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Scoparone/滨蒿内酯 {[allProObj[0].p_purity_real_show]}

货号:A332142 同义名: Aesculetin dimethyl ether; 6,7-Dimethylesculetin

Scoparone是从 Artemisia scoparia 中提取的天然产物,具有抗真菌、抗心绞痛、抗氧化、免疫抑制和血管舒张作用,可防止四氯化碳引起的肝损伤,是紫外辐射诱导脂质过氧化的有效抑制剂。

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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Scoparone/滨蒿内酯 化学结构 CAS号:120-08-1
Scoparone/滨蒿内酯 化学结构
CAS号:120-08-1
Scoparone/滨蒿内酯 3D分子结构
CAS号:120-08-1
Scoparone/滨蒿内酯 化学结构 CAS号:120-08-1
Scoparone/滨蒿内酯 3D分子结构 CAS号:120-08-1
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Scoparone/滨蒿内酯 纯度/质量文件 产品仅供科研

货号:A332142 标准纯度: {[allProObj[0].p_purity_real_show]}
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Scoparone/滨蒿内酯 生物活性

描述 Scoparone, a natural product isolated and purified from the herbs of Artemisia scoparia, with antifungal, antianginal, antioxidant, immunosuppression and vasorelaxation effects, protects against carbon tetrachloride-induced liver injury, is a very efficient inhibitor of ultraviolet radiation -induced lipid peroxidation and damage, and a phytoalexin associated with resistance of citrus to Phytophthora citrophthora.

Scoparone/滨蒿内酯 细胞实验

Cell Line
Concentration Treated Time Description References
bone marrow-derived macrophages (BMDMs) bone marrow-derived macrophages (BMDMs) significantly inhibited caspase-1 cleavage, GSDMD-mediated pyroptosis, mature IL-1β secretion and the formation of ASC specks Acta Pharmacol Sin. 2023 Jun;44(6):1238-1251.
mouse macrophage J774A.1 cells mouse macrophage J774A.1 cells significantly inhibited caspase-1 cleavage, GSDMD-mediated pyroptosis, mature IL-1β secretion and the formation of ASC specks Acta Pharmacol Sin. 2023 Jun;44(6):1238-1251.
Huh7 cells Huh7 cells Scoparone significantly potentiated the activation of the BSEP promoter by CDCA, and this potentiation was enhanced in cells transfected with CYP1A2. Br J Pharmacol. 2011 Nov;164(5):1547-57.
Primary human hepatocytes Primary human hepatocytes Scoparone significantly increased CYP2B6 mRNA expression at 100 μM but had no significant effect on UGT1A1 or BSEP expression. Br J Pharmacol. 2011 Nov;164(5):1547-57.
HepG2 cells HepG2 cells Inhibited STAT3 transcriptional activity, reduced cyclin D and M67 promoter activity Exp Mol Med. 2015 Mar 6;47(3):e145.
vascular smooth muscle cells (VSMCs) vascular smooth muscle cells (VSMCs) Inhibited serum-stimulated VSMC proliferation, significantly reduced S phase cell accumulation, increased G0/G1 phase cell proportion, and decreased expression of cyclin D1, phosphorylated Rb, and survivin Exp Mol Med. 2015 Mar 6;47(3):e145.
AML12 cells AML12 cells To observe the effect of scoparone on lipotoxic injured hepatocytes. Results showed that scoparone significantly improved PA-induced lipid deposition and apoptosis in hepatocytes. Front Pharmacol. 2022 May 3;13:863756.
HepG2 cells HepG2 cells To observe the effect of scoparone on lipotoxic injured hepatocytes. Results showed that scoparone significantly improved PA-induced lipid deposition and apoptosis in hepatocytes. Front Pharmacol. 2022 May 3;13:863756.

Scoparone/滨蒿内酯 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6J mice Bacterial enteritis and septic shock models Intraperitoneal injection and intragastric administration 50 mg/kg Single dose followed by observation after 12 hours for septic shock model; continuous administration for 9 days for enteritis model Scoparone significantly improved the survival rate of mice infected with bacteria, inhibited the secretion of IL-1β and TNF-α in serum, and reduced the infiltration of inflammatory cells in the lung, colon and liver Acta Pharmacol Sin. 2023 Jun;44(6):1238-1251.
Mice Mice Intraperitoneal injection 10 mg/kg Twice, 12 hours apart Scoparone robustly activated the human BSEP promoter and significantly enhanced the expression of the endogenous mouse bsep gene. Br J Pharmacol. 2011 Nov;164(5):1547-57.
C57BL/6J mice HFD-induced NASH model Oral 25, 50, and 100 mg/kg Once daily for 8 weeks To investigate the effect of scoparone on NASH mice. Results showed that scoparone significantly improved histopathological changes of liver tissues including mitochondrial number and morphology, lipid peroxide content, hepatosteatosis and inflammation, and decreased serum lipid and transaminase levels. Front Pharmacol. 2022 May 3;13:863756.
New Zealand rabbits Hyperlipidaemic diabetic rabbit model Subcutaneous injection 5 mg/kg Once daily for 6 weeks Scoparone significantly reduced plasma lipid and lipoprotein cholesterol levels and protected against pathological alterations in vascular morphology and reactivity in hyperlipidaemic diabetic rabbits. Br J Pharmacol. 1993 Dec;110(4):1508-14
Mice Maximal electroshock-induced (MES) tonic-clonic seizure model Intraperitoneal injection 199.8 mg/kg to 320.1 mg/kg 15, 30, 60 and 120 minutes To evaluate the anticonvulsant effects of Scoparone in the mouse maximal electroshock model Int J Mol Sci. 2023 Jan 11;24(2):1395

Scoparone/滨蒿内酯 参考文献

[1]Park S, Kim JK, et al. Scoparone interferes with STAT3-induced proliferation of vascular smooth muscle cells. Exp Mol Med. 2015 Mar 6;47:e145.

[2]Lee SH, Jang HD. Scoparone attenuates RANKL-induced osteoclastic differentiation through controlling reactive oxygen species production and scavenging. Exp Cell Res. 2015 Feb 15;331(2):267-77.

Scoparone/滨蒿内酯 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.85mL

0.97mL

0.48mL

24.25mL

4.85mL

2.42mL

48.50mL

9.70mL

4.85mL

Scoparone/滨蒿内酯 技术信息

CAS号120-08-1
分子式C11H10O4
分子量 206.19
SMILES Code O=C1C=CC2=CC(OC)=C(OC)C=C2O1
MDL No. MFCD00006871
别名 Aesculetin dimethyl ether; 6,7-Dimethylesculetin; Escoparone; 6,7-Dimethoxycoumarin
运输蓝冰
InChI Key GUAFOGOEJLSQBT-UHFFFAOYSA-N
Pubchem ID 8417
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry,2-8°C

溶解方案

DMSO: 50 mg/mL(242.49 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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