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• W4319160980 endingPage "106616" @default.
• W4319160980 startingPage "106616" @default.
• W4319160980 abstract "Microsomal prostaglandin E synthase-1 (mPGES-1) is an inducible prostaglandin E synthase expressed following exposure to pro-inflammatory stimuli. The mPGES-1 enzyme represents a new target for the therapeutic treatment of acute and chronic inflammatory disorders and cancer. In the present study, compounds from the ZINC15 database with an indole scaffold were docked at the mPGES-1 binding site using Glide (high-throughput virtual screening [HTVS], standard precision [SP] and extra precision [XP]), and the stabilities of the complexes were determined by molecular simulation studies. Following HTVS, the top 10% compounds were retained and further screened by SP. Again, the top 10% of these compounds were retained. Finally, the Glide XP scores of the compounds were determined, 20% were analyzed, and the Prime MM-GBSA total free binding energies of the compounds were calculated. The molecular simulations (100 ns) of the reference ligand, LVJ, and the two best-scoring compounds were performed with the Desmond program to analyze the dynamics of the target protein-ligand complexes. In human lung cells treated with the hit compounds, cell viability by colorimetric method and PGE2 levels by immunoassay method were determined. These in vitro experiments demonstrated that the two indole-containing hit compounds are potential novel inhibitors of mPGES-1 and are, therefore, potential therapeutic agents for cancer/inflammation therapies. Moreover, the compounds are promising lead mPGES-1 inhibitors for novel molecule design." @default.
• W4319160980 created "2023-02-04" @default.
• W4319160980 creator A5054290911 @default.
• W4319160980 creator A5067394775 @default.
• W4319160980 date "2023-03-01" @default.
• W4319160980 modified "2023-10-18" @default.
• W4319160980 title "Virtual screening, molecular simulations and bioassays: Discovering novel microsomal prostaglandin E Synthase-1 (mPGES-1) inhibitors" @default.
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• W4319160980 doi "https://doi.org/10.1016/j.compbiomed.2023.106616" @default.
• W4319160980 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36780799" @default.
• W4319160980 hasPublicationYear "2023" @default.
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