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Astragaloside I

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Chemical Structure| 84680-75-1 同义名 : Astrasieversianin IV;Cyclosieversioside B;AST-I;AS-I;AstragalosideⅠ
CAS号 : 84680-75-1
货号 : A719044
分子式 : C45H72O16
纯度 : 98%
分子量 : 869.044
MDL号 : MFCD30478908
存储条件:

粉末 Keep in dark place,Sealed in dry,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 50 mg/mL(57.53 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 Astragaloside I (As-I), one of the main active ingredients in Astragalus membranaceus, has osteogenic properties. As-I stimulated the expression of β-catenin and Runx2 in MC3T3-E1 cells. Furthermore, As-I also increased BMP-2, BGP and OPG/RANKL expression, which are also activated by Wnt/β-catenin signaling pathway. Astragaloside I stimulates osteoblast differentiation through the Wnt/β-catenin signaling pathway. Astragaloside I (10-40 μM) upregulates the express of β-catenin, Runx2, BGP and OPG, RANKL (osteogenesis marker genes) in MC3T3-E1 cells[2]. Astragaloside I (A), levistilide A (L) and calycosin (C) produced synergistic proliferation inhibition on LX-2 cells and TGF-β1-activated LX-2 cells. Administration of the ALC formula markedly decreased collagen deposition, hydroxyproline (Hyp) content and α-SMA expression levels in the liver tissues compared to the model mice. Astragaloside I, levistilide A and calycosin may be the 3 main bioactive components in DBT(Danggui Buxue Tang); their combination exerts anti-liver fibrosis effects in vitro and in vivo[3].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

1.15mL

0.23mL

0.12mL

5.75mL

1.15mL

0.58mL

11.51mL

2.30mL

1.15mL

参考文献

[1]Cheng X, Wei B, et al. Astragaloside I Stimulates Osteoblast Differentiation Through the Wnt/β-catenin Signaling Pathway. Phytother Res. 2016 Oct;30(10):1680-1688.

[2]Cheng X, Wei B, Sun L, Hu X, Liang J, Chen Y. Astragaloside I Stimulates Osteoblast Differentiation Through the Wnt/β-catenin Signaling Pathway. Phytother Res. 2016 Oct;30(10):1680-1688

[3]Guo T, Liu ZL, Zhao Q, Zhao ZM, Liu CH. A combination of astragaloside I, levistilide A and calycosin exerts anti-liver fibrosis effects in vitro and in vivo. Acta Pharmacol Sin. 2018 Sep;39(9):1483-1492