Pricing updated 2019-07-17. Prices are subject to change without notice.
SW203668 is an irreversible inhibitor of stearoyl-CoA desaturase (IC50 = 54 nM).1 It is selectively cytotoxic to H2122, H460, HCC44, and HCC95 cell lines that express cytochrome P450 (CYP) isoform CYP4F11 over eight other cancer cell lines that lack CYP4F11 in vitro (IC50s = 22-116 and >10,000 nM, respectively) and ectopic expression of CYP4F11 in SW203668-insensitive H1155 cells results in sensitization to SW203668. In vivo, SW203668 reduces tumor growth rate without reducing sebocyte production in the H2122 wild-type and nonobese diabetic severe combined immunodeficiency (NOD-SCID) mouse xenograft models when administered at doses of 20 and 6 mg/kg, respectively.
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Theodoropoulos, P.C., Gonzales, S.S., Winterton, S.E., et al. Discovery of tumor-