Simple stochastic fingerprints towards mathematical modelling in biology and medicine.: 1.: The treatment of coccidiosis

被引:48
作者
Díaz, HG
Bastida, I
Castañedo, N
Nasco, O
Olazabal, E
Morales, A
Serrano, HS
De Armas, RR
机构
[1] Univ Cent Las Villas, CBQ, Chem Bioact Ctr, Dept Drug Design, Santa Clara 54830, Villa Clara, Cuba
[2] Univ Cent Las Villas, Chem Bioact Ctr, Dept Parasitol, Santa Clara 54830, Villa Clara, Cuba
[3] Univ Cent Las Villas, Chem & Pharm Fac, Dept Chem, Santa Clara 54830, Villa Clara, Cuba
关键词
D O I
10.1016/j.bulm.2003.12.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have developed a classification function that is capable of discriminating between anticoccidial and nonanticoccidial compounds with different structural patterns. For this purpose, we calculated the Markovian electron delocalization negentropies of several compounds. These molecular descriptors, which act as molecular fingerprints, are derived from an electronegativity-weighted stochastic matrix ((1)Pi). The method attempts to describe the delocalization of electrons with time during the process of molecule formation by considering the 3D environment of the atoms. Accordingly, the entropies of this random process are used as molecular descriptors. The present study involves a stochastic generalization of the original idea described by Kier, which concerned the use of molecular negentropies in QSAR. Linear discriminant analysis allowed us to fit the discriminant function. This function has given rise to a good classification of 82.35% (28 anticoccidials out of 34) and 91.8% of inactive compounds (56/61) in training series. An overall classification of 88.42% (84/95) was achieved. Validation of the model was carried out by means of an external predicting series and this gave a global predictability of 93.1%. Finally, we report the experimental assay (more than 95% of lesion control) of two compounds selected from a large data set through virtual screening. We conclude that the approach described here seems to be a promising 3D-QSAR tool based on the mathematical theory of stochastic processes. (C) 2003 Published by Elsevier Ltd on behalf of Society for Mathematical Biology.
引用
收藏
页码:1285 / 1311
页数:27
相关论文
共 74 条
[1]   Prediction of enantiomeric selectivity in chromatography - Application of conformation-dependent and conformation-independent descriptors of molecular chirality [J].
Aires-de-Sousa, J ;
Gasteiger, J .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 2002, 20 (05) :373-388
[2]  
[Anonymous], 2007, ORGANIC CHEM DRUGS T
[3]  
[Anonymous], CHEMOMETRIC METHODS
[4]   Deriving a quantitative chirality measure from molecular similarity indices [J].
Benigni, R ;
Cotta-Ramusino, M ;
Gallo, G ;
Giorgi, F ;
Giuliani, A ;
Varì, MR .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (20) :3699-3703
[5]  
Bharucha-Reid AT, 1960, MCGRAWHILL SERIES PR, P167
[6]   INFORMATION-THEORY, DISTANCE MATRIX, AND MOLECULAR BRANCHING [J].
BONCHEV, D ;
TRINAJSTIC, N .
JOURNAL OF CHEMICAL PHYSICS, 1977, 67 (10) :4517-4533
[7]   Use of automatic relevance determination in QSAR studies using Bayesian neural networks [J].
Burden, FR ;
Ford, MG ;
Whitley, DC ;
Winkler, DA .
JOURNAL OF CHEMICAL INFORMATION AND COMPUTER SCIENCES, 2000, 40 (06) :1423-1430
[8]   Evaluation of the efficacy of anticoccidial drugs against Eimeria species in the fowl [J].
Chapman, HD .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1998, 28 (07) :1141-1144
[9]   COMPARATIVE MOLECULAR-FIELD ANALYSIS (COMFA) .1. EFFECT OF SHAPE ON BINDING OF STEROIDS TO CARRIER PROTEINS [J].
CRAMER, RD ;
PATTERSON, DE ;
BUNCE, JD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (18) :5959-5967
[10]   QSAR study on the contribution of log P and Es to the in vitro antiprotozoal activity of glutathione derivatives [J].
Daunes, S ;
D'Silva, C ;
Kendrick, H ;
Yardley, V ;
Croft, SL .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (18) :2976-2983