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顯示項目 316046-316055 / 2348973 (共234898頁)
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| 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
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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
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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?
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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
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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
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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
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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. |
顯示項目 316046-316055 / 2348973 (共234898頁)
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