Lipophilicity and antiproliferative activity profiling of 2-benzylidencycloalkanones

被引:13
|
作者
Hallgas, Balazs
Dobos, Zsofia
Agocs, Attila
Idei, Miklos
Keri, Gyoergy
Lorand, Tamas
Meszaros, Gyoergy
机构
[1] Semmelweis Univ, Dept Med Chem, H-1088 Budapest, Hungary
[2] Semmelweis Univ, Hungarian Acad Sci, Dept Med Chem, Peptidbiochem Res Grp, H-1088 Budapest, Hungary
[3] Univ Pecs, Fac Med, Dept BIochem & Med Chem, H-7624 Pecs, Hungary
[4] Semmelweis Univ, Cooperat Res Ctr, H-1062 Budapest, Hungary
关键词
cycloalkanone; molecular library; lipophilicity; retention factor; CLOGP calculation; drug-likeness; antiproliferative screening; QSAR;
D O I
10.1016/j.jchromb.2007.05.027
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
High performance liquid chromatographic (HPLC) method has been developed to separate the members of a library including 24 benzylidenecycloalkanone-type structures and to characterize their lipophilicity. The experimental lipophilicity data (k) of the compounds have been compared with their calculated lipophilicity parameters (CLOGP). In general, good correlations between the measured and calculated lipophilicities have been found and these results were in good accordance with our previously data obtained in case of structurally related molecular libraries. In addition, cytotoxicity screening has been performed to determine the antiproliferative activity of these compounds. Some of the investigated compounds possessed noticeable inhibitory potential. Based on the correlation between the antiproliferative activity and experimentally determined lipophilicity of the molecules investigated, limited structural demands to obtain more potent compounds can be exhibited to support the synthetic design. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:148 / 155
页数:8
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