Dehydroglyasperin C,99.0%

产品编号:Bellancom-N7335| CAS NO:199331-35-6| 分子式:C21H22O5| 分子量:354.40

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货号 包装 价格 库存与货期 购买量 操作
Bellancom-N7335
5250.00 杭州 北京(现货)
Bellancom-N7335
14350.00 杭州 北京(现货)

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Dehydroglyasperin C

产品介绍 Dehydroglyasperin C 是一种异黄酮,是一种有效的 NAD(P)H:氧化醌还原酶 (NQO1) 和 phase 2 酶诱导剂。Dehydroglyasperin C 具有抗氧化、神经保护、癌症化学预防和抗炎活性。
生物活性

Dehydroglyasperin C, a isoflavone, is a potent NAD(P)H:oxidoquinone reductase (NQO1) and phase 2 enzyme inducer. Dehydroglyasperin C has antioxidant, neuroprotective, cancer chemopreventive, and anti-inflammatory activities.

体外研究

Dehydroglyasperin C (0.1-1 μM; 24 h) blocks the PDGF-induced progression through the G0/G1 to S phase of the cell cycle, and down-regulates the expression of CDK; 2, cyclin E, CDK4 and cyclin D1. Dehydroglyasperin C significantly attenuates PDGF-stimulated phosphorylation of PDGF receptor-β, phospholipase C-γ1, AKT and extracellular-regulated kinase 1/2, and DGC inhibits cell migration and the dissociation of actin filaments by PDGF.
Dehydroglyasperin C (0.1-1 μM; 24 h) treatment significantly decreases PDGF-induced cell number and DNA synthesis in a dose-dependent manner without any cytotoxicity in human aortic smooth muscle cells (HASMC).

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cycle Analysis

Cell Line: Human aortic smooth muscle cells (HASMC)
Concentration: 0.1 μM, 0.5 μM, 1 μM
Incubation Time: 24 hours
Result: Blocked the PDGF-induced progression through the G0/G1 to S phase of the cell cycle.

Western Blot Analysis

Cell Line: Human aortic smooth muscle cells (HASMC)
Concentration: 0.1 μM, 0.5 μM, 1 μM
Incubation Time: 24 hours
Result: Down-regulated the expression of CDK; 2, cyclin E, CDK4 and cyclin D1.
体内研究
(In Vivo)

In ICR mice, Dehydroglyasperin C (5 mg/kg; once) combined with CCl4 shows reduced lipid droplet formation in liver tissue, as assessed by histological examination. Further, DGC demonstrated a slight protective effect against centrilobular injury caused by CCl4 injection, perhaps through suppression of CYP2E1 expression[4].

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

In ICR mice, Dehydroglyasperin C (5 mg/kg; once) combined with CCl4 shows reduced lipid droplet formation in liver tissue, as assessed by histological examination. Further, DGC demonstrated a slight protective effect against centrilobular injury caused by CCl4 injection, perhaps through suppression of CYP2E1 expression[4].

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

In ICR mice, Dehydroglyasperin C (5 mg/kg; once) combined with CCl4 shows reduced lipid droplet formation in liver tissue, as assessed by histological examination. Further, DGC demonstrated a slight protective effect against centrilobular injury caused by CCl4 injection, perhaps through suppression of CYP2E1 expression[4].

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

性状Solid
溶解性数据
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

参考文献

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