Tolperisone: Difference between revisions

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{{Drugbox
{{Drugbox
|IUPAC_name = 2-methyl-1-(4-methylphenyl)-3-(1-piperidyl)propan-1-one
| IUPAC_name = 2-methyl-1-(4-methylphenyl)-3-(1-piperidyl)propan-1-one
| image=Tolperisone.svg
| image=Tolperisone.svg
| width = 120
| width = 120
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* {{cite journal | author = Ribi C, Vermeulen C, Hauser C | title = Anaphylactic reactions to tolperisone (Mydocalm). | journal = Swiss Med Wkly | volume = 133 | issue = 25-26 | pages = 369-71 | year = 2003 | id = PMID 12947534}}
* {{cite journal | author = Ribi C, Vermeulen C, Hauser C | title = Anaphylactic reactions to tolperisone (Mydocalm). | journal = Swiss Med Wkly | volume = 133 | issue = 25-26 | pages = 369-71 | year = 2003 | id = PMID 12947534}}


{{Muscle relaxants}}


{{Muscle relaxants}}
[[Category:Drug]]

Revision as of 14:41, 8 April 2015

Tolperisone
File:Tolperisone.svg
Clinical data
ATC code
Identifiers
CAS Number
PubChem CID
E number{{#property:P628}}
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Chemical and physical data
FormulaC16H23NO
Molar mass245.36 g/mol

WikiDoc Resources for Tolperisone

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Tolperisone, a piperidine derivative, is a centrally acting muscle relaxant. Brand names include Mydocalm and Mydeton.

External links

  • Hofer D, Lohberger B, Steinecker B, Schmidt K, Quasthoff S, Schreibmayer W (2006). "A comparative study of the action of tolperisone on seven different voltage dependent sodium channel isoforms". Eur J Pharmacol. 538 (1–3): 5–14. PMID 16650844.
  • Kocsis P, Farkas S, Fodor L, Bielik N, Thán M, Kolok S, Gere A, Csejtei M, Tarnawa I (2005). "Tolperisone-type drugs inhibit spinal reflexes via blockade of voltage-gated sodium and calcium channels". J Pharmacol Exp Ther. 315 (3): 1237–46. PMID 16126840.
  • Ribi C, Vermeulen C, Hauser C (2003). "Anaphylactic reactions to tolperisone (Mydocalm)". Swiss Med Wkly. 133 (25–26): 369–71. PMID 12947534.