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IRX5010

Chemical Structure : IRX5010

CAS No.: 856683-59-5

IRX5010 (IRX4647F)

Catalog No.: PC-23692Not For Human Use, Lab Use Only.

IRX5010 (IRX4647F) is a second generation, potent, highly selective RARγ agonist with EC50 of <0.1 nM in RARγ transactivation reporter assays, >1000-fold selective over RARα.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

IRX5010 (IRX4647F) is a second generation, potent, highly selective RARγ agonist with EC50 of <0.1 nM in RARγ transactivation reporter assays, >1000-fold selective over RARα.
IRX5010 demonstrates no significant inhibitory activity in vitro on EMT-6 proliferation at concentrations lower than 20-100 uM.
IRX5010 demonstrates substantial dose dependent treatment effects relative to vehicle control (59-73%) on inhibition of growth of EMT-6 syngeneic murine triple negative breast cancer in vivo.
IRX5010 induces tumor infiltrating T-lymphocytes of effector memory phenotypes, demonstrating immunity promoting effects in the tumor immune microenvironment.

Physicochemical Properties

M.Wt 395.47
Formula C24H26FNO3
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

10 mM in DMSO

Chemical Name/SMILES

3-fluoro-4-((1E,3E)-3-(hydroxyimino)-3-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)prop-1-en-1-yl)benzoic acid

References

1. Martin Sanders, et al. Cancer Res (2024) 84 (9_Supplement): PO5-24-12.

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