WHI-P258

CAS No. 21561-09-1

WHI-P258( WHI-P258 | WHI-P 258 | WHI-P-258 | WHIP 258 )

Catalog No. M13440 CAS No. 21561-09-1

WHI-P258 is a dimethoxyquinazoline inhibitor of JAK3.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 32 In Stock
5MG 28 In Stock
10MG 46 In Stock
25MG 88 In Stock
50MG 137 In Stock
100MG 233 In Stock
200MG 341 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    WHI-P258
  • Note
    Research use only, not for human use.
  • Brief Description
    WHI-P258 is a dimethoxyquinazoline inhibitor of JAK3.
  • Description
    WHI-P258 is a dimethoxyquinazoline inhibitor of JAK3. This compound binds JAK3 weakly and may be used as a JAK binding negative control in the development of new therapeutics.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    WHI-P258 | WHI-P 258 | WHI-P-258 | WHIP 258
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    EGFR| JAK3
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    21561-09-1
  • Formula Weight
    281.31
  • Molecular Formula
    C16H15N3O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: <1.2mg/mL
  • SMILES
    COC1=CC2=NC=NC(NC3=CC=CC=C3)=C2C=C1OC
  • Chemical Name
    6,7-Dimethoxy-N-phenylquinazolin-4-amine

Shipping & Storage Information

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

Reference

1.Fry DW, et al. Science. 1994, 265(5175), 1093-1095.
molnova catalog
related products
  • Mobocertinib

    Mobocertinib is a potent ?inhibitor of epidermal growth factor receptor (EGFR) and an antineoplastic agent.

  • Olmutinib

    Olmutinib is a Novel Epidermal Growth Factor Receptor Tyrosine Kinase InhibitorOlmutinib at 3 μM significantly reversed drug resistance mediated by ABCG2, but not by ABCB1 and ABCC1, by antagonizing the drug efflux function in ABCG2-overexpressing cells.?

  • Avitinib maleate

    Avitinib maleate (AC-0010MA, AC0010 maleate) is an?orally available, irreversible, and mutant-selective EGFR inhibitor with IC50 of 0.18 nM against EGFR L858R/T790M.