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Cav1.x Channel Blockers

CaV1.x channels (L-type) are high-voltage activated Ca2+ channels that are sensitive to blockade by dihydropyridines. This family has four members, each composed of an α1, α2/δ, β and γ subunit.

CaV1.1 channels are specific to skeletal muscle where they interact with ryanodine receptors on the sarcoplasmic reticulum and trigger Ca2+ influx, Ca2+-activated Ca2+ release and muscle contraction. Mutations in CaV1.1 α1-subunit have been linked to hypokalemic periodic ...

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Allosteric Calcium-sensing receptor (CaSR) agonist; also CYP2D2 inhibitor and Ca2+ channel blocker; orally bioavailable

Alternate Names: AMG 073
Chemical Name: N-[(1R)-1-(1-Naphthyl)ethyl]-3-[3-(trifluoromethyl)phenyl]propan-1-amine hydrochloride
Purity: ≥98%
Allosteric Calcium-sensing receptor (CaSR) agonist; also CYP2D2 inhibitor and Ca2+ channel blocker; orally bioavailable
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