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(±)-Methoxyverapamil . hydrochloride

Ca2+ channel inhibitor
ALX-550-255-M005 5 mg 10.00 USD
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Selectively blocks L-type Ca2+ channels.

Product Specification

Alternative Name:(α-3-[[2-(3,4-Dimethoxyphenyl)ethyl]methylamino]propyl-3,4,5-trimethoxy-α-(1-methylethyl)benzeneacetonitrile . HCl, D600, Gallopamil
Formula:C28H40N2O5 . HCl
MI:14: 4356
Purity:≥98% (HPLC)
Appearance:White to off-white solid.
Solubility:Soluble in water or methanol.
Long Term Storage:Ambient
Handling:Protect from light.
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Product Literature References

Mode of action and comparative efficacy of pharmacological agents that inhibit calcium-dependent dehydration of sickle cells: J.C. Ellory, et al.; Br. J. Pharmacol. 106, 972 (1992), Abstract;
Physiological and pharmacological correlates of calcium antagonist receptors: J.A. Wagner, et al.; J. Cardiovasc. Pharmacol. 10, S1 (1987), Abstract;
A pharmacological explanation of the use-dependency of the verapamil (and D-600) block of slow calcium channels: G.B. Frank; J. Pharmacol. Exp. Ther. 236, 505 (1986), Abstract;

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