| 國立臺灣大學 |
2002 |
Design, Synthesis and Biological Evaluation of Heterocycle-Conjugated Styrene Derivatives as Protein Tyrosine Kinase Inhibitors and Free Radical Scavengers
|
陳建樹; 賴信羽; 徐佩霜; 蔡正昱; 方春旺; 蘇銘嘉; 鄭逢吉; 高佳麟; 陳基旺; CHEN, CHIEN-SHU; LAI, SHIN-YU; HSU, PEI- SHUANG; TSAI, CHENG-YU; FANG, CHUEN-WANG; SU, MING-JAI; CHENG, FONG-CHI; KAO, CHAI-LIN; CHERN, JI-WANG |
| 臺大學術典藏 |
2021-05-31T06:18:16Z |
Design, synthesis and biological evaluation of heterocycle-conjugated styrene derivatives as protein tyrosine kinase inhibitors and free radical scavengers
|
Chen C.-S.; Lai S.-Y.; Hsu P.-S.; Tsai C.-Y.; Fang C.-W.; MING-JAI SU; Cheng F.-C.; Kao C.-L.; Chern J.-W. |
| 國立臺灣大學 |
2002 |
Design, synthesis and biological evaluation of heterocycle-conjugated styrene derivatives as protein tyrosine kinase inhibitors and free radical scavengers.
|
Chen, CS; Lai, SY; Hsu, PS; Tsai, CY; Fang, CW; Su, MJ; Cheng, FC; Kao, CL; Chern, JW. |
| 國家衛生研究院 |
2005 |
Design, synthesis and biological evaluation of novel carbapenems
|
Hakimelahi, GH;Moosavi-Movahedi, AA;Saboury, AA;Osetrov, V;Khodarahmi, GA;Shia, KS |
| 中國醫藥大學 |
2014-01-23 |
Design, Synthesis and Biological Evaluation of Novel Curcumin Glucoside Derivatives as Anticancer Agents
|
(Hsin-Yu Chen);謝閔凔(Min-Tsang Hsieh);(Huei-Wen Chen);(Ling-Chu Chang);郭盛助(Sheng-Chu Kuo) |
| 臺大學術典藏 |
2018-09-10T15:27:37Z |
Design, synthesis and biological evaluation of tetracyclic azafluorenone derivatives with topoisomerase I inhibitory properties as potential anticancer agents
|
Chen, T.-C.;Yu, D.-S.;Chen, S.-J.;Chen, C.-L.;Lee, C.-C.;Hsieh, Y.-Y.;Chang, L.-C.;Guh, J.-H.;Lin, J.-J.;Huang, H.-S.; JIH-HWA GUH; JING-JER LIN |
| 臺大學術典藏 |
2019 |
Design, synthesis and biological evaluation of tetracyclic azafluorenone derivatives with topoisomerase I inhibitory properties as potential anticancer agents
|
Chen T.-C.;Yu D.-S.;Chen S.-J.;Chen C.-L.;Lee C.-C.;Hsieh Y.-Y.;Chang L.-C.;Guh J.-H.;Jing-Jer Lin;Huang H.-S.; Huang H.-S.; JING-JER LIN; Guh J.-H.; Chang L.-C.; Hsieh Y.-Y.; Chen T.-C.; Yu D.-S.; Chen S.-J.; Chen C.-L.; Lee C.-C. |
| 臺大學術典藏 |
2021-06-02T05:43:21Z |
Design, synthesis and biological evaluation of tetracyclic azafluorenone derivatives with topoisomerase I inhibitory properties as potential anticancer agents
|
Chen T.-C.;Yu D.-S.;Chen S.-J.;Chen C.-L.;Lee C.-C.;Hsieh Y.-Y.;Chang L.-C.;Jih-Hwa Guh;Lin J.-J.;Huang H.-S.; Chen T.-C.; Yu D.-S.; Chen S.-J.; Chen C.-L.; Lee C.-C.; Hsieh Y.-Y.; Chang L.-C.; JIH-HWA GUH; Lin J.-J.; Huang H.-S. |
| 臺大學術典藏 |
2022-04-14T23:27:22Z |
Design, synthesis and biological evaluations of niclosamide analogues against SARS-CoV-2
|
Juang, Yu Pu; Chou, Yu Ting; Lin, Ru Xian; Ma, Hsiu Hua; Chao, Tai Ling; Jan, Jia Tsrong; SUI-YUAN CHANG; PI-HUI LIANG |
| 臺大學術典藏 |
2022-05-12T03:43:44Z |
Design, synthesis and biological evaluations of niclosamide analogues against SARS-CoV-2
|
Juang, Yu-Pu; Chou, Yu-Ting; Lin, Ru-Xian; Ma, Hsiu-Hua; Chao, Tai-Ling; Jan, Jia-Tsrong; SUI-YUAN CHANG; Liang, Pi-Hui |
| 國立中山大學 |
2007 |
Design, Synthesis and Biological Evaluations of Novel Series of Enediynes Constituted with DNA Cleavage, Alkylating and DNA Binding Agents via Varies Spacers
|
C.F. Lin; M. Hwang; Y.H. Kuo; M.J. Wu |
| 國立中山大學 |
2005 |
Design, Synthesis and Biological Evaluations of Squamostolide and Its Related Analogs
|
C.L. Lee; C.F. Lin; W.R. Lin; K.S. Wang; Y.H. Chang; S.R. Lin; Y.C. Wu; M.J. Wu |
| 元智大學 |
Oct-21 |
Design, synthesis and Characterization of Novel Benzothiadiazine-1,1’-dioxide based organic emitter for thermally activated delayed fluorescence based OLED
|
Jatin J. Lade; Shian-Sung Chiou; Yeh-Hsiang Tseng; Meng-Hsuan Chiu; Yi-Fan Lin; Chih-Hao Chang*; Prabhakar Chetti; Atul C. Chaskara* |
| 臺大學術典藏 |
2021-06-02T05:43:29Z |
Design, synthesis and cytotoxic activity of N-Modified oleanolic saponins bearing A glucosamine
|
Lin Y.-Y.; Chan S.-H.; Juang Y.-P.; Hsiao H.-M.; JIH-HWA GUH; Liang P.-H. |
| 中國醫藥大學 |
2012-01 |
Design, synthesis and cytotoxic activity of novel spin-labeled rotenone derivatives
|
(Ying-Qian Liu)*;(Emika Ohkoshi);(Lin-Hai Li);(Liu Yang);李國雄(Kuo-Hsiung Lee)* |
| 國立成功大學 |
2005-05-16 |
Design, synthesis and cytotoxic effect of hydroxy- and 3-alkylaminopropoxy-9,10-anthraquinone derivatives
|
Teng, Chi-Huang; Won, Shen-Jeu; Lin, Shen-Jeu |
| 國家衛生研究院 |
2015-09 |
Design, synthesis and diversification of natural product-inspired hydantoin-fused tetrahydroazepino indoles
|
Barve, IJ;Dalvi, PB;Thikekar, TU;Chanda, K;Liu, YL;Fang, CP;Liu, CC;Sun, CM |
| 國立交通大學 |
2019-04-03T06:35:54Z |
Design, synthesis and diversification of natural product-inspired hydantoin-fused tetrahydroazepino indoles
|
Barve, Indrajeet J.; Dalvi, Prashant B.; Thikekar, Tushar Ulhas; Chanda, Kaushik; Liu, Yu-Li; Fang, Chiu-Ping; Liu, Chia-Chen; Sun, Chung-Ming |
| 臺大學術典藏 |
2020-02-27T06:39:35Z |
Design, synthesis and evaluation of cationic poly(N-substituent acrylamide)s for in vitro gene delivery
|
Young T.-H.; Wei M.-F.; MING-JIUM SHIEH; Ke J.-H.; Ke J.-H. ;Wei M.-F. ;Ming-Jium Shieh ;Young T.-H. |
| 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
|
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
|
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
|
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 |
