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Senicapoc

Senicapoc Structural

What is Senicapoc?

Description

Senicapoc is an inhibitor of intermediate conductance calcium-activated potassium (IKCa1/KCa3.1) channels. It inhibits rubidium efflux from and dehydration of isolated human red blood cells (RBCs) induced by the calcium ionophore A23187 (; IC50s = 11 and 30 nM, respectively). Senicapoc (10 mg/kg twice per day) reduces IKCa1/KCa3.1 channel activity, increases potassium levels in RBCs, and decreases erythrocyte density in the SAD transgenic mouse model of sickle cell disease. It inhibits IL-2, IFN-γ, IL-12, and IL-17A production in CD3+ T cells stimulated with phorbol 12-myristate 13-acetate (PMA; ) and ionomycin (Item Nos. 10004974 | 11932) when used at a concentration of 1 μM. Senicapoc (100 mg/kg) increases the paw withdrawal threshold in a rat model of chronic constriction injury (CCI) of the sciatic nerve.

The Uses of Senicapoc

Treatment of disorders mediated by a calcium activated intermediate conductance potassium ion channel antagonist.

Properties of Senicapoc

Melting point: 180-181 °C(Solv: hexane (110-54-3); dichloromethane (75-09-2))
Boiling point: 460.7±45.0 °C(Predicted)
Density  1.250±0.06 g/cm3(Predicted)
storage temp.  Sealed in dry,Store in freezer, under -20°C
solubility  DMSO : 50 mg/mL (154.64 mM; Need ultrasonic)
form  Powder
pka 15.41±0.50(Predicted)
color  White to yellow

Safety information for Senicapoc

Computed Descriptors for Senicapoc

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