| Cat. No. |
Product Name |
Information |
| PC-36028 |
SAK3
|
SAK3 (T-VGCC enhancer SAK3) is a potent, orally acitve enhancer of T-type voltage-gated Ca2+ channel (T-VGCC), enhances CaV3.1 and CaV3.3, but not CaV3.2 activity at concentrations of 0.01-10 nM in neuro2A cells in vitro. |
| PC-35298 |
FPL64176
|
FPL64176 (ARC-64176) is a potent L-type Ca++ channel activator with EC50 of 16 nM. |
| PC-63283 |
JTV-519 fumarate
|
JTV-519 (K201) is a Ca2+-dependent blocker of SERCA and a partial agonist of ryanodine receptors (RyRs). |
| PC-63282 |
JTV-519 hydrochloride
|
JTV-519 (K201) is a Ca2+-dependent blocker of SERCA and a partial agonist of ryanodine receptors (RyRs). |
| PC-43084 |
Nicardipine hydrochloride
|
Nicardipine(YC-93) is a calcium channel blocker that has been widely used to control blood pressure in severe hypertension following events such as ischemic stroke, traumatic brain injury, and intracerebral hemorrhage.. |
| PC-43083 |
Nicardipine
|
Nicardipine(YC-93) is a calcium channel blocker that has been widely used to control blood pressure in severe hypertension following events such as ischemic stroke, traumatic brain injury, and intracerebral hemorrhage.. |
| PC-43071 |
Efonidipine hydrochloride
|
Efonidipine (NZ-105) is a potent, dual T-type and L-type calcium channel blocker, exhibits antihypertensive effect through vasodilatation. |
| 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. |
