SF-1126

CAS No. 936487-67-1

SF-1126( SF 1126 | SF1126 )

Catalog No. M16703 CAS No. 936487-67-1

SF-1126?is a pan PI3K/BRD4 inhibitor, RGDS-conjugated LY294002 prodrug that exhibits increased solubility and binds to specific integrins.

Purity : >98% (HPLC)

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Biological Information

  • Product Name
    SF-1126
  • Note
    Research use only, not for human use.
  • Brief Description
    SF-1126?is a pan PI3K/BRD4 inhibitor, RGDS-conjugated LY294002 prodrug that exhibits increased solubility and binds to specific integrins.
  • Description
    SF-1126?is a pan PI3K/BRD4 inhibitor, RGDS-conjugated LY294002 prodrug that exhibits increased solubility and binds to specific integrins; blocks expression levels of c-Myc in HCC cells, inhibits proliferation, cell cycle, apoptosis, PI3K/AKT/mTOR and Ras/Raf/MAPK pathway; shows significant antitumor activity in vivo.Liver Cancer Phase 1 Clinical.
  • In Vitro
    SF1126 (0-6 μM; 48 hours) inhibits Hep3B, HepG2, SK-Hep1, and Huh7 cells proliferation with IC50s of 5.05, 6.89, 3.14, and 2.14 μM, respectively.SF1126 (1-10 μM; 24 hours) results in cell-cycle arrest with a proportional increase in G0-G1 and a decrease in the number of cells in the S-phase in Hep 3B, Hep G2, SK-Hep1, and Huh7 cells.SF1126 (0.5-2.5 μM; pre-30 minutes) and sorafenib suggests that combined treatment of SF1126 and sorafenib blocks multiple key enzymes in PI3K/AKT/mTOR and Ras/Raf/MAPK pathway. Cell Viability Assay Cell Line:Hep3B, HepG2, SK-Hep1, and Huh7 cells Concentration:0 μM; 1 μM; 2 μM; 3 μM; 4 μM; 5 μM; 6 μM Incubation Time:48 hours Result:Resulted in an increased inhibition of HCC proliferation. Cell Cycle Analysis Cell Line:Hep3B, HepG2, SK-Hep1, and Huh7 cells Concentration:1 μM; 5 μM; 10 μM Incubation Time:24 hours Result:Induced cell-cycle arrest.Western Blot Analysis Cell Line:Hep3B, HepG2, SK-Hep1, and Huh7 cells Concentration:0.5 μM and 2.5 μM Incubation Time:Pre-30 mins Result:Suppressed phosphorylation of AKT, p70S6K, 4EBP1, and ERK in all the cell lines together with sorafenib.
  • In Vivo
    ——
  • Synonyms
    SF 1126 | SF1126
  • Pathway
    PI3K/Akt/mTOR signaling
  • Target
    PI3K
  • Recptor
    PI3K
  • Research Area
    Cancer
  • Indication
    Liver Cancer

Chemical Information

  • CAS Number
    936487-67-1
  • Formula Weight
    852.84
  • Molecular Formula
    C39H48N8O14
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C([O-])[C@H](CO)NC([C@H](CC(O)=O)NC(CNC([C@H](CCCNC(N)=N)NC(CCC(OC[N+]1(C2=CC(C3=C(O2)C(C4=CC=CC=C4)=CC=C3)=O)CCOCC1)=O)=O)=O)=O)=O
  • Chemical Name
    (4-oxo-4-((4-(4-oxo-8-phenyl-4H-chromen-2-yl)morpholino-4-ium)methoxy)butanoyl)-L-arginylglycyl-L-aspartyl-L-serinate

Shipping & Storage Information

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

Reference

1. Garlich JR, et al. Cancer Res. 2008 Jan 1;68(1):206-15. 2. Dittmann A, et al. ACS Chem Biol. 2014 Feb 21;9(2):495-502. 3. Erdreich-Epstein A, et al. Oncotarget. 2016 Nov 16. doi: 10.18632/oncotarget.13386.
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