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CH5138303

Cat. No. M3776

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CH5138303 Structure
Size Price Availability
2mg USD 110 Out of stock
5mg USD 200 Out of stock
10mg USD 350 Out of stock
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Quality Control & Documentation
Biological Activity

CH5138303 is an orally available Hsp90 inhibitor with Kd of 0.48 nM. CH5138303 showed high binding affinity for N-terminal Hsp90α (Kd=0.52nM) and strong in vitro cell growth inhibition against human cancer cell lines (HCT116 IC50=0.098μM, NCI-N87 IC50=0.066μM) and also displayed high oral bioavailability in mice (F=44.0%) and potent antitumor efficacy in a human NCI-N87 gastric cancer xenograft model (tumor growth inhibition=136%).

Protocol (for reference only)
Cell Experiment
Cell lines HCT116 and NCI-N87 cell lines
Preparation method Culturing HCT116 cell line and NCI-N87 cell line according to the supplier’s instructions. Suspending cells in a medium are added to solutions which contains various concentrations of the test substance, and culturing the cells at 37 °C in 5% CO2. Four days later, adding cell Counting Kit-8 solution and measuring absorbance at 450 nm with Microplate-Reader iMark. Calculating antiproliferative activity by the formula (1−T/C) × 100 (%), where T represents the absorbance of drug-treated cells and C that of untreated control cells at 450 nm. Using Microsoft Excel 2007 to calculate the 50% inhibition concentration (IC50) values
Concentrations ~10 μM
Incubation time 4 days
Animal Experiment
Animal models Mice with human NCI-N87 gastric cancer xenograft.
Formulation
Dosages 50 mg/kg
Administration p.o.
Chemical Information
Molecular Weight 415.9
Formula C19H18ClN5O2S
CAS Number 959763-06-5
Solubility (25°C) DMSO
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Suda A, et al. Bioorg Med Chem. Design and synthesis of 2-amino-6-(1H,3H-benzo[de]isochromen-6-yl)-1,3,5-triazines as novel Hsp90 inhibitors.

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  Catalog
Abmole Inhibitor Catalog




Keywords: CH5138303 supplier, HSP, inhibitors, activators

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