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顯示項目 316041-316090 / 2348973 (共46980頁)
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每頁顯示[10|25|50]項目
| 國立臺灣大學 |
2011 |
Design, Synthesis and Evaluation of Cationic Polyn-Substituent Acrylamides for in Vitro Gene Delivery
|
柯錦和; 魏名峰; 謝銘鈞; 楊台鴻; KE, JIN-HE; WEI, MING-FENG; SHIEH, MING-JIUM; YOUNG, TAI-HORNG |
| 臺大學術典藏 |
2020-02-06T10:53:31Z |
Design, synthesis and evaluation of telomerase inhibitory, hTERT repressing, and anti-proliferation activities of symmetrical 1,8-disubstituted amidoanthraquinones
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Lee C.-C.; Huang K.-F.; Chang D.-M.; Hsu J.-J.; Huang F.-C.; Shih K.-N.; Chen C.-L.; Chen T.-C.; Chen R.-H.; JING-JER LIN; Huang H.-S. |
| 國立臺灣大學 |
2009 |
Design, Synthesis and Evaluation of Tetrahydroisoquinolines as New Kinesin Spindle Protein Inhibitors
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陳基旺; CHERN, JI-WANG |
| 臺北醫學大學 |
2010 |
Design, Synthesis and Pharmacological Evaluation of Rutaecarpine Derivatives toward Topoisomerase I
|
林俊茂 |
| 國家衛生研究院 |
2005-03 |
Design, synthesis and sar of indole-based PPAR agonists
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Hsieh, HP;Mahindroo, N;Coumar, MS;Wang, CC;Huang, CF;Lien, TW;Tsai, CH;Lin, YT;Lee, LH;Prakash, E;Hsu, TA;Chen, X;Wu, SY;Chen, CT;Chao, YS |
| 臺大學術典藏 |
2021-07-05T03:30:12Z |
Design, synthesis and the structure-activity relationship of agonists targeting on the ALDH2 catalytic tunnel
|
Cheng M.-C.; Lo W.-C.; Chang Y.-W.; Lee S.-S.; CHIA-CHUAN CHANG |
| 臺大學術典藏 |
2021-07-16T06:17:56Z |
Design, synthesis and the structure-activity relationship of agonists targeting on the ALDH2 catalytic tunnel
|
Cheng M.-C.; Lo W.-C.; Chang Y.-W.; SHOEI-SHENG LEE; Chang C.-C. |
| 國家衛生研究院 |
2009-04-01 |
Design, synthesis, and anti-HCV activity of thiourea compounds
|
Kang, IJ;Wang, LW;Lee, CC;Lee, YC;Chao, YS;Hsu, TA;Chern, JH |
| 國家衛生研究院 |
2023-02-03 |
Design, synthesis, and anticancer evaluation of 1-benzo[1,3]dioxol-5-yl-3-N-fused heteroaryl indoles
|
Yao, CH;Wu, MH;Chang, PW;Wu, SH;Song, JS;Huang, HH;Chen, YC;Lee, JC |
| 國家衛生研究院 |
2005-05-19 |
Design, synthesis, and antipicornavirus activity of 1-[5-(4-arylphenoxy)alkyl]-3-pyridin-4-ylimidazolidin-2-one derivatives
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Chang, CS; Lin, YT; Shih, SR; Lee, CC; Lee, YC; Tai, CL; Tseng, SN; Chern, JH |
| 中國醫藥大學 |
2005-01-? |
Design, Synthesis, and Antipicornavirus Activity of 1-[5-(4-Arylphenoxy)alkyl]-3-pyridin-4-ylimidazolidin-2-one Derivatives?
|
張誌祥(Chih-Shiang Chang); 林英廷(Ying-Ting Lin); (Shih-Ru Shih); (Chung-Chi Lee); (Yen-Chun Lee); (Chia-Liang Tai); (Sung-Nien Tseng); (Jyh-Haur Chern)*? |
| 中國醫藥大學 |
2015-01 |
Design, Synthesis, and Bioevaluation of Paeonol Derivatives as Potential Anti-HBV Agents
|
黃琮竣(Tsurng-Juhn Huang);(Hong Chuang);(Yu-Chuan Liang);(Hui-Hsien Lin);(Jia-Cherng Horng);郭于誠(Yu-Cheng, Kuo);陳嘉雯(Chia-Wen Chen);(Fu-Yuan Tsai);(Shih-Chieh Yen);(Shih-Ching Chou);(Ming-Hua Hsu)* |
| 國家衛生研究院 |
2023-08 |
Design, synthesis, and biological activity of dual monoamine oxidase A and heat shock protein 90 inhibitors, N-Methylpropargylamine-conjugated 4-isopropylresorcinol for glioblastoma
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Tseng, HJ;Banerjee, S;Qian, B;Lai, MJ;Wu, TY;Hsu, TI;Lin, TE;Hsu, KC;Chuang, KH;Liou, JP;Shih, JC |
| 中國醫藥大學 |
2002 |
Design, synthesis, and biological evaluation of a cephalosporin-monohydroguaiaretic acid prodrug activated by a monoclonal antibody-beta-lactamase conjugate
|
Hakimelahi, GH; Shia, KS; Pasdar, M; Hakimelahi, S; Khalafi-Nezhad, A; Soltani, MN; Mei, NW; Mei, HC; Saboury, AA; Rezaei-Tavirani, M; Moosavi-Movahedi, AA |
| 臺大學術典藏 |
2022-03-14T12:48:15Z |
Design, synthesis, and biological evaluation of heterotetracyclic quinolinone derivatives as anticancer agents targeting topoisomerases
|
Lee J.-F.; Chang T.-Y.; Liu Z.-F.; Lee N.-Z.; Yeh Y.-H.; Chen Y.-S.; Chen T.-C.; Chou H.-S.; TSAI-KUN LI; Lee S.-B.; Lin M.-H. |
| 衛生福利部國家中醫藥研究所 |
2008 |
Design, synthesis, and biological evaluation of Mannich bases of heterocyclic chalcone analogs as cytotoxic agents
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Reddy, M.Vijaya Bhaskar; Su, Chung-Ren; Chiou, Wen-Fei; Liu, Yi-Nan; Chen, Rosemary Yin-Hwa; Kenneth, F.Bastow; Lee, Kuo-Hsiung; Wu, Tian-Shung |
| 國立成功大學 |
2008-08-01 |
Design, synthesis, and biological evaluation of Mannich bases of heterocyclic chalcone analogs as cytotoxic agents
|
Reddy, M. Vijaya Bhaskar; Su, Chung-Ren; Chiou, Wen-Fei; Liu, Yi-Nan; Chen, Rosemary Yin-Hwa; Bastow, Kenneth F.; Lee, Kuo-Hsiung; Wu, Tian-Shung |
| 中國醫藥大學 |
2008-08 |
Design, synthesis, and biological evaluation of Mannich bases of heterocyclic chalcone analogs as cytotoxic Agents.
|
(M. V. B. Reddy); (C. R. Su); (W. F. Chiou); (Y. N. Liu); (R. Y. H. Chen); (K. F. Bastow); (K. H. Lee); 吳天賞* |
| 國家衛生研究院 |
2008-02-07 |
Design, synthesis, and biological evaluation of novel alkenylthiophenes as potent and selective CB1 cannabinoid receptor antagonists
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Tai, CL; Hung, MS; Pawar, VD; Tseng, SL; Song, JS; Hsieh, WP; Chiu, HH; Wu, HC; Hsieh, MT; Kuo, CW; Hsieh, CC; Tsao, JP; Chao, YS; Shia, KS |
| 臺大學術典藏 |
2021-11-17T08:13:36Z |
Design, synthesis, and biological evaluation of novel alkenylthiophenes as potent and selective CB1 cannabinoid receptor antagonists
|
Cheng-Ming Chu, Ming-Shiu Hung, Min-Tsang Hsieh, Chun-Wei Kuo, Suja T. D., Jen-Shin Song, Hua-Hao Chiu, Yu-Sheng Chao and Kak-Shan Shia; Cheng-Ming Chu; Hsieh CC |
| 中國醫藥大學 |
2001 |
Design, synthesis, and biological evaluation of novel nucleoside and nucleotide analogues as agents against DNA viruses and/or retroviruses
|
Hakimelahi, GH; Ly, TW; Moosavi-Movahedi, AA; Jain, ML; Zakerinia, M; Davari, H; Mei, HC; Sambaiah, T; Moshfegh, AA; Hakimelahi, S |
| 臺北醫學大學 |
2025-05-29 |
Design, Synthesis, and Biological Evaluation of Novel Quercetin Analogs: Discovery of a Hybrid Molecule with Potent Antitumor Activity in Non-Small Cell Lung Cancer
|
Sumitra, Maryam Rachmawati |
| 中國醫藥大學 |
2011-01 |
Design, synthesis, and biological evaluation of novel water-soluble N-mustards as potential anticancer agents.
|
(Kapuriya, N); (Kakadiya, R.); (Dong, H.); (Kumar, A.); 李培志(Lee, P-C.); (Zhang, X.); 周廷朝(Chou, T.-C.); 李德章(Lee, T.-C.); 陳靜煌(Chen, C.-H.); (Lam, K.); (Marvania, B.); (Shah, A.); 蘇燦隆* |
| 國立臺灣大學 |
2010 |
Design, synthesis, and biological studies of novel derivatives of indolin-2-one for acute myeloid leukemia
|
Wang, Hsiao-Chun; Khanwelkar, Rahul R.; Chen, Grace Shiahuy; Chen, Chien-Shu; Chen, Yen-Chun; Chou, Nien-Tzu; Ko, Ching-Huai; Lee, On; Lin, Mai-Wei; Liu, Chih-Peng; Hwang, Chrong-Shiong; Chern, Ji-Wang |
| 嘉南藥理大學 |
2013 |
Design, Synthesis, and Characterization of Novel Thiol-Derivatized Ibuprofen Monolayer Protected Gold Clusters
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Lee, Kuan-Han; Lin, Yu-Sheng; Huang, Po-Jui |
| 臺大學術典藏 |
2020-03-02T07:40:24Z |
Design, Synthesis, and Electrofluorochromism of New Triphenylamine Derivatives with AIE-Active Pendent Groups
|
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
|
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
|
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
|
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
|
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
|
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
|
(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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
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
|
(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
|
YI-TSU CHAN; Wesdemiotis, C.; Newkome, G.R.; Moorefield, C.N.; Carri, G.A.; Yu, J.; Chan, Y.-T.; Li, X. |
顯示項目 316041-316090 / 2348973 (共46980頁)
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每頁顯示[10|25|50]項目
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