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Merck KGaA
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31 May 2012
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Cell-permeable, non-competitive adenylate cyclase inhibitor (IC50 = 3 µM), that binds to the adenosine P1 binding site. Blocks positive inotropic and chronotropic effects of β-adrenergic agents.
| Product information | |||
|---|---|---|---|
| Form | White solid | ||
| Primary Target | adenylate cyclase | ||
| Primary Target IC50 | 3 µM | ||
| Molar mass | 235.2 | ||
| Cell permeable | Yes | ||
| Purity | ≥98% by HPLC | ||
| Solubility | DMSO | ||
| Chemical formula | C10H13N5O2 | ||
| CAS number | 6698-26-6 | ||
| Store and ship information | |||
|---|---|---|---|
| Storage | +2°C to +8°C | ||
| Ship |
Ambient Temperature Only
Standard Handling |
||
