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Ginsenoside F1/人参皂苷 F1 {[allProObj[0].p_purity_real_show]}

货号:A194392 同义名: 20(S)-Ginsenoside F1; GF1

Ginsenoside F1, a metabolite of ginsenoside Rg1 isolated and purified from the roots of Panax ginseng C.A.Mey., is reported to be antiaging and antioxidative, and to have beneficial effects on skin.

Ginsenoside F1/人参皂苷 F1 化学结构 CAS号:53963-43-2
Ginsenoside F1/人参皂苷 F1 化学结构
CAS号:53963-43-2
Ginsenoside F1/人参皂苷 F1 3D分子结构
CAS号:53963-43-2
Ginsenoside F1/人参皂苷 F1 化学结构 CAS号:53963-43-2
Ginsenoside F1/人参皂苷 F1 3D分子结构 CAS号:53963-43-2
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Ginsenoside F1/人参皂苷 F1 纯度/质量文件 产品仅供科研

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Ginsenoside F1/人参皂苷 F1 生物活性

描述 Ginsenoside F1, a pharmaceutical component of ginseng, is known to have antiaging, antioxidant, anticancer, and keratinocyte protective effects[3]. Ginsenoside F1 (GF1) has been shown to flaunt anticancer, anti-aging, and antioxidant effects and has demonstrated competitive inhibition of CYP3A4 activity and weaker inhibition of CYP2D6 activity. The cell viabilities are 68% at the highest concentration of ginsenoside F1 (200 μM) in MTT assays[4]. ApoE-/- mice were fed a high fat diet and orally treated with GF1 (50 mg/kg/day) for 8 weeks. The treatment with GF1 induced a remarkable reduction in the atherosclerotic lesion area, LOX-1, TLR4 expression and decreased the MPO distribution. GF1 treatment greatly increased ox-LDL-injured endothelial cell viability, ameliorated LOX-1, TLR4 expression levels and reduced monocytes adhesion. Protein microarray demonstrated that GF1 significantly inhibited G-CSF, ICAM-1, MIP-1δ, IL-1α, IL-15, IL-16 levels[5].

Ginsenoside F1/人参皂苷 F1 参考文献

[1]Kim JH, Baek EJ, et al. Ginsenoside F1 attenuates hyperpigmentation in B16F10 melanoma cells by inducing dendrite retraction and activating Rho signalling. Exp Dermatol. 2015 Feb;24(2):150-2.

[2]Lee EH, Cho SY, et al. Ginsenoside F1 protects human HaCaT keratinocytes from ultraviolet-B-induced apoptosis by maintaining constant levels of Bcl-2. J Invest Dermatol. 2003 Sep;121(3):607-13.

[3]Wang Y, Choi KD, Yu H, Jin F, Im WT. Production of ginsenoside F1 using commercial enzyme Cellulase KN. J Ginseng Res. 2016;40(2):121-126

[4]Wang DD, Jin Y, Wang C, et al. Rare ginsenoside Ia synthesized from F1 by cloning and overexpression of the UDP-glycosyltransferase gene from Bacillus subtilis: synthesis, characterization, and in vitro melanogenesis inhibition activity in BL6B16 cells. J Ginseng Res. 2018;42(1):42-49

[5]Qin M, Luo Y, Lu S, et al. Ginsenoside F1 Ameliorates Endothelial Cell Inflammatory Injury and Prevents Atherosclerosis in Mice through A20-Mediated Suppression of NF-kB Signaling. Front Pharmacol. 2017;8:953. Published 2017 Dec 22

Ginsenoside F1/人参皂苷 F1 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.57mL

0.31mL

0.16mL

7.83mL

1.57mL

0.78mL

15.65mL

3.13mL

1.57mL

Ginsenoside F1/人参皂苷 F1 技术信息

CAS号53963-43-2
分子式C36H62O9
分子量 638.87
SMILES Code O[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)[C@@H]1O[C@](CC/C=C(C)/C)(C)[C@@H]2[C@]([C@H](O)C3)([H])[C@](CC2)(C)[C@]4([C@@]3([H])[C@](CC5)(C)[C@@](C(C)(C)[C@H]5O)([H])[C@@H](O)C4)C
MDL No. MFCD06410947
别名 20(S)-Ginsenoside F1; GF1; Panaxoside A Progenin
运输蓝冰
InChI Key XNGXWSFSJIQMNC-FIYORUNESA-N
Pubchem ID 9809542
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: 105 mg/mL(164.35 mM),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
方案一
方案二
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