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SR1001

Chemical Structure : SR1001

CAS No.: 1335106-03-0

SR1001 (SR-1001)

Catalog No.: PC-43525Not For Human Use, Lab Use Only.

SR1001 is a higly potent, specific, inverse agonist of both RORα and RORγt with binding Ki of 172 and 111 nM, does not binds RORβ and devoid of LXR activity.

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Biological Activity

SR1001 is a higly potent, specific, inverse agonist of both RORα and RORγt with binding Ki of 172 and 111 nM, does not binds RORβ and devoid of LXR activity.
SR1001 inhibits the development of murine T(H)17 cells by inhibition of IL-17A gene expression and protein production, also inhibits the expression of cytokines when added to differentiated murine or human T(H)17 cells.
SR1001 modulates the expression of ROR target genes by decreasing coactivator recruitment (SRC2).
SR1001 effectively suppresses the clinical severity of autoimmune disease in mice.

Physicochemical Properties

M.Wt 477.40
Formula C15H13F6N3O4S2
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: ≥ 39 mg/mL

Chemical Name/SMILES

Acetamide, N-[4-methyl-5-[[[4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl]amino]sulfonyl]-2-thiazolyl]-

References

1. Solt LA, et al. Nature. 2011 Apr 28;472(7344):491-4.

2. Solt LA, et al. Endocrinology. 2015 Mar;156(3):869-81.

3. Beurel E, et al. Biol Psychiatry. 2013 Apr 1;73(7):622-30.

4. Ding Q, et al. BMC Immunol. 2015 May 29;16:32.

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