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Ispinesib is a cell-permeable, allosteric inhibitor of Eg5 (Ki app = 2.3 nM) with >10,000-fold selectivity for Eg5 over a range of other mitotic kinesins.1,2 It induces a monopolar spindle phenotype, leading to the activation of a spindle assembly checkpoint, mitotic arrest, and subsequent cell death (GI50s = 22-82 nM in colon, pancreas, prostrate, and lung cancer cells in vitro).3 At 10 mg/kg, ispinesib produces tumor regression of breast cancer cell xenografts in mice.4 It has also been used to halt the growth of treatment-resistant glioblastoma tumor-initiating cells, to prevent tumor initiation and self-renewal of a cancer stem cell population (EC50 = 1.15 nM), and to reduce glioma cell invasion.5
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1. Optimized S-
2. Triphenylbutanamines: Kinesin spindle protein inhibitors with in vivo antitumor activity. J. Med. Chem. 55, 1511-1525 (2012).
3. Elucidating the functionality of kinesins: An overview of small molecule inhibitors. Semin. Cell Dev. Biol. 22(9), 935-945 (2011).
4. Activity of the kinesin spindle protein inhibitor ispinesib (SB-
5. The mitotic kinesin KIF11 is a driver of invasion, proliferation, and self-