SR 9238

Discontinued Product

5854 has been discontinued.

View all LXR-like Receptors products.
Description: Potent and selective LXR inverse agonist
Chemical Name: Ethyl 5-[[[[3'-(Methylsulfonyl)[1,1'-biphenyl]-4-yl]methyl][(2,4,6-trimethylphenyl)sulfonyl]amino]methyl]-2-furancarboxylate
Purity: ≥98% (HPLC)
Datasheet
Citations (2)
Reviews

Biological Activity for SR 9238

SR 9238 is a potent and selective LXR inverse agonist (IC50 values are 43 and 214 nM for LXRβ and LXRα, respectively). Selectively inhibits liver LXR over peripheral LXR. Exhibits selectivity for LXR over a panel of 20 other nuclear receptors, including FXR. Reduces hepatic steatosis in obese mice.

Compound Libraries for SR 9238

SR 9238 is also offered as part of the Tocriscreen 2.0 Max. Find out more about compound libraries available from Tocris.

Technical Data for SR 9238

M. Wt 595.73
Formula C31H33NO7S2
Storage Store at +4°C
Purity ≥98% (HPLC)
CAS Number 1416153-62-2
PubChem ID 71478195
InChI Key HDZWHJYZJWLTAG-UHFFFAOYSA-N
Smiles CCOC(C1=CC=C(O1)CN(S(=O)(C2=C(C=C(C=C2C)C)C)=O)CC3=CC=C(C4=CC(S(C)(=O)=O)=CC=C4)C=C3)=O

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

Tocris products are intended for laboratory research use only, unless stated otherwise.

References for SR 9238

References are publications that support the biological activity of the product.

Griffett et al (2013) A liver-selective LXR inverse agonist that suppresses hepatic steatosis. ACS Chem.Biol. 8 559 PMID: 23237488

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Keywords: SR 9238, SR 9238 supplier, SR9238, potent, selective, LXR, inverse, agonist, liver, obesity, receptors, LXR-like, Receptors, 5854, Tocris Bioscience

2 Citations for SR 9238

Citations are publications that use Tocris products. Selected citations for SR 9238 include:

Bruschi et al (2019) PNPLA3 I148M Variant Impairs Liver X Receptor Signaling and Cholesterol Homeostasis in Human Hepatic Stellate Cells. Hepatol Commun 3 1191 PMID: 31497741

Ning et al (2023) Nuclear receptor modulators inhibit osteosarcoma cell proliferation and tumour growth by regulating the mTOR signaling pathway. Cell Death Dis 14 51 PMID: 36681687


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