Cerdulatinib

CAS No. 1198300-79-6

Cerdulatinib ( PRT2070;PRT-062070; Cerdulatinib )

Catalog No. M17872 CAS No. 1198300-79-6

Cerdulatinib is an novel oral dual Syk/JAK inhibitor.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 45 In Stock
5MG 65 In Stock
10MG 97 In Stock
25MG 176 In Stock
50MG 286 In Stock
100MG 492 In Stock
200MG 633 In Stock
500MG 972 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Cerdulatinib
  • Note
    Research use only, not for human use.
  • Brief Description
    Cerdulatinib is an novel oral dual Syk/JAK inhibitor.
  • Description
    Cerdulatinib, also known as PRT2070 and PRT062070, is a n ovel, oral, dual spleen tyrosine kinase (Syk) and janus kinase (JAK) inhibitor. Cerdulatinib preferentially inhibited JAK1 and JAK3 dependent cytokine mediated signaling and functional responses in various cell types. IL2 mediated STAT5 Y694 was inhibited with an IC50 of 0.27μM, while IL4 mediated signaling to STAT6 Y641 and functional responses in B cells and monocytes, namely CD69, CD25, and CD23 up-regulation, were inhibited with IC50’s within the range of 0.11μM to 0.57μM. It is currently being studied in patients with genetically-defined hematologic cancers, as well as for patients who have failed therapy due to relapse or acquired mutations.
  • Synonyms
    PRT2070;PRT-062070; Cerdulatinib
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    JAK1; JAKs; Syk
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1198300-79-6
  • Formula Weight
    445.54
  • Molecular Formula
    C20H27N7O3S
  • Purity
    98%
  • Solubility
    DMSO : ≥ 30 mg/mL; 67.33 mM
  • SMILES
    CCS(=O)(=O)N1CCN(CC1)c1ccc(cc1)Nc1ncc(C(=O)N)c(NC2CC2)n1
  • Chemical Name
    4-(cyclopropylamino)-2-((4-(4-(ethylsulfonyl)piperazin-1-yl)phenyl)amino)pyrimidine-5-carboxamide

Shipping & Storage Information

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

Reference

1. Coffey G, et al. J Pharmacol Exp Ther. 2014 Dec;351(3):538-48.
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