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XCT790

Chemical Structure : XCT790

CAS No.: 725247-18-7

XCT790 (XCT 790;XCT-790)

Catalog No.: PC-42580Not For Human Use, Lab Use Only.

XCT790 (XCT-790) is a potent and selective ERRα inverse agonist with IC50 of 300-500 nM in transient transfection assays.

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1 mg (Free Sample) $28 In stock
10 mg $98 In stock
25 mg $158 In stock
50 mg $268 In stock
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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

XCT790 (XCT-790) is a potent and selective ERRα inverse agonist with IC50 of 300-500 nM in transient transfection assays.
XCT790 shows no significant antagonist activity on related nuclear receptors (ERRγ or ERα, LXRα, LXRβ, FXR, PPARα, PPARδ, PPARγ, Nurr1, RARα, RORα, and RXRα) at 10 uM.
XCT790 inhibits PGC-1α regulation of ERRα and ERRα target gene expression.
XCT790 inhibits proliferation in cellular models of breast cancer.

Physicochemical Properties

M.Wt 596.4249
Formula C23H13F9N4O3S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: 21 mg/mL

Chemical Name/SMILES

2-Propenamide, 3-[4-[[2,4-bis(trifluoromethyl)phenyl]methoxy]-3-methoxyphenyl]-2-cyano-N-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]-

References

1. Willy PJ, et al. Proc Natl Acad Sci U S A. 2004 Jun 15;101(24):8912-7.

2. Busch BB, et al. J Med Chem. 2004 Nov 4;47(23):5593-6.

3. Lanvin O, et al. J Biol Chem. 2007 Sep 28;282(39):28328-34.

4. Chang CY, et al. Cancer Cell. 2011 Oct 18;20(4):500-10.

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