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- W3080315322 abstract "Thirty novel triaryl compounds were designed and synthesized based on the known proteasome inhibitor PI-1840. Most of them showed significant inhibition against the β5c subunit of human 20S proteasome, and five of them exhibited IC50 values at the sub-micromolar level, which were comparable to or even more potent than PI-1840. The most active two (1c and 1d) showed IC50 values of 0.12 and 0.18 μM against the β5c subunit, respectively, while they displayed no obvious inhibition against the β2c, β1c and β5i subunits. Molecular docking provided informative clues for the subunit selectivity. The potent and subunit selective proteasome inhibitors identified herein represent new chemical templates for further molecular optimization." @default.
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- W3080315322 date "2020-11-01" @default.
- W3080315322 modified "2023-10-10" @default.
- W3080315322 title "Design, synthesis and biological evaluation of triaryl compounds as novel 20S proteasome inhibitors" @default.
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- W3080315322 doi "https://doi.org/10.1016/j.bmcl.2020.127508" @default.
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