UNC3866

CAS No. 1872382-47-2

UNC3866 ( UNC 3866;UNC-3866 )

Catalog No. M12899 CAS No. 1872382-47-2

A potent, selective PRC1 chromodomains antagonist that binds to CBX4 and CBX7 with Kd of 100 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 63 In Stock
5MG 105 In Stock
10MG 178 In Stock
25MG 357 In Stock
50MG 533 In Stock
100MG 761 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    UNC3866
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective PRC1 chromodomains antagonist that binds to CBX4 and CBX7 with Kd of 100 nM.
  • Description
    A potent, selective PRC1 chromodomains antagonist that binds to CBX4 and CBX7 with Kd of 100 nM; displays 6- to 18-fold selectivity versus other CBX (CBX2/6/8) and CDY chromodomains, highly selectivity versus >250 other taergets in a Kme reader panel; inhibits PC3 cell proliferation with EC50 of 340 nM.
  • Synonyms
    UNC 3866;UNC-3866
  • Pathway
    Chromatin/Epigenetic
  • Target
    HMTase
  • Recptor
    CBX7-H3
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1872382-47-2
  • Formula Weight
    795.02
  • Molecular Formula
    C43H66N6O8
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 27 mg/mL
  • SMILES
    CC(C)(C)C1=CC=C(C(N[C@@H](CC2=CC=CC=C2)C(N[C@@H](C)C(N[C@@H](CC(C)C)C(N[C@@H](CCCCN(CC)CC)C(N[C@@H](CO)C(OC)=O)=O)=O)=O)=O)=O)C=C1
  • Chemical Name
    L-Serine, N-[4-(1,1-dimethylethyl)benzoyl]-L-phenylalanyl-L-alanyl-L-leucyl-N6,N6-diethyl-L-lysyl-, methyl ester

Shipping & Storage Information

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

Reference

1. Stuckey JI, et al. Nat Chem Biol. 2016 Mar;12(3):180-7.
2. Barnash KD, et al. ACS Chem Biol. 2016 Sep 16;11(9):2475-83.
molnova catalog
related products
  • MI-2-2 hydrochloride

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

  • EBI-2511

    EBI-2511 is a highly potent and orally active EZH2 inhibitor with IC50 of 4 nM against mutant EZH2 A677G.

  • UNC-1079

    The piperidine analog of UNC1021; structurally similar but significantly less potent inhibitor for use as a negative control in cellular studies.