MI-2-2 hydrochloride

CAS No. ——

MI-2-2 hydrochloride( —— )

Catalog No. M17067 CAS No. ——

MI-2-2 hydrochloride is a potent inhibitor of the menin-MLL interaction that binds to menin with low nanomolar affinity (Kd=22 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    MI-2-2 hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    MI-2-2 hydrochloride is a potent inhibitor of the menin-MLL interaction that binds to menin with low nanomolar affinity (Kd=22 nM).
  • Description
    MI-2-2 hydrochloride is a potent inhibitor of the menin-MLL interaction that binds to menin with low nanomolar affinity (Kd=22 nM); inhibits the interaction of menin with MLL-AF9 in HEK293 cells in a dose-dependent manner with 4-fold potentcy improvement over MI-2; suppresses growth of MLL-AF9–transformed BMCs; causes MV4:11 cells growth inhibition of with GI50 of 3 uM.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Chromatin/Epigenetic
  • Target
    HMTase
  • Recptor
    HMTase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    ——
  • Formula Weight
    451.955
  • Molecular Formula
    C17H21ClF3N5S2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    4-(4-(5,5-Dimethyl-4,5-dihydrothiazol-2-yl)piperazin-1-yl)-6-(2,2,2-trifluoroethyl)thieno[2,3-d]pyrimidine hydrochloride

Shipping & Storage Information

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

Reference

1. Arkin MR, et al. Chem Biol. 2014 Sep 18;21(9):1102-14. 2. Shi A, et al. Blood. 2012 Nov 29;120(23):4461-9.
molnova catalog
related products
  • CN-SAH

    CN-SAH is a potent and selective inhibitor of histone methyl transferase DOT1L with IC50 of 26 nM.

  • 3-Deazaneplanocin A ...

    A highly potent and competitive S-adenosylhomocysteine hydrolase inhibitor with Ki of 0.05 nM.

  • MS-453

    A potent, selective. covalent protein lysine methyltransferase SETD8 inhibitor with IC50 of 804 nM.