Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus
Por um escritor misterioso
Last updated 24 outubro 2024
Frontiers Inhibitors Targeting Multiple Janus Kinases From Zanthoxylum simulans Mediate Inhibition and Apoptosis Against Gastric Cancer Cells via the Estrogen Pathway
TK4g is a JAK Inhibitor for Leukemia Cancer Research
Molecules, Free Full-Text
Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus Kinase (JAK) and Histone Deacetylase (HDAC) Based on Ruxolitinib and Vorinostat.
Structures of monovalent inhibitors as well as the natural ligand
Frontiers Immunomodulation—a general review of the current state-of-the-art and new therapeutic strategies for targeting the immune system
Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus Kinase (JAK) and Histone Deacetylase (HDAC) Based on Ruxolitinib and Vorinostat
IJMS, Free Full-Text
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
Privileged Scaffolds in Medicinal by Bräse, Stefan
Design, Synthesis, and Biological Evaluation of Quinazolin-4-one-Based Hydroxamic Acids as Dual PI3K/HDAC Inhibitors
Treating inflammation with the Janus Kinase inhibitor CP-690,550: Trends in Pharmacological Sciences
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