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Calcium Channel

Chemical Structure Cat. No. Product Name CAS No.
(+/-)-BAY K 8644 Chemical Structure
BCP39708 (+/-)-BAY K 8644 93468-89-4
VK-II-86 Chemical Structure
BCP37839 VK-II-86 955371-84-3
VK-II-86 inhibit spontaneous Ca2+ release from the sarcoplasmic reticulum (SR).
Verapamil Chemical Structure
BCP37129 Verapamil 52-53-9
Verapamil is a calcium channel blocker that is a class IV anti-arrhythmia agent.
Isourolithin B Chemical Structure
BCP36684 Isourolithin B 855255-55-9
Urolithin C Chemical Structure
BCP36683 Urolithin C 165393-06-6
Urolithin C, a gut-microbial metabolite of Ellagic acid, is a glucose-dependent activator of insulin secretion.
Cyclic ADP-ribose Chemical Structure
BCP35557 Cyclic ADP-ribose 119340-53-3
Cyclic ADP-ribose is a cyclic purine nucleotide that is synthesised from NAD+ by ADP-ribosyl cyclase; acts as an agonist at ryanodine receptors.
Carboxyamidotriazole Orotate Chemical Structure
BCP34906 Carboxyamidotriazole Orotate 187739-60-2
Carboxyamidotriazole Orotate is the orotate salt form of Carboxyamidotriazole (CAI), an orally bioavailable signal transduction inhibitor. Carboxyamidotriazole Orotate is a cytostatic inhibitor of nonvoltage-operated calcium channels and calcium channel-mediated signaling pathways. Carboxyamidotriazole Orotate shows anti-tumor, anti-inflammatory and antiangiogenic effects.
Cav 2.2 blocker 1 Chemical Structure
BCP34882 Cav 2.2 blocker 1 1567335-29-8
Cav 2.2 blocker 1 is a N-type calcium channel (Cav 2.2) blocker for the treatment of pain, with an IC50 of 1 nM.
Bepridil hydrochloride hydrate Chemical Structure
BCP34263 Bepridil hydrochloride hydrate 74764-40-2
Bepridil is an amine Calcium channel antagonist that used to treat angina. But it is no longer sold in the United States. It may be a possible option in the treatment of atrial fibrillation.
Efonidipine hydrochloride ethanolate Chemical Structure
BCP33396 Efonidipine hydrochloride ethanolate 111011-76-8
Efonidipine hydrochloride monoethanolate is a dual T-type and L-type calcium channel blocker (CCB).The hydrochloride monoethanolate salt form of Efonidipine which has been launched for hypertension and discontinued for cerebrovascular disorders.
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