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Cat. No. Product Name Information
PC-45686

ABT-639

T-type calcium channel inhibitor

ABT-639 is a novel, peripherally acting, selective T-type calcium channel blocker, blocks recombinant human Cav 3.2 in a voltage-dependent fashion (IC50=2 uM).
PC-45854

NNC 55-0396

T-type calcium channel inhibitor

NNC 55-0396 is a potent and selective T-type calcium channel antagonist that blocks recombinant alpha(1)G T-type channels in human embryonic kidney 293 cellswith IC50 of 7 uM.
PC-42314

MK-8998

T-type calcium channel inhibitor

MK-8998 (Suvecaltamide, CX-8998) is a potent and selective antagonist of the T-type calcium channel for the treatment of schizophrenia.
PC-42385

NS-638

Sodium channel inhibitor

NS-638 is a nonpeptide calcium channel blocker that dose dependently inhibits AMPA-stimulated [3H]GABA-release from cultured cortical neurons with IC50 of 4.3 uM.
PC-24336

KT-362

Calcium antagonist

KT-362 is a small molecule intracellular calcium antagonist, inhibits NE-induced contractions and IP accumulation.
PC-23959

SERCA1 inhibitor CKP2

SERCA1 inhibitor

SERCA1 inhibitor CKP2 is a novel specific inhibitor of sarco/endoplasmic reticulum (ER) calcium ATPase 1 (SERCA1), induces severe ER stress-mediated apoptosis in metastatic PTC cells.
PC-23958

SERCA1 inhibitor CKP1

SERCA1 inhibitor

SERCA1 inhibitor CKP1 is a novel specific inhibitor of sarco/endoplasmic reticulum (ER) calcium ATPase 1 (SERCA1), induces severe ER stress-mediated apoptosis in metastatic PTC cells.
PC-23714

Ziconotide acetate

N-type calcium channel antagonist

Ziconotide acetate (SNX-111 acetate) is a potent and selective block of N-type calcium channels antagonist, reduces synaptic transmission.
PC-23713

ZC88

CaV2.2 inhibitor

ZC88 is a selective N-type calcium channel (CaV2.2) blocker, inhibits recombinant human N-type voltage-sensitive calcium channels (α1B/β1b/α2δ) transiently expressed in HEK-293 cells with IC50 of 0.45 uM.
PC-23712

C2230

CaV2.2 inhibitor

C2230 is a potent, specific CaV2.2 (N-type) calcium channel inhibitor/antagonist with IC50 of 1.3 uM (depolarizing Vh of -50 mV), preferably binds to the inactivated CaV2.2 channels.
PC-23650

ML218

T-type calcium channel inhibitor

ML218 (CID 45115620) is a selective, centrally active T-type Ca(2+) channel inhibitor with IC50 of 310 nM and 270 nM for Cav3.2 and Cav3.3 respectively in patch clamp electrophysiology.
PC-23295

Dicoumarol

VRAC inhibitor

Dicoumarol (Dicumarol) is an inhibitor of both NAD(P)H:quinone oxidoreductase 1 (NQO1) and PDK1 with IC50 of 0.37 and 19.42 uM respectively, also is a potent VRAC inhibitor.

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