THE EFFECT OF CHEMICAL SYMPATHECTOMY ON ACUTE LIVER-INJURY INDUCED BY CARBON-TETRACHLORIDE IN SPONTANEOUSLY HYPERTENSIVE RATS

中國醫藥大學機構典藏 China Medical University Repository, Taiwan > 醫學院 > 醫學系 > 期刊論文 > Item 310903500/30534

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题名:	THE EFFECT OF CHEMICAL SYMPATHECTOMY ON ACUTE LIVER-INJURY INDUCED BY CARBON-TETRACHLORIDE IN SPONTANEOUSLY HYPERTENSIVE RATS
作者:	HSU, CT;SHICHIJO, K;ITO, M;SEKINE, I
贡献者:	醫學院醫學系病理學科;HSU, CT, CHINA MED COLL,SCH MED,DEPT PATHOL,91 HSUEH SHIH RD,TAICHUNG,TAIWAN
日期:	1993
上传时间:	2010-09-24 14:57:14 (UTC+8)
出版者:	ELSEVIER SCIENCE BV
摘要:	A series of 1,6,7,8-substituted 2-(4'-substituted phenyl)-4-quinolones and related compounds been synthesized and evaluated as cytotoxic compounds and as antimitotic agents interacting with tubulin. The 2-phenyl-4-quinolones (22-30) with substituents (e.g. F, Cl, and OCH3) at C-6, C-7, and C-8 show, in general, potent cytotoxicity against human lung carcinoma (A-549), ileocecal carcinoma (HCT-8), melanoma (RPMI-7951), and epidermoid carcinoma of the nasopharynx (KB) and two murine leukemia lines (P-388 and L1210). Introduction of alkyl groups at N-1 or C-4 oxygen led to inactive compounds (35-43 and 50). In addition, compounds 24, 26, and 27 were evaluated in the National Cancer Institute's 60 human tumor cell line in vitro screen. These compounds demonstrated the most marked effects in the screen on two colon carcinoma cell lines (COLO-205 and KM-2OL2) and on a central nervous system tumor cell line (SF-539) with compound 26 the most potent of the three agents. Compounds 24, 26, and 27 were potent inhibitors of tubulin polymerization, with activity nearly comparable to that of the potent antimitotic natural products colchicine, podophyllotoxin, and combretastatin A-4. The three agents also inhibited the binding of radiolabeled colchicine to tubulin, but this inhibition was less potent than that obtained with the natural products.
關聯:	JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM 43(2):91-96
显示于类别:	[醫學系] 期刊論文

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