YK-4-279

CAS No. 1037184-44-3

YK-4-279( YK-4-279 | YK4-279 | YK 4-279 | YK 4279 )

Catalog No. M17770 CAS No. 1037184-44-3

YK 4-279, an inhibitor of RNA Helicase A (RHA), binds to the oncogenic transciption factor EWS-FLI1.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 49 In Stock
10MG 71 In Stock
25MG 133 In Stock
50MG 249 In Stock
100MG 442 In Stock
200MG 676 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    YK-4-279
  • Note
    Research use only, not for human use.
  • Brief Description
    YK 4-279, an inhibitor of RNA Helicase A (RHA), binds to the oncogenic transciption factor EWS-FLI1.
  • Description
    YK-4-279 is a ETV1 inhibitor, which inhibitor protein-protein interactions between ES-FLI1 and RHA.YK-4-279 effectively antagonizes EWS-FLI1 induced leukemia in a transgenic mouse model. YK-4-279 demonstrates specificity in targeting the oncogene EWS-FLI1. YK-4-279, prevents prostate cancer growth and metastasis in a mouse xenograft model.(In Vitro):YK-4-279 (3-30 μM; overight) dissociates EWS-FLI1 from RHA in Ewing’s sarcoma family tumor (ESFT) cells.YK-4-279 (3-30 μM; 14 h) nearly eliminates cyclin D1 in TC32 cells.YK-4-279 (3-30 μM; 72 h) potently and specifically inhibits ESFTs.YK-4-279 (50 μM; 6 h) induces substantial apoptosis of ESFT cells.YK-4-279 (0.1-30 μM; 72 h) inhibits the growth of ESFT, prostate, breast and pancreatic cancer cells.(In Vivo):YK-4-279 (1.5 mg; i.p. once) inhibited ESFT tumor growth.
  • In Vitro
    Cell Viability Assay Cell Line:TC32, ES925, GUES1, TC71, A673, A4573, CHP100, PANC1, ASP1, MCF-7, MDA-MB-231, PC-3, HFK and HEC cell lines Concentration:3-30 μM Incubation Time:72 h Result:Inhibited cell growth with IC50s of 900 nM, 1 μM and 8 μM for TC32, ES925 and GUES1 cells, respectively.Apoptosis Analysis Cell Line:TC32, HEK, HEC and HFK cell lines Concentration:50 μM Incubation Time:6 h Result:Induced apoptosis of ESFT cells and increased caspase-3 activity.Cell Viability Assay Cell Line:TC32, TC71, RDES, SKES, MMH-ES-1, STA-ET 7.2, A4573, PC3, MCF7, MDA-MB-231, PANC1 and ASPC1 cell lines Concentration:0.1-30 μM Incubation Time:72 h Result:Inhibited cell growth with IC50s of 0.94, 1.83, 1.03, 0.33, 0.94, 0.60, 1.46, 4.95, 22.82, 0.82, 1.514 and 14.28 μM for TC32, TC71, RDES, SKES, MMH-ES-1, STA-ET 7.2, A4573, PC3, MCF7, MDA-MB-231, PANC1 and ASPC1 cells, respectively.
  • In Vivo
    Animal Model:Beige mice with orthotopic ESFT and ESFT xenografts Dosage:1.5 mg Administration:Intraperitoneal injection; 1.5 mg once Result:Effectively redeced tumor volume of CHP100 and ESFT xenografts (TC71 and CHP100).
  • Synonyms
    YK-4-279 | YK4-279 | YK 4-279 | YK 4279
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    RNA helicase A
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1037184-44-3
  • Formula Weight
    366.2
  • Molecular Formula
    C17H13Cl2NO4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 25 mg/mL. 68.27 mM;
  • SMILES
    COC1=CC=C(C=C1)C(=O)CC1(O)C(=O)NC2=C(Cl)C=CC(Cl)=C12
  • Chemical Name
    4,7-dichloro-1,3-dihydro-3-hydroxy-3-[2-(4-methoxyphenyl)-2-oxoethyl]-2H-indole-2-one

Shipping & Storage Information

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

Reference

1. Erkizan HV, et al. Nat Med. 2009, 15(7), 750-756.2. Rahim S, et al. PLoS One. 2011, 6(4), e19343.
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