Windorphen

CAS No. 19881-70-0

Windorphen( —— )

Catalog No. M13107 CAS No. 19881-70-0

A potent, selective inhibitor of p300 histone acetyltransferase (IC50=4.2 uM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 43 Get Quote
10MG 65 Get Quote
25MG 115 Get Quote
50MG 175 Get Quote
100MG 261 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Windorphen
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective inhibitor of p300 histone acetyltransferase (IC50=4.2 uM).
  • Description
    A potent, selective inhibitor of p300 histone acetyltransferase (IC50=4.2 uM); displays >10-fold selectivity over other histone acetyltransferases; inhibits Wnt3a-inducible TOPFLASH-luciferase activity with IC50 of 1.5 uM, exhibits remarkable specificity toward β-catenin-1 function and selectively blocks the Wnt signal required for ventral development; robustly and selectively kills cancer cells that harbor Wnt-activating mutations.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Chromatin/Epigenetic
  • Target
    HAT
  • Recptor
    HAT
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    19881-70-0
  • Formula Weight
    302.75
  • Molecular Formula
    C17H15ClO3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 62.5 mg/mL (206.44 mM)
  • SMILES
    COC1=CC=C(C=C1)C(=C(C2=CC=C(C=C2)OC)Cl)C=O
  • Chemical Name
    (Z)-3-chloro-2,3-bis(4-methoxyphenyl)acrylaldehyde

Shipping & Storage Information

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

Reference

1. Hao J, et al. Cell Rep. 2013 Sep 12;4(5):898-904.
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