Puerarin

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Chemical Structure| 3681-99-0 同义名 : Kakonein; NPI 031G
CAS号 : 3681-99-0
货号 : A228947
分子式 : C21H20O9
纯度 : 97%
分子量 : 416.38
MDL号 : MFCD00063399
存储条件:

Pure form Inert atmosphere, 2-8°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 50 mg/mL(120.08 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

动物实验配方:
生物活性
描述 Puerarin is the major bioactive ingredient derived from the root of the Pueraria lobata .The neuroprotective effect of puerarin against Aβ‐induced neurotoxicity is related to suppression of apoptosis. Puerarin had a cerebral vasodilatory effect on rat basilar artery rings precontracted with U46619 (100 nm), which brought out 50% inhibition (IC50) of 304 ± 49 µm. Additionally, puerarin (10–160 µm) decreased NO production in rat aortic cells in a concentration‐dependent manner.Puerarin enhanced the mRNA expression of osteoprotegerin and alkaline phosphotase (ALP), whereas it impeded the mRNA expression of receptor activator of NF‐κB ligand in rat osteoblast‐like UMR106 cells[3].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.40mL

0.48mL

0.24mL

12.01mL

2.40mL

1.20mL

24.02mL

4.80mL

2.40mL

参考文献

[1]Yan LP, Chan SW, et al. Puerarin decreases serum total cholesterol and enhances thoracic aorta endothelial nitric oxide synthase expression in diet-induced hypercholesterolemic rats. Life Sci. 2006 Jun 20;79(4):324-30.

[2]Overstreet DH, Kralic JE, et al. NPI-031G (puerarin) reduces anxiogenic effects of alcohol withdrawal or benzodiazepine inverse or 5-HT2C agonists. Pharmacol Biochem Behav. 2003 Jun;75(3):619-25.

[3]Zhou YX, Zhang H, Peng C. Puerarin: a review of pharmacological effects. Phytother Res. 2014 Jul;28(7):961-75. doi: 10.1002/ptr.5083. Epub 2013 Dec 13. PMID: 24339367.