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Methantheline Bromide

Catalog No. T33314   CAS 53-46-3
Synonyms: Frenogastrico, Dixamone bromide, Banthine, Asabaine, Methanthelinium bromide

Methantheline Bromide is a synthetic spasmolytic used to relieve cramps or spasms of the stomach, bowel, and bladder. It is also useful for intestinal or gastric ulcers (peptic ulcer disease), intestinal problems, pancreatitis, gastritis, biliary dysmotility, pyloric or urinary problems.

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Methantheline Bromide Chemical Structure
Methantheline Bromide, CAS 53-46-3
Pack Size Availability Price/USD Quantity
25 mg 6-8 weeks $ 1,520.00
50 mg 6-8 weeks $ 1,980.00
100 mg 6-8 weeks $ 2,500.00
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This compound is a customized synthesis product. We have a strong synthesis team with excellent synthesis technology and capabilities. However, due to various objective factors, there is a low probability that the synthesis will not be successful. If you need to learn more, please feel free to consult us, we will serve you wholeheartedly.
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Methantheline Bromide is a synthetic spasmolytic used to relieve cramps or spasms of the stomach, bowel, and bladder. It is also useful for intestinal or gastric ulcers (peptic ulcer disease), intestinal problems, pancreatitis, gastritis, biliary dysmotility, pyloric or urinary problems.
Synonyms Frenogastrico, Dixamone bromide, Banthine, Asabaine, Methanthelinium bromide
Molecular Weight 420.34
Formula C21H26BrNO3
CAS No. 53-46-3

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. Müller C, Berensmeier A, Hamm H, Dirschka T, Reich K, Fischer T, Rzany B. Efficacy and safety of methantheline bromide (Vagantin(®) ) in axillary and palmar hyperhidrosis: results from a multicenter, randomized, placebo-controlled trial. J Eur Acad Dermatol Venereol. 2013 Oct;27(10):1278-84. doi: 10.1111/j.1468-3083.2012.04708.x. Epub 2012 Sep 25. PubMed PMID: 23004926. 2. [Hyperhidrosis. Effective reduced sweating with methantheline bromide]. MMW Fortschr Med. 2012 May 31;154(10):68-9. German. PubMed PMID: 22803247. 3. Newburger J, Kotenbauder HB. The effect of ion-pair formation on the lethal dose of methantheline bromide. Life Sci. 1977 Feb 15;20(4):627-30. PubMed PMID: 14290. 4. NOGAMI H, AWAZU S, IWATSURU M. STUDIES ON DECOMPOSITION AND STABILIZATION OF DRUGS IN SOLUTION. XIV. STABILIZATION OF METHANTHELINE BROMIDE AND CHOLINE DERIVATIVES IN AQUEOUS SOLUTION BY SURFACE-ACTIVE AGENTS. Chem Pharm Bull (Tokyo). 1963 Oct;11:1251-5. PubMed PMID: 14075277.

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Keywords

Methantheline Bromide 53-46-3 Frenogastrico Dixamone bromide Banthine Dixamone Bromide Asabaine Methanthelinium Bromide Methanthelinium bromide inhibitor inhibit

 

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