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Peficitinib

🥰Excellent
Catalog No. T6933Cas No. 944118-01-8
Alias JNJ-54781532, ASP015K

Peficitinib (ASP015K) (ASP015K, JNJ-54781532) is an orally bioavailable JAK inhibitor. Phase 3.

Peficitinib

Peficitinib

🥰Excellent
Purity: 99.4%
Catalog No. T6933Alias JNJ-54781532, ASP015KCas No. 944118-01-8
Peficitinib (ASP015K) (ASP015K, JNJ-54781532) is an orally bioavailable JAK inhibitor. Phase 3.
Pack SizePriceAvailabilityQuantity
2 mg$34In Stock
5 mg$60In Stock
10 mg$106In Stock
25 mg$192In Stock
50 mg$297In Stock
100 mg$463In Stock
200 mg$678In Stock
1 mL x 10 mM (in DMSO)$67In Stock
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Purity:99.4%
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Product Introduction

Bioactivity
Description
Peficitinib (ASP015K) (ASP015K, JNJ-54781532) is an orally bioavailable JAK inhibitor. Phase 3.
Targets&IC50
JAK3:0.7 nM, JAK2:5.0 nM, JAK1:3.9 nM, TYK2:4.8 nM
In vitro
ASP015K suppresses the IL-2-induced proliferation of human T cells with greater potency than EPO-induced proliferation of human erythroleukemia cells. In human whole blood, ASP015K inhibits STAT5 phosphorylation (pSTAT5). [1]
In vivo
In the rat AIA model, ASP015K (p.o.) significantly decreases paw swelling and ankle bone destruction score. [1]
AliasJNJ-54781532, ASP015K
Chemical Properties
Molecular Weight326.39
FormulaC18H22N4O2
Cas No.944118-01-8
Smiles[H][C@]12CC3C[C@]([H])(CC(O)(C3)C1)C2Nc1c(cnc2[nH]ccc12)C(N)=O
Relative Density.no data available
Storage & Solubility Information
Storagekeep away from direct sunlight,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: <1 mg/mL
Ethanol: <1 mg/mL
DMSO: 60 mg/mL (183.8 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0638 mL15.3191 mL30.6382 mL153.1910 mL
5 mM0.6128 mL3.0638 mL6.1276 mL30.6382 mL
10 mM0.3064 mL1.5319 mL3.0638 mL15.3191 mL
20 mM0.1532 mL0.7660 mL1.5319 mL7.6595 mL
50 mM0.0613 mL0.3064 mL0.6128 mL3.0638 mL
100 mM0.0306 mL0.1532 mL0.3064 mL1.5319 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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