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Pectolinarin/柳穿鱼叶苷 {[allProObj[0].p_purity_real_show]}

货号:A501874 同义名: 大蓟苷

Pectolinarin是一种从日本蓍草(Cirsium japonicum DC.)中分离的天然产物,具有肝保护和抗炎活性。

Pectolinarin/柳穿鱼叶苷 化学结构 CAS号:28978-02-1
Pectolinarin/柳穿鱼叶苷 化学结构
CAS号:28978-02-1
Pectolinarin/柳穿鱼叶苷 3D分子结构
CAS号:28978-02-1
Pectolinarin/柳穿鱼叶苷 化学结构 CAS号:28978-02-1
Pectolinarin/柳穿鱼叶苷 3D分子结构 CAS号:28978-02-1
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Pectolinarin/柳穿鱼叶苷 纯度/质量文件 产品仅供科研

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Pectolinarin/柳穿鱼叶苷 生物活性

描述 Pectolinarigenin, a natural product isolated and purified from the herbs of Cirsium japonicum DC., possesses hepatoprotective and anti-inflammatory activity.

Pectolinarin/柳穿鱼叶苷 细胞实验

Cell Line
Concentration Treated Time Description References
Staphylococcus aureus 0.39 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
Streptococcus sobrinus 1.4 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
Streptococcus mutans 1.2 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
Escherichia coli 0.25 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
Enterococcus faecium 0.19 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
Enterococcus faecalis 0.39 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
T24 cells 0.01–50 μg/mL 24 hours Reduced bacterial adherence Antibiotics (Basel). 2022 Apr 29;11(5):598
Porphyromonas gingivalis 9.0 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
Cutibacterium acnes 12.5 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
Pseudomonas aeruginosa 0.9 μg/mL (IC50) 24 hours Inhibited biofilm formation Antibiotics (Basel). 2022 Apr 29;11(5):598
SARS-CoV 3CLpro 37.78 µM 16 hours Inhibition of SARS-CoV 3CLpro enzymatic activity J Enzyme Inhib Med Chem. 2020 Dec;35(1):145-151
L-929 fibroblasts 20 μg/mL 2 hours Evaluate the antioxidant capacity of Pectolinarin, results showed that 20 μg/mL of Pectolinarin effectively counteracted the detrimental effects of reactive oxygen species (ROS). J Cell Mol Med. 2024 Feb;28(4):e18130
SH-SY5Y neuronal cells 1, 2.5, 5, 10 µg/mL 24 hours To investigate the protective effects of Pectolinarin against H2O2-induced oxidative stress. Results showed that Pectolinarin significantly increased cell viability and reduced ROS production and LDH release. Molecules. 2023 Aug 2;28(15):5826
EA.hy926 endothelial cells 25, 50, 100, 200 μg/mL 24, 48, 72 hours Assess the effect of Pectolinarin on endothelial cell proliferation, results showed that 50 μg/mL of Pectolinarin significantly promoted endothelial cell proliferation. J Cell Mol Med. 2024 Feb;28(4):e18130

Pectolinarin/柳穿鱼叶苷 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 female mice Ovariectomy model Oral 20 mg/kg Once daily for 8 weeks To evaluate the protective effects of Pectolinarin on ovariectomy-induced osteoporosis, results showed Pectolinarin inhibited bone resorption and promoted bone formation. Int J Mol Sci. 2023 Jan 13;24(2):1620
Mice LPS-induced acute liver and kidney injury model Intraperitoneal injection 25 mg/kg and 50 mg/kg Once daily for 3 days To evaluate the protective effect of Pectolinarin on LPS-induced acute liver and kidney injury. Results showed that Pectolinarin significantly alleviated histopathological injuries in liver and kidney and reduced serum TNF-α levels. Molecules. 2022 Dec 8;27(24):8695
Sprague Dawley (SD) rats Full-thickness skin defect model Topical administration 50 μg/mL Replenished every 3 days for 14 days Evaluate the effect of Pectolinarin hydrogel on wound healing and scar formation, results showed that 50 μg/mL of Pectolinarin hydrogel significantly promoted wound healing and minimized scar formation. J Cell Mol Med. 2024 Feb;28(4):e18130

Pectolinarin/柳穿鱼叶苷 参考文献

[1]Lim H, Son KH, et al. Anti-inflammatory activity of pectolinarigenin and pectolinarin isolated from Cirsium chanroenicum. Biol Pharm Bull. 2008 Nov;31(11):2063-7.

[2]Martinez-Vazquez M, Ramirez Apan TO, et al. A comparative study of the analgesic and anti-inflammatory activities of pectolinarin isolated from Cirsium subcoriaceum and linarin isolated from Buddleia cordata. Planta Med. 1998 Mar;64(2):134-7.

Pectolinarin/柳穿鱼叶苷 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.61mL

0.32mL

0.16mL

8.03mL

1.61mL

0.80mL

16.06mL

3.21mL

1.61mL

Pectolinarin/柳穿鱼叶苷 技术信息

CAS号28978-02-1
分子式C29H34O15
分子量 622.57
SMILES Code O=C1C=C(C2=CC=C(OC)C=C2)OC3=CC(O[C@H]4[C@@H]([C@H]([C@@H]([C@@H](CO[C@H]5[C@@H]([C@@H]([C@H]([C@H](C)O5)O)O)O)O4)O)O)O)=C(OC)C(O)=C13
MDL No. MFCD12407436
别名 大蓟苷
运输蓝冰
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: 30 mg/mL(48.19 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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