Name | L791943 |
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Description | L791943 is a potent, selective Phosphodiesterase-4 (PDE4) inhibitor with an IC50 of 4.2 nM. |
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Related Catalog | |
Target |
IC50: 4.2 nM (Phosphodiesterase-4)[1] |
In Vitro | The extent of metabolism of L791943 is evaluated in vitro in rat hepatocytes and compared to the data obtaine with CDP-840. In our standard incubation conditions, >98% of the parent drug remain in the case of L791943 whereas only 11% of CDP-840 is left intact[2]. |
References |
Molecular Formula | C24H17F10NO4 |
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Molecular Weight | 573.38 |
Storage condition | 2-8℃ |