Discovery of novel, non-acidic mPGES-1 inhibitors by virtual screening with a multistep protocol (original) (raw)

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ARTICLE pubs.acs.org/jmc Pharmacophore Modeling and Virtual Screening for Novel Acidic

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Identification of Key Residues Determining Species Differences in Inhibitor Binding of Microsomal Prostaglandin E Synthase-1*

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Human microsomal prostaglandin E synthase-1 (mPGES-1) binding with inhibitors and the quantitative structure-activity correlation

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Success of prostaglandin E2 in structure-function is a challenge for structure-based therapeutics

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Amide Hydrolysis of a Novel Chemical Series of Microsomal Prostaglandin E Synthase-1 Inhibitors Induces Kidney Toxicity in the Rat

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Homo-timeric structural model of human microsomal prostaglandin E synthase-1 and characterization of its substrate/inhibitor binding interactions

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Design, synthesis, and discovery of 5-((1,3-diphenyl-1H-pyrazol-4-yl)methylene)pyrimidine-2,4,6(1H,3H,5H)-triones and related derivatives as novel inhibitors of mPGES-1

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