Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus
Por um escritor misterioso
Last updated 27 setembro 2024
A lymphatic-absorbed multi-targeted kinase inhibitor for myelofibrosis therapy
Design and Synthesis of Ligand Efficient Dual Inhibitors of Janus Kinase (JAK) and Histone Deacetylase (HDAC) Based on Ruxolitinib and Vorinostat
Full article: In silico computational drug discovery: a Monte Carlo approach for developing a novel JAK3 inhibitors
Dual-target Janus kinase (JAK) inhibitors: Comprehensive review on the JAK-based strategies for treating solid or hematological malignancies and immune-related diseases - ScienceDirect
Structure-based design of a phosphotyrosine-masked covalent ligand targeting the E3 ligase SOCS2
Discovery of 4-piperazinyl-2-aminopyrimidine derivatives as dual inhibitors of JAK2 and FLT3 - ScienceDirect
Magnetite‐based Janus nanoparticles, their synthesis and biomedical applications - Madadi - WIREs Nanomedicine and Nanobiotechnology - Wiley Online Library
Evolving cognition of the JAK-STAT signaling pathway: autoimmune disorders and cancer
A ) Triaminotriazine-acridine conjugate 1 designed for selective
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