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
  • EPZ 025654

    EPZ025654 (GSK 35336023) is a potent, selective arginine methyltransferase CARM1 inhibitor with IC50 of 3 nM.

  • GSK3326595

    A potent, selective, reversible and orally active PRMT5 inhibitor with IC50 of 22 nM.

  • EPZ5676

    EPZ-5676 is an S-adenosyl methionine (SAM) competitive inhibitor of protein methyltransferase DOT1L with Ki of 80 pM.