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Cytisine-Pterocarpan-Derived Compounds: Biomimetic Synthesis and Apoptosis-Inducing Activity in Human Breast Cancer Cells.


ABSTRACT: Cytisine-pterocarpan-derived compounds were biomimetically synthesized with (-)-cytisine and (-)-maackiain via a N,N-4-dimethyl-4-aminopyridine (DMAP)-mediated synthetic strategy in a mild manner. In the present study, tonkinensine B (4) was elaborated in good and high yields with the optimized reaction conditions. The in vitro cytotoxicity of compound 4 was evaluated against breast cancer cell lines and showed that 4 had a better cytotoxicity against MDA-MB-231 cells (IC50 = 19.2 ?M). Depending on the research on cytotoxicities of 4 against RAW 264.7 and BV2 cells, it was suggested that 4 produced low cytotoxic effects on the central nervous system. Further study indicated that 4 demonstrated cytotoxic activity against MDA-MB-231 cells and the cytotoxic activity was induced by apoptosis. The results implied that the apoptosis might be induced by mitochondrion-mediated apoptosis via regulating the ratio of Bax/Bcl-2 and promoting the release of cytochrome c from the mitochondrion to the cytoplasm in MDA-MB-231 cells.

SUBMITTER: Peng TT 

PROVIDER: S-EPMC6321416 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Cytisine-Pterocarpan-Derived Compounds: Biomimetic Synthesis and Apoptosis-Inducing Activity in Human Breast Cancer Cells.

Peng Ting-Ting TT   Sun Xuan-Rong XR   Liu Ren-Hao RH   Hua Lu-Xia LX   Cheng Dong-Ping DP   Mao Bin B   Li Xing-Nuo XN  

Molecules (Basel, Switzerland) 20181122 12


Cytisine-pterocarpan-derived compounds were biomimetically synthesized with (-)-cytisine and (-)-maackiain via a <i>N</i>,<i>N</i>-4-dimethyl-4-aminopyridine (DMAP)-mediated synthetic strategy in a mild manner. In the present study, tonkinensine B (<b>4</b>) was elaborated in good and high yields with the optimized reaction conditions. The in vitro cytotoxicity of compound <b>4</b> was evaluated against breast cancer cell lines and showed that <b>4</b> had a better cytotoxicity against MDA-MB-23  ...[more]

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