Synthesis and antitumor evaluation of fluoroquinolone C3 fused heterocycles (II): From triazolothiadiazines to pyrazolotriazoles
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Xiao-yi Wen | Wen-long Huang | Guoqiang Wang | Guo-qiang Hu | Yong Yang | Nan-nan Duan | Li-li Hou | Songqiang Xie | L. Yi | T. Y. Chao
[1] J. Chern,et al. Discovery of a novel series of quinolone and naphthyridine derivatives as potential topoisomerase I inhibitors by scaffold modification. , 2009, Journal of medicinal chemistry.
[2] S. Kuo,et al. Design and synthesis of 2-(3-benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one analogues as potent antitumor agents that inhibit tubulin assembly. , 2009, Journal of medicinal chemistry.
[3] A. Shafiee,et al. N-Substituted piperazinyl quinolones as potential cytotoxic agents: structure-activity relationships study. , 2009, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[4] Mei Xu,et al. HL-37, a novel anthracene derivative, induces Ca(2+)-mediated apoptosis in human breast cancer cells. , 2008, Toxicology.
[5] Y. A. Ibrahim,et al. Pyrolytic desulfurization ring contraction of condensed thiadiazines as a general route towards pyrazoloazines and pyrazoloazoles with a bridgehead (ring junction) nitrogen atom , 2008 .