Discovery of anilinopyrimidine-based naphthamide derivatives as potent VEGFR-2 inhibitors
Vascular endothelial growth factor receptor-2 (VEGFR-2) plays an important role in tumor angiogenesis, and inhibition of the VEGFR-2 signaling pathway has emerged as an attractive strategy for the treatment of cancer. Herein, we describe the design, synthesis, and biological evaluation of anilinopyr...
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Veröffentlicht in: | MedChemComm 2015-01, Vol.6 (7), p.1375-1380 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Vascular endothelial growth factor receptor-2 (VEGFR-2) plays an important role in tumor angiogenesis, and inhibition of the VEGFR-2 signaling pathway has emerged as an attractive strategy for the treatment of cancer. Herein, we describe the design, synthesis, and biological evaluation of anilinopyrimidine-based naphthamide derivatives as potent VEGFR-2 inhibitors. Among the new derivatives, compound
3k
exhibited high VEGFR-2 inhibitory potency in both enzymatic and VEGF-induced HUVEC cellular proliferation assays (IC
50
= 0.5 and 9.8 nM, respectively). Kinase selectivity profiling revealed that
3k
was a highly selective VEGFR-2 inhibitor. Moreover,
3k
effectively inhibited angiogenesis in HUVEC tube formationassay. |
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ISSN: | 2040-2503 2040-2511 |
DOI: | 10.1039/C5MD00191A |