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Salvianolic acid A/丹酚酸A {[allProObj[0].p_purity_real_show]}

货号:A695449 同义名: Salvianolic Acid; Dan Phenolic Acid A

Salvianolic acid A, a natural product isolated and purified from the root of Salvia miltiorrhiza Bge. with antioxidant and protective activity, significantly improves glucose metabolism and inhibit oxidative injury as well as protect against impaired vascular responsiveness in STZ-induced diabetic rats, inhibits platelet activation via the inhibition of PI3K, and attenuates arterial thrombus formation in vivo, suggesting that it may be developed as a therapeutic agent for the prevention of thrombotic disorders. Salvianolic acid A is also a matrix metalloproteinase-9 inhibitor, can prevents cardiac remodeling in spontaneously hypertensive rats, and inhibits PDGF-BB-activated HSC proliferation, partially through apoptosis induction while exerting no direct cytotoxicity on primary hepatocytes and HSC-T6 cells under experimental concentrations.

Salvianolic acid A/丹酚酸A 化学结构 CAS号:96574-01-5
Salvianolic acid A/丹酚酸A 化学结构
CAS号:96574-01-5
Salvianolic acid A/丹酚酸A 3D分子结构
CAS号:96574-01-5
Salvianolic acid A/丹酚酸A 化学结构 CAS号:96574-01-5
Salvianolic acid A/丹酚酸A 3D分子结构 CAS号:96574-01-5
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Salvianolic acid A/丹酚酸A 纯度/质量文件 产品仅供科研

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Salvianolic acid A/丹酚酸A 生物活性

描述 Salvianolic acid A (Sal A or SAA) is a hydrophilic polyphenolic derivative isolated from Salvia miltiorrhiza Bunge as an anti-cancer and cardio-protective herbal medicine. The IC50 values were determined as 5.7 µM in the HEK293/ETAR cell line and 3.14 µM in HeLa cells, respectively[3]. in vitro, SAA enhances the activation of the Akt/GSK-3β/Nrf2 signaling pathway in H2O2-Induced HK-2 Cells. in vivo, administration of SAA significantly increased the activities of T-SOD, GPx, and CAT[4]. It also can inhibit platelet activation via the inhibition of PI3K, and attenuates arterial thrombus formation in vivo, suggesting that it may be developed as a therapeutic agent for the prevention of thrombotic disorders[5]. Salvianolic acid A is also a matrix metalloproteinase-9 inhibitor, can prevents cardiac remodeling in spontaneously hypertensive rats, and inhibits PDGF-BB-activated HSC proliferation, partially through apoptosis induction while exerting no direct cytotoxicity on primary hepatocytes and HSC-T6 cells under experimental concentrations[6].

Salvianolic acid A/丹酚酸A 参考文献

[1]Wang X, Wang C, et al. Salvianolic acid A shows selective cytotoxicity against multidrug-resistant MCF-7 breast cancer cells. Anticancer Drugs. 2015 Feb;26(2):210-23.

[2]Cai J, Chen S, et al. Salvianolic acid A reverses paclitaxel resistance in human breast cancer MCF-7 cells via targeting the expression of transgelin 2 and attenuating PI3 K/Akt pathway. Phytomedicine. 2014 Oct 15;21(12):1725-32.

[3]Zhang Q, Wang S, Yu Y, et al. Salvianolic Acid A, as a Novel ETA Receptor Antagonist, Shows Inhibitory Effects on Tumor in Vitro. Int J Mol Sci. 2016;17(8):1244. Published 2016 Aug 2.

[4]Zhang HF, Wang JH, Wang YL, et al. Salvianolic Acid A Protects the Kidney against Oxidative Stress by Activating the Akt/GSK-3β/Nrf2 Signaling Pathway and Inhibiting the NF-κB Signaling Pathway in 5/6 Nephrectomized Rats. Oxid Med Cell Longev. 2019;2019:2853534. Published 2019 Mar 18.

[5]Huang ZS, Zeng CL, Zhu LJ, Jiang L, Li N, Hu H. Salvianolic acid A inhibits platelet activation and arterial thrombosis via inhibition of phosphoinositide 3-kinase. J Thromb Haemost. 2010;8(6):1383-1393.

[6]Jiang B, Li D, Deng Y, et al. Salvianolic acid A, a novel matrix metalloproteinase-9 inhibitor, prevents cardiac remodeling in spontaneously hypertensive rats. PLoS One. 2013;8(3):e59621.

Salvianolic acid A/丹酚酸A 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.02mL

0.40mL

0.20mL

10.11mL

2.02mL

1.01mL

20.22mL

4.04mL

2.02mL

Salvianolic acid A/丹酚酸A 技术信息

CAS号96574-01-5
分子式C26H22O10
分子量 494.45
SMILES Code O=C(O)[C@H](OC(/C=C/C1=CC=C(O)C(O)=C1/C=C/C2=CC=C(O)C(O)=C2)=O)CC3=CC=C(O)C(O)=C3
MDL No. MFCD08458447
别名 Salvianolic Acid; Dan Phenolic Acid A
运输蓝冰
InChI Key YMGFTDKNIWPMGF-UCPJVGPRSA-N
Pubchem ID 5281793
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Sealed in dry, store in freezer, under -20°C

溶解方案 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
方案一
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