Aloisine A (RP107) is a a potent cyclin-dependent kinase ( CDK ) inhibitor with IC 50 s of 0.15 μM, 0.12 μM, 0.4 μM, 0.16 μM for CDK1/cyclin B, CDK2/cyclin A, CDK2/cyclin E, CDK5/p35, respectively. Aloisine A ininhibits GSK-3α ( IC 50 =0.5 μM) and GSK-3β ( IC 50 =1.5 μM). Aloisine A stimulates wild-type CFTR and mutated CFTR , with submicromolar affinity by a cAMP-independent mechanism. Aloisine A has the potential for CFTR-related diseases, including cystic fibrosis research.
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