Valperinol |
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- In general: non-regulated
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(1R,3R,4S,6R,7S,8R,10R)-8-methoxy-10-methyl-3-(1-piperidinylmethyl)-2,9-dioxatricyclo[4.3.1.03,7]decan-4-ol
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| Formula | C16H27NO4 |
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| Molar mass | 297.395 g·mol−1 |
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| 3D model (JSmol) | |
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O1[C@@H](OC)[C@@H]2[C@@]3(O[C@H]1[C@@H]([C@H]2C[C@@H]3O)C)CN4CCCCC4
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InChI=1S/C16H27NO4/c1-10-11-8-12(18)16(9-17-6-4-3-5-7-17)13(11)15(19-2)20-14(10)21-16/h10-15,18H,3-9H2,1-2H3/t10-,11-,12+,13-,14+,15-,16-/m1/s1 Key:KZSHXABWNBVUTK-GBIHRFPISA-N
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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
- ^ 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.
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| Calcium | | VDCCsTooltip Voltage-dependent calcium channels | |
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| Potassium | | VGKCsTooltip Voltage-gated potassium channels | |
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| IRKsTooltip Inwardly rectifying potassium channel | | Blockers | |
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| Activators |
- GIRKTooltip G protein-coupled inwardly rectifying potassium channel-specific: ML-297 (VU0456810)
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| KCaTooltip Calcium-activated potassium channel | |
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| K2PsTooltip Tandem pore domain potassium channel | |
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| Sodium | | VGSCsTooltip Voltage-gated sodium channels | |
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| ENaCTooltip Epithelial sodium channel | |
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| ASICsTooltip Acid-sensing ion channel | |
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| Chloride | | CaCCsTooltip Calcium-activated chloride channel | |
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| CFTRTooltip Cystic fibrosis transmembrane conductance regulator | |
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| Unsorted | |
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| Others | | TRPsTooltip Transient receptor potential channels | |
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| LGICsTooltip Ligand gated ion channels | |
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See also: Receptor/signaling modulators • Transient receptor potential channel modulators |