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SR 1903 Sale

目录号 : GC45567

A modulator of RORγ and LXR receptors

SR 1903 Chemical Structure

Cas No.:1414248-06-8

规格 价格 库存 购买数量
1mg
¥496.00
现货
5mg
¥1,867.00
现货
10mg
¥3,477.00
现货

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Sample solution is provided at 25 µL, 10mM.

Description

SR 1903 is a modulator of retinoic acid receptor-related orphan receptor γ (RORγ) and liver X receptor (LXR).1 It is an inverse agonist of RORγ (IC50 = ~100 nM in a cell-based reporter assay) and an agonist of LXR. It also binds to peroxisome proliferator-activated receptor γ (PPARγ; IC50 = 209 nM) but does not activate it. SR 1903 (10 μM) inhibits LPS-induced expression of triggering receptor expressed on myeloid cells 1 (TREM-1) in RAW 264.7 cells. It also inhibits LPS-induced expression of the LXR target genes IL-6 and IL-33 and increases expression of ABCG1, FASN, and SCD-1 in RAW 264.7 cells. SR 1903 (20 mg/kg twice per day) reduces severity score in a mouse model of collagen-induced arthritis. It reduces blood glucose levels in a glucose tolerance test, serum levels of total cholesterol and LDL, body weight, and fat mass in a mouse model of high-fat diet-induced obesity.

References
1. Chang, M.R., Ciesla, A., Strutzenberg, T.S., et al. Unique polypharmacology nuclear receptor modulator blocks inflammatory signaling pathways. ACS Chem. Biol. 14(5), 1051-1062 (2019).

化学性质

Cas No. 1414248-06-8 SDF
Canonical SMILES CC1=C(C2=CC=C(C(O)(C(F)(F)F)C(F)(F)F)C=C2)C=CC(CN(CC3)CCN3CC4=CC=NC=C4)=C1
分子式 C27H27F6N3O 分子量 523.5
溶解度 DMF: 20 mg/ml,DMSO: 20 mg/ml,Ethanol: 10 mg/ml 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 1.9102 mL 9.5511 mL 19.1022 mL
5 mM 0.382 mL 1.9102 mL 3.8204 mL
10 mM 0.191 mL 0.9551 mL 1.9102 mL
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