This is an old revision of this page, as edited by Beetstra (talk | contribs) at 10:07, 29 July 2011 (Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: ChEMBL.). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
Revision as of 10:07, 29 July 2011 by Beetstra (talk | contribs) (Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: ChEMBL.)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)This article does not cite any sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. Find sources: "Methylscopolamine bromide" – news · newspapers · books · scholar · JSTOR (December 2009) (Learn how and when to remove this message) |
It has been suggested that this article be merged with Methylscopolamine. (Discuss) Proposed since October 2009. |
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Elimination half-life | 3 - 4hr |
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.005.314 |
Chemical and physical data | |
Formula | C18H24NO4 |
Molar mass | 318.388 g/mol g·mol |
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Methscopolamine, usually provided as a bromide salt (Pamine), is an oral medication used along with other medications to treat peptic ulcers by reducing stomach acid secretion. With the advent of proton pump inhibitors and antihistamine medications it is rarely used for this anymore. It can also be used for stomach or intestinal spasms, to reduce salivation, and to treat motion sickness. Methscopolamine is also commonly used as a drying agent, to dry up post-nasal drip, in cold,irritable bowel syndrome and allergy medications (Extendryl, AlleRx, Rescon).
Methscopolamine, a methylated derivative of scopolamine, is a muscarinic antagonist structurally similar to the neurotransmitter acetylcholine. Its mechanism of action involves blocking the muscarinic acetylcholine receptors.
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