Peficitinib
CAS No. 944118-01-8
Peficitinib( ASP-015K | JNJ-54781532 )
Catalog No. M16761 CAS No. 944118-01-8
Peficitinib (ASP-015K, JNJ-54781532) is a potent JAK inhibitor with IC50s of 3.9 and 0.7 nM for JAK1 and JAK3 respectively; inhibits IL-2-dependent T cell proliferation in vitro and STAT5 phosphorylation in vitro and ex vivo.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 65 | In Stock |
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| 10MG | 113 | In Stock |
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| 50MG | 332 | In Stock |
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| 100MG | 551 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NamePeficitinib
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NoteResearch use only, not for human use.
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Brief DescriptionPeficitinib (ASP-015K, JNJ-54781532) is a potent JAK inhibitor with IC50s of 3.9 and 0.7 nM for JAK1 and JAK3 respectively; inhibits IL-2-dependent T cell proliferation in vitro and STAT5 phosphorylation in vitro and ex vivo.
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DescriptionPeficitinib (ASP-015K, JNJ-54781532) is a potent JAK inhibitor with IC50s of 3.9 and 0.7 nM for JAK1 and JAK3 respectively; inhibits IL-2-dependent T cell proliferation in vitro and STAT5 phosphorylation in vitro and ex vivo; dose-dependently suppresses bone destruction and paw swelling in an adjuvant-induced arthritis model in rats; orally bioactive.Rheumatoid Arthritis Phase 3 Clinical.
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In VitroPeficitinib hydrobromide (0-100 nM; 3 days) inhibits IL-2-induced T cell proliferation in a concentration-dependent manner.Peficitinib hydrobromide (10-1000 nM) inhibits IL-2-induced STAT5 phosphorylation in a concentration-dependent manner with a mean IC50 of 124 nM in rat whole blood, and inhibits STAT5 phosphorylation with a mean IC50 of 127 nM in human lymphocytes. Cell Proliferation Assay Cell Line:Splenocytes from male Lewis rats Concentration:0-100 nM Incubation Time:3 days Result:Inhibited IL-2-induced T cell proliferation in a concentration-dependent manner with an IC50 of 10 nM.
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In VivoPeficitinib hydrobromide (1-30 mg/kg; p.o.; once daily for 24 days) shows dose-dependent efficacy both in prophylactic and therapeutic dosing regimens in an adjuvant-induced arthritis rat model. Animal Model:Seven-weeks-old female Lewis rats, adjuvant-induced arthritis (AIA) model Dosage:1, 3, 10, and 30 mg/kg Administration:Oral administration, once daily for 24 days Result:Significantly inhibited the increase in paw volume at doses of 1 mg/kg or greater with an ED50 value of 2.7 mg/kg (95% confidence interval: 1.5–4.2 mg/kg). Significantly reduced the bone destruction score at 10 mg/kg or greater and almost fully ameliorated both paw swelling and bone destruction scores at 30 mg/kg.
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SynonymsASP-015K | JNJ-54781532
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PathwayAngiogenesis
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TargetJAK
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RecptorJAK
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Research AreaInflammation/Immunology
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IndicationRheumatoid Arthritis
Chemical Information
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CAS Number944118-01-8
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Formula Weight326.3929
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Molecular FormulaC18H22N4O2
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 60 mg/mL
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SMILESC1C2CC3CC(C2)(CC1C3NC4=C5C=CNC5=NC=C4C(=O)N)O
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Chemical Name1H-Pyrrolo[2,3-b]pyridine-5-carboxamide, 4-[(5-hydroxytricyclo[3.3.1.13,7]dec-2-yl)amino]-, stereoisomer
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Oda K, et al. Xenobiotica. 2015;45(6):488-94.
2. Takeuchi T, et al. Ann Rheum Dis. 2016 Jun;75(6):1057-64.
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