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CAS:480-19-3 Isorhamnetin 异鼠李素
发布时间:2024-04-01     作者:kx   分享到:

中文名 异鼠李素

英文名 isorhamnetin

中文别名 3,5,7-三羟基-2-(4-羟基-3-甲氧基苯基)苯并吡喃-4-酮

密度 1.6±0.1 g/cm3

沸点 599.4±50.0 °C at 760 mmHg

熔点 307°C

分子式 C16H12O7

分子量 316.262

闪点 227.8±23.6 °C

精确质量 316.058289

PSA 120.36000

LogP 1.76

外观性状 固体;Light yellow to Amber to Dark green powder to crystal

蒸汽压 0.0±1.8 mmHg at 25°C

折射率 1.741

储存条件 密封储存,储存于阴凉、干燥的库房。

稳定性 常温常压下稳定,避免与强氧化剂接触。

"Isorhamnetin on experimental IBD via PXR-mediated up-regulation of xenobiotic metabolism and down-regulation of NF-κB signaling.

Isorhamnetin is efficacious in protecting hepatocytes against oxidative stress by Nrf2 activation and in inducing the expressions of its downstream genes.

Isorhamnetin may contribute to blockade of the host-destructive processes mediated by IL-6 and could be a highly efficient modulator of the host response in the treatment of inflammatory periodontal disease. 

Isorhamnetin has anti-tumor activity, has cytotoxic effect on BEL-7402 cells  with IC50 equal to 74.4±1.13 ug/ml after treatment with isorhamnetin for 72 h. 

Isorhamnetin and quercetin prevent angiotensin II (AngII)-induced endothelial dysfunction by inhibiting the overexpression of p47(phox) and the subsequent increases O2-production, resulting in increased nitric oxide bioavailability.

Isorhamnetin, kaempferol, and quercetin preferentially inhibit the in vitro catalytic activity of human CYP1B1.

Isorhamnetin has anti-adipogenic effects in mouse 3T3-L1 cells, it inhibits the adipogenic differentiation of hAMSCs and that its mechanisms are mediated by the stabilization of β-catenin.

8. Isorhamnetin inhibits the H(2)O(2)-induced activation of the intrinsic apoptotic pathway via ROS scavenging and ERK inactivation, thus, it is a promising reagent for the treatment of ROS-induced cardiomyopathy."

CAS:480-19-3  Isorhamnetin	异鼠李素

包装:100mg,500mg,1g,10g,100g以及kg级别等公斤级大包装

纯度:99%

配送:惯例下常温**

包装:袋装

厂家:西安齐岳生物科技有限公司

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