101143-87-7
Chemical Structure
Ep vinyl quinidine
Synonym(s): 3-Epiquinine; Epivinylquinidine
- CAS No.: 101143-87-7
- Formula:C20H24N2O2
- Molecular Weight:324.42
IUPAC Name: (S)-(6-methoxyquinolin-4-yl)((1S,2R,4S,5S)-5-vinylquinuclidin-2-yl)methanol
InChIKey: LOUPRKONTZGTKE-ITHTXLDVSA-N
SMILES: O[C@H]([C@]1([H])[N@@]2C[C@H]([C@@H](CC2)C1)C=C)C3=CC=NC4=C3C=C(OC)C=C4
Biological Activity: Ep vinyl quinidine (3-Epiquinine) is an epi-vinyl stereoisomer of Quinidine. Quinidine is an antiarrhythmic agent. Quinidine is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine is also a K+ channel blocker with an IC50 of 19.9 μM. Quinidine can be used for malaria research[1][2][3].
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Ep vinyl quinidine | Ep vinyl quinidine (3-Epiquinine) is an epi-vinyl stereoisomer of Quinidine. Quinidine is an antiarrhythmic agent. Quinidine is a potent, orally active, selective cytochrome P450db inhibitor. Quinidine is also a K+ channel blocker with an IC50 of 19.9 μM. Quinidine can be used for malaria research. | |||||||||||||||||||||
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References
- [1]. Hu B, et al. Origin of and a Solution for Uneven Efficiency by Cinchona Alkaloid-Derived, Pseudoenantiomeric Catalysts for Asymmetric Reactions. J Am Chem Soc. 2018 Oct 24;140(42):13913-13920. [Content Brief]
- [2]. Kehl SJ. Quinidine-induced inhibition of the fast transient outward K+ current in rat melanotrophs. Br J Pharmacol. 1991 Jul;103(3):1807-13. [Content Brief]
- [3]. Roden DM, et al. Class I antiarrhythmic agents: quinidine, procainamide and N-acetylprocainamide, disopyramide. Pharmacol Ther. 1983;23(2):179-91. [Content Brief]
