Sinensetin

目录号: GN10280纯度: >98.00%同义词: 5,6,7,3',4'-五甲氧基黄酮,Pedalitin permethyl ether
An anti-inflammatory flavone

Sinensetin
Cas No.: 2306-27-6
规格价格库存数量操作
20mg¥1,565.00现货
1

文献被引

本产品暂无引用记录;以下为 GlpBio 产品在 Nature / Cell / Science 等顶刊的客户引用样例
  • Nature cover
    Nature
    641, 529–536 (2025)
  • Nature cover
    Nature
    628, 630–638 (2024)
  • Nature cover
    Nature
    632, 686–694 (2024)
  • Nature cover
    Nature
    618, 1017–1023 (2023)
  • Nature cover
    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
  • Science cover
    Science
    388(6745) (2025)
  • Science cover
    Science
    387(6739) (2025)
  • Science cover
    Science
    387(6734) (2025)
  • Cell Research cover
    Cell Research
    35, 97–116 (2025)
  • Cell Research cover
    Cell Research
    34, 683–706 (2024)
  • Cell Research cover
    Cell Research
    33, 273–287 (2023)
  • Cell Research cover
    Cell Research
    33, 546–561 (2023)
  • Cell Research cover
    Cell Research
    33, 904–922 (2023)
  • Cell Research cover
    Cell Research
    31, 1291–1307 (2021)

产品描述 Description

Sinensetin is a selective inhibitor of α-glucosidase with IC50 value of 0.66 mg/ml [1].
Sinensetin is a family of the major polymethoxyflavones (PMFs) that mainly contained in the citrus peels. It has been reported that sinensetin has various bioactivities, including antifungal, antimutagenic, anticancer, and anti-inflammatory [2] [3].
When tested with human cytochrome P450 1A2 (CYP1A2), sinensetin treatment significantly inhibited the activity of CYP1A2 [4]. Using a method modified by Apostolidis, incubation of sinensetin solution and phosphate buffer (pH 6.9) containing α-glucosidase solution in 96-well plates at 25°C for 10 min markedly inhibitedα-glucosidase [1]. In Human umbilical vein endothelial cells, administration of sinensetin inhibited cell proliferation via inducing cell cycle arrest in the G0/G1 phase which means it has antiangiogenesis activity with low toxicity [2]. When tested with RAW 264.7 cells, sinensetin inhibited inflammatory activity through regulating κB-α expression in protein level [3]. Treated human AGS gastric cancer cells with sinensetin showed that it increased p53 and p21 expression and resulted in the inhibited proliferation and apoptosis [5].
In animal model of zebrafish, sinensetin treatment downregulated the expression of flt1, kdrl, and hras that associated with angiogenesis in mRNA level [2].
References:
[1].    Mohamed, E.A., et al., Potent alpha-glucosidase and alpha-amylase inhibitory activities of standardized 50% ethanolic extracts and sinensetin from Orthosiphon stamineus Benth as anti-diabetic mechanism. BMC Complement Altern Med, 2012. 12: p. 176.
[2].    Lam, I.K., et al., In vitro and in vivo structure and activity relationship analysis of polymethoxylated flavonoids: identifying sinensetin as a novel antiangiogenesis agent. Mol Nutr Food Res, 2012. 56(6): p. 945-56.
[3].    Shin, H.S., et al., Sinensetin attenuates LPS-induced inflammation by regulating the protein level of IkappaB-alpha. Biosci Biotechnol Biochem, 2012. 76(4): p. 847-9.
[4].    Pan, Y., et al., In vitro effect of important herbal active constituents on human cytochrome P450 1A2 (CYP1A2) activity. Phytomedicine, 2014. 21(12): p. 1645-50.
[5].    Dong, Y., et al., [Effects of sinensetin on proliferation and apoptosis of human gastric cancer AGS cells]. Zhongguo Zhong Yao Za Zhi, 2011. 36(6): p. 790-4.

产品文档 Product Documents

Purity:>98.00%

化学性质Chemical Properties

CAS 号
2306-27-6
同义词
5,6,7,3',4'-五甲氧基黄酮,Pedalitin permethyl ether
化学名
2-(3,4-dimethoxyphenyl)-5,6,7-trimethoxychromen-4-one
SMILES
COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC
分子式
C20H20O7
分子量
372.37 g/mol
溶解性
DMF: 0.5 mg/mL
保存条件
Store at 2-8°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol