2D-autocorrelation descriptors for predicting cytotoxicity of naphthoquinone ester derivatives against oral human epidermoid carcinoma

被引:117
作者
Saiz-Urra, Liane
Gonzalez, Maykel Perez [1 ]
Teijeira, Marta
机构
[1] Cent Univ Las Villas, Chem Bioact Ctr, Santa Clara 54830, Villa Clara, Cuba
[2] Vigo Univ, Dept Organ Chem, Vigo 36200, Spain
[3] Expt Sugar Cane Stn, Serv Unit, Ranchuelo 53100, Villa Clara, Cuba
关键词
QSAR; naphthoquinone esters; anticancer activity; 2D-autocorrelation descriptors; cluster analysis;
D O I
10.1016/j.bmc.2007.02.032
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
A QSAR study was developed, employing 2D-autocorrelation descriptors and a set of 37 naphthoquinone ester derivatives, in order to model the cytotoxicity of these compounds against oral human epidermoid carcinoma (KB). A comparison with other approaches such as the BCUT, Galvez topological charge indexes, Randie molecular profile, Geometrical, and RDF descriptors was carried out. Mathematical models were obtained by means of the multiple regression analysis (MRA) and the variables were selected using genetic algorithm. Based on the statistical results the 2D-autocorrelation descriptors were considered the best and were able to describe more than 84.2% of the variance in the experimental activity once we controlled for outliers. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3565 / 3571
页数:7
相关论文
共 34 条
[1]   NEW LOOK AT STATISTICAL-MODEL IDENTIFICATION [J].
AKAIKE, H .
IEEE TRANSACTIONS ON AUTOMATIC CONTROL, 1974, AC19 (06) :716-723
[2]  
Akaike H, 1973, 2 INT S INF THEOR
[3]   Design, synthesis, and biological evaluation of novel naphthoquinone derivatives with CDC25 phosphatase inhibitory activity [J].
Brun, MP ;
Braud, E ;
Angotti, D ;
Mondésert, O ;
Quaranta, M ;
Montes, M ;
Miteva, M ;
Gresh, N ;
Ducommun, B ;
Garbay, C .
BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (16) :4871-4879
[4]   MOLECULAR-IDENTIFICATION NUMBER FOR SUBSTRUCTURE SEARCHES [J].
BURDEN, FR .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1989, 29 (03) :225-227
[5]   A chemically intuitive molecular index based on the eigenvalues of a modified adjacency matrix [J].
Burden, FR .
QUANTITATIVE STRUCTURE-ACTIVITY RELATIONSHIPS, 1997, 16 (04) :309-314
[6]   THE DEVELOPMENT AND USE OF QUANTUM-MECHANICAL MOLECULAR-MODELS .76. AM1 - A NEW GENERAL-PURPOSE QUANTUM-MECHANICAL MOLECULAR-MODEL [J].
DEWAR, MJS ;
ZOEBISCH, EG ;
HEALY, EF ;
STEWART, JJP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (13) :3902-3909
[7]  
FRANK J, 1993, SEILER RES LAB
[8]  
Friedman J., 1990, 102 STANF U
[9]   TOPOLOGICAL APPROACH TO DRUG DESIGN [J].
GALVEZ, J ;
GARCIADOMENECH, R ;
DEJULIANORTIZ, JV ;
SOLER, R .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1995, 35 (02) :272-284
[10]   CHARGE INDEXES - NEW TOPOLOGICAL DESCRIPTORS [J].
GALVEZ, J ;
GARCIA, R ;
SALABERT, MT ;
SOLER, R .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 1994, 34 (03) :520-525