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Cat. No. Product Name Information
PC-38082

Etripamil

Calcium channel blocker

Etripamil (MSP-2017) is a novel intranasal non-dihydropyridine calcium channel blocker that has begun phase III clinical trials for the treatment of paroxysmal supraventricular tachycardias..
PC-35727

BTT-369

Cav2.2 inhibitor

BTT-369 (BTT369) is a voltage-gated CaV2.2 calcium channel inhibitor that disrupts the CaVα·CaVβ3 protein-protein interaction with Ki of 2.0 uM in FP assays.
PC-35726

BTT-266

Cav2.2 inhibitor

BTT-266 (BTT266) is a voltage-gated CaV2.2 calcium channel inhibitor that disrupts the CaVα·CaVβ3 protein-protein interaction, directly binds to CaVβ3 with Kd of 3.6 uM.
PC-35299

CDN1163

SERCA2 activator

CDN1163 (CDN-1163) is a small molecule, allosteric activator of SERCA2, dose-dependently increases the Vmax of SERCA2 Ca2+-ATPase activity in ER microsomes.
PC-35298

FPL64176

L-type Ca2+ channel activator

FPL64176 (ARC-64176) is a potent L-type Ca2+ channel activator with EC50 of 16 nM.
PC-63469

RU1968

CatSper inhibitor

RU1968 is a potent, cross-species sperm-specific Ca2+ channel CatSper inhibitor that is selective for CatSper over Slo3.
PC-63283

JTV-519 hemifumarate

SERCA inhibitor, RyR2 inhibitor

JTV-519 hemifumarate (K201) is a Ca2+-dependent blocker of SERCA and a ryanodine receptor 2 (RyR2) inhibitor.
PC-63282

JTV-519 hydrochloride

SERCA inhibitor, RyR2 inhibitor

JTV-519 hydrochloride (K201) is a Ca2+-dependent blocker of SERCA and a ryanodine receptor 2 (RyR2) inhibitor.
PC-63281

JTV-519

SERCA inhibitor, RyR2 inhibitor

JTV-519 (K201) is a Ca2+-dependent blocker of SERCA and a ryanodine receptor 2 (RyR2) inhibitor.
PC-50011

Mirogabalin besylate

Calcium channel α2δ ligand

Mirogabalin besylate (DS-5565) is a novel potent, selective ligand of the α2δ subunit of voltage-gated calcium channels with Kd of 13.5/22.7/27.0/47.6 nM for huamn α2δ-1, human α2δ-2, rat α2δ-1 and rat α2δ-2 subunits, respectively.
PC-43138

Mirogabalin

Calcium channel α2δ ligand

Mirogabalin (DS-5565) is a potent, selective ligand of the α2δ subunit of voltage-gated calcium channels with Kd of 13.5/22.7/27.0/47.6 nM for huamn α2δ-1, human α2δ-2, rat α2δ-1 and rat α2δ-2 subunits, respectively.
PC-43100

Dantrolene sodium hemiheptahydrate

Glutathione reductase inhibitor, RyR antagonist

Dantrolene is a postsynaptic muscle relaxant that lessens excitation-contraction coupling in muscle cells, inhibits Ca2+ ions release from sarcoplasmic reticulum stores by antagonizing ryanodine receptors.

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