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- W4313200975 abstract "17-trifluoromethylphenyl trinor prostaglandin F2α (17-CF3PTPGF2α) was reported recently to exhibit in vitro and in vivo anticancer activity. Based solely on the results of in silico molecular docking, it was claimed that this compound is NK1 receptor (NK1R) antagonist and that its activity is through this receptor. In this contribution we show that 17-CF3PTPGF2α is only a very weak NK1R ligand (IC50 > 200 μM). In connection with that we discuss the issue of this compound's molecular target. Finally, we briefly narrate on the proper use of molecular docking in biomedical research." @default.
- W4313200975 created "2023-01-06" @default.
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- W4313200975 date "2023-02-01" @default.
- W4313200975 modified "2023-10-14" @default.
- W4313200975 title "Docking is not enough: 17-trifluoromethylphenyl trinor PGF2α is only a very weak ligand of neurokinin-1 receptor" @default.
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- W4313200975 doi "https://doi.org/10.1016/j.yexmp.2022.104849" @default.
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