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Merck
CN

B7273

Sigma-Aldrich

苯扎贝特

≥98%, solid

别名:

2- [4- [2-(4-氯苯甲酰胺基)苄]苯氧基] -2-甲基丙酸

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About This Item

经验公式(希尔记法):
C19H20ClNO4
CAS号:
分子量:
361.82
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

方案

≥98%

表单

solid

溶解性

DMF: soluble
deionized water: insoluble
methanol: soluble

创始人

Roche

SMILES字符串

CC(C)(Oc1ccc(CCNC(=O)c2ccc(Cl)cc2)cc1)C(O)=O

InChI

1S/C19H20ClNO4/c1-19(2,18(23)24)25-16-9-3-13(4-10-16)11-12-21-17(22)14-5-7-15(20)8-6-14/h3-10H,11-12H2,1-2H3,(H,21,22)(H,23,24)

InChI key

IIBYAHWJQTYFKB-UHFFFAOYSA-N

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应用

苯扎贝特已被用于:
  • 小鼠标准饲料 (SD) 中的补充剂,用于研究其对糖尿病的影响
  • 评估其对丙型肝炎病毒 (HCV) 组装和分泌的影响
  • 评估其对斑马鱼性腺类固醇生成和精子生成的影响,也用作 HPLC 的标准

生化/生理作用

苯扎贝特具有抑制 HCV 组装和分泌的能力。它用于治疗血脂异常。
苯扎贝特是过氧化物酶体增殖物激活受体活化剂,用于PPARα、PPARδ和PPARγ。脂蛋白脂酶(LPL)激活剂。
过氧化物酶体增殖物激活受体(PPAR)是类固醇核受体超家族成员之一。苯扎贝特是过氧化物酶体增殖物激活受体活化剂,用于PPARα、PPARδ和PPARγ。脂蛋白脂酶(LPL)激活剂。
PPARgamma激动剂(包括苯扎贝特)在抑制RSV感染期间的炎症反应中具有有益作用,因此在重度RSV感染过程中可能具有临床疗效。

特点和优势

该化合物由Roche开发。要浏览其他药物开发化合物和批准的药物/候选药物列表,单击此处
这种化合物是基因调控研究的特色产品。点击此处发现更多特色基因调控产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Zhihong Ye et al.
Water research, 184, 115986-115986 (2020-07-20)
This work reports the novel application of an Fe-based 2D metal-organic framework (MOF), prepared with 2,2'-bipyridine-5,5'-dicarboxylate (bpydc) as organic linker, as highly active catalyst for heterogeneous photoelectro-Fenton (PEF) treatment of the lipid regulator bezafibrate in a model matrix and urban
Bezafibrate ameliorates diabetes via reduced steatosis and improved hepatic insulin sensitivity in diabetic TallyHo mice
Franko A, et al.
Molecular Metabolism, 6(3), 256-266 (2017)
Marc Engelen et al.
PloS one, 7(7), e41013-e41013 (2012-08-23)
X-linked adrenoleukodystrophy (X-ALD) is caused by mutations in the ABCD1 gene and is characterized by impaired beta-oxidation of very-long-chain fatty acids (VLCFA) and subsequent VLCFA accumulation in tissues. In adulthood X-ALD most commonly manifests as a gradually progressive myelopathy, (adrenomyeloneuropathy;
Magali Dumont et al.
Human molecular genetics, 21(23), 5091-5105 (2012-08-28)
Peroxisome proliferator-activated receptors (PPARs) are ligand-mediated transcription factors, which control both lipid and energy metabolism and inflammation pathways. PPARγ agonists are effective in the treatment of metabolic diseases and, more recently, neurodegenerative diseases, in which they show promising neuroprotective effects.
Akira Honda et al.
Hepatology (Baltimore, Md.), 57(5), 1931-1941 (2012-08-23)
Bezafibrate is a widely used hypolipidemic agent and is known as a ligand of the peroxisome proliferator-activated receptors (PPARs). Recently this agent has come to be recognized as a potential anticholestatic medicine for the treatment of primary biliary cirrhosis (PBC)

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