Pages that link to "Q27677295"

The following pages link to Implications of Promiscuous Pim-1 Kinase Fragment Inhibitor Hydrophobic Interactions for Fragment-Based Drug Design (Q27677295):

Displaying 10 items.

• Discovery of novel benzylidene-1,3-thiazolidine-2,4-diones as potent and selective inhibitors of the PIM-1, PIM-2, and PIM-3 protein kinases (Q27681337) (← links)
• Increasing Chemical Space Coverage by Combining Empirical and Computational Fragment Screens (Q27683679) (← links)
• Fragment-based screening by protein crystallography: successes and pitfalls (Q34314898) (← links)
• Protein crystallography and fragment-based drug design. (Q34353117) (← links)
• Finding novel pharmaceuticals in the systems biology era using multiple effective drug targets, phenotypic screening and knowledge of transporters: where drug discovery went wrong and how to fix it. (Q34646772) (← links)
• Palladium-catalyzed chemoselective synthesis of indane-1,3-dione derivatives via tert-butyl isocyanide insertion (Q35640706) (← links)
• Prospective evaluation of shape similarity based pose prediction method in D3R Grand Challenge 2015. (Q36092809) (← links)
• Synthesis of new thieno[2,3-b]pyridine derivatives as pim-1 inhibitors. (Q38751047) (← links)
• Discovery and identification of PIM-1 kinase inhibitors through a hybrid screening approach (Q39024729) (← links)
• Binding mode information improves fragment docking (Q64062455) (← links)