SKA-121

1820708-73-3

C12H10N2O

DMSO : >= 42.86 mg/mL (216.22 mM)

Membrane Transporter/Ion Channel

SKA-121 is a selective K_Ca3.1 activator. SKA-121 exhibits EC₅₀s of 109 nM and 4.4 uM for K_Ca3.1 and K_Ca2.3, respectively. IC50 & Target: EC50: 109 nM (K_Ca3.1), 4.4 uM (K_Ca2.3)^[1] In Vitro: SKA-121, a compound generated through an isosteric replacement approach. SKA-121 is a typical positive-gating modulator and shifts the calcium-concentration response curve of K_Ca3.1 to the left. SKA-121 displays 41-fold selectivity for K_Ca3.1 (EC₅₀ 109 nM+/-14 nM) over K_Ca2.3 (EC₅₀ 4.4 +/- 1.6 uM). SKA-121 is 200- to 400-fold selective over representative K_V (K_V1.3, K_V2.1, K_V3.1, and K_V11.1), Na_V (Na_V1.2, Na_V1.4, Na_V1.5, and NaV1.7), as well as Ca_V1.2 channels^[1]. In Vivo: In blood pressure telemetry experiments, SKA-121 (100 mg/kg i.p.) significantly lowers mean arterial blood pressure in normotensive and hypertensive wild-type but not in K_Ca3.1^-/- mice. SKA-121 can be used as a new K_Ca3.1 selective pharmacological tool compound despite its relatively short half-life in mice. A lower dose of 30 mg/kg of SKA-121 does not produce significant alterations in MAP. The vehicle, peanut oil/DMSO (9:1 v/v, for SKA-121), does not cause significant alterations in MAP or HR. SKA-121 has a short half-life (ca.20 minutes), and plasma decay is extremely rapid (21.3+/-2.4 uM at 5 minutes; 483+/-231 nM at 1 hour and 53+/-44 nM at 4 hours). Since SKA-121 is relatively well soluble (logP=1.79) and can potentially be added to drinking water in animal experiments, it orally is also administered, and find that it has an oral availability of roughly 25%^[1].