AZD-1480
CAS No. 935666-88-9
AZD-1480( AZD1480 | AZD 1480 )
Catalog No. M16692 CAS No. 935666-88-9
A potent, selective, ATP competitive JAK2 inhibitor with Ki of 0.26 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 47 | In Stock |
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| 10MG | 73 | In Stock |
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| 25MG | 129 | In Stock |
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| 100MG | Get Quote | 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 NameAZD-1480
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NoteResearch use only, not for human use.
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Brief DescriptionA potent, selective, ATP competitive JAK2 inhibitor with Ki of 0.26 nM.
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DescriptionA potent, selective, ATP competitive JAK2 inhibitor with Ki of 0.26 nM; demonstrates significant JAK2 selectivity over JAK3 and marginal selectivity over JAK1; blocks STAT3 phosphorylation in a panel of human solid tumor cell lines, potently inhibits the growth of the TEL-Jak2 cell line (GI50=60 nM); suppresses the growth of human solid tumor xenografts harboring persistent Stat3 activity.Liver Cancer Phase 1 Discontinued.
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In Vitro——
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In Vivo——
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SynonymsAZD1480 | AZD 1480
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PathwayAngiogenesis
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TargetJAK
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RecptorJAK2
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Research AreaCancer
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IndicationLiver Cancer
Chemical Information
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CAS Number935666-88-9
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Formula Weight348.766
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Molecular FormulaC14H14ClFN8
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESCC1=CC(NC2=NC(N[C@H](C3=NC=C(F)C=N3)C)=NC=C2Cl)=NN1
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Chemical Name2,4-Pyrimidinediamine, 5-chloro-N2-[(1S)-1-(5-fluoro-2-pyrimidinyl)ethyl]-N4-(5-methyl-1H-pyrazol-3-yl)-
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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Pumecitinib
Pumecitinib is a Janus kinase (JAK) inhibitor. Pumecitinib exhibits anti-inflammatory activity.
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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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Oclacitinib
Oclacitinib(PF03394197) is a potent and selective JAKs inhibitor with IC50 of 10-99 nM.
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