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Protopanaxatriol

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Product Overview
Product Name Protopanaxatriol
CAS34080-08-5
FormulaC30H52O4
MW476.73
Appearance 白色结晶粉末
Melting point242-244 °C
Boiling point590.0±50.0 °C | Condition: Press: 760 Torr
PKa14.73±0.70 | Condition: Most Acidic Temp: 25 °C
Product details

WKQ-0000703

中文名称:原人参三醇

中文别名:20(S)-原人参三醇;(S型)原人参三醇;S-原人参三醇;(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-((S)-2-羟基-6-甲基庚-5-烯-2-基)-4,4,8,10,14-五甲基十六氢-1H-环戊[a]菲-3,6,12-三醇

英文名称:Protopanaxatriol

英文别名: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号:34080-08-5

纯度:HPLC≥98%

熔点:242-244 °C

沸点:590.0±50.0 °C | Condition: Press: 760 Torr

密度:1.079±0.06 g/cm3 | Condition: Temp: 20 °C Press: 760 Torr

酸系度数:14.73±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

供应电话:028-81700200/4008005713

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Related literature
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.

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.

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