Discovery of AZD2932, a new Quinazoline Ether Inhibitor with high affinity for VEGFR-2 and PDGFR tyrosine kinases
- PMID: 22153662
- DOI: 10.1016/j.bmcl.2011.11.019
Discovery of AZD2932, a new Quinazoline Ether Inhibitor with high affinity for VEGFR-2 and PDGFR tyrosine kinases
Abstract
A new series of Quinazoline Ether Inhibitor which potently inhibits VEGFR-2 and PDGFR tyrosine kinases is described here. In vitro, pharmacokinetics and in vivo evaluations led to the selection of AZD2932.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Similar articles
-
Discovery of new quinoline ether inhibitors with high affinity and selectivity for PDGFR tyrosine kinases.Bioorg Med Chem Lett. 2012 May 1;22(9):3050-5. doi: 10.1016/j.bmcl.2012.03.074. Epub 2012 Mar 28. Bioorg Med Chem Lett. 2012. PMID: 22497760
-
Synthesis of a novel biotin-tagged photoaffinity probe for VEGF receptor tyrosine kinases.Bioorg Med Chem Lett. 2006 Jan 1;16(1):129-33. doi: 10.1016/j.bmcl.2005.09.036. Epub 2005 Oct 10. Bioorg Med Chem Lett. 2006. PMID: 16216503
-
Pharmacological characterization of CP-547,632, a novel vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for cancer therapy.Cancer Res. 2003 Nov 1;63(21):7301-9. Cancer Res. 2003. PMID: 14612527
-
Impact of aryloxy-linked quinazolines: a novel series of selective VEGFR-2 receptor tyrosine kinase inhibitors.Bioorg Med Chem Lett. 2011 Apr 1;21(7):2106-12. doi: 10.1016/j.bmcl.2011.01.137. Epub 2011 Feb 3. Bioorg Med Chem Lett. 2011. PMID: 21353546
-
Design, synthesis and antitumor activity of 4-aminoquinazoline derivatives targeting VEGFR-2 tyrosine kinase.Bioorg Med Chem Lett. 2012 Jan 1;22(1):110-4. doi: 10.1016/j.bmcl.2011.11.061. Epub 2011 Nov 23. Bioorg Med Chem Lett. 2012. PMID: 22169262
Cited by
-
Functionalisation of Fe3O4 nanoparticles by 2-((pyrazol-4-yl) methylene) hydrazinecarbothioamide enhances the apoptosis of human breast cancer MCF-7 cells.IET Nanobiotechnol. 2020 Aug;14(6):508-518. doi: 10.1049/iet-nbt.2019.0199. IET Nanobiotechnol. 2020. PMID: 32755961 Free PMC article.
-
Kinase Inhibitory Activities and Molecular Docking of a Novel Series of Anticancer Pyrazole Derivatives.Molecules. 2018 Nov 24;23(12):3074. doi: 10.3390/molecules23123074. Molecules. 2018. PMID: 30477238 Free PMC article.
-
Design, synthesis, and bioactivity evaluation of antitumor sorafenib analogues.RSC Adv. 2018 Nov 8;8(66):37643-37651. doi: 10.1039/c8ra08246d. eCollection 2018 Nov 7. RSC Adv. 2018. PMID: 35558629 Free PMC article.
-
Synthesis, molecular docking and biological potentials of new 2-(4-(2-chloroacetyl) piperazin-1-yl)-N-(2-(4-chlorophenyl)-4-oxoquinazolin-3(4H)-yl)acetamide derivatives.BMC Chem. 2019 Sep 5;13(1):113. doi: 10.1186/s13065-019-0629-0. eCollection 2019 Dec. BMC Chem. 2019. PMID: 31517312 Free PMC article.
-
Small Molecule c-KIT Inhibitors for the Treatment of Gastrointestinal Stromal Tumors: A Review on Synthesis, Design Strategies, and Structure-Activity Relationship (SAR).Int J Mol Sci. 2023 May 29;24(11):9450. doi: 10.3390/ijms24119450. Int J Mol Sci. 2023. PMID: 37298401 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Chemical Information
Miscellaneous