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SR 33805 oxalate

Cat no: S-105

SR 33805 oxalate

SR 33805 oxalate.
A Specific L-type Cav Channel Blocker.

Two types of voltage-gatedпїЅCa2+ channels (VGCC, Cav) are found in most nonexcitable cells, T-type and the L-type Ca2+ channels.
SR 33805, a fantofarone derivative, is a potent Ca2+ channel antagonist. It binds allosterically to the alpha1-subunit of L-type Ca2+ channels (Kd = 20 pM), at a site distinct from other types of blocker. It potently inhibits the Ca2+пїЅchannel, and hence prevents Ca2+пїЅinflux, in primary mouse cardiac myocytes cultures with IC50 valuesпїЅranging from 4.1 to 33 nM.
SR 33805 shows selectivity for vascular smooth muscle, inducing vasorelaxation without producing inotropic or chronotropic effects. It inhibits PDGF-stimulated smooth muscle cell proliferation and the associated rise in intracellular Ca2+пїЅconcentration with IC50 values of 0.2 μM and 0.3 μM, respectively.
Despite its strong Ca2+-antagonistic properties, SR33805 increases cardiac cell contractile activity as a consequence of its Ca2+-sensitizing effects. These effects are attributable to both an increase in the maximal Ca2+-activated force and a length-dependent Ca2+-sensitization.
Alomone Labs is pleased to offer SR 33805 oxalate (#S-105).

Ion Channel Modulators; Voltage - Gated Ca2+ Channel Blockers

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SPECIFICATIONS

Catalog Number

S-105

Size

10 mg

Purity

>96%

Concentration

1 nM - 10 uM

Shipping Temp

Room Temperature

Molecular Weight

654.77 Da

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