N-(3-fluoro-4-(2-arylthieno[3,2- b]pyridin-7-yloxy)phenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: A novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors
A series of N-(3-fluoro-4-(2-arylthieno[3,2- b]pyridin-7-yloxy)phenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides ( II) targeting c-Met and VEGFR2 tyrosine kinases, based on our previous acetylthiourea series ( I), was designed and synthesized. The new compounds were potent against these two enzymes...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2009-03, Vol.19 (5), p.1323-1328 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A series of
N-(3-fluoro-4-(2-arylthieno[3,2-
b]pyridin-7-yloxy)phenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides (
II) targeting c-Met and VEGFR2 tyrosine kinases, based on our previous acetylthiourea series (
I), was designed and synthesized. The new compounds were potent against these two enzymes with IC
50 values in the low nanomolar range
in vitro, possessed favorable pharmacokinetic profiles and showed high efficacy
in vivo in several human tumor xenograft models in mice.
A series of
N-(3-fluoro-4-(2-arylthieno[3,2-
b]pyridin-7-yloxy)phenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides targeting c-Met and VEGFR2 tyrosine kinases was designed and synthesized. The compounds were potent against these two enzymes with IC
50 values in the low nanomolar range in vitro, possessed favorable pharmacokinetic profiles and showed high efficacy in vivo in several human tumor xenograft models in mice. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2009.01.068 |