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新型硼酸查耳酮衍生物作为抗肿瘤剂的设计、合成与评价

Design, synthesis, and evaluation of novel boronic-chalcone derivatives as antitumor agents.

作者信息

Kumar Srinivas K, Hager Erin, Pettit Catherine, Gurulingappa Hallur, Davidson Nancy E, Khan Saeed R

机构信息

Division of Experimental Therapeutics, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland 21231, USA.

出版信息

J Med Chem. 2003 Jul 3;46(14):2813-5. doi: 10.1021/jm030213+.

DOI:10.1021/jm030213+
PMID:12825923
Abstract

A series of boronic-chalcone derivatives were synthesized and tested for antitumor activity against human breast cancer cell lines. The results show the boronic-chalcones are more toxic to breast cancer cells compared to normal breast cells than other known chalcones.

摘要

合成了一系列硼酸查尔酮衍生物,并测试了它们对人乳腺癌细胞系的抗肿瘤活性。结果表明,与其他已知查尔酮相比,硼酸查尔酮对乳腺癌细胞的毒性比对正常乳腺细胞的毒性更大。

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