Le informazioni sugli articoli di fonte ISI sono coperte da copyright

Per ulteriori informazioni selezionare i riferimenti di interesse.

1. Cheng, MY; De, B; Pikul, S; Almstead, NG; Natchus, MG; Anastasio, MV; McPhail, SJ; Snider, CE; Taiwo, YO; Chen, LY; Dunaway, CM; Gu, F; Dowty, ME; Mieling, GE; Janusz, MJ; Wang-Weigand, S
   Design and synthesis of piperazine-based matrix metalloproteinase inhibitors
   JOURNAL OF MEDICINAL CHEMISTRY
   
   M.Y. Cheng et al., "Design and synthesis of piperazine-based matrix metalloproteinase inhibitors", J MED CHEM, 43(3), 2000, pp. 369-380
2. Chen, LY; Rydel, TJ; Gu, F; Dunaway, CM; Pikul, S; Dunham, KM; Barnett, BL
   Crystal structure of the stromelysin catalytic domain at 2.0 angstrom resolution: Inhibitor-induced conformational changes
   JOURNAL OF MOLECULAR BIOLOGY
   
   L.Y. Chen et al., "Crystal structure of the stromelysin catalytic domain at 2.0 angstrom resolution: Inhibitor-induced conformational changes", J MOL BIOL, 293(3), 1999, pp. 545-557
3. Cheng, MY; De, B; Almstead, NG; Pikul, S; Dowty, ME; Dietsch, CR; Dunaway, CM; Gu, F; Hsieh, LC; Janusz, MJ; Taiwo, YO; Natchus, MG; Hudlicky, T; Mandel, M
   Design, synthesis, and biological evaluation of matrix metalloproteinase inhibitors derived from a modified proline scaffold
   JOURNAL OF MEDICINAL CHEMISTRY
   
   M.Y. Cheng et al., "Design, synthesis, and biological evaluation of matrix metalloproteinase inhibitors derived from a modified proline scaffold", J MED CHEM, 42(26), 1999, pp. 5426-5436
4. Almstead, NG; Bradley, RS; Pikul, S; De, B; Natchus, MG; Taiwo, YO; Gu, F; Williams, LE; Hynd, BA; Janusz, MJ; Dunaway, CM; Mieling, GE
   Design, synthesis, and biological evaluation of potent thiazine- and thiazepine-based matrix metalloproteinase inhibitors
   JOURNAL OF MEDICINAL CHEMISTRY
   
   N.G. Almstead et al., "Design, synthesis, and biological evaluation of potent thiazine- and thiazepine-based matrix metalloproteinase inhibitors", J MED CHEM, 42(22), 1999, pp. 4547-4562
5. Pikul, S; Dunham, KLM; Almstead, NG; De, B; Natchus, MG; Anastasio, MV; McPhail, SJ; Snider, CE; Taiwo, YO; Chen, LY; Dunaway, CM; Gu, F; Mieling, GE
   Design and synthesis of phosphinamide-based hydroxamic acids as inhibitorsof matrix metalloproteinases
   JOURNAL OF MEDICINAL CHEMISTRY
   
   S. Pikul et al., "Design and synthesis of phosphinamide-based hydroxamic acids as inhibitorsof matrix metalloproteinases", J MED CHEM, 42(1), 1999, pp. 87-94
6. NATCHUS MG; CHENG MY; WAHL CT; PIKUL S; ALMSTEAD NG; BRADLEY RS; TAIWO YO; MIELING GE; DUNAWAY CM; SNIDER CE; MCIVER JM; BARNETT BL; MCPHAIL SJ; ANASTASIO MB; DE B
   DESIGN AND SYNTHESIS OF CONFORMATIONALLY-CONSTRAINED MMP INHIBITORS
   Bioorganic & medicinal chemistry letters
   
   M.G. Natchus et al., "DESIGN AND SYNTHESIS OF CONFORMATIONALLY-CONSTRAINED MMP INHIBITORS", Bioorganic & medicinal chemistry letters, 8(16), 1998, pp. 2077-2080
7. PIKUL S; DUNHAM KLM; ALMSTEAD NG; DE B; NATCHUS MG; ANASTASIO MV; MCPHAIL SJ; SNIDER CE; TAIWO YO; RYDEL T; DUNAWAY CM; GU F; MIELING GE
   DISCOVERY OF POTENT, ACHIRAL MATRIX METALLOPROTEINASE INHIBITORS
   Journal of medicinal chemistry
   
   S. Pikul et al., "DISCOVERY OF POTENT, ACHIRAL MATRIX METALLOPROTEINASE INHIBITORS", Journal of medicinal chemistry, 41(19), 1998, pp. 3568-3571
8. SCHRAG JD; LI YG; CYGLER M; LANG DM; BURGDORF T; HECHT HJ; SCHMID R; SCHOMBURG D; RYDEL TJ; OLIVER JD; STRICKLAND LC; DUNAWAY CM; LARSON SB; DAY J; MCPHERSON A
   THE OPEN CONFORMATION OF A PSEUDOMONAS LIPASE
   Structure
   
   J.D. Schrag et al., "THE OPEN CONFORMATION OF A PSEUDOMONAS LIPASE", Structure, 5(2), 1997, pp. 187-202