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Details

Stereochemistry ACHIRAL
Molecular Formula C23H33N2O.Cl
Molecular Weight 388.974
Optical Activity NONE
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISOPROPAMIDE CHLORIDE

SMILES

[Cl-].CC(C)[N+](C)(CCC(C(N)=O)(C1=CC=CC=C1)C2=CC=CC=C2)C(C)C

InChI

InChIKey=YDLRIMWTVADYID-UHFFFAOYSA-N
InChI=1S/C23H32N2O.ClH/c1-18(2)25(5,19(3)4)17-16-23(22(24)26,20-12-8-6-9-13-20)21-14-10-7-11-15-21;/h6-15,18-19H,16-17H2,1-5H3,(H-,24,26);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 C23H33N2O
Molecular Weight 353.5209
Charge 1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity NONE

Isopropamide is a quaternary ammonium antimuscarinic with peripheral effects similar to those of atropine. It has been used as an adjunct in the treatment of peptic ulcer disease, in the relief of gastro-intestinal and urinary tract disorders associated with smooth muscle spasm, in rhinitis, and the relief of symptoms of cold.

Originator

Curator's Comment: reference retrieved from http://www.drugfuture.com/chemdata/isopropamide-iodide.html

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
DARBID

Approved Use

Isopropamide (I) is a quaternary ammonium antimuscarinic with peripheral effects similar to those of atropine. It has been used as an adjunct in the treatment of peptic ulcer disease, in the relief of gastro-intestinal and urinary tract disorders associated with smooth muscle spasm, in rhinitis, and the relief of symptoms of cold.

Launch Date

1957
Primary
DARBID

Approved Use

Isopropamide (I) is a quaternary ammonium antimuscarinic with peripheral effects similar to those of atropine. It has been used as an adjunct in the treatment of peptic ulcer disease, in the relief of gastro-intestinal and urinary tract disorders associated with smooth muscle spasm, in rhinitis, and the relief of symptoms of cold.

Launch Date

1957
Doses

Doses

DosePopulationAdverse events​
40 mg single, oral
MTD
Dose: 40 mg
Route: oral
Route: single
Dose: 40 mg
Sources:
unhealthy, 27-53
Health Status: unhealthy
Age Group: 27-53
Sex: M+F
Sources:
PubMed

PubMed

TitleDatePubMed
Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010-12
2-Hydroxy-N,N'-diisopropylpropane-1,3-diaminium dichloride.
2010-06-23
Spectrophotometric determination of isopropamide iodide and trifluoperazine hydrochloride in presence of trifluoperazine oxidative degradate.
2010-04
Simultaneous RP-HPLC Estimation of Trifluoperazine Hydrochloride and Chlordiazepoxide in Tablet Dosage Forms.
2009-09
Annotation of novel neuropeptide precursors in the migratory locust based on transcript screening of a public EST database and mass spectrometry.
2006-08-09
Evaluation of antimotility effect of Lantana camara L. var. acuelata constituents on neostigmine induced gastrointestinal transit in mice.
2005-09-17
Derivative spectrophotometric, thin layer chromatographic-densitometric and high performance liquid chromatographic determination of trifluoperazine hydrochloride in presence of its hydrogen peroxide induced-degradation product.
2002-01-01
Spectrophotometric determination of trifluoperazine HCl and isopropamide iodide in binary mixture using second derivative and second derivative of the ratio spectra methods.
2001-09
Patents

Sample Use Guides

Unknown
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:55:09 GMT 2025
Edited
by admin
on Mon Mar 31 22:55:09 GMT 2025
Record UNII
F97R3WDS0Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZENEPROPANAMINIUM, .GAMMA.-(AMINOCARBONYL)-N-METHYL-N,N-BIS(1-METHYLETHYL)-.GAMMA.-PHENYL-, CHLORIDE (1:1)
Preferred Name English
ISOPROPAMIDE CHLORIDE
Common Name English
NSC-15548
Code English
Code System Code Type Description
DRUG BANK
DBSALT002274
Created by admin on Mon Mar 31 22:55:09 GMT 2025 , Edited by admin on Mon Mar 31 22:55:09 GMT 2025
PRIMARY
FDA UNII
F97R3WDS0Q
Created by admin on Mon Mar 31 22:55:09 GMT 2025 , Edited by admin on Mon Mar 31 22:55:09 GMT 2025
PRIMARY
PUBCHEM
32320
Created by admin on Mon Mar 31 22:55:09 GMT 2025 , Edited by admin on Mon Mar 31 22:55:09 GMT 2025
PRIMARY
CAS
24353-18-2
Created by admin on Mon Mar 31 22:55:09 GMT 2025 , Edited by admin on Mon Mar 31 22:55:09 GMT 2025
PRIMARY
NSC
15548
Created by admin on Mon Mar 31 22:55:09 GMT 2025 , Edited by admin on Mon Mar 31 22:55:09 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY