Details
Stereochemistry | ACHIRAL |
Molecular Formula | C21H23NO3.ClH |
Molecular Weight | 373.873 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CN(C)CCOC(=O)C(OCC#C)(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=RSBGQTFIHFGTSY-UHFFFAOYSA-N
InChI=1S/C21H23NO3.ClH/c1-4-16-25-21(18-11-7-5-8-12-18,19-13-9-6-10-14-19)20(23)24-17-15-22(2)3;/h1,5-14H,15-17H2,2-3H3;1H
Pargeverine (also known as a propinox) is an antispasmodic drug that was studied for the treatment of disorders of the gastrointestinal tract, the uterus, and the gallbladder. Pargeverine showed a dual mechanism of action, it binds to muscarinic and calcium receptors that can be related to its antispasmodic activity. The clinical trial has shown that pargeverine was an effective drug in the treatment of moderate to severe colic pain of biliary origin. In addition, its efficacy and tolerability were determined in patients with moderate-to-severe acute intestinal colic pain. As a result, no differences in blood pressure or heart rate were found among treatments. The incidence of mouth dryness was significantly more frequent with the 20 mg and 30 mg doses of propinox than with the placebo or the 10 mg dose. Information about the current development of this drug is not available.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL1075061 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10797855 |
1.2 µM [Ki] | ||
Target ID: 1.0072804E8 Gene Symbol: Chrm1 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10797855 |
100.0 µM [Ki] | ||
Target ID: CHEMBL5498 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10797855 |
1.5 µM [Ki] |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11146900
propinox (PARGEVERINE) administered i.v. (10 mg, 20 mg and 30 mg)
Route of Administration:
Intravenous
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NCI_THESAURUS |
C29698
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ACTIVE MOIETY
SUBSTANCE RECORD