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Cat. No. Product Name Information
PC-43070

Efonidipine hydrochloride monoethanolate

Efonidipine (NZ-105) is a potent, dual T-type and L-type calcium channel blocker, exhibits antihypertensive effect through vasodilatation.
PC-43069

Efonidipine

Efonidipine (NZ-105) is a potent, dual T-type and L-type calcium channel blocker, exhibits antihypertensive effect through vasodilatation.
PC-43065

GV-58

GV-58 is a potent, selective N-Type and P/Q-type Ca2+ Channel agonist with EC50 of 7.2 and 8.8 uM, shows no acitivity for L-type calcium channels (EC50>100 uM).
PC-62318

Tetrandrine

Tetrandrine (NSC 77037.
PC-61834

Imagabalin hydrochloride

Imagabalin (PD 0332334) is a novel ligand for the α2δ subunit of the voltage-dependent calcium channel (VDCC) with some selectivity for the α2δ1 subunit over α2δ2.
PC-61833

Imagabalin

Imagabalin (PD 0332334) is a novel ligand for the α2δ subunit of the voltage-dependent calcium channel (VDCC) with some selectivity for the α2δ1 subunit over α2δ2.
PC-61832

Atagabalin

Atagabalin (PD 0200390) is a novel ligand of the voltage-dependent calcium channel (VDCC) α2δ subunit (1 and 2) for treatment for insomnia..
PC-61779

SERCA2a activator A

SERCA2a activator A is a novel sarco/endoplasmic reticulum Ca2+-dependent ATPase 2a (SERCA2a) activator that activates the Ca2+-dependent ATPase activity of cardiac SR vesicles but not that of skeletal muscle SR vesicles that lack of phospholamban (PLN).
PC-60979

AMG1

A novel specific CRAC channel inhibitor that blocks function of effector but not regulatory T cells in vitro and attenuates the pogression and severity of EAE in vivo.
PC-60224

Synta-66

A potent, selective CRAC channel Orai1 blocker with IC50 of 3 uM.
PC-60006

A-1048400

A novel potent, selective, orally active N-type and T-type calcium channel blocker with IC50 of 1.4 and 1.2 uM, respectively.
PC-44016

Dantrolene sodium

A postsynaptic muscle relaxant that inhibits Ca2+ ions release from sarcoplasmic reticulum stores.

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