of cardiopulmonary and acid-base variables during long-term balanced anesthesia for experimental surgery in dogs.
1997 Dec
Gas chromatographic-mass spectrometric analysis of veterinary tranquillizers in urine: evaluation of method performance.
1999 Oct 29
Trypanosoma cruzi trypanothione reductase is inactivated by peroxidase-generated phenothiazine cationic radicals.
2001 Apr
Spectrophotometric determination of vanadium(V) in minerals, steels, soil and biological samples using phenothiazine derivatives.
2001 Aug
[The opinion of O. Habler].
2001 Aug
[Acute normovolemic hemodilution (ANH). Der Anaesthesist (2000) 49: 939-948].
2001 Aug
[Inactivation of Trypanosoma cruzi trypanothione reductase by phenothiazine cationic free radicals].
2001 Jan-Mar
Analysis of promazines in bovine livers by high performance liquid chromatography with ultraviolet and fluorimetric detection.
2003 Feb 6
Development of a rapid screening test for veterinary sedatives and the beta-blocker carazolol in porcine kidney by ELISA.
2004 Feb
Stability of the tranquilizer drug propionylpromazine hydrochloride in formulated products.
2005 Jun
Comprehensive screening and quantification of veterinary drugs in milk using UPLC-ToF-MS.
2008 Jul
Rapid method for the determination of tranquilizers and a beta-blocker in porcine and bovine kidney by liquid chromatography with tandem mass spectrometry.
2009 Apr 1
Effects of inosine on reperfusion injury after cardiopulmonary bypass.
2010 Nov 8
Patents

Sample Use Guides

Dogs: Administer 0.5 to 2.0 milligrams per pound of body weight once or twice daily, depending upon the degree of tranquilization desired.
Route of Administration: Oral
10 uM Propiopromazine produced 95-100% inactivation of Trypanosoma cruzi trypanothione reductase (TR).
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:24:23 GMT 2023
Edited
by admin
on Fri Dec 15 15:24:23 GMT 2023
Record UNII
U0BND6SD2I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROPIOPROMAZINE HYDROCHLORIDE
GREEN BOOK  
Common Name English
PROPIOPROMAZINE HCL
Common Name English
PROPIOPROMAZINE HYDROCHLORIDE [GREEN BOOK]
Common Name English
1-(10-(3-(DIMETHYLAMINO)PROPYL)-10H-PHENOTHIAZIN-2-YL)-1-PROPANONE
Systematic Name English
PROPIONYLPROMAZINE HYDROCHLORIDE
Common Name English
1-PROPANONE, 1-(10-(3-(DIMETHYLAMINO)PROPYL)-10H-PHENOTHIAZIN-2-YL)-, MONOHYDROCHLORIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29710
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
CFR 21 CFR 522.2002
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
Code System Code Type Description
DRUG BANK
DBSALT001697
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
PRIMARY
EPA CompTox
DTXSID4045187
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
PRIMARY
PUBCHEM
24351
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
PRIMARY
NCI_THESAURUS
C84114
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
PRIMARY
FDA UNII
U0BND6SD2I
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
PRIMARY
CAS
7681-67-6
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
PRIMARY
MESH
C026328
Created by admin on Fri Dec 15 15:24:23 GMT 2023 , Edited by admin on Fri Dec 15 15:24:23 GMT 2023
PRIMARY
Related Record Type Details
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