Valperinol: Difference between revisions
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{{Short description|Chemical compound}} |
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{{Drugbox |
{{Drugbox |
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| IUPAC_name = (1''R'',3''R'',4''S'',6''R'',7''S'',8''R'',10''R'')-8-methoxy-10-methyl-3-(1-piperidinylmethyl)-2,9-dioxatricyclo[4.3.1.0<sup>3,7</sup>]decan-4-ol |
| IUPAC_name = (1''R'',3''R'',4''S'',6''R'',7''S'',8''R'',10''R'')-8-methoxy-10-methyl-3-(1-piperidinylmethyl)-2,9-dioxatricyclo[4.3.1.0<sup>3,7</sup>]decan-4-ol |
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| image = Valperinol.svg |
| image = Valperinol.svg |
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| CAS_number_Ref = {{cascite|correct|CAS}} |
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| CAS_number = 64860-67-9 |
| CAS_number = 64860-67-9 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 580OD29R6M |
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| ATC_prefix = None |
| ATC_prefix = None |
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| ATC_suffix = |
| ATC_suffix = |
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'''Valperinol''' ([[International Nonproprietary Name|INN]]; '''GA 30-905''') is a [[drug]] which acts as a [[calcium channel blocker]].<ref name="pmid6543120">{{cite journal |vauthors=Thies PW, Asai A, Bán I, David S, Finner E | title = [The synthesis of valperinol and various 3-aminomethyl derivatives of 2,9-dioxatricyclo[4,3,1,0(3,7)]decane from didrovaltrate] | language = |
'''Valperinol''' ([[International Nonproprietary Name|INN]]; '''GA 30-905''') is a [[drug]] which acts as a [[calcium channel blocker]].<ref name="pmid6543120">{{cite journal |vauthors=Thies PW, Asai A, Bán I, David S, Finner E | title = [The synthesis of valperinol and various 3-aminomethyl derivatives of 2,9-dioxatricyclo[4,3,1,0(3,7)]decane from didrovaltrate] | language = de | journal = Arzneimittel-Forschung | volume = 34 | issue = 11 | pages = 1460–3 | year = 1984 | pmid = 6543120 }}</ref><ref name="pmid6098282">{{cite journal | author = Dose M | title = [Calcium antagonist properties of valperinol] | language = de | journal = Arzneimittel-Forschung | volume = 34 | issue = 11 | pages = 1464–6 | year = 1984 | pmid = 6098282 }}</ref> It was patented as a possible [[sedative]], [[antiepileptic]], and/or [[Management of Parkinson's disease#Medication|antiparkinsonian]] agent, but was never marketed.<ref name="isbn978-0-412-46630-4">{{cite book | title = Dictionary of Pharmacological Agents Volume 2 | url = https://books.google.com/books?id=A0THacd46ZsC&pg=PA2104 | access-date = 22 April 2012 | publisher = CRC Press | isbn = 978-0-412-46630-4 | page = 2104|date = 1996-11-21}}</ref> |
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== References == |
== References == |
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[[Category:Ethers]] |
[[Category:Ethers]] |
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[[Category: |
[[Category:1-Piperidinyl compounds]] |
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{{heterocyclic-stub}} |
Latest revision as of 15:57, 24 July 2024
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Formula | C16H27NO4 |
Molar mass | 297.395 g·mol−1 |
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Valperinol (INN; GA 30-905) is a drug which acts as a calcium channel blocker.[1][2] It was patented as a possible sedative, antiepileptic, and/or antiparkinsonian agent, but was never marketed.[3]
References
[edit]- ^ Thies PW, Asai A, Bán I, David S, Finner E (1984). "[The synthesis of valperinol and various 3-aminomethyl derivatives of 2,9-dioxatricyclo[4,3,1,0(3,7)]decane from didrovaltrate]". Arzneimittel-Forschung (in German). 34 (11): 1460–3. PMID 6543120.
- ^ Dose M (1984). "[Calcium antagonist properties of valperinol]". Arzneimittel-Forschung (in German). 34 (11): 1464–6. PMID 6098282.
- ^ Dictionary of Pharmacological Agents Volume 2. CRC Press. 1996-11-21. p. 2104. ISBN 978-0-412-46630-4. Retrieved 22 April 2012.