| 2010 | Novel ALK5 Inhibitor Inhibits Breast Tumor Metastasis and Increases the Interactions of SnoN and Ski to the Promoters of TGF beta Target Genes. | 신윤용; 김대기 | Meeting Abstract |
| 2016 | Novel oral transforming growth factor- signaling inhibitor EW-7197 eradicates CML-initiating cells | 신윤용; 김대기 | Article |
| 2009 | Ozone Induces Pulmonary Fibrosis via a TGF-beta Signaling Pathway | 김대기 | Meeting Abstract |
| 2008 | Pharmacokinetics and tissue distribution of 3-((5-(6-methylpyridin-2-yl)-4- (quinoxalin-6-yl)-1H-imidazol-2-yl)methyl)benzamide; a novel ALK5 inhibitor and a potential anti-fibrosis drug | 신윤용; 이화정; 김대기 | Article |
| 2015 | Phosphorylation status determines the opposing functions of Smad2/Smad3 as STAT3 cofactors in T(H)17 differentiation | 김대기 | Article |
| 2006 | Potent in vivo anti-breast cancer activity of IN-2001, a novel inhibitor of histone deacetylase, in MMTV/c-Neu Mice | 신윤용; 김대기 | Article |
| 2011 | Role of IN-1233 in the prevention of neointimal hyperplasia after stent placement in a rat artery model | 김대기 | Article |
| 2004 | Site-specific Tc-99m-labeling of antibody using dihydrazinophthalazine (DHZ) conjugation to Fc region of heavy chain | 김대기 | Article |
| 2011 | Synthesis and biological evaluation of 1-substituted-3(5)-(6-methylpyridin- 2-yl)-4-(quinolin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기 | Article |
| 2011 | Synthesis and biological evaluation of 1-substituted-3(5)-(6-methylpyridin- 2-yl)-4-(quinoxalin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기 | Article |
| 2011 | Synthesis and biological evaluation of 1-substituted-3-(6-methylpyridin-2- yl)-4-([1,2,4triazolo[1,5-apyridin-6-yl)pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기 | Article |
| 2012 | Synthesis and biological evaluation of 2-benzylamino-4(5)-(6-methylpyridin- 2-yl)-5(4)-([1,2,4]triazolo[1,5-a]-pyridin-6-yl)thiazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기; 김승원 | Article |
| 2010 | Synthesis and biological evaluation of 2-pyridyl-substituted pyrazoles and imidazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 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 |
| 2007 | Synthesis and biological evaluation of 4(5)-(6-alkylpyridin-2-yl)imidazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 김대기 | Article |
| 2010 | Synthesis and biological evaluation of 4(5)-(6-methylpyridin-2-yl)imidazoles and -pyrazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 신윤용; 김대기 | Article |
| 2015 | Synthesis and biological evaluation of 5-(fluoro-substituted-6-methylpyridin-2-yl)-4-([1,2,4]triazolo[1,5-alpha]pyridin-6-yl)imidazoles as inhibitors of transforming growth factor-beta type I receptor kinase | 신윤용; 김대기 | Article |
| 2008 | Synthesis and biological evaluation of 5-(pyridin-2-yl)thiazoles as transforming growth factor-β type1 receptor kinase inhibitors | 김대기 | Article |
| 2009 | Synthesis and biological evaluation of benzenesulfonamide-substituted 4-(6-alkylpyridin-2-yl)-5-(quinoxalin-6-yl)imidazoles as transforming growth factor-β type 1 receptor kinase inhibitors | 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 |
| 2004 | Synthesis and biological evaluation of novel tert-azido or ten-amino substituted penciclovir analogs | 정낙신; 김대기 | Article |
| 2008 | Synthesis and biological evaluation of trisubstituted imidazole derivatives as inhibitors of p38α mitogen-activated protein kinase | 김대기 | Article |
| 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 |
| 2006 | Synthesis of 5-ethyl-2-{5-[4-(2-hydroxyethyl)piperazin-1-ylsulfonyl]-2-n- propoxyphenyl}-7-n-propyl-3,5-dihydro-4H-pyrrolo[3,2-d]-[2-14C] pyrimidin-4-one · 2 HCl (14C-SK3530 · 2 HCl) | 김대기 | Article |
| 2004 | Synthesis of D- and L-apio nucleoside analogues with 2′-hydroxyl group as potential anti-HIV agents | 정낙신; 김대기 | Article |
| 2020 | Synthesis, biological evaluation and molecular modelling of 2,4-disubstituted-5-(6-alkylpyridin-2-yl)-1H-imidazoles as ALK5 inhibitors | 이화정; 김대기 | Article |
| 2016 | TGF-beta Type I Receptor Kinase Inhibitor EW-7197 Suppresses Cholestatic Liver Fibrosis by Inhibiting HIF1 alpha-Induced Epithelial Mesenchymal Transition | 신윤용; 김대기 | Article |
| 2016 | TGF-β type i receptor kinase inhibitor EW-7197 suppresses cholestatic liver fibrosis by inhibiting HIF1α-induced epithelial mesenchymal transition | 신윤용; 김대기 | Article |
| 2013 | Transforming growth factor-β1 receptor inhibition preserves glomerulotubular integrity during ureteral obstruction in adults but worsens injury in neonatal mice | 김대기 | Article |
| 2004 | Trichostatin A, a histone deacetylase inhibitor stimulate CYP3A4 proximal promoter activity in hepa-l cells | 신윤용; 김대기 | Article |
