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Calcium Channel

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Calcium Channel

Chemical Structure Cat. No. Product Name CAS No.
Amlodipine besylate Chemical Structure
 BCP21993 Amlodipine besylate 111470-99-6
Amlodipine besylate is a long-acting calcium channel blocker.
Manidipine Chemical Structure
 BCP21717 Manidipine 120092-68-4
Manidipine is a calcium channel blocker that is used clinically as an antihypertensive.
Berbamine Chemical Structure
 BCP29709 Berbamine 478-61-5
Berbamine is a calcium channel blocker.
Fantofarone Chemical Structure
 BCP29553 Fantofarone 114432-13-2
Fantofarone is a highly potent Calcium Channel antagonist.
S(-)-BAY K8644 Chemical Structure
 BCP23923 S(-)-BAY K8644 98625-26-4
(S)-(-)-Bay-K-8644 is an agonist of L-type Ca2+ channel. Bay-K-8644 (S)-(-)- activates Ba2+ currents (IBa) (EC50=32 nM).
R(+)-BAY K 8644 Chemical Structure
 BCP23924 R(+)-BAY K 8644 98791-67-4
(R)-(+)-Bay-K-8644 is a calcium channel inhibitor. Bay-K-8644 (R)-(+)- inhibits Ba2+ currents (IBa) (IC50=975 nM).
GV-58 Chemical Structure
 BCP23927 GV-58 1402821-41-3
GV-58 is a potent, selective N- and P/Q-type Ca2+ channels agonist with EC50 of 7.21/8.81 uM for N-type/P-Q-type Ca2+ channel; 20-fold less potent CDK inhibitor activity.
HC-056456 Chemical Structure
 BCP29452 HC-056456 7733-96-2
HC-056456 is a CatSper channel modulator.
ST271 Chemical Structure
 BCP20728 ST271 106392-48-7
ST271 is a potent inhibitor of protein tyrosine kinase (PTK).
Mirogabalin besylate Chemical Structure
 BCP29292 Mirogabalin besylate 1138245-21-2
Mirogabalin besylate is a selective and orally available ligand for the α2δ subunit of voltage-gated calcium channels, with Kds of 13.5 nM, 22.7 nM, 27 nM, and 47.6 nM for human α2δ-1, human α2δ-2, rat α2δ-1, and rat α2δ-2, respectively.
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