UNC0631

CAS No. 1320288-19-4

UNC0631( UNC0631, UNC 0631, UNC-0631 )

Catalog No. M17245 CAS No. 1320288-19-4

UNC0631 is a effectvie histone methyltransferase G9a inhibitor (IC50=4 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 61 In Stock
5MG 101 In Stock
10MG 177 In Stock
25MG 378 In Stock
50MG 556 In Stock
100MG 777 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    UNC0631
  • Note
    Research use only, not for human use.
  • Brief Description
    UNC0631 is a effectvie histone methyltransferase G9a inhibitor (IC50=4 nM).
  • Description
    UNC-0631 is a novel G9a inhibitor with excellent potency in a variety of cell lines and excellent separation of functional potency versus cell toxicity. Protein lysine methyltransferase G9a plays key roles in the transcriptional repression of a variety of genes via dimethylation of lysine 9 on histone H3 (H3K9me2) of chromatin as well as dimethylation of nonhistone proteins including tumor suppressor p53.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    UNC0631, UNC 0631, UNC-0631
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    G9a
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    1320288-19-4
  • Formula Weight
    635.93
  • Molecular Formula
    C37H61N7O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 16.67 mg/mL. 26.21 mM; H2O : < 0.1 mg/mL
  • SMILES
    COc1c(OCCCN2CCCCC2)cc2nc(nc(NC3CCN(CC4CCCCC4)CC3)c2c1)N1CCCN(CC1)C(C)C
  • Chemical Name
    N-(1-(cyclohexylmethyl)piperidin-4-yl)-2-(4-isopropyl-1,4-diazepan-1-yl)-6-methoxy-7-(3-(piperidin-1-yl)propoxy)quinazolin-4-amine

Shipping & Storage Information

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

Reference

1. Liu F, et al. J Med Chem. 2011, 54(17), 6139-6150.
molnova catalog
related products
  • EGFR/ErbB2 Inhibitor

    EGFR/ErbB2 Inhibitor is a cell-permeable inhibitor of EGFR and c-ErbB2 (IC50s = 20 and 79 nM, respectively)

  • EGFR-IN-1 hydrochlor...

    EGFR-IN-1 hydrochloride is an irreversible and specific inhibitor of L858R/T790M mutant EGFR, with 100-fold selectivity over wild-type EGFR.

  • Lifirafenib

    Lifirafenib is a potent inhibitor of RAF family kinases and EGFR in biochemical assays with IC50 of 23, 29 and 495 nM for the recombinant BRAFV600E kinase domain, EGFR and EGFR T790M/L858R mutant respectively.