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Details

Stereochemistry ACHIRAL
Molecular Formula C23H33N2O
Molecular Weight 353.5209
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of ISOPROPAMIDE

SMILES

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

InChI

InChIKey=JTPUMZTWMWIVPA-UHFFFAOYSA-O
InChI=1S/C23H32N2O/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)/p+1

HIDE SMILES / InChI

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

-3.85948811E11
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

-3.85948811E11
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
Evaluation of antimotility effect of Lantana camara L. var. acuelata constituents on neostigmine induced gastrointestinal transit in mice.
2005 Sep 17
Annotation of novel neuropeptide precursors in the migratory locust based on transcript screening of a public EST database and mass spectrometry.
2006 Aug 9
Spectrophotometric determination of isopropamide iodide and trifluoperazine hydrochloride in presence of trifluoperazine oxidative degradate.
2010 Apr
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 Fri Dec 15 16:14:43 UTC 2023
Edited
by admin
on Fri Dec 15 16:14:43 UTC 2023
Record UNII
8B9I31H724
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ISOPROPAMIDE
VANDF   WHO-DD  
Common Name English
ISOPROPAMIDE ION
Common Name English
BENZENEPROPANAMINIUM, .GAMMA.-(AMINOCARBONYL)-N-METHYL-N,N-BIS(1-METHYLETHYL)-.GAMMA.-PHENYL-
Systematic Name English
(3-CARBAMOYL-3,3-DIPHENYLPROPYL)DIISOPROPYLMETHYLAMMONIUM
Systematic Name English
ISOPROPAMIDE CATION
Common Name English
Isopropamide [WHO-DD]
Common Name English
ISOPROPAMIDE [VANDF]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 520.1921
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
CFR 21 CFR 520.1920
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
WHO-ATC A03CA01
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
WHO-VATC QA03AB09
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
CFR 21 CFR 522.1920
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
WHO-ATC A03AB09
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
WHO-VATC QA03CA01
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
NCI_THESAURUS C66880
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
Code System Code Type Description
WIKIPEDIA
ISOPROPAMIDE
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
EPA CompTox
DTXSID9023174
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
NCI_THESAURUS
C73139
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
RXCUI
89784
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY RxNorm
PUBCHEM
3775
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
FDA UNII
8B9I31H724
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
CAS
7492-32-2
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
DRUG BANK
DB01625
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
SMS_ID
100000086458
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
DRUG CENTRAL
1500
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
ECHA (EC/EINECS)
231-316-9
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
EVMPD
SUB02799MIG
Created by admin on Fri Dec 15 16:14:43 UTC 2023 , Edited by admin on Fri Dec 15 16:14:43 UTC 2023
PRIMARY
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ACTIVE MOIETY