Dimethylenastron is an inhibitor of the mitotic kinesin Eg5 (IC50 = 200 nM in an ATPase assay).1 It is selective for Eg5 over other kinesin subfamilies from four different organisms. Dimethylenastron induces accumulation of HeLa cells in the G2/M phase (75% at a concentration of 1 μM). It inhibits spindle formation and induces radial arrangement of chromosomes in Xenopus oocytes. Dimethylenastron inhibits migration and growth of PANC-1 pancreatic cancer cells in a concentration-dependent manner.2 Dimethylenastron also inhibits angiogenesis and induces severe circulation defects in zebrafish embryos.3
1.Gartner, M., Sunder-Plassmann, N., Seiler, J., et al.Development and biological evaluation of potent and specific inhibitors of mitotic Kinesin Eg5Chembiochem6(7)1173-1177(2005) 2.Sun, X.-d., Shi, X.-j., Sun, X.-o., et al.Dimethylenastron suppresses human pancreatic cancer cell migration and invasion in vitro via allosteric inhibition of mitotic kinesin Eg5Acta Pharmacol. Sin.32(12)1543-1548(2011) 3.Exertier, P., Javerzat, S., Wang, B., et al.Impaired angiogenesis and tumor development by inhibition of the mitotic kinesin Eg5.Oncotarget4(12)2302-2316(2013)
















