| Name | (2R)-1,1,1-trifluoro-2-[3-[(2R)-4-[4-fluoro-2-(trifluoromethyl)phenyl]-2-methylpiperazin-1-yl]sulfonylphenyl]propan-2-ol |
|---|---|
| Synonyms | hsd-016 |
| Description | HSD-016 is a potent, selective and orally active 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitor with IC50 values of 11, 1 and 8 nM against human, mouse and rat 11β-HSD1, respectively. HSD-016 can be used for type 2 diabetes research[1]. |
|---|---|
| Related Catalog | |
| Target |
IC50: 1 nM (mouse 11β-HSD1), 8 nM (rat 11β-HSD1), 11 nM (human 11β-HSD1)[1] |
| References |
| Molecular Formula | C21H21F7N2O3S |
|---|---|
| Molecular Weight | 514.45700 |
| Exact Mass | 514.11600 |
| PSA | 69.23000 |
| LogP | 5.59740 |