| 國立成功大學 |
2012 |
Design and Synchronization of Master-Slave Electronic Horizontal Platform System
|
Kuo, Hang-Hong; Liao, Teh-Lu; Yan, Jun-Juh |
| 嘉南藥理大學 |
2017 |
Design and synthesis a water-soluble group for ether-linkage of 10-hydroxycamptothecin prodrug
|
邱沛芳; 林偉琪; 陳國輝; 呂玉玲 |
| 中國醫藥大學 |
2014-09-28 |
Design and Synthesis Indole-3-carbinol Analogues as Potential Anticancer Agents
|
張誌祥(Chih-Shiang Chang)*;黃建富(Chien-Fu Huang);湯智昕(Tang Chih-Hsin);張凱惟(Kai-Wei Chang) |
| 國家衛生研究院 |
2016-07-28 |
Design and synthesis of 1,2,3-triazole-containing N-acyl zanamivir analogs as potent neuraminidase inhibitors
|
Das, A;Adak, AK;Ponnapalli, K;Lin, CH;Hsu, KC;Yang, JM;Hsu, TA;Lin, CC |
| 國立交通大學 |
2017-04-21T06:56:48Z |
Design and synthesis of 1,2,3-triazole-containing N-acyl zanamivir analogs as potent neuraminidase inhibitors
|
Das, Anindya; Adak, Avijit K.; Ponnapalli, Kalyankumar; Lin, Chien-Hung; Hsu, Kai-Cheng; Yang, Jinn-Moon; Hsu, Tsu-An; Lin, Chun-Cheng |
| 國立成功大學 |
2002-02 |
Design and synthesis of 1,2,4-oxadiazole derivatives as non-steroidal 5 alpha-reductase inhibitors
|
Chang, Chih-Shiang; Kan, Wai-Ming; Chen, Chiu-Liang; Wang, K. C.; Chern, Ji-Wang |
| 國立臺灣大學 |
2002 |
Design and Synthesis of 1,2,4-Oxadiazole Derivatives as Non-Steroidal 5 Alpha-Reductase Inhibitors
|
陳基旺; CHERN, JI-WANG |
| 國立中山大學 |
2008 |
Design and Synthesis of 1-(6-(2-(2-Arylethynyl)phenyl)hexyn-5-yl)piperidin-2-ones as Antitumor Agents that Induce Apoptotic Progress
|
I.L. Lin; I.H. Chen; C.F. Lin; Y.H. Lo; S.H. Yang; S.R. Lin; M.J. Wu |
| 國立成功大學 |
2022-07-13 |
Design and Synthesis of 1-O- and 6 '-C-Modified Heparan Sulfate Trisaccharides as Human Endo-6-O-Sulfatase 1 Inhibitors
|
Tseng;Kuei-Yao;Tzeng;Zheng-Hao;Cheng;Rachel, Ting-Jen;Liang;Pi-Hui;Hung;Shang-Cheng |
| 國立成功大學 |
2022 |
Design and Synthesis of 1-O- and 6′-C-Modified Heparan Sulfate Trisaccharides as Human Endo-6-O-Sulfatase 1 Inhibitors
|
Tseng, K.-Y.;Tzeng, Z.-H.;Cheng, T.-J.R.;Liang, P.-H.;Hung, S.-C. |
| 國立臺灣大學 |
2008-05 |
Design and Synthesis of 2- and 3-Substituted-3-phenylpropyl Analogs of 1-[2-[Bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine and 1-[2-(Diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine: Role of Amino, Fluoro, Hydroxyl, Meth
|
Hsin, L.-W.; Chang, L.-T.; Rothman, R. B.; Dersch, C. M.; Jacobson, A. E.; Rice, K. C. |
| 臺大學術典藏 |
2021-07-07T05:13:10Z |
Design and synthesis of 2- and 3-substituted-3-phenylpropyl analogs of 1-[2-[bis(4-fluorophenyl)methoxy]ethyl]-4-(3-phenylpropyl)piperazine and 1-[2-(diphenylmethoxy)ethyl]-4-(3-phenylpropyl)piperazine: Role of amino, fluoro, hydroxyl, methoxyl, methyl, methylene, and oxo substituents on affinity for the dopamine and serotonin transporters
|
LING-WEI HSIN; Chang L.-T.; Rothman R.B.; Dersch C.M.; Jacobson A.E.; Rice K.C. |
| 中國醫藥大學 |
2010-02-05 |
Design and Synthesis of 2-(3-Benzo[b]thienyl)-6,7- methylenedioxyquinolin-4-one Analogs as Potent Antitumor Agents that Inhibit Tubulin Assembly
|
張昱勛(Yu-Hsun Chang);(Mei-Hua Hsu);周立琛(Li-Chen Chou);(Sheng-Hung Wang);黃麗嬌(Li-Jiau Huang);(Keduo Qian);(Susan L. Morris-Natschke);(Ernest Hamel);李國雄(Kuo-Hsiung Lee);郭盛助(Sheng-Chu Kuo)* |
| 中國醫藥大學 |
2009-07 |
Design and synthesis of 2-(3-benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one analogues as potent antitumor agents that inhibit tubulin assembly
|
(Yu-Hsun Chang); (Mei-Hua Hsu); (Sheng-Hung Wang); 黃麗嬌(Li-Jiau Huang); (Keduo Qian); (Susan L. Morris-Natschke); (Ernest Hamel); 郭盛助(Sheng-Chu Kuo)*; (Kuo-Hsiung Lee)* |
| 國立臺灣大學 |
1993 |
Design and Synthesis of 2-Amino-4-methyl-5-(4-substituted-1-piperazinyl) pyrimidin-6-ones As Lipophilic Folate Antimetabolites
|
王惠珀; Wang, Hui-Po |
| 高雄醫學大學 |
2006 |
Design and Synthesis of 2-Phenybenzothiazoles as Anticancer Agents
|
羅曉萍;蔡逸民;王志鉦 |
| 高雄醫學大學 |
2007 |
Design and Synthesis of 2-Phenybenzothiazoles as Anticancer Agents
|
羅曉萍;王志鉦 |
| 高雄醫學大學 |
2006 |
Design and Synthesis of 2-Phenylbenzothiazoles as Antitumor Agents
|
羅曉萍;蔡逸民;王志鉦 |
| 淡江大學 |
2007-12 |
Design and Synthesis of 2-Styrylchromone Derivatives as a Novel Class of Anticancer Agents
|
蕭永政 |
| 國立成功大學 |
2005-04 |
Design and synthesis of 3-aryl-5-alicylic-[1,2,4]-oxadiazoles as novel platelet aggregation inhibitors
|
Chern, Ching-Yuh; Chen, Shinn-Jyh; Kan, Wai-Ming |
| 臺大學術典藏 |
2020 |
Design and Synthesis of 3-Benzylaminocoumarin-7-O-Sulfamate Derivatives as Steroid Sulfatase Inhibitors
|
Liang, Pi-Hui |
| 臺大學術典藏 |
2021-01-09T09:27:08Z |
Design and synthesis of 3-benzylaminocoumarin-7-O-sulfamate derivatives as steroid sulfatase inhibitors
|
Hng, Yue; Hng, Yue;Lin, Mei-Hsiang;Lin, Tzung-Sheng;Liu, I-Chen;Lin, I-Chun;Lu, Yeh-Lin;Chang, Chiao-Nien;Chiu, Pei-Fang;Tsai, Keng-Chang;Mei-Jou Chen;Pi-Hui Liang; Lin, Mei-Hsiang; Lin, Tzung-Sheng; Liu, I-Chen; Lin, I-Chun; Lu, Yeh-Lin; Chang, Chiao-Nien; Chiu, Pei-Fang; Tsai, Keng-Chang; MEI-JOU CHEN; PI-HUI LIANG |
| 臺大學術典藏 |
2021-03-02T05:49:30Z |
Design and synthesis of 3-benzylaminocoumarin-7-O-sulfamate derivatives as steroid sulfatase inhibitors
|
Hng, Yue; Lin, Mei-Hsiang; Lin, Tzung-Sheng; Liu, I-Chen; Lin, I-Chun; Lu, Yeh-Lin; Chang, Chiao-Nien; Chiu, Pei-Fang; Tsai, Keng-Chang; MEI-JOU CHEN; Liang, Pi-Hui |
| 東海大學 |
1999 |
Design and synthesis of 3-fluoro-2-oxo-3-phenylpropionic acid derivatives as potent inhibitors of 4-hydroxyphenylpyruvate dioxygenase from pig liver
|
Ling, T.-S., Shiu, S., Yang, D.-Y. |
| 中國醫藥大學 |
2008-07-28 |
Design and Synthesis of 3-Phenyl-4H-1-benzopyran-4-ones Derivatives for Bone Cancer
|
劉如芳(Ju-Fang Liu); 林敏生(Min-Sheng Lin); 湯智昕(Tang Chih-Hsin); 張誌祥(Chih-Shiang Chang)*; 張誌祥(Chih-Shiang Chang) |
