Topomer CoMFA 3D-QSAR and Docking Studies of Pyrimidine Inhibitors of Pneumocystis Carinii Dihydrofolate Reductase

Title:Topomer CoMFA 3D-QSAR and Docking Studies of Pyrimidine Inhibitors of Pneumocystis Carinii Dihydrofolate Reductase

Volume: 13 Issue: 10

Author(s): Jianbo Tong, Pei Zhan, Tuanli Yao, Lanbing Ma and Min Bai

Affiliation:

Keywords: 3D-QSAR, dihydrofolate reductase, pyrimidine derivatives, topomer CoMFA, molecular docking.

Abstract: P. carinii dihydrofolate reductase (PcDHFR) inhibitors are used for the treatment of P. carinii pneumonia (PCP) in humans with acquired immunodeficiency syndrome (AIDS). Translocation comparative molecular field vector analysis (Topomer CoMFA) 3D-QSAR and molecular docking were applied for a series of pyrimidine derivatives. 64 Pyrimidine derivatives were analyzed and the relationship between the structures and bioactivities was explored. Topomer CoMFA was used to build 3D-QSAR model, the results show that cross-validation q2 = 0.721, SDCV = 0.52, the non-crossvalidated r2 = 0.922, SD = 0.28, and the correlation coefficient of external validation Q2 ext = 0.934, this indicated that model generated form Topomer CoMFA was reasonable, and had good prediction ability. The mechanism of action of drug was studied by molecular docking. It showed that the pyrimidine compounds and GLU32, ILE123, LYS37 sites of PcDHFR have interactions. These results have provided an insight for the design of new potent inhibitors of PcDHFR.

Cite this article as:

Tong Jianbo, Zhan Pei, Yao Tuanli, Ma Lanbing and Bai Min, Topomer CoMFA 3D-QSAR and Docking Studies of Pyrimidine Inhibitors of Pneumocystis Carinii Dihydrofolate Reductase, Letters in Drug Design & Discovery 2016; 13 (10) . https://dx.doi.org/10.2174/1570180813666160324154549

DOI https://dx.doi.org/10.2174/1570180813666160324154549	Print ISSN 1570-1808
Publisher Name Bentham Science Publisher	Online ISSN 1875-628X