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• W2082298210 abstract "There is an urgent need to design and develop new and more potent EGFR inhibitors with improved anti-tumor activity. Here we describe the design and synthesis of two series of 4-benzothienyl amino quinazolines as new analogues of the EGFR inhibitor Gefitinib. The anti-tumor activity of these novel Gefitinib analogues in 6 human cancer cell lines was examined. Compared with the parental Gefitinib, most of the new compounds show a markedly increased cytotoxicity to cancer cells. Furthermore, several of the series B compounds that side chains at position 7 contain either a methyl or ethyl group are potent pan-RTK inhibitors. Two representative compounds in this class, 15 and 17, have an enhanced capability to inhibit cancer cell growth and induce apoptosis in vitro and inhibit tumor formation in vivo in human cancer cells with high HER-2, as compared with the parental Gefitinib. Thus they may be promising lead compounds to be developed as an alternative for current Gefitinib therapy or for Gefitinb-resistant patients, potentially via simultaneously blocking multiple RTK signaling pathways." @default.
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• W2082298210 date "2010-06-01" @default.
• W2082298210 modified "2023-10-16" @default.
• W2082298210 title "Design and synthesis of novel Gefitinib analogues with improved anti-tumor activity" @default.
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• W2082298210 doi "https://doi.org/10.1016/j.bmc.2010.04.046" @default.
• W2082298210 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2890262" @default.
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