| Cat.No. | Name | Information |
|---|---|---|
| M3621 | Ionomycin | Ionomycin is a calcium ionophor and an antibiotic produced by Streptomyces conglobatus. |
| M3807 | Ionomycin (Calcium salt) | Ionomycin is a calcium ionophor and an antibiotic produced by Streptomyces conglobatus. |
| M7409 | Thapsigargin | Thapsigargin is an endoplasmic reticulum (ER) stress inducer, it is also an inhibitor of microsomal Ca2+-ATPase. |
| M5073 | (R)-(+)-BAY K 8644 | (R)-(+)-BAY K 8644 is a calcium channel inhibitor, inhibits Ba2+ currents (IBa) with IC50 of 975 nM. |
| M5922 | Ranolazine | Ranolazine (CVT 303) is an anti-angina and anti-ischemia agent that works by inhibiting the late effects of inward sodium current (IC50 values of 6 μM and 12 μM for INa and IKr, respectively) without affecting heart rate or blood pressure. Ranolazine is also a partial inhibitor of fatty acid oxidation (FAO). |
| M5756 | L-Phenylalanine | L-Phenylalanine is an antagonist at α2δ calcium channels with a Ki of 980 nM. |
| M5738 | Levosimendan | Levosimendan is a calcium sensitizer acting through calcium-dependent binding to cardiac troponin C (cTnC), provides treatment for heart failure. |
| M5733 | Lercanidipine hydrochloride | Lercanidipine hydrochloride is a calcium channel blocker of the dihydropyridine class. |
| M5723 | Lacidipine | Lacidipine is a L-type calcium channel blocker, used for treating high blood pressure. |
| M5717 | Isradipine | Isradipine is a potent and selective L-type voltage-gated calcium channel blocker, used to treat high blood pressure. |
| M5654 | Flunarizine 2HCl | Flunarizine 2HCl is a dihydrochloride salt form which is a calcium channel blocker with a Ki of 68 nM. |
| M5640 | Fendiline HCl | Fendiline is a nonselective calcium channel blocker. |
| M5629 | Ethosuximide | Ethosuximide is a succinimide anticonvulsant, used mainly in absence seizures; A calcium channel blocker. |
| M5607 | Efonidipine hydrochloride monoethanolate | Efonidipine(NZ-105) Hcl monoethanolate is a dual T-type and L-type calcium channel blocker (CCB). |
| M5550 | Dantrolene sodium hemiheptahydrate | Dantrolene sodium hemiheptahydrate ia a skeletal muscle relaxant that acts by interfering with excitation-contraction coupling in the muscle fiber. |
| M5439 | Butamben | Butamben is a long-duration local anesthetic used for the treatment of chronic pain. |
| M5411 | Amlodipine Besylate | Amlodipine Besylate is a long-acting calcium channel blocker, used to lower blood pressure and prevent chest pain. |
| M5205 | ML204 | ML204 is a novel potent antagonist that selectively modulates native TRPC4/C5 ion channels. |
| M5139 | Amlodipine | Amlodipine is a long-acting calcium channel blocker, used to lower blood pressure and prevent chest pain. |
| M5080 | Efonidipine hydrochloride | Efonidipine Hcl is a dual T-type and L-type calcium channel blocker . |
| M5077 | (S)-(-)-BAY K 8644 | (S)-(-)-BAY K 8644 is a Ca2+ channel activator; L-type Ca2+ channel activator. |
| M5075 | GV-58 | GV-58 is a potent, selective N- and P/Q-type Ca2(addition) channels agonist with EC50 of 7.21/8.81 uM for N-type/P-Q-type Ca2(addition) channel; 20-fold less potent CDK inhibitor activity. |
| M4514 | Tetrandrine | Tetrandrine (NSC-77037; D-tetrandrine (D-Tetrandrine) is a diphenylisoquinoline alkaloid that inhibits voltage-gated calcium channels (ICa) and Ca2+ -activated potassium channels. |
| M4485 | (-)-pareruptorin-A | (±) -praeruptorin A is A diesterification product of cis-lactone (CKL), and is the main active component of Peucedani Radix composed of dried Peucedanum praeruptorumDunn. |
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