Molecular Formula | C31H40N4O6 |
Molar Mass | 564.67 |
Density | 1.227 |
pKa | pKa 7.04(H2O tunde?ned Iunde?ned) (Uncertain) |
Storage Condition | 2-8℃ |
MDL | MFCD00871548 |
In vivo study | DMP-777-treated rats show a marked decrease in H/K-ATPase staining parietal cells. DMP-777-induced loss of parietal cells is significantly ameliorated with coadministration of omeprazole. DMP-777-treated animals demonstrates marked foveolar hyperplasia in the fundus with prominent expansion of diastase-resistant, PAS-positive surface mucous cells. When DMP-777 is coadministeredwith omprazole, there is a significant decrease in BrdUpositive S-phase cells compared with rats thatreceive DMP-777 alone. After oral dosing of monkeys at 40 mg/kg with DMP-777 the only stereoisomer detected in the post-dose plasma samples is the starting material DMP-777, and no inversion of the configuration at positions 'a' and 'b' of DMP-777 has occurred in vivo. Mist1-/- mice treated with DMP-777 show fewer chief cell to SPEM transitions. Mist1-/- mice treated with L635 demonstrates significantly fewer proliferative SPEM cells compared to control mice. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 1.771 ml | 8.854 ml | 17.709 ml |
5 mM | 0.354 ml | 1.771 ml | 3.542 ml |
10 mM | 0.177 ml | 0.885 ml | 1.771 ml |
5 mM | 0.035 ml | 0.177 ml | 0.354 ml |
biological activity | DMP 777 is a potent, selective, orally available human leucocyte elastase (HLE) inhibitors. |
Target | Human leucocyte elastase (HLE) |