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。
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+ |
规格 | 价格 | 会员价 | 库存 | 数量 | |||
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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. |
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. |
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 |
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 |
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 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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