JAK3i

CAS No. 1918238-72-8

JAK3i( JAK3 inhibitor JAK3i )

Catalog No. M13007 CAS No. 1918238-72-8

JAK3i is a selective, covalent JAK3 kinase inhibitor with IC50 of 0.43 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 745 Get Quote
10MG 1017 Get Quote
25MG 1431 Get Quote
50MG 1782 Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    JAK3i
  • Note
    Research use only, not for human use.
  • Brief Description
    JAK3i is a selective, covalent JAK3 kinase inhibitor with IC50 of 0.43 nM.
  • Description
    JAK3i is a selective, covalent JAK3 kinase inhibitor with IC50 of 0.43 nM, shows high selectivity (>3,000-fold) against the closely related kinase domains in JAK1, JAK2, or TYK2, displays 1,300-fold, 600-fold, and 50-fold over EGFR, ITK, and BTK respectively.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    JAK3 inhibitor JAK3i
  • Pathway
    Angiogenesis
  • Target
    JAK
  • Recptor
    JAK
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1918238-72-8
  • Formula Weight
    354.34
  • Molecular Formula
    C18H15FN4O3
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(C1=CNC2=NC=NC(C3=CC(NC(C=C)=O)=CC=C3F)=C21)OCC
  • Chemical Name
    Ethyl 4-(5-acrylamido-2-fluorophenyl)-7H-pyrrolo[2,3-d]pyrimidine-5-carboxylate

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Smith GA, et al. Nat Chem Biol. 2016 May;12(5):373-9.
molnova catalog
related products
  • SHR0302

    SHR0302 is a JAK inhibitor that binds JAK1 with stronger affinity than others (Selectivity for JAK1 is more than 10 times for JAK2, 77 times for JAK3, 420 times for Tyk2).

  • WHI-P97 HCl 211555-0...

    WHI-P97 HCl is a potent and selective JAK-3 inhibitor.?WHI-P97 had an estimated Ki value of 0.09 microM from modeling studies and a measured IC50 value of 2.5 microM in EGFR kinase inhibition assays.?WHI-P97 effectively inhibited the in vitro invasiveness of EGFR-positive human cancer cells in a concentration-dependent manner.

  • AZD-1480

    A potent, selective, ATP competitive JAK2 inhibitor with Ki of 0.26 nM.