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BC13 is a dual inhibitor of cyclin-dependent kinase 6 (Cdk6) and bromodomain-containing protein 4 (BRD4, IC50s = 36. 234. and 137. nM for Cdk6 and BRD4 bromodomain 1 (BD1) and BD2), respectively). It is selective for Cdk6 over Cdk1-Cdk5 at 500 nM and for BD1 and BD2 in BRD4 over those in BRD2 and BRD3 (IC50s = >1,000, >1,000, 863. and 967. nM, respectively). It inhibits the proliferation of MDA-MB-231 and BT-549 triple-negative breast cancer (TNBC) cells (IC50s = 2,250 and 980 nM, respectively) but not non-cancerous MCF-10A cells (IC50 = >16. µM). BC13 (2 µM) in combination with the ferroptosis inducer RSL3 (Cay-19288) synergistically reduces colony formation of MDA-MB-231 cells. It also reduces tumor growth in an MDA-MB-231 mouse xenograft model when administered at a dose of 25 mg/kg every other day.. Solulibility: Chloroform: Sparingly Soluble: 1-10 mg/ml: .
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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