PF-06263276
CAS No. 1421502-62-6
PF-06263276( PF 06263276 | PF06263276 | PF 6263276 )
Catalog No. M11766 CAS No. 1421502-62-6
PF-06263276 (PF06263276, PF 6263276) is a potent, selective pan JAK inhibitor with IC50 of 2.2, 23.1, 59.9 and 29.7 nM for JAK1, JAK2, JAK3, and TYK2, respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
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| 100MG | 1071 | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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Biological Information
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Product NamePF-06263276
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NoteResearch use only, not for human use.
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Brief DescriptionPF-06263276 (PF06263276, PF 6263276) is a potent, selective pan JAK inhibitor with IC50 of 2.2, 23.1, 59.9 and 29.7 nM for JAK1, JAK2, JAK3, and TYK2, respectively.
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DescriptionPF-06263276 (PF06263276, PF 6263276) is a potent, selective pan JAK inhibitor with IC50 of 2.2, 23.1, 59.9 and 29.7 nM for JAK1, JAK2, JAK3, and TYK2, respectively; demonstrates good JAK potency and kinase selectivity, exhibts inhibitory potency in human whole blood versus various stimulatory cytokines (IFNα, IL-23, IL-4, IL-6 and GM-CSF) with IC50 of 0.6-5.2 uM; suitable for inhaled and topical delivery in vivo.Psoriasis Phase 1 Discontinued.
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In Vitro——
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In Vivo——
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SynonymsPF 06263276 | PF06263276 | PF 6263276
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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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Indication——
Chemical Information
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CAS Number1421502-62-6
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Formula Weight566.64
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Molecular FormulaC31H31FN8O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 33.33 mg/mL (58.82 mM)
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SMILESFC1=C(O)C=C(CC)C(C2=CC(NN=C3C4=NC5=C(CN(C(C6=NC=C(N7CCCCC7)N=C6)=O)CC5)N4)=C3C=C2)=C1
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Chemical Name(2-(6-(2-ethyl-5-fluoro-4-hydroxyphenyl)-1H-indazol-3-yl)-3,4,6,7-tetrahydro-5H-imidazo[4,5-c]pyridin-5-yl)(5-(piperidin-1-yl)pyrazin-2-yl)methanone
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. Jones P, et al. J Med Chem. 2017 Jan 26;60(2):767-786.
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