2004 | Synthesis and phosphodiesterase 5 inhibitory activity of new sildenafil analogues containing a phosphonate group in the 5′-sulfonamide moiety of phenyl ring | 김대기 | Article |
2004 | Synthesis and biological evaluation of novel 2-pyridinyl-[1,2,3]triazoles as inhibitors of transforming growth factor β1 type 1 receptor | 김대기 | Article |
2003 | Synthesis and Biological Evaluation of 3-(4-Substituted-phenyl)-N-hydroxy-2-propenamides, a New Class of Histone Deacetylase Inhibitors | 김대기 | Article |
2004 | Synthesis and biological evaluation of novel tert-azido or ten-amino substituted penciclovir analogs | 정낙신; 김대기 | Article |
2004 | Design, synthesis, and biological evaluation of novel 2-pyridinyl-[1,2,4] triazoles as inhibitors of transforming growth factor β1 type 1 receptor | 김대기 | Article |
2004 | Synthesis of D- and L-apio nucleoside analogues with 2′-hydroxyl group as potential anti-HIV agents | 정낙신; 김대기 | Article |
2012 | A-62176, a potent topoisomerase inhibitor, inhibits the expression of human epidermal growth factor receptor 2 | 김대기; 권영주; 전규연 | Article |
2015 | Combinatorial TGF-beta attenuation with paclitaxel inhibits the epithelial-to-mesenchymal transition and breast cancer stem-like cells | 신윤용; 김대기; 임우성 | Article |
2015 | Combinatorial TGF-β attenuation with paclitaxel inhibits the epithelial-to-mesenchymal transition and breast cancer stem-like cells | 신윤용; 김대기; 임우성 | Article |
2014 | EW-7197 inhibits hepatic, renal, and pulmonary fibrosis by blocking TGF-β/Smad and ROS signaling | 신윤용; 김대기; 우현애 | Article in Press |