
Fosifidancitinib
CAS No. 1237168-58-9
Fosifidancitinib( —— )
Catalog No. M28194 CAS No. 1237168-58-9
Fosifidancitinib is a potent inhibitor of JAK 1 and JAK 3.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 302 | Get Quote |
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10MG | 447 | Get Quote |
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25MG | 714 | Get Quote |
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50MG | 1017 | Get Quote |
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100MG | 1368 | Get Quote |
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200MG | Get Quote | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameFosifidancitinib
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NoteResearch use only, not for human use.
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Brief DescriptionFosifidancitinib is a potent inhibitor of JAK 1 and JAK 3.
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DescriptionFosifidancitinib is a potent inhibitor of JAK 1 and JAK 3.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayAngiogenesis
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TargetJAK
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number1237168-58-9
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Formula Weight505.39
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Molecular FormulaC21H21FN5O7P
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Purity>98% (HPLC)
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Solubility——
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SMILESCc1cc(Nc2ncc(C)c(Nc(cc3)cc(N4COP(O)(O)=O)c3OC4=O)n2)cc(OC)c1F
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference



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PF-06651600
PF-06651600 is a novel potent, selective JAK3 inhibitor with IC50 of 0.346 nM, displays >1,000-fold selectivity over JAK1 and JAK2; inhibits Th1 and Th17 cell differentiation and function, reduces disease pathology in rat adjuvant-induced arthritis as well as in mouse experimental autoimmune encephalomyelitis models; selectively targets γc cytokine pathways while preserving JAK1-dependent anti-inflammatory signaling such as the IL-10 suppressive functions following LPS treatment in macrophages and the suppression of TNFα and IL-1β production in IL-27-primed macrophages.Rheumatoid ArthritisPhase 2 Clinical
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Ifidancitinib
Ifidancitinib (ATI-50002) is a specific JAK kinase 1/3 inhibitor that induces hair growth in AA-affected C3H/HeJ mice.Ifidancitinib can be used to study autoimmune diseases.
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Tofacitinib
Tofacitinib (CP-690550) is a potent, specific, orally active inhibitor of JAK3 with IC50 of 1 nM in cell-free assays; displays 20- to 100-fold less potency for JAK2 and JAK1 (IC50=20 nM and 112 nM, respectively).