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Merck
CN

G5048

Sigma-Aldrich

替普瑞酮(异构体混合物)

别名:

6,10,14,18-四甲基-5,9,13,17-十九碳四烯-2-酮,(5E,9E,13E)和(5Z,9E,13E)异构体混合物, GGA, UNII-S8S8451A4O, 戊四烯酮, 替普瑞酮

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关于此项目

经验公式(希尔记法):
C23H38O
化学文摘社编号:
分子量:
330.55
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
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方案

≥98% (HPLC)

质量水平

表单

oil

储存条件

protect from light

颜色

clear

溶解性

DMSO: >5 mg/mL

储存温度

−20°C

SMILES字符串

C\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CCC(C)=O

InChI

1S/C23H38O/c1-19(2)11-7-12-20(3)13-8-14-21(4)15-9-16-22(5)17-10-18-23(6)24/h11,13,15,17H,7-10,12,14,16,18H2,1-6H3/b20-13+,21-15+,22-17+

InChI key

HUCXKZBETONXFO-NJFMWZAGSA-N

应用

替普瑞酮已被用作热休克蛋白70 (HSP70)的诱导剂,以分析对局部缺血/再灌注(I/R)的保护作用。

生化/生理作用

替普瑞酮可以诱导 HSP70、HSPB8 和 HSPB1 的表达。
替普瑞酮可以诱导 HSP70、HSPB8 和 HSPB1 的表达。诱导 HSP70 表达可预防各种疾病的发展,例如炎症性肠病、缺氧/缺血性脑损伤,以及脊髓和延髓性肌萎缩(细胞保护和抗炎作用)。 报告表明,GGA 可通过诱导 HSP70 表达来预防 NSAID 诱导的胃和肠损伤。其他研究表明,GGA 可以诱导 HSPB5 R120G TG 小鼠中 HSPB8 和 HSPB1 的表达,并减少淀粉样蛋白低聚物以及不溶性聚集体的形成。
替普瑞酮是一种无环聚异戊二烯类化合物,研究表明对再灌注损伤、炎症和器官移植具有保护作用。它是一种抗溃疡剂,参与保护胃黏膜。

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Fu-Cheng Luo et al.
Free radical biology & medicine, 52(7), 1218-1227 (2012-01-31)
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Deli Zhang et al.
Journal of molecular and cellular cardiology, 51(3), 381-389 (2011-07-13)
The most common clinical tachycardia, Atrial Fibrillation (AF), is a progressive disease, caused by cardiomyocyte remodeling, which finally results in contractile dysfunction and AF persistence. Recently, we identified a protective role of heat shock proteins (HSPs), especially the small HSPB1
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The mechanisms underlying mitochondrial impairment in the failing heart are not yet clear. In a previous study, we found that the levels of small heat shock proteins (HSP) such as mitochondrial HSPB1 and HSPB8 in the failing heart following myocardial

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