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SC66

🥰Excellent
Catalog No. T3132Cas No. 871361-88-5

SC66 is a AKT inhibitor in HepG2, HA22T/VGH, and PLC/PRF/5 cells (IC50: about 0.75 μg/ml, at 72 h).

SC66

SC66

🥰Excellent
Purity: 100%
Catalog No. T3132Cas No. 871361-88-5
SC66 is a AKT inhibitor in HepG2, HA22T/VGH, and PLC/PRF/5 cells (IC50: about 0.75 μg/ml, at 72 h).
Pack SizePriceAvailabilityQuantity
5 mg$40In Stock
10 mg$56In Stock
25 mg$97In Stock
50 mg$152In Stock
100 mg$222In Stock
500 mg$552In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
SC66 is a AKT inhibitor in HepG2, HA22T/VGH, and PLC/PRF/5 cells (IC50: about 0.75 μg/ml, at 72 h).
Targets&IC50
Akt:0.75 μg/ml
In vitro
HepG2, HA22T/VGH, and PLC/PRF/5 cells had similar IC50 values of approximately 0.85 and 0.75 μg/ml at 48 and 72 hours for SC66, respectively. The most resistant cell line was Huh7(IC50: 3.1/2.8 μg/ml, at 48/72 h), while the Hep3B cell line was found to be the most sensitive, (IC50: 0.75/0.5 μg/ml, at 48/72 h). SC66 reduced cell viability in a time- and dose-dependent manner inhibited colony formation and induced apoptosis in HCC cells. SC66 treatment led to a reduction in total and phospho-AKT levels. In addition, SC66 induces the production of reactive oxygen species (ROS) and DNA damage. SC66 significantly potentiates the effects of both conventional chemotherapeutic and targeted agents, doxorubicin and everolimus, respectively. [1]
In vivo
In xenograft models, SC66 can inhibit tumor growth of Hep3B cells.
Chemical Properties
Molecular Weight276.33
FormulaC18H16N2O
Cas No.871361-88-5
SmilesO=C1\C(CCC\C1=C/c1ccncc1)=C\c1ccncc1
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: <1 mg/mL (insoluble or slightly soluble)

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