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(R)-(+)-Bay-K-8644 is a Ca2+ channel and dihydropyridine agonist that inhibits Ba2+ currents (IBa), induces central respiratory depression in cats, and inhibits platelet activation through competitive antagonism of thromboxane A2-prostaglandin H2 receptors.

| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $54 | 5 days | |
| 5 mg | $129 | In Stock |
| Description | (R)-(+)-Bay-K-8644 is a Ca2+ channel and dihydropyridine agonist that inhibits Ba2+ currents (IBa), induces central respiratory depression in cats, and inhibits platelet activation through competitive antagonism of thromboxane A2-prostaglandin H2 receptors. |
| Targets&IC50 | Iba:957 nM |
| In vitro | (R)-(+)-Bay-K-8644, a component of the racemic mixture Bay K 8644, is a well-known L-type Ca2+ channel agonist but functions as an inhibitor of Ba2+ currents (IBa) with an IC50 of 975 nM. At a concentration of 0.5 μM, it reduces IBa to 71±10% of the control level, demonstrating its efficacy in inhibiting Ba2+ currents. Notably, this compound acts as a calcium channel inhibitor, crucial for modulating calcium channel activity [2]. |
| Synonyms | (R)-(+)-Bay K 8644 |
| Molecular Weight | 356.3 |
| Formula | C16H15F3N2O4 |
| Cas No. | 98791-67-4 |
| Smiles | COC(=O)C1=C(C)NC(C)=C([C@@H]1c1ccccc1C(F)(F)F)[N+]([O-])=O |
| Relative Density. | 1.37g/cm3 |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 100 mg/mL (280.66 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (11.23 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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