| 英文名稱(chēng) | Ginsenoside F2 |
|---|---|
| 中文名稱(chēng) | 人參皂苷F2/人參皂甙F2/20(s)人參皂苷F2/20(S)-人參皂苷F2/20-(S)-人參皂苷F2 |
| CAS號 | 62025-49-4 |
| 分子式 | C42H72O13 |
| 分子量 | 785.01 |
| 外觀(guān) | 白色粉末 |
| 沸點(diǎn) | 871.5±65.0 °C | Condition: Press: 760 Torr |
| 酸度系數pKa | 12.91±0.70 | Condition: Most Acidic Temp: 25 °C |
WKQ-0000461
中文名稱(chēng)：人參皂苷F2
中文別稱(chēng)：人參皂甙F2/20(s)人參皂苷F2/20(S)-人參皂苷F2/20-(S)-人參皂苷F2
英文名稱(chēng)：Ginsenoside F2
英文別名：(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號：62025-49-4
純度：HPLC≥98%
沸點(diǎn)：871.5±65.0 °C | Condition: Press: 760 Torr
密度：1.30±0.1 g/cm3 | Condition: Temp: 20 °C Press: 760 Torr
酸系度數：12.91±0.70 | Condition: Most Acidic Temp: 25 °C
儲存條件：-20℃，干燥、避光、密封
規格：5mg10mg20mg50mg100mg500mg1g2g等應客戶(hù)需求包裝
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| 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 | ||
| 來(lái)源：SCI：JOURNAL OF ETHNOPHARMACOLOGY | 作者：Kewen Ding | 備注：影響因子：4.36 |
| 引用描述 | ||
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) | ||
| 來(lái)源：SCI：TOXICOLOGY AND APPLIED PHARMACOLOGY | 作者：Zhong-Ze Fang | 備注：影響因子：3.975 |
| 引用描述 | ||
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 | ||
| 來(lái)源：SCI：Journal of Natural Medicines | 作者：Suzuki, Toshiaki | 備注：影響因子：1.982 |
| 引用描述 | ||
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 | ||
| 來(lái)源：SCI：Journal of Natural Medicines | 作者：Gao, Shengli | 備注：影響因子：1.67 |
| 引用描述 | ||
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 | ||
| 來(lái)源：SCI：Journal of Natural Medicines | 作者：Suzuki, Toshiaki | 備注：影響因子：1.593 |
| 引用描述 | ||
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. | ||
