CDK9-IN-36 (Compound T7) is a potent, selective and metabolically stable CDK9 inhibitor with an IC50 value of 1.2 nM. CDK9-IN-36 effectively suppresses cell proliferation, reduces colony formation, and induces apoptosis in Osimertinib (HY-15772)-resistant NSCLC cells by downregulating Mcl-1. CDK9-IN-36 also demonstrates antitumor efficacy in a tumor xenograft model[1].
Molekulargewicht:
565.61
Formel:
C30H33F2N5O4
Target-Kategorie:
Apoptosis,CDK
Anwendungsbeschreibung:
MCE Product type: Reference compound
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