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Ginsenoside F2

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Product Overview
Product Name Ginsenoside F2
CAS62025-49-4
FormulaC42H72O13
MW785.01
Appearance 白色粉末
Boiling point871.5±65.0 °C | Condition: Press: 760 Torr
PKa12.91±0.70 | Condition: Most Acidic Temp: 25 °C
Product details

WKQ-0000461

中文名称:人参皂苷F2

中文别称:人参皂甙F2/20(s)人参皂苷F2/20(S)-人参皂苷F2/20-(S)-人参皂苷F2

英文名称:Ginsenoside F2

英文别名:(3β,12β)-12-Hydroxydammar-24-ene-3,20-diyl bis-β-D-glucopyranoside;Dammarane, β-D-glucopyranoside deriv.;3-O-Glucosylginsenoside C K;Ginsenoside F2;

分子式:C42H72O13

分子量:785.01

CAS号:62025-49-4

纯度:HPLC≥98%

沸点:871.5±65.0 °C | Condition: Press: 760 Torr

密度:1.30±0.1 g/cm3 | Condition: Temp: 20 °C Press: 760 Torr

酸系度数:12.91±0.70 | Condition: Most Acidic Temp: 25 °C

储存条件:-20℃,干燥、避光、密封

规格:5mg10mg20mg50mg100mg500mg1g2g等应客户需求包装

供应单位:四川省维克奇生物科技有限公司

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Related literature
Effect of steam-processing of the Panax ginseng root on its inducible activity on granulocyte-colony stimulating factor secretion in intestinal epithelial cells in vitro
Source:SCI:JOURNAL OF ETHNOPHARMACOLOGY Author:Kewen Ding Notes:影响因子:4.36
Reference description

Isomaltose was purchased from Tokyo Chemical Industry (Tokyo, Japan). Protopanaxatriol and protopanaxadiol were obtained from ChromaDex (Irvine, CA). Compound K, ginsenosides Rh1, Rd, F1, F2, Rg3, and Rh2 were obtained from Sichuan Weikeqi Biological Technology (Chengdu, Sichuam, China). Lectin from Phytolacca americana (pokeweed mitogen, PWM), dextran standards certified according to Deutsches Institut für Normung (molecular weight; 668 kDa), Dulbecco’s modified Eagle’s medium

Structure–inhibition relationship of ginsenosides towards UDP-glucuronosyltransferases (UGTs)
Source:SCI:TOXICOLOGY AND APPLIED PHARMACOLOGY Author:Zhong-Ze Fang Notes:影响因子:3.975
Reference description

Recombinant human UGT isoforms (UGT1A1, UGT1A6, UGT1A7, UGT1A8, UGT1A9, UGT1A10, UGT2B7, UGT2B15) expressed in baculovirus-infected insect cells were obtained from BD Gentest Corp. (Woburn, MA, USA). Ginsenosides Rb1, Rb2, Rc, Rd, Rg3, Rh2, C-K, ppd, ppt, Re, Rg1, Rh1, F1, and F2 were purchased from Sichuan Weikeqi Biotechnology Company (Chengdu, Sichuan, China). The purity of these compounds was above 95%. All other reagents were of HPLC grade or of the highest grade commercially available.

Effect of ninjin’yoeito and ginseng extracts on oxaliplatin-induced neuropathies in mice
Source:SCI:Journal of Natural Medicines Author:Suzuki, Toshiaki Notes:影响因子:1.982
Reference description

The water layer was further partitioned with water-saturated BuOH three times, yielding the BuOH and water fractions (0.20 and 4.4 g, respectively). Ginsenosides F1, F2, Rd, Rg3, Rh1, Rh2, protopanaxadiol, and protopanaxatriol were obtained from Sichuan Weikeqi Biological Technology (Chengdu, Sichuan, China); ginsenosides Rg1 and Rb1 were obtained from Wako Pure Chemical Industries (Osaka, Japan)

Ginsenosides, ingredients of the root of Panax ginseng, are not substrates but inhibitors of sodium-glucose transporter 1
Source:SCI:Journal of Natural Medicines Author:Gao, Shengli Notes:影响因子:1.67
Reference description

Ginsenosides Rg1 and Rb1 were obtained from Wako Pure Reagents (Osaka). Compound K was obtained from ChromaDex (Irvine, CA, USA). Ginsenosides F1, F2, Rd, Rg3, Rh1, Rh2, protopanaxadiol and protopanaxatriol were obtained from Sichuan Weikeqi Biological Technology (Chengdu, Sichuam, China). Chemical structures of ginsenosides used in the present study are shown in Fig. 1.

Ninjin’yoeito and ginseng extract prevent oxaliplatin-induced neurodegeneration in PC12 cells
Source:SCI:Journal of Natural Medicines Author:Suzuki, Toshiaki Notes:影响因子:1.593
Reference description

Ginsenosides Rg1 and Rb1 were obtained from Wako Pure Reagents (Osaka, Japan). Compound K was obtained from ChromaDex (Irvine, CA). Ginsenosides Rd, Rh1, F1, and F2 were obtained from Sichuan Weikeqi Biological Technology (Chengdu, Sichuam, China). The chemical structures of these ginsenosides are shown in Fig. 2.

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