Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus
Por um escritor misterioso
Last updated 13 maio 2024
Design and optimization of a series of 4-(3-azabicyclo[3.1.0]hexan-3-yl)pyrimidin-2-amines: Dual inhibitors of TYK2 and JAK1 - ScienceDirect
Chemical structures of JAK1/2 dual inhibitor Compound 1 and JAK2
Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus Kinase (JAK) and Histone Deacetylase (HDAC) Based on Ruxolitinib and Vorinostat
Discovery of 4-piperazinyl-2-aminopyrimidine derivatives as dual inhibitors of JAK2 and FLT3 - ScienceDirect
TK4g is a JAK Inhibitor for Leukemia Cancer Research
Discovery of Janus Kinase 2 (JAK2) and Histone Deacetylase (HDAC) Dual Inhibitors as a Novel Strategy for the Combinational Treatment of Leukemia and Invasive Fungal Infections
Structure-based design of a phosphotyrosine-masked covalent ligand targeting the E3 ligase SOCS2
Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus Kinase (JAK) and Histone Deacetylase (HDAC) Based on Ruxolitinib and Vorinostat
Treating inflammation with the Janus Kinase inhibitor CP-690,550: Trends in Pharmacological Sciences
Molecules, Free Full-Text
The role of ligand efficiency metrics in drug discovery
Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus Kinase (JAK) and Histone Deacetylase (HDAC) Based on Ruxolitinib and Vorinostat.
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