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GSK5182

Cat. No. M20777

All AbMole products are for research use only, cannot be used for human consumption.

GSK5182 Structure
Size Price Availability Quantity
5mg USD 128  USD128 In stock
10mg USD 185  USD185 In stock
25mg USD 330  USD330 In stock
50mg USD 500  USD500 In stock
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Quality Control & Documentation
Biological Activity

GSK5182 is a 4-Hydroxytamoxifen analog and a highly potent, selective, orally active estrogen-related receptor gamma (ERRγ) inverse agonist with an IC50 value of 79 nM.GSK5182 does not interact with other nuclear receptors, including ERRα and ERα. In addition, GSK5182 inhibits proinflammatory cytokine-induced catabolic factors and increases ROS production in liver cancer cells. cytokine-induced catabolic factors and increased ROS production in hepatocellular carcinoma cells.

Chemical Information
Molecular Weight 417.54
Formula C27H31NO3
CAS Number 877387-37-6
Solubility (25°C) DMSO 84 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Soon-Young Na, et al. Int J Mol Sci. An Inverse Agonist GSK5182 Increases Protein Stability of the Orphan Nuclear Receptor ERRγ via Inhibition of Ubiquitination

[2] Hyun-Ju Kim, et al. BMB Rep. The estrogen-related receptor γ modulator, GSK5182, inhibits osteoclast differentiation and accelerates osteoclast apoptosis

[3] Yunhui Min, et al. Pharmaceuticals (Basel). GSK5182, 4-Hydroxytamoxifen Analog, a New Potential Therapeutic Drug for Osteoarthritis

[4] Mathieu Vernier, et al. Genes Dev. Estrogen-related receptors are targetable ROS sensors

[5] Jinhyuk Choi, et al. Gastroenterology. Estrogen-Related Receptor γ Maintains Pancreatic Acinar Cell Function and Identity by Regulating Cellular Metabolism

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Keywords: GSK5182 supplier, Estrogen Receptor, inhibitors, activators

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