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Aloisine A
CAS No. : 496864-16-5
Biological Activity:Aloisine A (RP107) is a a potent cyclin-dependent kinase (CDK) inhibitor with IC50s 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 (IC50=0.5 µM) and GSK-3β (IC50=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[2].
Research Area:Cancer|Inflammation/Immunology
Targets:CFTR|CDK|GSK-3|JNK|ERK
Related Small Molecules:Akt/NF-κB/JNK-IN-1;DB0614;TCS2002;JNK3 inhibitor-2;Dinaciclib;AR-A014418;SNS-032;CC-671;PG01;(E/Z)-Zotiraciclib;CFTR corrector 8;CDK1-IN-4;CCT-251921;BS-181;Samuraciclib hydrochloride hydrate;CP-628006;T025;Flavopiridol;CDK8-IN-3;CDK9-IN-12;FLT3/CDK4-IN-1;GFB-12811;GSK 3 Inhibitor IX;Corynoxeine;Eciruciclib;JIP-1(153-163) TFA;CDK-IN-6;Lerociclib dihydrochloride
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