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
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
Molecular Formula | C23H33N2O |
Molecular Weight | 353.5209 |
Charge | 1 |
Count |
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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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13259723
Curator's Comment: reference retrieved from http://www.drugfuture.com/chemdata/isopropamide-iodide.html
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2094109 Sources: http://www.genome.jp/dbget-bin/www_bget?dr:D01005 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Primary | DARBID Approved UseIsopropamide (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 Date1957 |
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Primary | DARBID Approved UseIsopropamide (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 Date1957 |
PubMed
Title | Date | PubMed |
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Spectrophotometric determination of isopropamide iodide and trifluoperazine hydrochloride in presence of trifluoperazine oxidative degradate. | 2010 Apr |
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Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method. | 2010 Dec |
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2-Hydroxy-N,N'-diisopropylpropane-1,3-diaminium dichloride. | 2010 Jun 23 |
Patents
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/29133
Unknown
Substance Class |
Chemical
Created
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admin
on
Edited
Fri Dec 15 16:14:43 GMT 2023
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Fri Dec 15 16:14:43 GMT 2023
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Record UNII |
8B9I31H724
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Record Status |
Validated (UNII)
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Record Version |
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CFR |
21 CFR 520.1921
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CFR |
21 CFR 520.1920
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WHO-ATC |
A03CA01
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WHO-VATC |
QA03AB09
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CFR |
21 CFR 522.1920
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WHO-ATC |
A03AB09
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WHO-VATC |
QA03CA01
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NCI_THESAURUS |
C66880
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Code System | Code | Type | Description | ||
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ISOPROPAMIDE
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DTXSID9023174
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PRIMARY | |||
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C73139
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89784
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3775
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8B9I31H724
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7492-32-2
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DB01625
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100000086458
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1500
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PRIMARY | |||
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231-316-9
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SUB02799MIG
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PRIMARY |
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SALT/SOLVATE -> PARENT | |||
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |