| 中國醫藥大學 |
2002 |
Synthesis and Biological Activity of 2,6- and 2,7-Disubstituted Anthraquinones.
|
(C. S. Wu); 邱文謙(W. C. Chiu); 王繼平; 郭盛助(Sheng-Chu Kuo) |
| 中國醫藥大學 |
2003-12-07 |
Synthesis and Biological Activity of 2-(p-Substituted Phenylmercapto)-5-Substituted Benzoic Acids
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng))*; 高嘉園; 張國志 |
| 中國醫藥大學 |
2001-07-31 |
Synthesis and Biological Activity of 2-Substituted furo[2,4-b]chromones
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng)); 王繼平 |
| 中國醫藥大學 |
2005-12-17? |
Synthesis and Biological Activity of 5-(2'-Alkoxycarbonyl substituteds phenoxy) furfural Derivatives (論文編號PA-08)?
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng))*? |
| 中國醫藥大學 |
2002-04 |
Synthesis and Biological Activity of 5-(2'-Alkoxycarbonyl substituted phenoxy)furan-2-carboxylic Acid Derivatives
|
張嘉麟; 吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng))*; 王賢文; 王繼平 |
| 中國醫藥大學 |
2002-04 |
Synthesis and Biological Activity of 5-(2-Alkoxycarbonyl substituted phenoxy)furan-2-carboxylic Acid Derivatives
|
張嘉麟(Chang, L. C.); 吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng))*; 王賢文(Wang, S. W.); 王繼平(Wang, J. P.) |
| 中國醫藥大學 |
2002-07-31 |
Synthesis and Biological Activity of 5-(2’-Carboxyl substituted phenoxy)-2-furanacrylic Acids
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng)); 王繼平 |
| 中國醫藥大學 |
2002-12-21 |
Synthesis and Biological Activity of 5-(2′-Alkoxycarbonyl substituted Phenoxy)furfurals
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng))*; 張嘉麟; 張國志 |
| 中國醫藥大學 |
2003-07-31 |
Synthesis and Biological Activity of 5-(Disubstituted phenoxy)-furfural Derivatives
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng)); 張國志 |
| 中國醫藥大學 |
2007-05-18 |
Synthesis and biological activity of ethyl 2-[N-substitutedbenzyl-4'(or 3')-bromo]anilino-4-oxo-4,5-dihydrofuran-3-carboxylate
|
李世良(Shi-Liang Li); 林宗平; 蘇怡芳(I-Fang Su); 黃安正(An-Cheng Huang); 黃士鳴(Shih-Ming Huang); 張建平(Chien-Ping Chang); 張國志(Gwo-Jyh Chang); 蘇銘嘉(Ming-Jai Su) |
| 臺大學術典藏 |
2018-09-10T03:23:36Z |
Synthesis and biological activity of fluoro-substituted pyrrolo[2,3-d]pyrimidines: The development of potential positron emission tomography imaging agents for the corticotropin-releasing hormone type 1 receptor
|
Hsin, L.-W.;Webster, E.L.;Chrousos, G.P.;Gold, P.W.;Eckelman, W.C.;Contoreggi, C.;Rice, K.C.; LING-WEI HSIN |
| 臺大學術典藏 |
2021-07-07T05:13:15Z |
Synthesis and biological activity of fluoro-substituted pyrrolo[2,3-d]pyrimidines: The development of potential positron emission tomography imaging agents for the corticotropin-releasing hormone type 1 receptor
|
LING-WEI HSIN; Webster E.L.; Chrousos G.P.; Gold P.W.; Eckelman W.C.; Contoreggi C.; Rice K.C. |
| 國立臺灣大學 |
2012 |
Synthesis and biological activity of obatoclax derivatives as novel and potent SHP-1 agonists
|
Su, Jung-Chen; Chen, Kuen-Feng; Chen, Wei-Lin; Liu, Chun-Yu; Huang, Jui-Wen; Tai, Wei-Tien; Chen, Pei-Jer; Kim, Inki; Shiau, Chung-Wai; 陳昆鋒; 陳培哲 |
| 臺大學術典藏 |
2021-07-03T03:34:29Z |
Synthesis and biological activity of obatoclax derivatives as novel and potent SHP-1 agonists
|
Su J.-C.; Chen K.-F.; Chen W.-L.; Liu C.-Y.; Huang J.-W.; Tai W.-T.; PEI-JER CHEN; Kim I.; Shiau C.-W. |
| 中國醫藥大學 |
2008-07-28 |
Synthesis and Biological Activity of Phloroglucinol Derivatives
|
湯智昕(Tang Chih-Hsin); 郭盛助(Sheng-Chu Kuo); 張誌祥(Chih-Shiang Chang)* |
| 臺北醫學大學 |
1983 |
Synthesis and biological activity of potential antimalarial agents containing a 2,4-pyrimidinediamine moiety. Synthesis of Dihydrothioxanthenedione analogs as potential antimalarial agents
|
王惠珀; Hung Wang JHP |
| 中國醫藥大學 |
2002-06 |
Synthesis and Biological Activity of Some 2-Substituted Thioxanthone 10,10-Dioxides
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng))*; 王繼平(Wang, J. P.) |
| 中國醫藥大學 |
1994-07-31 |
Synthesis and Biological Activity of Some 2-Substituted Thioxanthone 10,10-Dioxides
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng)); 王繼平 |
| 中國醫藥大學 |
2002-12 |
Synthesis and Biological Activity of Some 2-Substituted-methylthioxanthones
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng))*; 朱培龍(Chu, P. L.); 王繼平(Wang, J. P.) |
| 中國醫藥大學 |
1995-07-31 |
Synthesis and Biological Activity of Some 2-Substituted-methylthioxanthones
|
吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng)); 王繼平 |
| 中國醫藥大學 |
1998-12-19 |
Synthesis and Biological Activity of Substituted Furyl Substituted Phenyl Ethers
|
張嘉麟; 吳錦生(Wu, Chin-Sheng (Wu, Jiin-Sheng))*; 王繼平; 鄧哲明 |
| 國立交通大學 |
2018-08-21T05:53:56Z |
Synthesis and biological assay of erlotinib analogues and BSA-conjugated erlotinib analogue
|
Boobalan, Ramalingam; Liu, Kuang-Kai; Chao, Jui-I.; Chen, Chinpiao |
| 中國醫藥大學 |
2014-12-06 |
Synthesis and biological evaluation of 1,3-dioxolo[4,5-g]quinoline derivatives as anti-Helicobacter pylori agents
|
黃姿燕(Tzu-Yen Huang);李之瑀(Chih-Yu Lee);賴志河(Chih-Ho Lai);張誌祥(Chih-Shiang Chang)*;張誌祥(Chih-Shiang Chang) |
| 國立成功大學 |
2011-09 |
Synthesis and biological evaluation of 1-(4 '-Indolyl and 6 '-Quinolinyl) indoles as a new class of potent anticancer agents
|
Lai, Mei-Jung |
| 臺北醫學大學 |
2011 |
Synthesis and biological evaluation of 1-(4'-Indolyl and 6'-Quinolinyl) indoles as a new class of potent anticancer agents
|
Lai;M, J.;Chang;J, Y.;Lee;H, Y.;Kuo;C, C. C.;Lin;M, H.;Hsieh;H, P.;Chang;C, Y.;Wu;J, S.;Wu;S, Y.;Shey;K, S.;Liou;J, P. |
| 臺北醫學大學 |
2011 |
Synthesis and biological evaluation of 1-(4'-Indolyl and 6'-Quinolinyl) indoles as a new class of potent anticancer agents
|
Lai;M.J.;Chang;J.Y.;Lee;H.Y.;Kuo;C.C.;Lin;M.H.;Hsieh;H.P.;Chang;C.Y.;Wu;J.S.;Wu;S.Y.;Shey;K.S.;Liou;J.P. |
| 臺北醫學大學 |
2011 |
Synthesis and biological evaluation of 1-(40-Indolyl and 60-Quinolinyl) indoles as a new class of potent anticancer agents.
|
MJ, Lai;JY, Chang;HY, Lee;CC, Kuo;MH, Lin;HP, Hsieh;CY, Chang;JS, Wu;SY, Wu;Shey;KS;JP, Liou |
| 臺北醫學大學 |
2011 |
Synthesis and biological evaluation of 1-(40-Indolyl and 60-Quinolinyl) indoles as a new class of potent anticancer agents.
|
Lai, MJ;Chang, JY;Lee, HY;Kuo, CC;Lin, MH;Hsieh, HP;Chang, CY;Wu, JS;Wu, SY;Shey;KS;Liou, JP |
| 臺北醫學大學 |
2011 |
Synthesis and Biological Evaluation of 1-(4’-Indolyl and 6’-Quinolinyl)indoles as a New Class of Potent Anticancer Agents
|
MJ, Lia;JY, Chang;HY, Lee;CC, Kuo;MH, Lin;HP, Hsieh;CY, Chang;JS, Wu;SY, Wu;KS, Shey;JP, Liou |
| 臺北醫學大學 |
2011 |
Synthesis and Biological Evaluation of 1-(4’-Indolyl and 6’-Quinolinyl)indoles as a New Class of Potent Anticancer Agents
|
Lia, MJ;Chang, JY;Lee, HY;Kuo, CC;Lin, MH;Hsieh, HP;Chang, CY;Wu, JS;Wu, SY;Shey, KS;Liou, JP |
| 國家衛生研究院 |
2011-09 |
Synthesis and biological evaluation of 1-(4′-Indolyl and 6′-Quinolinyl) indoles as a new class of potent anticancer agents
|
Lai, MJ;Chang, JY;Lee, HY;Kuo, CC;Lin, MH;Hsieh, HP;Chang, CY;Wu, JS;Wu, SY;Shey, KS;Liou, JP |
| 臺北醫學大學 |
2012 |
Synthesis and Biological Evaluation of 1-Arylsulfonyl-5-(N-hydroxyacrylamide) indoles as Potent Histone Deacetylase Inhibitors with Antitumor Activity in vivo
|
Lai;M, J.;Huang;H, L.;Pan;S, L.;Liu;Y, M.;Peng;C, Y.;Lee;H, Y.;Yeh;T, K.;Hung;P, H.;Teng;C, M.;Chen;S, H.;Chuang;H, Y.;Liou;J, P. |
| 臺北醫學大學 |
2012 |
Synthesis and Biological Evaluation of 1-Arylsulfonyl-5-(N-hydroxyacrylamide) indoles as Potent Histone Deacetylase Inhibitors with Antitumor Activity in vivo
|
Lai;M.J.;Huang;H.L.;Pan;S.L.;Liu;Y.M.;Peng;C.Y.;Lee;H.Y.;Yeh;T.K.;Hung;P.H.;Teng;C.M.;Chen;S.H.;Chuang;H.Y.;Liou;J.P. |
| 國家衛生研究院 |
2012-04 |
Synthesis and biological evaluation of 1-Arylsulfonyl-5-(N-hydroxyacrylamide)indoles as potent histone deacetylase inhibitors with antitumor activity in vivo
|
Lai, MJ;Huang, HL;Pan, SL;Liu, YM;Peng, CY;Lee, HY;Yeh, TK;Huang, PH;Teng, CM;Chen, CS;Chuang, HY;Liou, JP |
| 中國醫藥大學 |
2012-03 |
Synthesis and Biological Evaluation of 1-Arylsulfonyl-5-(N-hydroxyacrylamide)indoles as Potent Histone Deacetylase Inhibitors with Antitumor Activity in Vivo
|
(Lai MJ);(Huang HL); (Pan SL);(Liu YM);彭婕妤(Chieh-Yu Peng);(Lee HY);(Yeh TK);(Huang PH); (Teng CM);(Chen CS);(Chuang HY);(Liou JP)* |
| 國家衛生研究院 |
2008-03-13 |
Synthesis and biological evaluation of 1-methyl-2-(3 ',4 ',5 '-trimethoxybenzoyl)-3-aminoindoles as a new class of antimitotic agents and tubulin inhibitors
|
Romagnoli, R; Baraldi, PG; Sarkar, T; Carrion, MD; Cara, CL; Cruz-Lopez, O; Preti, D; Tabrizi, MA; Tolomeo, M; Grimaudo, S; Di Cristina, A; Zonta, N; Balzarini, J; Brancale, A; Hsieh, HP; Hamel, E |
| 高雄醫學大學 |
2012 |
Synthesis and Biological Evaluation of 2-(5-Nitrofuranyl)vinyl-8-hydroxyquinoline Analogues as Antitumor Agent
|
方昱文;高佳麟;陳惠亭 |
| 國家衛生研究院 |
2012-02 |
Synthesis and biological evaluation of 2-amino-1-thiazolyl imidazoles as orally active anticancer agents
|
Li, WT;Hwang, DR;Song, JS;Chen, CP;Chen, TW;Lin, CH;Chuu, JJ;Lien, TW;Hsu, TA;Huang, CL;Tseng, HY;Lin, CC;Lin, HL;Chang, CM;Chao, YS;Chen, CT |
| 臺大學術典藏 |
2021-02-02T00:46:44Z |
Synthesis and biological evaluation of 2′,5′-dimethoxychalcone derivatives as microtubule-targeted anticancer agents
|
Tu H.-Y.;Huang A.-M.;Hour T.-C.;Yang S.-C.;Yeong-Shiau Pu;Lin C.-N.; Tu H.-Y.; Huang A.-M.; Hour T.-C.; Yang S.-C.; YEONG-SHIAU PU; Lin C.-N. |
| 中國醫藥大學 |
1999-05-07 |
Synthesis and Biological Evaluation of 3’,6,7-Substituted 2,3-dihydro-2- phenyl-4-quinazoli-nones an
|
侯曼貞(Hour,Mann-Jen); (M. J.; Huang); (L. J.; Chang); (C. Y.; Lai); (Y. Y.; Lee); (K. H.; Kuo); 廖世傑(Shih-Chieh Liao) |
| 朝陽科技大學 |
2009 |
Synthesis and biological evaluation of 3′,4′,5′-trimethoxychalcone analogues as inhibitors of nitric oxide production and tumor cell proliferation.
|
曾耀銘; Rao YK; Fang SH; Tzeng YM |
| 國家衛生研究院 |
2011-03-07 |
Synthesis and biological evaluation of 4-aroyl-6,7,8-trimethoxyquinolines as a novel class of anticancer agents
|
Hsieh, CC;Lee, HY;Nien, CY;Kuo, CC;Chang, CY;Chang, JY;Liou, JP |
| 臺北醫學大學 |
2011 |
Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
|
Hsieh;C, C. C.;Lee;H, Y.;Nien;C, Y.;Kuo;C, C. C.;Chang;C, Y.;Chang;J, Y.;Liou;J, P. |
| 臺北醫學大學 |
2011 |
Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
|
CC, Hsieh;HY, Lee;CY, Nien;CC, Kuo;CY, Chang;JY, Chang;JP, Liou |
| 臺北醫學大學 |
2011 |
Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
|
Hsieh, CC;Lee, HY;Nien, CY;Kuo, CC;Chang, CY;Chang, JY;Liou, JP |
| 臺北醫學大學 |
2011 |
Synthesis and Biological Evaluation of 4-Aroyl-6,7,8-Trimethoxyquinolines as a Novel Class of Anticancer Agents
|
Hsieh;C.C.;Lee;H.Y.;Nien;C.Y.;Kuo;C.C.;Chang;C.Y.;Chang;J.Y.;Liou;J.P. |
| 國家衛生研究院 |
2010-08 |
Synthesis and biological evaluation of 7-arylindoline-1-benzenesulfonamides as a novel class of potent anticancer agents
|
Chang, JY;Lai, MJ;Chang, YT;Lee, HY;Cheng, YC;Kuo, CC;Su, MC;Chang, CY;Liou, JP |
| 嘉南藥理大學 |
2011 |
Synthesis and Biological Evaluation of Agents
|
Chia-Hao Lu (呂家豪); Yi-Cheng Chan (詹沂澄); Tzung-Han Tang (湯宗翰); Fong-Pin Liang (梁峰賓); P. Shin-Hun Juang (莊聲宏); Chih-Shiang Chang (張誌祥) |
| 臺大學術典藏 |
2020-02-06T10:53:26Z |
Synthesis and biological evaluation of anthra[1,9-cd]pyrazol-6(2H)-one scaffold derivatives as potential anticancer agents
|
Chen T.-C.;Guh J.-H.;Hsu H.-W.;Chen C.-L.;Lee C.-C.;Wu C.-L.;Lee Y.-R.;Jing-Jer Lin;Yu D.-S.;Huang H.-S.; Chen T.-C.; Guh J.-H.; Hsu H.-W.; Chen C.-L.; Lee C.-C.; Wu C.-L.; Lee Y.-R.; JING-JER LIN; Yu D.-S.; Huang H.-S. |
| 臺大學術典藏 |
2021-06-02T05:43:21Z |
Synthesis and biological evaluation of anthra[1,9-cd]pyrazol-6(2H)-one scaffold derivatives as potential anticancer agents
|
Chen T.-C.;Jih-Hwa Guh;Hsu H.-W.;Chen C.-L.;Lee C.-C.;Wu C.-L.;Lee Y.-R.;Lin J.-J.;Yu D.-S.;Huang H.-S.; Chen T.-C.; JIH-HWA GUH; Hsu H.-W.; Chen C.-L.; Lee C.-C.; Wu C.-L.; Lee Y.-R.; Lin J.-J.; Yu D.-S.; Huang H.-S. |
