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Details

Stereochemistry ACHIRAL
Molecular Formula C23H33N2O.Cl
Molecular Weight 388.974
Optical Activity NONE
Defined Stereocenters 0 / 0
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 / 0
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 (max)
MTD
Dose: 40 mg
Route: oral
Route: single
Dose: 40 mg
Sources: Page: p.537
unhealthy, 27-53
n = 7
Health Status: unhealthy
Condition: Duodenal ulcer
Age Group: 27-53
Sex: M+F
Population Size: 7
Sources: Page: p.537
PubMed

PubMed

TitleDatePubMed
Spectrophotometric determination of trifluoperazine HCl and isopropamide iodide in binary mixture using second derivative and second derivative of the ratio spectra methods.
2001 Sep
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 Jan 1
Annotation of novel neuropeptide precursors in the migratory locust based on transcript screening of a public EST database and mass spectrometry.
2006 Aug 9
Simultaneous RP-HPLC Estimation of Trifluoperazine Hydrochloride and Chlordiazepoxide in Tablet Dosage Forms.
2009 Sep
Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method.
2010 Dec
2-Hydroxy-N,N'-diisopropylpropane-1,3-diaminium dichloride.
2010 Jun 23
Patents

Sample Use Guides

Unknown
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:55:40 GMT 2023
Edited
by admin
on Sat Dec 16 09:55:40 GMT 2023
Record UNII
F97R3WDS0Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ISOPROPAMIDE CHLORIDE
Common Name English
NSC-15548
Code English
BENZENEPROPANAMINIUM, .GAMMA.-(AMINOCARBONYL)-N-METHYL-N,N-BIS(1-METHYLETHYL)-.GAMMA.-PHENYL-, CHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
DRUG BANK
DBSALT002274
Created by admin on Sat Dec 16 09:55:40 GMT 2023 , Edited by admin on Sat Dec 16 09:55:40 GMT 2023
PRIMARY
FDA UNII
F97R3WDS0Q
Created by admin on Sat Dec 16 09:55:40 GMT 2023 , Edited by admin on Sat Dec 16 09:55:40 GMT 2023
PRIMARY
PUBCHEM
32320
Created by admin on Sat Dec 16 09:55:40 GMT 2023 , Edited by admin on Sat Dec 16 09:55:40 GMT 2023
PRIMARY
CAS
24353-18-2
Created by admin on Sat Dec 16 09:55:40 GMT 2023 , Edited by admin on Sat Dec 16 09:55:40 GMT 2023
PRIMARY
NSC
15548
Created by admin on Sat Dec 16 09:55:40 GMT 2023 , Edited by admin on Sat Dec 16 09:55:40 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY