| Product Name | Protopanaxatriol |
|---|---|
| CAS | 34080-08-5 |
| Formula | C30H52O4 |
| MW | 476.73 |
| Appearance | 白色結(jié)晶粉末 |
| Melting point | 242-244 °C |
| Boiling point | 590.0±50.0 °C | Condition: Press: 760 Torr |
| PKa | 14.73±0.70 | Condition: Most Acidic Temp: 25 °C |
| Product Name | Protopanaxatriol |
|---|---|
| CAS | 34080-08-5 |
| Formula | C30H52O4 |
| MW | 476.73 |
| Appearance | 白色結(jié)晶粉末 |
| Melting point | 242-244 °C |
| Boiling point | 590.0±50.0 °C | Condition: Press: 760 Torr |
| PKa | 14.73±0.70 | Condition: Most Acidic Temp: 25 °C |
WKQ-0000703
中文名稱：原人參三醇
中文別名：20(S)-原人參三醇；(S型)原人參三醇；S-原人參三醇；(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-((S)-2-羥基-6-甲基庚-5-烯-2-基)-4,4,8,10,14-五甲基十六氫-1H-環(huán)戊[a]菲-3,6,12-三醇
英文名稱：Protopanaxatriol
英文別名：Dammar-24-ene-3β,6α,12β,20-tetrol, (20S)- (8CI);(3β,6α,12β)-Dammar-24-ene-3,6,12,20-tetrol;(20S)-Protopanaxatriol;20(S)-APPT;Panaxoside A aglycone Aφ;
分子式：C30H52O4
分子量：476.73
CAS號(hào)：34080-08-5
純度：HPLC≥98%
熔點(diǎn)：242-244 °C
沸點(diǎn)：590.0±50.0 °C | Condition: Press: 760 Torr
密度：1.079±0.06 g/cm3 | Condition: Temp: 20 °C Press: 760 Torr
酸系度數(shù)：14.73±0.70 | Condition: Most Acidic Temp: 25 °C
儲(chǔ)存條件：-20℃，干燥、避光、密封
規(guī)格：5mg10mg20mg50mg100mg500mg1g2g等應(yīng)客戶需求包裝
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供應(yīng)電話：028-81700200/4008005713
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| Effect of ninjin’yoeito and ginseng extracts on oxaliplatin-induced neuropathies in mice | ||
| Source:SCI：Journal of Natural Medicines | Author:Suzuki, Toshiaki | Notes：影響因子：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：影響因子：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. | ||
| Structure–inhibition relationship of ginsenosides towards UDP-glucuronosyltransferases (UGTs) | ||
| Source:SCI：TOXICOLOGY AND APPLIED PHARMACOLOGY | Author:Zhong-Ze Fang | Notes：影響因子：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. | ||
