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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Rg3/20(S)-人參皂苷RG3/人參皂苷20(S)-RG3/人參皂甙 Rg3/(20S)-人參皂苷Rg3/人參皂苷S型Rg3/人參皂苷Rg3(S型)/S型人參皂苷RG3

人參皂苷Rg3/20(S)-人參皂苷RG3/人參皂苷20(S)-RG3/人參皂甙 Rg3/(20S)-人參皂苷Rg3/人參皂苷S型Rg3/人參皂苷Rg3(S型)/S型人參皂苷RG3

Ginsenoside Rg3

產(chǎn)品編號:WKQ-0000472 CAS No.:14197-60-5 純度:HPLC≥98% 分子式:C42H72O13

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基本信息
英文名稱 Ginsenoside Rg3
中文名稱人參皂苷Rg3/20(S)-人參皂苷RG3/人參皂苷20(S)-RG3/人參皂甙 Rg3/(20S)-人參皂苷Rg3/人參皂苷S型Rg3/人參皂苷Rg3(S型)/S型人參皂苷RG3
CAS號14197-60-5
分子式C42H72O13
分子量785.02
外觀
熔點(diǎn)146-147 °C
沸點(diǎn)885.0±65.0 °C | Condition: Press: 760 Torr
酸度系數(shù)pKa12.85±0.70 | Condition: Most Acidic Temp: 25 °C
產(chǎn)品詳情

WKQ-0000472

中文名稱:人參皂苷Rg3

中文別名:20(S)-人參皂苷RG3;人參皂苷20(S)-RG3;人參皂甙 Rg3;(20S)-人參皂苷Rg3;人參皂苷S型Rg3;人參皂苷Rg3(S型);S型人參皂苷RG3

英文名稱:Ginsenoside Rg3

英文別名:Dammar-24-ene-12β,20-diol, 3β-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]- (8CI);(3β,12β)-12,20-Dihydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside;Dammarane, β-D-glucopyranoside deriv.;(20S)-Propanaxadiol;(3β,12β)-12,20-Dihydroxydammar-24-en-3-yl O-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside;20(S)-Ginsenoside-Rg3;20(S)-Rg3;20S-Ginsenoside Rg3;3-O-β-D-Glucopyranosyl-(1→2)-β-D-glucopyranosyldammar-24-ene-3β,12β,20S-triol;Ginsenoside 20-Rg3;Ginsenoside Rg3;Ginsenoside Rg3s;S-Ginsenoside Rg3;

分子式:C42H72O13

分子量:785.01

CAS號:14197-60-5

純度:HPLC≥98%

熔點(diǎn):146-147 °C

沸點(diǎn):885.0±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(shù):12.85±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(yīng)客戶需求包裝

供應(yīng)單位:四川省維克奇生物科技有限公司

供應(yīng)電話:028-81700200/4008005713

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Extracellular Vesicle Delivery of Neferine for the Attenuation of Neurodegenerative Disease Proteins and Motor Deficit in an Alzheimer’s Disease Mouse Model
來源:SCI:Pharmaceuticals 作者:Bin Tang 備注:影響因子:5.863
引用描述

The exosome-encapsulated compounds (Exo-Bai, Exo-Hed, Exo-Nef, Exo-Rg3, Exo-Rapa and Exo-Rb1) were prepared by the RT method, as described [22]. In brief, 100 μg Bai, Hed, Nef, Rg3 and Rb1 (purchased from Sichuan Weikeqi Biological Technology Co., Ltd., Sichuan, China) or Rapa (purchased from Guangzhou Tomums Life Science Co., Ltd., Guangdong, China) were incubated with exosomes (25 μg) in a ratio of 4:1 in PBS at 22 °C for 18 h before being subjected to quantitation.

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.

Ginsenoside Rg3 Alleviates Aluminum Chloride-Induced Bone Impairment in Rats by Activating the TGF-β1/Smad Signaling Pathway
來源:SCI:JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY 作者:Miao Song 備注:影響因子:5.279
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The administered dose of AlCl3

(Aladdin, Shanghai, China) was previously reported to exert a change

in bone activity.11 Rg3 (purity >98%; Weikeqi, Sichuan, China) was

dissolved in isotonic physiological saline (0.9% NaCl) and

administered for 30 days at a dose previously reported to influence

the bone activity


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
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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).

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AlCl3 (Aladdin, Shanghai, China) was administered in accordance with the dose previously reported for exerting a change in bone activity for 120 days [25]. Rg3 (Weikeqi, Sichuan, China) was dissolved in isotonic physiological saline (0.9% NaCl), and a dose administered in accordance with that previously reported as exerting an influence on bone, for 30 days [24].

Application of magnetically immobilized edible fungus for the biotransformation of panax notoginseng saponin Rb1 to Rd and Rg3
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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
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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)
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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.

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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)

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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.

Antidepressant-like effects of ginsenosides: A comparison of ginsenoside Rb3 and its four deglycosylated derivatives, Rg3, Rh2, compound K, and 20(S)-protopanaxadiol in mice models of despair
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The ginsenoside Rb3 (Rb3) was isolated from SCLPN, and its structure was characterized by spectroscopic analysis with both ESI-MS and 13C NMR. 20(S)-Ginsenoside Rg3 (Rg3, Lot No.: 14,197–60-5-15-1), 20(S)-ginsenoside Rh2 (Rh2, Lot No.: 78214-33-2-14-6), compound K (C-K, Lot No.: 39262-14-1-14-9) and 20(S)-protopanaxadiol (PPD, Lot No.: 30636-90-9-14-2) were supplied by Sichuan Weikeqi Biological Technology Co. Ltd. (Chengdu, China). These compounds are white powders with a purity of 98%, which was verified by high

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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.

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