Repository of Research and Investigative Information

Repository of Research and Investigative Information

Baqiyatallah University of Medical Sciences

QSAR and QSTR study of pyrimidine derivatives to improve their therapeutic index as antileishmanial agents

(2013) QSAR and QSTR study of pyrimidine derivatives to improve their therapeutic index as antileishmanial agents. Medicinal Chemistry Research. pp. 5029-5035. ISSN 1054-2523

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Abstract

In the treatment of leishmaniasis, chemotherapy is expensive and has various side effects. The major side effects are due to multiple injections that are required over a course of several weeks and non-selectivity of the drugs. In addition, there is no fully effective drug available against the cutaneous form of the disease. Experimental data of pyrimidine derivatives show that they are potent inhibitors of Leishmania growth. In the current study, a series of 2-pyridyl pyrimidine derivatives with Plasmodium falciparum methionine aminopeptidase 1b inhibitory activity was subjected to quantitative structure activity relationship (QSAR) and quantitative structure toxicity relationship (QSTR) analyses to identify the ideal physicochemical characteristics of potential anti Leishmania activity with limited cytotoxic effects. We also determined the physicochemical characteristics that affect antiparasitic activity and cytotoxicity to identify the best relationship model related to these two parameters. 2-Pyridyl pyrimidines with desirable properties were built using HyperChem program, and conformational studies were performed through the semi-empirical method followed by the PM3 force field. Different descriptors were calculated using Dragon and HyperChem software. Multilinear regression was used as a chemometric tool for QSAR and QSTR modeling and the developed models were shown to be statistically significant according to the validation parameters. Based on our computational studies, using lipophilic and electronegative moieties can improve the therapeutic index of pyrimidine derivatives. Quantitative structure activity relationships (QSAR) used to improve the therapeutic index of the pyrimidine derivatives as antileishmanial agents and Quantitative structure toxicity relationships (QSTR) used to improve the low cytotoxicity of the pyrimidine derivatives.

Item Type: Article
Keywords: Cytotoxicity Leishmaniasis 2-Pyridyl pyrimidines QSAR QSTR cutaneous leishmaniasis drug design 3d qsar 1,4-dihydropyridines chemotherapy substituent Pharmacology & Pharmacy
Divisions:
Page Range: pp. 5029-5035
Journal or Publication Title: Medicinal Chemistry Research
Journal Index: ISI
Volume: 22
Number: 10
Identification Number: https://doi.org/10.1007/s00044-013-0477-8
ISSN: 1054-2523
Depositing User: مهندس مهدی شریفی
URI: http://eprints.bmsu.ac.ir/id/eprint/5961

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