کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1396827 | 1501199 | 2009 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
3D-QSAR studies on the inhibitors of AP-1 and NF-κB mediated transcriptional activation
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آلی
پیش نمایش صفحه اول مقاله
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چکیده انگلیسی
Comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA) were performed on a series of 68 inhibitors of AP-1 and NF-κB mediated transcriptional activations. The CoMFA model produced statistically significant results with the cross-validated q2 of 0.594 and the conventional correlation coefficient r2 of 0.968. The best CoMSIA model was obtained by the combination use of steric, electrostatic, hydrogen-bond donor and acceptor fields. The corresponding q2 and r2 of CoMSIA model were 0.703 and 0.932, respectively. From the cross-validated results, it can be seen that the CoMSIA model has a better predictive ability than CoMFA model due to the importance of the hydrogen bonds for the activity of these inhibitors. The predictive abilities of the two models were further validated by a test set of 15 compounds. The models gave predicted correlation coefficient rpred2 of 0.891 for CoMFA model and 0.810 for CoMSIA model. Based on the above results, we identified the key structural features that may help to design potent inhibitors with improved activities: (1) the NH linker at the position R4 acts as important hydrogen-bond donor and any group on phenyl or 2-thienyl ring of R1 substituent decreases inhibitory activity, (2)further structural modification of compound 50 on the phenyl ring of the quinazoline ring considering steric, electrostatic and hydrogen-bond acceptor properties will influence the inhibitory activity.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Medicinal Chemistry - Volume 44, Issue 7, July 2009, Pages 2888-2895
Journal: European Journal of Medicinal Chemistry - Volume 44, Issue 7, July 2009, Pages 2888-2895
نویسندگان
Jin Qin, Huanxiang Liu, Jiazhong Li, Yueying Ren, Xiaojun Yao, Mancang Liu,