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JAK inhibitor Upadacitinib, Purity ≥98%

Cat. No.: X23-10-ZQ428

JAK inhibitor Upadacitinib, Purity ≥98%

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Synonym: Upadacitinib; 1310726-60-3; ABT-494; Rinvoq; Upadacitinib anhydrous; 4RA0KN46E0; UNII-4RA0KN46E0; JAK inhibitor

  • MDL: MFCD30502663
  • CAS Number: 1310726-60-3
  • Compound CID: 58557659
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Product Size
2 mg; 5 mg; 10 mg; 25 mg; 50 mg
Price
Datasheet
Datasheet
MSDS
MSDS
Properties
Description
Upadacitinib, soluble in DMSO and ethanol and insoluble in water, is an available JAK small molecule inhibitor with potential antineoplastic activity. It targets JAK1, JAK2, JAK3, and Tyk2.
Molecular Weight
380.37
Molecular Formula
C17H19F3N6O
Targets
JAK1: 0.043 μM; JAK2: 0.2 μM; JAK3: 2.3 μM; Tyk2: 4.7 μM
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 66 mg/mL (173.51 mM); Water: Insoluble; Ethanol: 66 mg/mL (173.51 mM)
Identity
Confirmed by NMR/HPLC/MS.
Applications
Upadacitinib can be used in research targeting JAK1 for treating autoimmune diseases.
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Dextran
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