公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2018 | Discovery of aliphatic-chain hydroxamates containing indole derivatives with potent class I histone deacetylase inhibitory activities | Chao S.-W.; Chen L.-C.; Yu C.-C.; Liu C.-Y.; Lin T.E.; JIH-HWA GUH ; Wang C.-Y.; Chen C.-Y.; Hsu K.-C.; Huang W.-J. | European Journal of Medicinal Chemistry | 20 | 17 | |
2015 | DUSP1 expression induced by HDAC1 inhibition mediates gefitinib sensitivity in non-small cell lung cancers | Lin Y.-C.; Lin Y.-C.; JIN-YUAN SHIH ; Huang W.-J.; Chao S.-W.; YIH-LEONG CHANG ; CHING-CHOW CHEN | Clinical Cancer Research | 36 | 34 | |
2014 | A novel small molecule hybrid of vorinostat and DACA displays anticancer activity against human hormone-refractory metastatic prostate cancer through dual inhibition of histone deacetylase and topoisomerase i | Yu C.-C.; Pan S.-L.; Chao S.-W.; SHIH-PING LIU ; Hsu J.-L.; Yang Y.-C.; TSAI-KUN LI ; Huang W.-J.; JIH-HWA GUH | Biochemical Pharmacology | 29 | 28 | |
2011 | Synthesis and evaluation of aliphatic-chain hydroxamates capped with osthole derivatives as histone deacetylase inhibitors | Huang W.-J.; CHING-CHOW CHEN ; Chao S.-W.; Yu C.-C.; Yang C.-Y.; JIH-HWA GUH ; Lin Y.-C.; Kuo C.-I.; Yang P.; Chang C.-I. | European Journal of Medicinal Chemistry | 37 | 35 | |
2010 | Synthesis of n-hydroxycinnamides capped with a naturally occurring moiety as inhibitors of histone deacetylase | Huang W.-J.; CHING-CHOW CHEN ; Chao S.-W.; SHOEI-SHENG LEE ; Hsu F.-L.; Lu Y.-L.; Hung M.-F.; Chang C.-I. | ChemMedChem | 40 | 38 | |
2015 | Total Synthesis of Hispidulin and the Structural Basis for Its Inhibition of Proto-oncogene Kinase Pim-1 | Chao S.-W.; Su M.-Y.; LIH-CHU CHIOU ; Chen L.-C.; Chang C.-I.; Huang W.-J. | Journal of Natural Products | 27 | 25 |