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Merck
CN

A1737

Sigma-Aldrich

A922500

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About This Item

经验公式(希尔记法):
C26H24N2O4
分子量:
428.48
UNSPSC代码:
12352204
NACRES:
NA.77

生物来源

synthetic (organic)

质量水平

检测方案

>95% (HPLC)

形式

powder

分子量

Mw 428.5

溶解性

DMSO: 10 mg/mL, clear, colorless to greenish-yellow

储存温度

−20°C

InChI

1S/C26H24N2O4/c29-24(22-7-4-8-23(22)25(30)31)19-11-9-17(10-12-19)18-13-15-21(16-14-18)28-26(32)27-20-5-2-1-3-6-20/h1-3,5-6,9-16,22-23H,4,7-8H2,(H,30,31)(H2,27,28,32)/t22-,23-/m1/s1

InChI key

BOZRFEQDOFSZBV-DHIUTWEWSA-N

应用

A922500 已用于抑制上皮人乳腺癌细胞系(MDA-MB-231)、毛地黄皂苷透化的人癌细胞、人肌管和巨噬细胞中的二酰基甘油酰基转移酶(DGAT)。

生化/生理作用

二酰基甘油酰基转移酶(DGAT-1)抑制剂; IC50 7 至 24 nM
二酰基甘油酰基转移酶(DGAT)1 抑制剂 A922500 在 0.03、0.3 和 3 mg/kg 浓度下可有效降低啮齿动物的餐后血清甘油三酯水平。这些结果表明 A922500 可能有助于降低心血管疾病风险。

外形

A922500 以结晶固体形式提供。

制备说明

储备溶液可以通过将 A922500 溶解在所选溶剂中来制备。A922500 可溶于乙醇、DMSO 和二甲基甲酰胺(DMF)等有机溶剂。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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A specific lipid metabolic profile is associated with the epithelial mesenchymal transition program
Giudetti AM, et al.
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, 1864(3), 344-357 (2019)
Andrew J King et al.
European journal of pharmacology, 637(1-3), 155-161 (2010-04-14)
Postprandial serum triglyceride concentrations have recently been identified as a major, independent risk factor for future cardiovascular events. As a result, postprandial hyperlipidemia has emerged as a potential therapeutic target. The purpose of this study was two-fold. Firstly, to describe
Lipid droplets induced by secreted phospholipase A2 and unsaturated fatty acids protect breast cancer cells from nutrient and lipotoxic stress
Jarc E, et al.
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, 1863(3), 247-265 (2018)
Increased triacylglycerol-Fatty acid substrate cycling in human skeletal muscle cells exposed to eicosapentaenoic acid
Lovsletten NG, et al.
PLoS ONE, 13(11), e0208048-e0208048 (2018)
A Snake Venom-Secreted Phospholipase A2 Induces Foam Cell Formation Depending on the Activation of Factors Involved in Lipid Homeostasis
Leiguez E, et al.
Mediators of Inflammation, 2018 (2018)

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