推荐产品
product name
罗格列酮, ≥98% (HPLC)
品質等級
化驗
≥98% (HPLC)
形狀
powder
溶解度
DMSO: ≥10 mg/mL
起源
GlaxoSmithKline
儲存溫度
2-8°C
SMILES 字串
CN(CCOc1ccc(CC2SC(=O)NC2=O)cc1)c3ccccn3
InChI
1S/C18H19N3O3S/c1-21(16-4-2-3-9-19-16)10-11-24-14-7-5-13(6-8-14)12-15-17(22)20-18(23)25-15/h2-9,15H,10-12H2,1H3,(H,20,22,23)
InChI 密鑰
YASAKCUCGLMORW-UHFFFAOYSA-N
基因資訊
human ... PPARG(5468)
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一般說明
Rosiglitazone is a member of the thiazolidinedione family. It effectively lowers glucose levels by enhancing the response of target cells to insulin, without causing increased stimulation and release of insulin by the pancreatic beta cells. Rosiglitazone functions by activating the nuclear peroxisome proliferator-activated (PPAR) receptor gamma, which plays a key role in regulating adipogenesis, glucose metabolism, and genetic networks. It exhibits high potency as a thiazolidinedione, with a binding affinity for PPAR-gamma that is 30-fold higher than pioglitazone. Furthermore, it increases insulin-stimulated IRS-1/2 in skeletal muscle and adipose tissue, leading to the expression of the GLUT4 glucose transporter.
應用
罗格列酮已被用于：
- 脂肪细胞分化的培养基成分
- 人结肠癌细胞的细胞增殖测定
- 脂肪细胞中Bcl-2样蛋白13（Bcl2113）的表达
- 作为过氧化物酶体增殖物激活受体γ（PPARγ）的配体
生化／生理作用
罗格列酮是PPARγ的强效激动剂，对人受体的EC50为43 nM。 它是一种抗糖尿病药，作为胰岛素增敏剂，可与脂肪细胞的PPARγ受体结合并使细胞对胰岛素更敏感。
特點和優勢
该化合物是ADME Tox和基因调控研究的特色产品。发现更多 ADME Tox 和 基因调控 特色产品。想要了解有关生物活性小分子在其他研究领域应用的更多信息，请访问 sigma.com/discover-bsm。
该化合物由 GlaxoSmithKline开发。想要浏览其他由制药公司开发的化合物以及已批准物/候选药物清单， 请单击此处。
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
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