| 臺大學術典藏 |
2022-03-14T12:48:25Z |
Synthesis, DNA binding, and cytotoxicity of 1,4-bis(2-amino-ethylamino)anthraquinone-amino acid conjugates
|
Hsin L.-W.; Wang H.-P.; Kao P.-H.; Lee O.; Chen W.-R.; Chen H.-W.; Guh J.-H.; Chan Y.-L.; His C.-P.; Yang M.-S.; TSAI-KUN LI; Lee C.-H. |
| 臺大學術典藏 |
2021-09-22T03:00:03Z |
Synthesis and structure-activity relationship of 6-arylureido-3-pyrrol-2- ylmethylideneindolin-2-one derivatives as potent receptor tyrosine kinase inhibitors
|
Khanwelkar R.R.; Chen G.S.; Wang H.-C.; CHAO-WU YU; Huang C.-H.; Lee O.; Chen C.-H.; Hwang C.-S.; Ko C.-H.; Chou N.-T.; Lin M.-W.; Wang L.-M.; Chen Y.-C.; Hseu T.-H.; Chang C.-N.; Hsu H.-C.; Lin H.-C.; Shih Y.-C.; Chou S.-H.; Tseng H.-W.; Liu C.-P.; Tu C.-M.; Hu T.-L.; Tsai Y.-J.; Chern J.-W. |
| 臺大學術典藏 |
2021-07-07T05:13:10Z |
Synthesis, DNA binding, and cytotoxicity of 1,4-bis(2-amino-ethylamino)anthraquinone-amino acid conjugates
|
LING-WEI HSIN; Wang H.-P.; Kao P.-H.; Lee O.; Chen W.-R.; Chen H.-W.; Guh J.-H.; Chan Y.-L.; His C.-P.; Yang M.-S.; Li T.-K.; Lee C.-H. |
| 臺大學術典藏 |
2021-06-02T05:43:57Z |
Synthesis, DNA binding, and cytotoxicity of 1,4-bis(2-amino-ethylamino)anthraquinone-amino acid conjugates
|
Hsin L.-W.; Wang H.-P.; Kao P.-H.; Lee O.; Chen W.-R.; Chen H.-W.; JIH-HWA GUH; Chan Y.-L.; His C.-P.; Yang M.-S.; Li T.-K.; Lee C.-H. |
| 臺大學術典藏 |
2018-09-10T07:39:52Z |
The synthesis of antigens and the production of antibodies against patulin derivatives
|
Sheu, F.; Lee, O.; Shyu, Y.T.; Sheu, F.; Lee, O.; Shyu, Y.T.; FUU SHEU |
| 臺大學術典藏 |
2018-09-10T06:55:29Z |
Synthesis, DNA binding, and cytotoxicity of 1,4-bis(2-amino-ethylamino)anthraquinone-amino acid conjugates
|
Hsin, L.-W.;Wang, H.-P.;Kao, P.-H.;Lee, O.;Chen, W.-R.;Chen, H.-W.;Guh, J.-H.;Chan, Y.-L.;His, C.-P.;Yang, M.-S.;Li, T.-K.;Lee, C.-H.; LING-WEI HSIN; JIH-HWA GUH; TSAI-KUN LI |
| 臺北醫學大學 |
2014 |
Novel Piperazinediones as Antitumor Agents
|
CL, Wang;Lee, O;Hsiao, G;JF, Lian;YW, Cheng |
| 臺北醫學大學 |
2014 |
Novel piperazinediones as antitumor agents
|
Wang, CL;Lee, O;Hsiao, G;Lian, JF;Cheng, YW |
| 國家衛生研究院 |
2013-02 |
Azatyrosinamides: Novel RAS-related anticancer agents
|
Wang, CL;Lee, O;Huang, CF;Li, EIC;Teng, CM;Pan, SL;Lian, JF;Chang, FS;Liou, JP;Wang, HP |
| 臺北醫學大學 |
2012 |
Histone Deacetylase Inhibitors
|
HP, Wang;Lee, O;YW, Cheng;CL, Wang;FS, Chang;CC, Hsiao |
| 臺北醫學大學 |
2012 |
組織蛋白去乙醯?抑制劑HISTONE DEACETYLASE INHIBITORS
|
HP, Wang;Lee, O;YW, Cheng;CL, Wang;FS, Chang;CC, Hsiao |
| 臺北醫學大學 |
2012 |
組蛋白去乙?化?抑製劑
|
HP, Wang;Lee, O;YW, Cheng;CL, Wang;FS, Chang;CC, Hsiao |
| 臺北醫學大學 |
2012 |
Histone Deacetylase Inhibitors
|
Wang, HP;Lee, O;Cheng, YW;Wang, CL;Chang, FS;Hsiao, CC |
| 臺北醫學大學 |
2012 |
組織蛋白去乙醯?抑制劑HISTONE DEACETYLASE INHIBITORS
|
Wang, HP;Lee, O;Cheng, YW;Wang, CL;Chang, FS;Hsiao, CC |
| 臺北醫學大學 |
2012 |
組蛋白去乙?化?抑製劑
|
Wang, HP;Lee, O;Cheng, YW;Wang, CL;Chang, FS;Hsiao, CC |
| 國立臺灣大學 |
2008-01 |
Synthesis, DNA binding, and cytotoxicity of 1,4-bis(2-amino-ethylamino)anthraquinone–amino acid conjugates
|
Hsin, L.-W.; Wang, H.-P.; Kao, P.-H.; Lee, O.; Chen, W.-R.; Chen, H.-W.; Guh, J.-H.; Chan, Y.-L.; His, C.-P.; Yang, M.-S.; Li, T.-K.; Lee, C.-H. |
| 臺北醫學大學 |
2008 |
Synthesis; DNA binding and cytotoxicity of 1; 4-bis(2-amino-tehylamino)anthraquinone-amino acid conjugates
|
王惠珀; Hsin LW; Wang HP; Kao PH; Lee O; Chen WR; Chen HW; Guh JH; Chan YL; His CP; Yang MS; Li a TK |
| 臺北醫學大學 |
2008 |
Piperazinedione compounds
|
王惠珀; Teng CM; Wang HP; Lee O; Chen HT; Guh JH; Pan SL; Fan YB |
| 國立臺灣大學 |
2008 |
Synthesis, DNA binding, and cytotoxicity of 1,4-bis(2-amino-ethylamino) anthraquinone-amino acid conjugates.
|
Hsin, LW; Wang, HP; Kao, PH; Lee, O; Chen, WR; Chen, HW; Guh, JH; Chan, YL; His, CP; Yang, MS; Li, T-K; Lee, CH. |
| 國立臺灣大學 |
2005-09 |
Selective cytotoxicity of azatyrosinamides against ras-transformed NIH 3T3 cells.
|
Wang, HP; Hwang, TL; Lee, O; Tseng, YJ; Shew, JY; Lee, SJ. |
| 臺北醫學大學 |
2005 |
Selective cytotoxicity of azatyrosinamides against ras-transformed NIH3T3 cell lines.
|
王惠珀; Wang HP; Huang TL; Lee O; Shu CY; Lee SJ; Chen YR |
| 國立臺灣大學 |
2000-12 |
Preparation and antitumor activities of beta-azatyrosinamides.
|
Wang, HP; Wu, MF; Shew, JY; Lee, O; Lee, SJ; Sung, CH. |
| 臺北醫學大學 |
2000 |
Preparation and antitumor activities of b-azatyrosinamides.
|
王惠珀; Wang HP; Wu MF; Shu CY; Lee O; Lee SJ; Sung CH |
| 臺北醫學大學 |
1999 |
Aminoacyl Antraquinones as potential antineoplastic agents.
|
王惠珀; Lee O; LeeLT; Wu HS; Wang HP |
| 臺北醫學大學 |
1999 |
Selective cytotoxicity of novel Azatyrosinamides.
|
王惠珀; Lee O; Li YI; Hwang CF; Wang HP |
| 臺北醫學大學 |
1999 |
b-Azatyrosinamides: Synthesis and Selective cytotoxicity
|
王惠珀; Lee O; Wang HP |
| 臺北醫學大學 |
1999 |
Synthesis and inhibition of pyrimidine analogues on bovine liver dihydrofolate redutase.
|
王惠珀; Lee O; Wu HS; Liu WC; Wang HP |
| 臺北醫學大學 |
1999 |
Selective cytotoxicity of novel Azatyrosinamides.
|
王惠珀; Lee O; Li YI; Hwang CF; Wang HP |
| 臺北醫學大學 |
1999 |
Synthesis and inhibition of pyrimidine analogues on bovine liver dihydrofolate redutase.
|
王惠珀; Lee O; Wu HS; Liu WC; Wang HP |
| 國立臺灣大學 |
1999 |
The synthesis of antigens and the production of antibodies against patulin derivatives.
|
Sheu, F.; Lee, O.; Shyu, Y.T. |
| 臺北醫學大學 |
1997 |
Inhibition of azatyrosine analogues on the growth of Ras-transformed tumor cells.
|
王惠珀; Lee O; Shu CY; Lee SJ; Wang HP |
| 臺北醫學大學 |
1997 |
Electrophilic Condensation of Pyrimidines with Cyclic Ketones.
|
王惠珀; Lee O; Wang HP |
| 臺北醫學大學 |
1997 |
Electrophilic Condensation of Pyrimidines with Cyclic Ketones.
|
王惠珀; Lee O; Wang HP |
| 臺北醫學大學 |
1997 |
Inhibition of azatyrosine analogues on the growth of Ras-transformed tumor cells.
|
王惠珀; Lee O; Shu CY; Lee SJ; Wang HP |
| 臺北醫學大學 |
1996 |
Electophilic Substitution of Pyrimidines with Cyclic Ketones.
|
王惠珀; Lee O; Wang HP |
| 臺北醫學大學 |
1995 |
A Convenient Synthesis of Antihyperlipo proteinemic Agent Gemfibrozil.
|
王惠珀; Wang HP; Lee O; Fan CT; Lee LT |
| 臺北醫學大學 |
1995 |
Derivatives and preparation of 2, 2-dimethyl-5-substituted phenoxypentanoic acid
|
王惠珀; Wang HP; Lee O; Fan CT; |
| 臺北醫學大學 |
1995 |
Synthesis of Open-Ring Analogues of N5,N10-Methylene- 5,6,7,8-Tetrahydro Folic Acid with Selective Activity against Human CNS Cancer in vitro.
|
王惠珀; Wang HP; Bai TS; Lee O; Ker KD |
| 臺北醫學大學 |
1995 |
Synthesis of Open-Ring Analogues of N5,N10-Methylene- 5,6,7,8-Tetrahydro Folic Acid with Selective Activity against Human brain cancer cell line.
|
王惠珀; Bai TS; Lee O; Ker KD; Wang HP |
| 國立臺灣大學 |
1994-11 |
A Convenient Synthesis of Antihyperlipoproteinemic Agent Gemfibrozil.
|
Lee, O.; Fan, C. T.; Lee, L. T.; 王惠珀; Lee, O.; Fan, C. T.; Lee, L. T.; Wang, Hui-Po |
| 國立臺灣大學 |
1994-10 |
Derivatives and Preparation of 2,2-dimethyl-5-substituted Phenoxypentanoic Acid
|
王惠珀; Lee, O.; Fan, C. C.; Wang, Hui-Po; Lee, O.; Fan, C. C. |
| 臺北醫學大學 |
1994 |
Synthesis and hypocholesteremic Activities of Gemfibrozil Analogues.
|
王惠珀; Lee O; Fan C; Lee LT; Wang HP |
| 臺北醫學大學 |
1994 |
Synthesis and hypocholesteremic Activities of Gemfibrozil Analogues.
|
王惠珀; Lee O; Fan C; Lee LT; Wang HP |
| 國立臺灣大學 |
1994 |
Synthesis and Hypocholesteremic Activities of Gemfibrozil Analogues
|
Lee, O.; Fan, C. T.; Lee, L. T.; 王惠珀; Lee, O.; Fan, C. T.; Lee, L. T.; Wang, Hui-Po |
