Name | upadacitinib |
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Synonyms |
upadacitinib
UNII-4RA0KN46E0 (3S,4R)-3-Ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)-1-pyrrolidinecarboxamide (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide 1-Pyrrolidinecarboxamide, 3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)-, (3S,4R)- ABT-494 UNII:4RA0KN46E0 |
Description | Upadacitinib (ABT-494) is a potent and selective Janus kinase (JAK) 1 inhibitor with an IC50 of 43 nM, being developed for the treatment of several autoimmune disorders. |
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Related Catalog | |
Target |
IC50: 43 nM (JAK1), 200 nM (JAK2)[1] |
In Vitro | In biochemical assays, Upadacitinib is 74-fold more selective for JAK-1 than for JAK-2 (which is involved in erythropoiesis) and 58-fold more selective for JAK-1 than for JAK-3 (which is involved in immunosurveillance)[1].. The enhanced selectivity of Upadacitinib for JAK-1 over JAK-2 and JAK-3 may offer an improved benefit–risk profile in patients with RA range[2]. |
References |
Density | 1.6±0.1 g/cm3 |
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Molecular Formula | C17H19F3N6O |
Molecular Weight | 380.368 |
Exact Mass | 380.157257 |
LogP | 3.06 |
Index of Refraction | 1.678 |
Hazard Codes | Xn |
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