Antifungal properties of new series of quinoline derivatives

被引:280
|
作者
Musiol, R
Jampilek, J
Buchta, V
Silva, L
Niedbala, H
Podeszwa, B
Palka, A
Majerz-Maniecka, K
Oleksyn, B
Polanski, J
机构
[1] Silesian Univ, Inst Chem, PL-40007 Katowice, Poland
[2] Zentiva AS, Prague 10237 10, Czech Republic
[3] Charles Univ Prague, Fac Pharm Hradec Kralove, Dept Biol & Med Sci, Hradec Kralove 50005, Czech Republic
[4] Jagiellonian Univ, Fac Chem, PL-30060 Krakow, Poland
关键词
quinoline derivatives; styrylquinoline analogues; in vitro antifungal activity; lipophilicity measurement; structure-activity relationships;
D O I
10.1016/j.bmc.2006.01.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The series of quinoline derivatives were prepared. The synthetic approach, analytical, and spectroscopic data of all synthesized compounds are presented. All the prepared derivatives were analyzed using the reversed-phase high performance liquid chromatography (RP-HPLC) method for the lipophilicity measurement. In the present study, the correlation between RP-HPLC retention parameter log K (the logarithm of capacity factor K) and various calculated log P data is shown. The relationships between the lipophilicity and the chemical structure of the studied compounds are discussed as well. The prepared compounds were tested for their in vitro antifungal activity. 2-[(3-Hydroxyphenylimino)methyl]quinolin-8-ol (8), 2-[(4-hydroxyphenylimino)methyl]quinolin-8-ol (9) and 2-[(2,5-dichloro-4-nitrophenylamino)methoxymethyl]quinolin-8-ol (10) showed in vitro antifungal activity comparable to or higher than that of the standard fluconazole. Structure-activity relationships among the chemical structure, the physical properties, and the biological activities of the evaluated compounds are discussed in the article. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3592 / 3598
页数:7
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