Product Data Sheet

T0070907

Catalog No. A11588

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T0070907 was identified as a potent and selective PPARgamma antagonist. With an apparent binding affinity (concentration at 50% inhibition of [(3)H]rosiglitazone binding or IC(50)) of 1 nm, T0070907 covalently modifies PPARgamma on cysteine 313 in helix 3 of human PPARgamma2.
Chemical Information
Catalog NumA11588
M. Wt277.66
FormulaC12H8ClN3O3
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.313516-66-4
SynonymsT 0070907
SMILESClC1=CC=C([N+]([O-])=O)C=C1C(NC2=CC=NC=C2)=O
Biological Activity
DescriptionT0070907 was identified as a potent and selective PPARgamma antagonist. With an apparent binding affinity (concentration at 50% inhibition of [(3)H]rosiglitazone binding or IC(50)) of 1 nm, T0070907 covalently modifies PPARgamma on cysteine 313 in helix 3 of human PPARgamma2.
Targets
TargetValue
Solubility
In vitro (25°C) DMSO24 mg/mL (86.43 mM)
WaterInsoluble
EthanolInsoluble
In vivo 5% DMSO+45% PEG 300+ddH2O 8 mg/mL
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
Preparing Stock Solutions
Concentration / Solvent Volume / Mass1 mg5 mg10 mg
0.1 mM36.02 mL180.08 mL360.15 mL
0.5 mM7.2 mL36.02 mL72.03 mL
1 mM3.6 mL18.01 mL36.02 mL
5 mM0.72 mL3.6 mL7.2 mL
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SHIPPING AND STORAGE
Adooq products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Adooq Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Adooq products are stable under the recommended conditions.