The identification of potent dual-target monopolar spindle 1 (MPS1) and histone deacetylase 8 (HDAC8) inhibitors through pharmacophore modeling, molecular docking, molecular dynamics simulations, and biological evaluation
BackgroundOverexpression of monopolar spindle 1 (MPS1) and histone deacetylase 8 (HDAC8) is associated with the proliferation of liver cancer cells, so simultaneous inhibition of both MPS1 and HDAC8 could offer a promising therapeutic approach for the treatment of liver cancer. Dual-targeted MPS1/HD...
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Main Authors: | , , , , , , , |
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Format: | Book |
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Frontiers Media S.A.,
2024-09-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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