XCT790 是ERRα的一种选择性反向激动剂，IC50值为 0.37 μM。它在化疗过程中诱导癌细胞死亡。

XCT790 is a potent, selective and inverse agonist of estrogen-related receptor alpha(ERRα).

The inhibition of SHP2 from the tested compounds (SHP099) concentrations varying from 0.003-100 μM is monitored using an assay in which 0.5 nM of SHP2 is incubated with of 0.5 μM of peptide IRS1_pY1172(dPEG8)pY1222. After 30-60 minutes incubation at the surrogate substrate, DiFMUP is added to the reaction and incubated at 25 °C for 30 minutes. The reaction is then quenched by the addition of 5 μL of a 160 μM solution of bpV(Phen). The fluorescence signal is monitored using a microplate reader using excitation and emission wavelengths of 340 nm and 450 nm, respectively[1].

725247-18-7

C23H13F9N4O3S

596.43

DMSO:21 mg/mL (35.21 mM),Need ultrasonic and warming
Powder: -20°C for 3 years
In solvent: -80°C for 2 years