Chemical Structure : IRX5010
CAS No.: 856683-59-5
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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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.
| M.Wt | 395.47 | |
| Formula | C24H26FNO3 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| 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 |
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1. Martin Sanders, et al. Cancer Res (2024) 84 (9_Supplement): PO5-24-12.

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