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- W2149188030 abstract "Microsomal prostablandin E synthase-1 (mPGES-1) has been recently investigated to be a novel and promising target for inflammation-related diseases. The quantitative structure-activity relationship (QSAR) study was used to explore the critical pharmacophore features of mPGES-1 by using a set of 35 azaphenanthrenone derivatives. Twenty four selected pharmacophore models derived from 240 hypotheses were employed to identify the critical features. The best two pharmacophore hypotheses exhibited the residuals of approximately 150 and the high correlation coefficient of 0.92. The selected four hypotheses all showed a confidence level of 95 % in the Fischerpsilas randomization test. The final four pharmacophore model showed that the four dominant features (hydrogen bond donor and 3 hydrophobic features, occasionally replaced by ring aromatic feature) had significant impact on activity of mPGES-1 inhibitors. The database virtual screening and drug design can be further implement to searching the novel mPGES-1 inhibitors." @default.
- W2149188030 created "2016-06-24" @default.
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- W2149188030 date "2008-09-01" @default.
- W2149188030 modified "2023-09-25" @default.
- W2149188030 title "Exploring 3D-QSAR pharmacophore mapping of azaphenanthrenone derivatives for mPGES-1 inhibition Using HypoGen technique" @default.
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- W2149188030 doi "https://doi.org/10.1109/cibcb.2008.4675780" @default.
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