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100Blair et al..
Structure-guided development of affinity probes for tyrosine kinases using chemical genetics, Nature Chemical Biology, 2007 Jingxian ZhangThe authors contributed equally to this work., Jia Jia, Feng Zhu, Xiaohua Ma, Bucong Han, Xiaona Wei, Chunyan Tan, Yuyang Jiang and Yuzong Chen.
Analysis of bypass signaling in EGFR pathway and profiling of bypass genes for predicting response to anticancer EGFR tyrosine kinase inhibitors, Mol. Biosyst., 2012, 8, 2645. Thomas Beckers, Siavosh Mahboobi, Andreas Sellmer, Matthias Winkler, Emerich Eichhorn, Herwig Pongratz, Thomas Maier, Thomas Ciossek, Thomas Baer, Gerhard Kelter, Heinz-Herbert Fiebig and Mathias Schm
idt.
Chimerically designed HDAC- and tyrosine kinase inhibitors. A series of erlotinib hybrids as dual-selective inhibitors of EGFR, HER2 and histone deacetylases, Med. Chem. Commun., 2012, 3, 829. Samuel M. Meier, Muhammad Hanif, Zenita Adhireksan, Verena Pichler, Maria Novak, Elisabeth Jirkovsky, Michael A. Jakupec, Vladimir B. Arion, Curt A. Davey, Bernhard K. Keppler and Christian G. Harting
er.
Novel metal(ii) arene 2-pyridinecarbothioamides: a rationale to orally active organometallic anticancer agents, Chem. Sci., 2013, 4, 1837. Xu Tianfeng, Peng Ting, Ren Xiaomei, Zhang Lianwen, Yu Lei, Luo Jinfeng, Zhang Zhang, Tu Zhengchao, Tong Linjiang, Huang Zhaoru, Lu Xiaoyun, Geng Meiyu, Xie Hua, Ding Jian, Ding Ke.
C5-substituted pyrido[2,3-d]pyrimidin-7-ones as highly specific kinase inhibitors targeting the clinical resistance-related EGFRT790M mutant, Med. Chem. Commun., 2015 Bagul chandrakant, Rao Garikapati Koteswara, Makani Venkata Krishna Kanth , Tamboli Jaki R , Bhadra Manika Pal, Kamal Ahmed.
Synthesis and biological evaluation of chalcone-linked pyrazolo[1,5-a]pyrimidines as potential anticancer agents, Med. Chem. Commun., 2017 Antitumor activity of HER1/EGFR tyrosine kinase inhibitor erlotinib, alone and in combination with CPT-11 (irinotecan) in human colorectal cancer xenograft models, Cancer Chemotherapy and Pharmacology