SML1510

SR9238

≥98% (HPLC)

• 別名: Ethyl 5-((2,4,6-trimethyl-N-((3′-(methylsulfonyl)-[1,1′-biphenyl]-4-yl)methyl)phenylsulfonamido)methyl)furan-2-carboxylate
• 実験式（ヒル表記法）: C₃₁H₃₃NO₇S₂
• CAS番号: 1416153-62-2
• 分子量: 595.73
• UNSPSCコード: 12352200
• NACRES: NA.77

特性

• 品質水準: 100
• アッセイ: ≥98% (HPLC)
• フォーム: powder
• 色: white to beige
• 溶解性: DMSO: 5 mg/mL, clear (warmed)
• 保管温度: 2-8°C
• SMILES記法: [S](=O)(=O)(N(Cc4[o]c(cc4)C(=O)OCC)Cc2ccc(cc2)c3cc(ccc3)[S](=O)(=O)C)c1c(cc(cc1C)C)C
• InChI: 1S/C31H33NO7S2/c1-6-38-31(33)29-15-14-27(39-29)20-32(41(36,37)30-22(3)16-21(2)17-23(30)4)19-24-10-12-25(13-11-24)26-8-7-9-28(18-26)40(5,34)35/h7-18H,6,19-20H2,1-5H3
• InChI Key: HDZWHJYZJWLTAG-UHFFFAOYSA-N

詳細

生物化学的／生理学的作用

SR9238 is liver selective LXR inverse agonist with high potency for both LXRα and LXRβ with an IC₅₀ of 214 nM for LXRα and 43 nM for LXRβ. Metabolic syndrome is often accompanied by liver problems, such as fatty liver (nonalcoholic hepatosteatosis), associated with increased lipogenesis. Liver X receptors α and β (LXRα and LXRβ) are known to induce lipogenesis by increasing transcription of lipogenic enzyme genes, so it was hoped LXR antagonists might be of use in fatty liver. In a mouse model of nonalcoholic hepatosteatosis, SR9238 reduced the expression of lipogenic genes, and suppressed hepatic lipogenesis, inflammation and hepatic lipid accumulation. It was also effective in reduction of hepatic fibrosis in another study. Additionally in diet induced obese mice, SR9238 suppressed plasma cholesterol levels.

SR9238 is liver selective LXR inverse agonist with high potency for both LXRα and LXRβ.

安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable