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CCT 018159

Cat. No. M6571
CCT 018159 Structure
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10mg USD 300  USD300 Custom Synthesis
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Quality Control & Documentation
Biological Activity

CCT 018159 is a novel inhibitor of heat shock protein 90 (Hsp90) ATPase activity (IC50 = 5.7 μM) that displays selectivity over human Hsp72 and topoisomerase II. Inhibits proliferation of HCT116 human colon tumor cells and produces upregulation of Hsp70 and downregulation of c-Raf and cdk4. More soluble than 17-AAG and is independent of NQO1/DT-diaphorase and P-glycoprotein expression.

Chemical Information
Molecular Weight 352.39
Formula C20H20N2O4
CAS Number 171009-07-7
Solubility (25°C) DMSO 35.24 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Heytler and Pritchard. Biochem Biophys Res Commun. A new class of uncoupling agents - carbonyl cyanide phenylhydrazones.

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Keywords: CCT 018159 supplier, HSP, inhibitors, activators


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