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)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 732 | Get Quote |
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| 100MG | Get Quote | Get Quote |
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| 200MG | Get Quote | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameSF-1126
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NoteResearch use only, not for human use.
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Brief DescriptionSF-1126 is a pan PI3K/BRD4 inhibitor, RGDS-conjugated LY294002 prodrug that exhibits increased solubility and binds to specific integrins.
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DescriptionSF-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.
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In VitroSF1126 (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.
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In Vivo——
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SynonymsSF 1126 | SF1126
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PathwayPI3K/Akt/mTOR signaling
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TargetPI3K
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RecptorPI3K
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Research AreaCancer
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IndicationLiver Cancer
Chemical Information
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CAS Number936487-67-1
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Formula Weight852.84
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Molecular FormulaC39H48N8O14
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Purity>98% (HPLC)
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Solubility——
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SMILESO=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
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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
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Storage(-20℃)
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ShippingWith Ice Pack
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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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