MMRi64

CAS No. 430458-66-5

MMRi64( MMRi64 )

Catalog No. M14460 CAS No. 430458-66-5

MMRi64 is a small molecule inhibitor that disrupts Mdm2-MdmX RING-RING interaction interactions in vitro and activates p53 in cancer cells.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 110 Get Quote
10MG 174 Get Quote
25MG 300 Get Quote
50MG 447 Get Quote
100MG 624 Get Quote
500MG 1305 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    MMRi64
  • Note
    Research use only, not for human use.
  • Brief Description
    MMRi64 is a small molecule inhibitor that disrupts Mdm2-MdmX RING-RING interaction interactions in vitro and activates p53 in cancer cells.
  • Description
    MMRi64 is a small molecule inhibitor that disrupts Mdm2-MdmX RING-RING interaction interactions in vitro and activates p53 in cancer cells; potently induces downregulation of Mdm2 and MdmX in leukemia cells, only induces the expression of pro-apoptotic gene PUMA (p53 upregulated modulator of apoptosis) with minimal induction of growth-arresting gene p21; selectively induces the apoptotic arm of the p53 pathway in leukemia/lymphoma cells; synergistically induces p53 and apoptosis in combination with Nutlin3a.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    MMRi64
  • Pathway
    Apoptosis
  • Target
    MDM2-p53
  • Recptor
    MDM2-p53
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    430458-66-5
  • Formula Weight
    410.298
  • Molecular Formula
    C22H17Cl2N3O
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (243.72 mM)
  • SMILES
    OC1=C2N=CC=CC2=CC=C1C(C3=CC=CC(Cl)=C3Cl)NC4=NC=CC(C)=C4
  • Chemical Name
    7-[(2,3-Dichlorophenyl)[(4-methyl-2-pyridinyl)amino]methyl]-8-quinolinol

Shipping & Storage Information

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

Reference

1. Wu W, et al. Cell Death Dis. 2015 Dec 31;6:e2035.
molnova catalog
related products
  • (Rac)-Nutlin-3

    A potent and selective Mdm2 inhibitor with IC50 of 90 nM.

  • UC2288

    UC2288 is a relatively selective p21 attenuator which is synthesized based Sorafenib. UC2288 attenuates p21 protein levels with minimal effect on p21 protein stability.

  • AA-115

    AA-115 (APG 115) is a potent and orally active MDM2 inhibitor with Ki <1 nM, potently inhibits SJSA-1 cell growth with IC50 of 60 nM.