Tazemetostat hydrobromide

CAS No. 1467052-75-0

Tazemetostat hydrobromide( EPZ-6438 hydrobromide | E-7438 hydrobromide )

Catalog No. M26837 CAS No. 1467052-75-0

Tazemetostat hydrobromide is a potent and selective EZH2 inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 72 In Stock
2MG 34 In Stock
5MG 52 In Stock
10MG 70 In Stock
50MG 90 In Stock
100MG 151 In Stock
200MG 226 In Stock
500MG 369 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Tazemetostat hydrobromide
  • Note
    Research use only, not for human use.
  • Brief Description
    Tazemetostat hydrobromide is a potent and selective EZH2 inhibitor.
  • Description
    Tazemetostat hydrobromide is a potent and selective EZH2 inhibitor. Tazemetostat hydrobromide inhibits the activity of human polycomb repressive complex 2 (PRC2)-containing wild-type EZH2 (Ki: 2.5 nM). Tazemetostat hydrobromide also inhibits EZH1 (IC50: 392 nM).(In Vitro):Tazemetostat hydrobromide inhibits Rat EZH2 (IC50: 4 nM). Tazemetostat hydrobromide inhibits EZH2 with IC50s of 11 and 16 nM in peptide assay and nucleosome assay, respectively. Tazemetostat hydrobromide inhibits multi wild-type and mutant lymphoma cell lines proliferation with IC50s of 0.49 nM-7.6 μM .(In Vivo):Tazemetostat (250 or 500 mg/kg twice daily for 21-28 days) practically eliminates the fast-growing G401 tumors .
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    EPZ-6438 hydrobromide | E-7438 hydrobromide
  • Pathway
    Chromatin/Epigenetic
  • Target
    Histone Demethylase
  • Recptor
    microtubule
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1467052-75-0
  • Formula Weight
    653.662
  • Molecular Formula
    C34H45BrN4O4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Br.CCN(C1CCOCC1)c1cc(cc(C(=O)NCc2c(C)cc(C)[nH]c2=O)c1C)-c1ccc(CN2CCOCC2)cc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Ekaterina Poluektova, et al. Curvulin and Phaeosphaeride A From Paraphoma Sp. VIZR 1.46 Isolated From Cirsium arvense as Potential Herbicides. Molecules. 2018 Oct 28;23(11):2795.
molnova catalog
related products
  • BAY-598

    BAY-598 is a selective inhibitor of SMYD2?with IC50 values of 27 nM.

  • GSK J5

    GSK J5 is an inhibitor of schistosomes and helminths and is often used as a trematode insecticide.GSK J5 promotes schistosome mortality in a dose- and time-dependent manner.

  • SNDX-5613

    SNDX-5613 is a potent and specific inhibitor of Menin-MLL(Ki of 0.149 nM and a cell based IC50 of 10-20 nM).