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首頁 > 產(chǎn)品目錄 > 對照品 > 中藥對照品 > 人參系列 > 人參皂苷Rh1/人參皂甙Rh1/S-人參皂苷Rh1/(S型)人參皂苷Rh1/20(S)-人參皂苷Rh1/(20S)-人參皂苷Rh1/(2R,3R,4S,5S,6R)-2-(((3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-二羥基-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-6-基)氧基)-6-(羥甲基)四氫-2H-吡喃-3,4,5-三醇

人參皂苷Rh1/人參皂甙Rh1/S-人參皂苷Rh1/(S型)人參皂苷Rh1/20(S)-人參皂苷Rh1/(20S)-人參皂苷Rh1/(2R,3R,4S,5S,6R)-2-(((3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-二羥基-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-6-基)氧基)-6-(羥甲基)四氫-2H-吡喃-3,4,5-三醇

Ginsenoside Rh1

產(chǎn)品編號:WKQ-0000473 CAS No.:63223-86-9 純度:HPLC≥98% 分子式:C36H62O9

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  • 相關(guān)文獻
基本信息
英文名稱 Ginsenoside Rh1
中文名稱人參皂苷Rh1/人參皂甙Rh1/S-人參皂苷Rh1/(S型)人參皂苷Rh1/20(S)-人參皂苷Rh1/(20S)-人參皂苷Rh1/(2R,3R,4S,5S,6R)-2-(((3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-二羥基-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-6-基)氧基)-6-(羥甲基)四氫-2H-吡喃-3,4,5-三醇
CAS號63223-86-9
分子式C36H62O9
分子量638.87
外觀 白色粉末
沸點755.1±60.0 °C | Condition: Press: 760 Torr
酸度系數(shù)pKa12.91±0.70 | Condition: Most Acidic Temp: 25 °C
產(chǎn)品詳情

WKQ-0000473

中文名稱:人參皂苷Rh1

中文別名:人參皂甙Rh1;S-人參皂苷Rh1;(S型)人參皂苷Rh1;20(S)-人參皂苷Rh1;(20S)-人參皂苷Rh1;(2R,3R,4S,5S,6R)-2-(((3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-3,12-二羥基-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-6-基)氧基)-6-(羥甲基)四氫-2H-吡喃-3,4,5-三醇

英文名稱:Ginsenoside Rh1

英文別名:(3β,6α,12β)-3,12,20-Trihydroxydammar-24-en-6-yl β-D-glucopyranoside;Dammarane, β-D-glucopyranoside deriv.;20(S)-Ginsenoside Rh1;Ginsenoside Rh1;Prosapogenin A2;Rh1 ginsenoside;Rh1 ginsenoside;S-Ginsenoside Rh1;Sanchinoside B2;Sanchinoside Rh1;

分子式:C36H62O9

分子量:638.87

CAS號:63223-86-9

純度:HPLC≥98%

沸點:755.1±60.0 °C | Condition: Press: 760 Torr

密度:1.23±0.1 g/cm3 | Condition: Temp: 20 °C Press: 760 Torr

酸系度數(shù):12.91±0.70 | Condition: Most Acidic Temp: 25 °C

儲存條件:-20℃,干燥、避光、密封

規(guī)格:5mg10mg20mg50mg100mg500mg1g2g等應客戶需求包裝

供應單位:四川省維克奇生物科技有限公司

供應電話:028-81700200/4008005713

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相關(guān)文獻
Steamed Panax notoginseng attenuates renal anemia in an adenine-induced mouse model of chronic kidney disease
來源:SCI:JOURNAL OF ETHNOPHARMACOLOGY 作者:Min Gao 備注:影響因子:4.36
引用描述

The reference standards of notoginsenoside R1, ginsenosides Rg1, Re, Rb1, Rc, 20(S)–Rh1, 20(R)-Rh1, Rd, Rg6, F4, Rk3, Rh4, 20(S)-Rg3, 20(R)-Rg3, Rk1, and Rg5, all with a purity ≥98%, were purchased from Sichuan Weikeqi Biological Technology Co., Ltd. (Chengdu, Sichuan, China). EPO was purchased from Chengdu Di'ao Jiuhong Pharmaceutical Factory (Chengdu, Sichuan, China). FEJ was purchased from Shandong Dong'e E'jiao Co., Ltd.

Rapid characterization and determination of isoflavones and triterpenoid saponins in Fu-Zhu-Jiang-Tang tablets using UHPLC-Q-TOF/MS and HPLC-UV
來源:SCI:Analytical Methods 作者:Yi Tao 備注:影響因子:1.915
引用描述

3′-Hydroxypuerarin, puerarin, 3′-methoxypuerarin, mirificin, daidzin and daidzein were obtained from Chengdu Purechem-standard Co. Ginsenoside Rg1, ginsenoside Rh1, ginsenoside Rd, astragaloside IV and 20(S)-ginsenoside Rg3 were purchased from Chendu Herbpurify Co. Astragalin was obtained from Sichuan Weikeqi Biotechnology Co. Linoleic acid and palmitic acid were purchased from Shanghai Ryon Biological Technology Co. HPLC-grade acetonitrile was obtained from Merck Co.

An integrated strategy of MS-network-based offline 2DLC-QTOF-MS/MS coupled with UHPLC-QTRAP®-MS/MS for the characterization and quantification of the non-polysaccharides in Sijunzi decoction
來源:SCI:ANALYTICAL AND BIOANALYTICAL CHEMISTRY 作者:Dong, Bangjian 備注:影響因子:4.157
引用描述

Liquiritin apioside, liquiritin, neoliquiritin, isoliquiritin apioside, isoliquiritin, ononin, naringin, liquiritigenin, poricoic acid A, poricoic acid B, poricoic acid C, glycyrrhetinic acid, dehydropachymic acid, pachymic acid, ginsenoside Re, ginsenoside Rg1, ginsenoside Rf, isoliquiritigenin, ginsenoside Rb1, ginsenoside Rg2, ginsenoside Rg3, ginsenoside Rg5, 20(S)-ginsenoside Rh1, notoginsenoside R1, ginsenoside Ro, ginsenoside Rc, formononetin, ginsenoside Rb2, glycyrrhizic acid, ginsenoside Rd, ginsenoside Rk1, and atractylenolide III were purchased from Chengdu DeSiTe Biological Technology Co., Ltd. (Chengdu, China) or Sichuan Weikeqi Biological Technology Co., Ltd. (Chengdu, China).

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

Steamed Panax notoginseng Attenuates Anemia in Mice With Blood Deficiency Syndrome via Regulating Hematopoietic Factors and JAK-STAT Pathway
來源:SCI:Frontiers in Pharmacology 作者:Yin Xiong, 備注:影響因子:4.225
引用描述

Qualitative and quantitative analyses of SPN were performed as previous report (Xiong et al., 2017a). In brief, notoginsenoside R1 and ginsenosides Rg1, Re, 20(R)-Rh1, Rb1, Rd, Rk3, Rh4, 20(S)-Rg3, 20(R)-Rg3 (Sichuan Weikeqi Biological Technology Co., Ltd. Sichuan, China) with purity ≧ 98% were used as standard compounds. The analysis was performed on an Agilent 1260HPLC system (Agilent Technologies) equipped with a G1311B Pump, a G4212B DAD detector, and a G1329B autosampler.

Structure–inhibition relationship of ginsenosides towards UDP-glucuronosyltransferases (UGTs)
來源: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.

Optimisation of Ethanol-Reflux Extraction of Saponins from Steamed Panax notoginseng by Response Surface Methodology and Evaluation of Hematopoiesis Effect
來源:SCI:MOLECULES 作者:Yupiao Hu 備注:影響因子:3.098
引用描述

Acetonitrile of chromatographic grade and ferrous chloride and hydrogen peroxide of analytical grade were purchased from Merck Chemical Co. (Darmstadt, Germany). Notoginsenoside R1, ginsenosides Rg1, Re, Rb1, Rd, Rh1, Rk3, Rh4, 20(S)-Rg3, and 20(R)-Rg3 (Sichuan Weikeqi Biological Technology Co., Ltd. Chengdu, China) with a purity ≥ 98% were used as the standard compounds.

Effect of ninjin’yoeito and ginseng extracts on oxaliplatin-induced neuropathies in mice
來源: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.

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