Pramiverine
From EverybodyWiki Bios & Wiki
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| Synonyms | Cintaverin, Monoverin, Propaminodiphene, Raptalgin, Sistalcin, Sistalgin, Syntaverin, EMD 9806, HSp 2986. |
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| E number | {{#property:P628}} |
| ECHA InfoCard | {{#property:P2566}} |
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| Formula | C21H27N |
| Molar mass | 293.454 g·mol−1 |
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Pramiverine is a spasmolytic and cholinolytic analgesic drug.
The structure is related to Budipine/Prodipine but instead of the more typical piperidine, it is based on an atypical cyclohexylamine ring system, where the amine is situated outside of the alicyclic ring. SIR-117 is another example of this unusual chemistry as was Lednicer's U-32,802A.
See also
References
- ↑ Morel CJ (April 1976). "[Experimental studies on pramiverine (author's transl)]". Arzneimittel-Forschung (in German). 26 (4b): 699–702. PMID 989018.CS1 maint: Unrecognized language (link)
- ↑ Enenkel HJ, Müller-Calgan H, Schorscher E (April 1976). "[On the cholinolytic activity of pramiverine]". Arzneimittel-Forschung (in German). 26 (4b): 690–6. PMID 821493.CS1 maint: Unrecognized language (link)
- ↑ Niemann H, Jakob G (April 1976). "[Eosphagomanometric finding in man after intravenous administration of a new cholinolytic (pramiverine), atropine and scopolamine butylbromide]". Arzneimittel-Forschung (in German). 26 (4b): 728–30. PMID 989022.CS1 maint: Unrecognized language (link)
- ↑ Chieri RA (April 1976). "[Animal experimental study on spasmolytic and analgesic activities of pramiverine, metamizole and their combination (author's transl)]". Arzneimittel-Forschung (in German). 26 (4b): 696–8. PMID 989017.CS1 maint: Unrecognized language (link)
- ↑ Koch E (April 1976). "[Profile comment on clinical and experimental studies of pramiverine and pramiverine/metamizole (author's transl)]". Arzneimittel-Forschung (in German). 26 (4b): 686–9. PMID 782469.CS1 maint: Unrecognized language (link)
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