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顯示項目 316066-316090 / 2348971 (共93959頁) << < 12638 12639 12640 12641 12642 12643 12644 12645 12646 12647 > >> 每頁顯示[10|25|50]項目
| 臺大學術典藏 |
2020-03-02T07:40:24Z |
Design, Synthesis, and Electrofluorochromism of New Triphenylamine Derivatives with AIE-Active Pendent Groups
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Lin, H.-T.; Huang, C.-L.; Liou, G.-S.; GUEY-SHENG LIOU |
| 淡江大學 |
2023-10-23T04:05:45Z |
Design, synthesis, and evaluation of 1,2,3-triazole-based benzenesulfonamide and flavonol hybrid molecules as anticancer agents
|
Shih, Tzenge-lien |
| 國家衛生研究院 |
2008-08-01 |
Design, synthesis, and evaluation of 3C protease inhibitors as anti-enterovirus 71 agents
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Kuo, CJ;Shie, JJ;Fang, JM;Yen, GR;Hsu, JTA;Liu, HG;Tseng, SN;Chang, SC;Lee, CY;Shih, SR;Liang, PH |
| 國立臺灣大學 |
2008 |
Design, synthesis, and evaluation of 3C protease inhibitors as anti-enterovirus 71 agents
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Kuo, Chih-Jung; Shie, Jiun-Jie; Fang, Jim-Min; Yen, Guei-Rung; Hsu, John T.-A.; Liu, Hun-Ge; Tseng, Sung-Nain; Chang, Shih-Cheng; Lee, Ching-Yin; Shih, Shin-Ru; Liang, Po-Huang |
| 臺大學術典藏 |
2018-09-10T07:00:21Z |
Design, synthesis, and evaluation of 3C protease inhibitors as anti-enterovirus 71 agents
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Liu, H.-G.; Tseng, S.-N.; Chang, S.-C.; Lee, C.-Y.; Shih, S.-R.; Liang, P.-H.; JIM-MIN FANG; Kuo, C.-J.; Shie, J.-J.; Fang, J.-M.; Yen, G.-R.; Hsu, J. T.-A. |
| 國立臺灣大學 |
2008-08 |
Design, Synthesis, and Evaluation of 3C Protease Inhibitors as Anti-Enterovirus 71 Agents.
|
Kuo, C.-J.; Shie, J.-J.; Fang, J.-M.; Yen, G.-R.; Hsu, J. T.-A.; Liu, H.-G.; Tseng, S.-N.; Chang, S.-C.; Lee, C.-Y.; Shih, S.-R.; Liang, P.-H. |
| 國立臺灣大學 |
2016 |
Design, synthesis, and evaluation of cell permeable probes for protein kinases
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Hsu, Yu-Ling; Yang, Chun-Chieh; Chou, Tzyy-Chao; Tai, Chih-Hsuan; Chen, Long-Yuan; Fu, Shu-Ling; Lin, Jing-Jer; Lo, Lee-Chiang; 林敬哲 |
| 臺大學術典藏 |
2018-09-10T15:31:47Z |
Design, synthesis, and evaluation of cell permeable probes for protein kinases
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Hsu, Y.-L.;Yang, C.-C.;Chou, T.-C.;Tai, C.-H.;Chen, L.-Y.;Fu, S.-L.;Lin, J.-J.;Lo, L.-C.; Hsu, Y.-L.; Yang, C.-C.; Chou, T.-C.; Tai, C.-H.; Chen, L.-Y.; Fu, S.-L.; Lin, J.-J.; Lo, L.-C.; LEE-CHIANG LO |
| 臺大學術典藏 |
2020-02-06T10:53:28Z |
Design, synthesis, and evaluation of cell permeable probes for protein kinases
|
Hsu Y.-L.; Yang C.-C.; Chou T.-C.; Tai C.-H.; Chen L.-Y.; Fu S.-L.; JING-JER LIN; Lo L.-C. |
| 中國醫藥大學 |
2010-11 |
Design, Synthesis, and Evaluation of Diarylpyridines and Diarylanilines as Potent Non-nucleoside HIV-1 Reverse Transcriptase Inhibitors
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(Xingtao Tian); (Bingjie Qin); (Zhiyuan Wu); (Xiaofeng Wang); (Hong Lu); (Susan L. Morris-Natschke); (Chin Ho Chen); (Shibo Jiang); 李國雄(Kuo-Hsiung Lee); (Lan Xie)* |
| 東海大學 |
2013-11 |
Design, Synthesis, and Evaluation of Fluorescent Cell-penetrating Peptidic Antagonists of Grb2 SH2 for Targeting MCF-7 Breast Cancer Cells
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趙偉廷; Hsiao, Yu-Cheng; Lee, Chen-Yu; Lin, Yi-Jhen; Tsai, Shu-Huai; Jeng, Lee-Ching G; Chao, Wei-Ting; Lung, Feng-Di T |
| 東海大學 |
2013 |
Design, synthesis, and evaluation of fluorescent cell-penetrating peptidic antagonists of Grb2-SH2 for targeting MCF-7 breast cancer cells
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Hsiao, Y.-C., Lee, C.-Y., Lin, Y.-J., Tsai, S.-H., Jeng, K.-C.G., Chao, W.-T., Lung, F.-D.T. |
| 東海大學 |
2013 |
Design, synthesis, and evaluation of fluorescent cell-penetrating peptidic antagonists of Grb2-SH2 for targeting MCF-7 breast cancer cells
|
Hsiao, Y.-C.; Lee, C.-Y.; Lin, Y.-J.; Tsai, S.-H.; Jeng, K.-C.G.; Chao, W.-T.; Lung, F.-D.T. |
| 東海大學 |
2002 |
Design, synthesis, and evaluation of postulated transient intermediate and substrate analogues as inhibitors of 4-hydroxyphenylpyruvate dioxygenase
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Lin, Y.-L., Huang, J.-L., Wu, C.-S., Liu, H.-G., Yang, D.-Y. |
| 國家衛生研究院 |
2017-07 |
Design, synthesis, and evaluation of thiazolidine-2,4-dione derivatives as a novel class of glutaminase inhibitors
|
Yeh, TK;Kuo, CC;Lee, YZ;Ke, YY;Chu, KF;Hsu, HY;Chang, HY;Liu, YW;Song, JS;Yang, CW;Lin, LM;Sun, MW;Wu, SH;Kuo, PC;Shih, C;Chen, CT;Tsou, LK;Lee, SJ |
| 國立臺灣大學 |
2008 |
Design, synthesis, and evaluation of trifluoromethyl ketones as inhibitors of SARS-CoV 3CL protease
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Shao, Yi-Ming; Yang, Wen-Bin; Kuo, Tun-Hsun; Tsai, Keng-Chang; Lin, Chun-Hung; Yang, An-Suei; Liang, Po-Huang; Wong, Chi-Huey |
| 國立成功大學 |
2013-09-15 |
Design, synthesis, and mechanism of action of 2-(3-hydroxy-5-methoxyphenyl)-6-pyrrolidinylquinolin-4-one as a potent anticancer lead
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Cheng, Yung-Yi; Liu, Chin-Yu; Tsai, Meng-Tung; Lin, Hui-Yi; Yang, Jai-Sing; Wu, Tian-Shung; Kuo, Sheng-Chu; Huang, Li-Jiau; Lee, Kuo-Hsiung |
| 中國醫藥大學 |
2011 |
Design, Synthesis, and Preclinical Evaluation of New 5,6?(or6,7?)Disubstituted?2?(fluorophenyl)quinolin?4?one Derivatives as Potent Antitumor Agents
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周立琛(Li-Chen Chou); 蔡孟東(Meng-Tung Tsai); (Mei-Hua Hsu); (Sheng-Hung Wang); 魏宗德(Tzong-Der Way); (Chi-Hung Huang); (Hui-Yi Lin); (Keduo Qian); (Yizhou Dong); 李國雄(Kuo-Hsiung Lee); 黃麗嬌(Li-Jiau Huang)*; 郭盛助(Sheng-Chu Kuo)* |
| 中國醫藥大學 |
2010-10 |
Design, Synthesis, and Preclinical Evaluation of New 5,6?(or6,7?)Disubstituted?2?(fluorophenyl)quinolin?4?one Derivatives as Potent Antitumor Agents
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周立琛(Li-Chen Chou); 蔡孟東(Meng-Tung Tsai); (Mei-Hua Hsu); (Sheng-Hung Wang); 魏宗德(Tzong-Der Way); (Chi-Hung Huang); (Hui-Yi Lin); (Keduo Qian); (Yizhou Dong); 李國雄(Kuo-Hsiung Lee); 黃麗嬌(Li-Jiau Huang)*; 郭盛助(Sheng-Chu Kuo)* |
| 國家衛生研究院 |
2012-03-25 |
Design, synthesis, and SAR studies of duel FLT-3 and Aurora kinase inhibitors
|
Hsieh, HP;Shiao, HY;Lin, WH;Hsu, JTA;Chao, YS |
| 國家衛生研究院 |
2002-04-11 |
Design, synthesis, and structure-activity relationship of pyridyl imidazolidinones: A novel class of potent and selective human enterovirus 71 inhibitors
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Shia, KS; Li, WT; Chang, CM; Hsu, MC; Chern, JH; Leong, MK; Tseng, SN; Lee, CC; Lee, YC; Chen, SJ; Peng, KC; Tseng, HY; Chang, YL; Tai, CL; Shih, SR |
| 國家衛生研究院 |
2002-08 |
Design, synthesis, and structure-activity relationship of pyridyl imidazolidinones: A novel class of potent and selective human enterovirus 71 inhibitors
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Shia, KS;Li, WT;Chang, CM;Hsu, MC;Chern, DH;Leong, MK;Tseng, SN;Lee, CC;Lee, YC;Chen, SJ;Peng, KC;Tseng, HY;Chang, YL;Tai, CL;Lin, CC;Shih, SR |
| 國家衛生研究院 |
2004-05-17 |
Design, synthesis, and structure-activity relationships of pyrazolo[3,4-d]pyrimidinies: a novel class of potent enterovirus inhibitors
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Chern, JH; Shia, KS; Hsu, TA; Tai, CL; Lee, CC; Lee, YC; Chang, CS; Tseng, SN; Shih, SR |
| 中國醫藥大學 |
2004-02 |
Design, synthesis, and structure–activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors
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(Jyh-Haur Chern)*; (Kak-Shak Shia); (Tsu-An Hsu); (Chia-Liang Tai); (Chyng-Chi Lee); (Yen-Chun Lee); 張誌祥(Chih-Shiang Chang); (Sung-Nien Tseng); (Shih-Ru Shih) |
| 臺大學術典藏 |
2018-09-10T08:34:49Z |
Design, synthesis, and traveling wave ion mobility mass spectrometry characterization of iron(II)- and ruthenium(II)-terpyridine metallomacrocycles
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YI-TSU CHAN; Wesdemiotis, C.; Newkome, G.R.; Moorefield, C.N.; Carri, G.A.; Yu, J.; Chan, Y.-T.; Li, X. |
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