异恶唑
部分
喹唑啉
体外
化学
组合化学
立体化学
药理学
生物化学
医学
作者
Jianping Yong,Can‐Zhong Lu,Xiao‐Yuan Wu
标识
DOI:10.2174/1871520614666140812105445
摘要
14 new structures of isoxazole-moiety-containing quinazoline derivatives(3a~3n) were synthesized for the first time and characterized by IR, (1)H NMR, (13)C NMR, ESI-MS. Subsequently, their in vitro anticancer activity against A549, HCT116 and MCF-7 cell lines was preliminarily evaluated using the MTT method. Among them, most compounds showed good to excellent anticancer activity, especially 3d, 3i, 3k and 3m exhibited the more potent anticancer activity against A549, HCT116 and MCF-7 cell lines, which can be regarded as the promising drug candidates for development of anticancer drugs.
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