UNC1999

CAS No. 1431612-23-5

UNC1999 ( UNC1999; UNC 1999; UNC-1999 )

Catalog No. M11830 CAS No. 1431612-23-5

UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM in cell-free assays, respectively.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 40 In Stock
5MG 59 In Stock
10MG 88 In Stock
25MG 168 In Stock
50MG 272 In Stock
100MG 489 In Stock
500MG 1071 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    UNC1999
  • Note
    Research use only, not for human use.
  • Brief Description
    UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM in cell-free assays, respectively.
  • Description
    UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM in cell-free assays, respectively, showing >1000-fold selectivity over a broad range of epigenetic and non-epigenetic targets.
  • Synonyms
    UNC1999; UNC 1999; UNC-1999
  • Pathway
    Chromatin/Epigenetic
  • Target
    HMTase
  • Recptor
    EZH1; EZH2
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1431612-23-5
  • Formula Weight
    569.74
  • Molecular Formula
    C33H43N7O2
  • Purity
    >98%(HPLC)
  • Solubility
    Ethanol: 100 mg/mL (175.51 mM); DMSO: 100 mg/mL (175.51 mM)
  • SMILES
    O=C(NCC1=C(CCC)C=C(C)NC1=O)C2=C3C(N(C(C)C)N=C3)=CC(C4=CC=C(N5CCN(C(C)C)CC5)N=C4)=C2
  • Chemical Name
    1-isopropyl-6-(6-(4-isopropylpiperazin-1-yl)pyridin-3-yl)-N-((6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl)-1H-indazole-4-carboxamide

Shipping & Storage Information

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

Reference

1.Konze KD, et al. ACS Chem. Biol. 2013, 8 (6), 1324–1334.
molnova catalog
related products
  • A-196

    A potent, selective and substrate-competitive inhibitor of protein lysine methyltransferases (PKMTs) SUV420H1 and SUV420H2 with IC50 of 25 nM and 144 nM, respectively.

  • PFI-2

    A first-in-class, potent and selective inhibitor of SETD7 methyltransferase with Ki app/IC50 of 0.33/2 nM.

  • MMSET-IN-1

    MMSET-IN-1 is a potent, selective epigenetic oncogene MMSET (aka NSD2 or WHSC1) inhibitor with Ki/IC50 of 1.6/3.3 uM.