Design, synthesis, biological activity evaluation of 3-(4-phenyl-1H-imidazol-2-yl)-1H-pyrazole derivatives as potent JAK 2/3 and aurora A/B kinases multi-targeted inhibitors
Authors:
- 1 January 2021
- journal article
- research article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 209, 112934
Abstract
No abstract availableKeywords
Funding Information
- National Natural Science Foundation of China
This publication has 63 references indexed in Scilit:
- Crystal Structure of Human Aurora B in Complex with INCENP and VX-680Journal of Medicinal Chemistry, 2012
- Phase I study of the Aurora B kinase inhibitor barasertib (AZD1152) to assess the pharmacokinetics, metabolism and excretion in patients with acute myeloid leukemiaCancer Chemotherapy and Pharmacology, 2012
- Potentiation of Nilotinib-mediated cell death in the context of the bone marrow microenvironment requires a promiscuous JAK inhibitor in CMLLeukemia Research, 2012
- The role of conformational entropy in molecular recognition by calmodulinNature Chemical Biology, 2010
- AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreadingJournal of Computational Chemistry, 2009
- AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibilityJournal of Computational Chemistry, 2009
- Antitumor activity of MLN8054, an orally active small-molecule inhibitor of Aurora A kinaseProceedings of the National Academy of Sciences, 2007
- Development and testing of a general amber force fieldJournal of Computational Chemistry, 2004
- The cellular geography of Aurora kinasesNature Reviews Molecular Cell Biology, 2003
- Comparison of simple potential functions for simulating liquid waterThe Journal of Chemical Physics, 1983