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Abstract Taking sophoridine as a lead compound, 58 sophoridine derivatives were designed, synthesized and evaluated for their antiproliferative activity in the HepG2 cancer cell line. Among the 58 compounds, 33 compounds showed potent antiproliferative activity with IC 50 less than 10 μM. Compound 5w showed the most potent anti-proliferative activity in the HepG2 cancer cell line. Thus, we further extended our characterization of the antiproliferative activity of 5w in six cancer cell lines (HepG2, SMMC-7721, Hela, CNE1, CNE2 and MCF7). The representative compound 5w displayed robust anti-proliferative activities in all the tested cell lines with IC 50 values in range of 0.93–1.89 μM which were much lower than that of sophoridine. Here, we report the structure–activity relationships (SAR) in a sophoridine series of compounds, which indicated that introduction of N-benzyl indole group on the 14-carbon atom of sophoridine can significantly enhance the antiproliferative activity. By molecular docking and enzymatic assay, compound 5w was found to be able to inhibit the activity of DNA Topo I. Furthermore, apoptosis assay displayed that compound 5w could significantly induce the apoptosis of HepG2 cells in a dose-dependent manner by activating caspase-3, increasing expression of cleaved caspase-3 and reducing the ratio of Bcl-2/Bax. The in vivo antitumor assay demonstrated that 5w suppressed the growth of HepG2 xenografts in nude mice without any obvious side effects. Graphical abstract Image 1 Highlights • 58 sophoridine derivatives were designed, synthesized and evaluated. • 5w exhibited potent antitumor activity in vitro. • 5w inhibited the activity of DNA Topo I. • 5w arrested tumor growth in vivo. [ABSTRACT FROM AUTHOR]

Using matrine ( 1 ) as the lead compound, a series of new 14-( N -substituted-2-pyrrolemethylene) matrine and 14-( N -substituted-indolemethylene) matrine derivatives was designed and synthesized for their potential application as anticancer agents. The structure of these compounds was characterized by 1 H NMR, 13 C NMR and ESI-MS spectral analyses. The target compounds were evaluated for their in vitro cytotoxicity against three human cancer cell lines (SMMC-7721, A549 and CNE2). The results revealed that compound A6 and B21 displayed the most significant anticancer activity against three cancer cell lines with IC 50 values in range of 3.42–8.05 μM, which showed better activity than the parent compound (Matrine) and positive control Cisplatin. Furthermore, the Annexin V-FITC/PI dual staining assay revealed that compound A6 and B21 could significantly induce the apoptosis of SMMC-7721 and CNE2 cells in a dose-dependent manner. The cell cycle analysis also revealed that compound A6 could cause cell cycle arrest of SMMC-7721 and CNE2 cells at G2/M phase. [ABSTRACT FROM AUTHOR]

Two triterpenoid acids, betulinic acid and ursolic acid, were purified from the ethanol extract ofEngelhardtia serrataBl. by bioassay-guided isolation. Their cytotoxic and apoptosis-inducing activities on the K562 cell line were evaluated by MTT and flow cytometric analysis. Betulinic acid and ursolic acid inhibited the growth of K562 tumor cell line with IC 50 values of 6.25 and 12.5  μg/ml and also induced 35%and 13%apoptosis at 25  μg/ml, respectively. [ABSTRACT FROM AUTHOR]