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. 2021 Feb 10;12:920. doi: 10.1038/s41467-021-21159-7

Fig. 4. SJF-0628 outperforms vemurafenib in inhibiting growth of cell lines expressing mutant BRAF.

Fig. 4

a Cell proliferation assay in SK-MEL-28 cells treated with increasing amounts of vemurafenib, SJF-0628, or SJF-0661 for 3 days (mean ± SD, n = 3 biologically independent samples). EC50 = 215 ± 1.09 nM, 37 ± 1.2 nM, and 243 ± 1.09 nM, respectively; vemurafenib = blue, SJF-0628 = burgundy, SJF-0661 = purple. b Cell proliferation assay in vemurafenib resistant SK-MEL-239-C4 cells treated with increasing amounts vemurafenib, SJF-0628, or SJF-0661 for 5 days (mean ± SD, n = 3 biologically independent samples); vemurafenib = blue, SJF-0628 = burgundy, SJF-0661 = purple. c Cell proliferation assay in SK-MEL-246 (Class 2) cells treated with increasing amounts vemurafenib, SJF-0628, or SJF-0661 for 5 days (mean ± SD, n = 3 biologically independent samples); vemurafenib = blue, SJF-0628 = burgundy, SJF-0661 = purple. d SJF-0628 EC50 = 218 nM ± 1.06 c,H1666 cells treated with SJF-0628, vemurafenib, or SJF-0661 for 5 days (mean ± SD, n = 3 biologically independent samples); vemurafenib = blue, SJF-0628 = burgundy, SJF-0661 = purple. e Treatment of CAL-12-T cells with vemurafenib, SJF-0628, or SJF-0661 for 5 days shows minimal effect on cell viability (mean ± SD, n = 3 biologically independent samples). f Results of an efficacy study in SK-MEL-246 tumor xenografts implanted in female athymic mice showing tumor regression with 50 mg/kg IP twice daily (mean ± SD, n = 3 biologically independent animals). g Scatter plot result of final tumor volumes of SKMEL-246 xenografts treated with SK-MEL-246 (mean ± SD, n = 3 biologically independent animals). P value calculated by unpaired t-test. Source data are provided as a Source Data file.