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Ion Channel/Membrane Transporter

Chemical Structure Cat. No. Product Name CAS No.
Clopidogrel Besylate Chemical Structure
BCP13469 Clopidogrel Besylate 744256-69-7
Clopidogrel besylate is a ticlopidine analog and platelet purinergic P2Y receptor antagonist that inhibits adenosine diphosphate-mediated PLATELET AGGREGATION.
Pilsicainide hydrochloride Chemical Structure
BCP09636 Pilsicainide hydrochloride 88069-49-2
Pilsicainide functions by blocking the fast inward movement of sodium ions through the Nav1.5 sodium channel that contributes to the rapid depolarization characteristic of phase 0 in the cardiac action potential.
Pilsicainide Chemical Structure
BCP13541 Pilsicainide 88069-67-4
Pilsicainide functions by blocking the fast inward movement of sodium ions through the Nav1.5 sodium channel that contributes to the rapid depolarization characteristic of phase 0 in the cardiac action potential.
Simendan Chemical Structure
BCP09589 Simendan 131741-08-7
Simendan is a hydrazone and pyridazine derivative; the levo-form is a phosphodiesterase III inhibitor, calcium-sensitizing agent, and inotropic agent that is used in the treatment of HEART FAILURE.
Lidocaine Chemical Structure
BCP09081 Lidocaine 137-58-6
Lidocaine, an amide local anesthetic, has anti-inflammatory properties in vitro and in vivo, possibly due to an attenuation of pro-inflammatory cytokines, intracellular adhesion molecule-1 (ICAM-1), and reduction of neutrophils influx.
Chlorotoxin Chemical Structure
BCP30217 Chlorotoxin 163515-35-3
Chlorotoxin is a 36 amino-acid peptide from the venom of the Israeli scorpion Leiurus quinquestriatus with anticancer activity.
Mivacurium chloride Chemical Structure
BCP13607 Mivacurium chloride 106861-44-3
Mivacurium chloride is an isoquinoline derivative that is used as a short-acting non-depolarizing agent.
Glibornuride Chemical Structure
BCP13008 Glibornuride 26944-48-9
Glibornuride is a blocker of adenosine 5'-triphosphate (ATP)-sensitive K+ channels (KATP channels).
Halofantrine Chemical Structure
BCP13777 Halofantrine 69756-53-2
Halofantrine has been shown to preferentially block open and inactivated HERG channels leading to some degree of cardiotoxicity.
Sergliflozin Etabonate Chemical Structure
BCP09291 Sergliflozin Etabonate 408504-26-7
Sergliflozin etabonate is a SGLT-2 inhibitor potentially for the treatment of type 2 diabetes and obesity.
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