| Name | Povorcitinib |
|---|---|
| Synonyms |
(S)-4-(3-(cyanomethyl)-3-(3',5'-dimethyl-1H,1'H-[4,4'-bipyrazol]-1-yl)azetidin-1-yl)-2,5-difluoro-N-(1,1,1-trifluoropropan-2-yl)benzamide
4-[3-(cyanomethyl)-3-[4-(3,5-dimethyl-1H-pyrazol-4-yl)-1-pyrazolyl]-1-azetidinyl]-2,5-difluoro-N-[(2S)-1,1,1-trifluoropropan-2-yl]benzamide |
| Description | Povorcitinib is a potent and selective inhibitor of JAK1. Povorcitinib has the potential for the research of disease selected from cutaneous lupus erythematosus (CLE) and Lichen planus (LP) (extracted from patent WO2021076124A1)[1]. |
|---|---|
| Related Catalog | |
| Target |
JAK1[1] |
| References |
| Molecular Formula | C23H22F5N7O |
|---|---|
| Molecular Weight | 507.46 |