Sodium Channel


Sodium channels are integral membrane proteins that form ion channels, conducting sodium ions (Na+) through a cell's plasma membrane. They are classified according to the trigger that opens the channel for such ions, i.e. either a voltage-change ("Voltage-gated", "voltage-sensitive", or "voltage-dependent" sodium channel also called "VGSCs" or "Nav channel") or a binding of a substance (a ligand) to the channel (ligand-gated sodium channels). In excitable cells such as neurons, myocytes, and certain types of glia, sodium channels are responsible for the rising phase of action potentials.
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    D-I03 is a selective inhibitor of RAD52 with a Kd value of 25.8 µM. D-I03 inhibits ssDNA annealing via RAD52 and D-loop formation, with IC50 values of 5 µM and 8 µM, respectively.

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  • RI-1 EY5005

    RI-1 (RAD51 inhibitor 1) is a RAD51 inhibitor with an IC₅₀ of 5 to 30 µM.

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  • Brompheniramine hydrogen maleate EY2861

    Brompheniramine hydrogen maleate is a histamine H1 receptors antagonist.

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  • Azelastine HCl EY2852

    Azelastine hydrochloride (Astelin) is a potent, second-generation, selective, histamine antagonist.

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  • Pemirolast potassium EY2796

    Pemirolast Potassium (BMY 26517) is a histamine H1 antagonist and mast cell stabilizer that acts as an antiallergic agent.

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