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Showing items 61-70 of 72 (8 Page(s) Totally)
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| 臺北醫學大學 |
2015 |
1-Arylsulfonyl-5-(N-hydroxyacrylamide)tetrahydroquinolines as potent histone deacetylase inhibitors suppressing the growth of prostate cancer cells
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Liu;Y, M.;Lee;H, Y.;Chen;C, H.;Lee;C, H.;Wang;L, T.;Pan;S, L.;Lai;M, J.;Yeh;T, K.;Liou;J, P. |
| 臺北醫學大學 |
2014 |
A novel action mechanism for MPT0G013, a derivative of arylsulfonamide, inhibits tumor angiogenesis through up-regulation of TIMP3 expression
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Wang;C, Y.;Liou;J, P;Tsai;A, C;Lai;M, J.;Liu;Y, M.;Lee;H, Y.;Wang;J, C.;Pan;S, L.;Teng;C, M. |
| 臺北醫學大學 |
2014 |
Effect of C7-substitution of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indolines on the selectivity towards a subclass of histone deacetylases
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Lee;H, Y.;Wang;L, T.;Li;Y, H.;Pan;S, L.;Chen;Y, L;Teng;C, M.;Liou;J, P. |
| 臺北醫學大學 |
2014 |
A novel action mechanism for MPT0G013, a derivative of arylsulfonamide, inhibits tumor angiogenesis through up-regulation of TIMP3 expression
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Wang;C.Y.;Liou;J.P;Tsai;A.C;Lai;M.J.;Liu;Y.M.;Lee;H.Y.;Wang;J.C.;Pan;S.L.;Teng;C.M. |
| 臺北醫學大學 |
2014 |
Effect of C7-substitution of 1-arylsulfonyl-5-(N-hydroxyacrylamide)indolines on the selectivity towards a subclass of histone deacetylases
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Lee;H.Y.;Wang;L.T.;Li;Y.H.;Pan;S.L.;Chen;Y.L;Teng;C.M.;Liou;J.P. |
| 臺北醫學大學 |
2013 |
The HDAC inhibitor, MPT0E028, enhances erlotinib-induced cell death in EGFR-TKI-resistant NSCLC cells
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Chen;M, C.;Chen;C, H.;Wang;J, C.;Tsai;A, C.;Liou;J, P.;Pan;S, L.;Teng;C, M. |
| 臺北醫學大學 |
2013 |
The HDAC inhibitor, MPT0E028, enhances erlotinib-induced cell death in EGFR-TKI-resistant NSCLC cells
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Chen;M.C.;Chen;C.H.;Wang;J.C.;Tsai;A.C.;Liou;J.P.;Pan;S.L.;Teng;C.M. |
| 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
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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
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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 |
2003 |
A novel antioxidant, octyl caffeate, suppression of LPS/IFN-gamma-induced inducible nitric oxide synthase gene expression in rat aortic smooth muscle cells
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鄭幼文; Hsiao; G.; Shen; M.Y.; Chang; W.C.; Cheng; Y.W.; Pan; S.L.; Kuo; Y.H.; Chen; T.F. and Sheu ; J.R. |
Showing items 61-70 of 72 (8 Page(s) Totally)
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