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Formula | C15H13F6N3O4S2 |
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Molecular Weight | 477.40 | CAS No. | 1335106-03-0 | |
Solubility (25°C)* | In vitro | DMSO | 95 mg/mL (198.99 mM) | |
Ethanol | 95 mg/mL (198.99 mM) | |||
Water | Insoluble | |||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
Description | SR1001 is a RORα inverse agonist with Ki values of 172 nM and 111 nM for RORα and RORγ respectively. | ||||
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Targets |
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In vitro | SR1001 binds specifically to the ligand binding domains (LBDs) of RORα and RORγt inducing a conformational change within the LBD that encompasses repositioning of helix 12 leading to diminished affinity for coactivators and increased affinity for corepressors resulting in suppression of the receptors transcriptional activity[2]. |
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In vivo | SR1001 suppresses the immune response, including TH17 cells in vitro and in vivo, TH1 cells in vivo, autoantibody production, maintains insulin levels, and increases Foxp3 expression[1]. SR1001 effectively protects against pathologic neovascularization in both oxygen-induced retinopathy and another angiogenic model of very-low-density lipoprotein receptor (Vldlr)-deficient (Vldlr −/−) mice with spontaneous subretinal neovascularization[3]. |
Animal Study: |
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