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Formula | C13H20N2O2 |
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Molecular Weight | 236.31 | CAS No. | 17692-31-8 | |
Solubility (25°C)* | In vitro | DMSO | 47 mg/mL (198.89 mM) | |
Ethanol | 47 mg/mL (198.89 mM) | |||
Water | 11 mg/mL (46.54 mM) | |||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | Dropropizine (UCB-1967,(±)- Dropropizine) is a racemic non-opiate antitussive agent, it is used as a cough suppressant. |
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In vitro | Dropropizine shows neither mutagenic nor clastogenic effects in Chinese hamster V79 and human EUE cells, while Lithium carbonicum manifestes a weak and mazindol a medium genotoxic response which is in both cases reduce in the presence of microsomal fraction S9. [1] |
In vivo | Dropropizine exhibits antitussive activity in cats noticeably lower than Pinacidil and Codeine. [2] Dropropizine (100 mg/kg, b.w., intraperitoneally) has similar antitussive activity as that of EEPF (200 mg/kg, b.w., orally). [3] Dropropizine exhibits antitussive activity of 28.3% in mechanically induced cough in nonanaesthetized cats, comparable to prenoxdiazine (24.7%).[4] Dropropizine (dropro–dose 100 mg/kg b.w.) exhibits comparable cough-suppressing effect of mucilage from S. althaeae. Dropropizine (dropro–dose 100 mg/kg b.w.) exhibits antitussive activity less than E. officinalis on the mechanically induced cough reflex under experimental conditions. [5] |
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SHIPPING AND STORAGE
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