Current Proceedings on Technology
Yazarlar: Nam Sook Kang, Joo Yun Lee, Kee Young Kim
Konular:-
Anahtar Kelimeler:11β-HSD1,Inhibitor,Pharmacophore,Docking,Thiazolidine
Özet: There is a difference in the sequence homology between the human and mouse 11β-HSD1 enzymes. Many researchers have had difficulties in identifying the compounds that are equivalently active towards both human and mouse 11β-HSD1 enzymes. The aim of this study was to build docking-based pharmacophore models that can demonstrate the differences of the structural features in human and mouse 11β-HSD1 enzymes using in-house compounds-thiazolidine derivatives as potential 11β-HSD1 inhibitors. It was possible to obtain new insights into the structural relationship of a series of compounds with the human and mouse 11β-HSD1 enzymes. High correlation coefficients of 0.64 and 0.70 were respectively obtained when comparing the activity of the thiazolidine derivatives with the actual measurements in human and mouse species.