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Synthesis and Evaluation of Novel 2-Pyrrolidone-Fused (2-Oxoindolin-3-ylidene)methylpyrrole Derivatives as Potential Multi-Target Tyrosine Kinase Receptor Inhibitors

机译：新型2-吡咯烷酮 - 稠合（2-氧代二氢吲哚-3-亚基）甲基吡咯衍生物作为潜在的多靶酪氨酸激酶受体抑制剂的合成与评价

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Ting-Hsuan Yang; Chun-I Lee; Wen-Hsin Huang; An-Rong Lee;
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年度 2017
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1. Synthesis and Evaluation of Novel 2-Pyrrolidone-Fused (2-Oxoindolin-3-ylidene)methylpyrrole Derivatives as Potential Multi-Target Tyrosine Kinase Receptor Inhibitors [J] . Ting-Hsuan Yang, Chun-I Lee, Wen-Hsin Huang, Molecules . 2017,第6期

机译：新型2-吡咯烷酮融合的（2-氧吲哚-3-亚甲基）甲基吡咯衍生物作为潜在的多靶酪氨酸激酶受体抑制剂的合成和评价
2. Synthesis and Evaluation of Novel 2-Pyrrolidone-Fused (2-Oxoindolin-3-ylidene)methylpyrrole Derivatives as Potential Multi-Target Tyrosine Kinase Receptor Inhibitors [J] . Yang Ting-Hsuan, Lee Chun-I, Huang Wen-Hsin, Molecules . 2017,第6期

机译：作为潜在的多靶酪氨酸激酶受体抑制剂的新型2-吡咯烷酮稠合（2-氧代吲哚-3- ylidene）甲基吡咯衍生物的合成与评价
3. Structural optimization and evaluation of novel 2-pyrrolidone-fused (2-oxoindolin-3-ylidene)methylpyrrole derivatives as potential VEGFR-2/PDGFRβ inhibitors [J] . Ting-Hsuan Yang, Chun-I Lee, Wen-Hsin Huang, Chemistry central journal . 2017,第1期

机译：新型2-吡咯烷酮-稠合的（2-氧代吲哚-3-亚基）甲基吡咯衍生物作为潜在的VEGFR-2 /PDGFRβ抑制剂的结构优化和评价
4. QSAR Study of Quinazoline Derivatives as Inhibitor of Epidermal Growth Factor Receptor-Tyrosine Kinase (EGFR-TK) [C] . La Ode Aman, Widisusanti Abdulkadir, Julitha Geybie Rembet, International Conference on Computation for Science and Technology . 2015

机译：喹唑啉衍生物作为表皮生长因子受体 - 酪氨酸激酶（EGFR-TK）抑制剂的QSAR研究
5. The multi-targeted receptor tyrosine kinase inhibitor, linifanib (ABT-869), induces apoptosis and inhibits proliferation of leukemia cells through phosphoinositide-3 kinase (PI3K)/AKT-dependent signaling pathways. [D] . Hernandez, Jenny Elizabeth. 2010

机译：多靶点受体酪氨酸激酶抑制剂利尼法尼（ABT-869）通过磷酸肌醇3激酶（PI3K）/ AKT依赖性信号传导途径诱导凋亡并抑制白血病细胞的增殖。
6. Structural optimization and evaluation of novel 2-pyrrolidone-fused (2-oxoindolin-3-ylidene)methylpyrrole derivatives as potential VEGFR-2/PDGFRβ inhibitors [O] . Ting-Hsuan Yang, Chun-I Lee, Wen-Hsin Huang, 2017

机译：新型2-吡咯烷酮稠合的（2-氧代吲哚-3-亚基）甲基吡咯衍生物作为潜在的VEGFR-2 /PDGFRβ抑制剂的结构优化和评价
7. Synthesis and In Vitro Cytotoxicity of the 4-(Halogenoanilino)-6-bromoquinazolines and Their 6-(4-Fluorophenyl) Substituted Derivatives as Potential Inhibitors of Epidermal Growth Factor Receptor Tyrosine Kinase [O] . Malose Jack Mphahlele, Hugues K. Paumo, Yee Siew Choong 2017

机译：4-（卤代苯胺基）-6-溴喹唑啉及其6-（4-氟苯基）取代衍生物作为表皮生长因子受体酪氨酸激酶的潜在抑制剂的合成和体外细胞毒性
8. Isolation and Analysis of Human Kekkon-Like Molecules, a Family of Potential Inhibitors of ErbB Receptor Tyrosine Kinases [R] . Kockel, L. 2005

机译：人类Kekkon样分子的分离和分析，一系列ErbB受体酪氨酸激酶的潜在抑制剂

Synthesis and Evaluation of Novel 2-Pyrrolidone-Fused (2-Oxoindolin-3-ylidene)methylpyrrole Derivatives as Potential Multi-Target Tyrosine Kinase Receptor Inhibitors

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