Novel VEGFR-2 inhibitors with an N-acylhydrazone scaffold
- PMID: 32667721
- DOI: 10.1002/ardp.202000130
Novel VEGFR-2 inhibitors with an N-acylhydrazone scaffold
Abstract
Vascular endothelial growth factor receptor 2 (VEGFR-2) is a tyrosine kinase that mediates a large number of cell responses associated with angiogenesis. The control of the angiogenic pathway in tumorigenesis by the inhibition of VEGFR-2 is considered a promising therapeutic strategy for the prevention and control of solid tumor growth. In this study, the design, synthesis, and biological evaluation of a novel series of VEGFR-2 inhibitors with an N-acylhydrazone (NAH) scaffold (9a-h) are reported. The molecular design is validated by docking studies and by in vitro inhibitory activity assays. Compounds 9b, 9c, 9d, and 9f effectively inhibited neovascularization induced by VEGF in the chorioallantoic membrane assay. Thus, these NAH derivatives are promising antiangiogenic prototypes.
Keywords: LASSBio-2027; N-acylhydrazone; VEGFR-2; angiogenesis inhibitor; kinase inhibitor.
© 2020 Deutsche Pharmazeutische Gesellschaft.
References
REFERENCES
-
- M. Rajabi, S. Mousa, Biomedicines 2017, 5, 34.
-
- S. Qin, A. Li, M. Yi, S. Yu, M. Zhang, K. Wu, J. Hematol. Oncol. 2019, 12, 1.
-
- L. M. Sherwood, E. E. Parris, J. Folkman, N. Engl. J. Med. 1971, 258, 1182.
-
- P. Carmeliet, R. K. Jain, Nature 2000, 407, 249.
-
- T. Tonini, F. Rossi, P. P. Claudio, Oncogene 2003, 22, 6549.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
