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Ginsenoside Rd

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Product Overview
Product Name Ginsenoside Rd
CAS52705-93-8
FormulaC48H82O18
MW947.15
Appearance 白色粉末
Melting point204-206 °C
Boiling point1015.6±65.0 °C | Condition: Press: 760 Torr
PKa12.85±0.70 | Condition: Most Acidic Temp: 25 °C
Product details

WKQ-0000467

中文名稱:人參皂苷Rd

中文別名:人參皂甙RD;絞股藍皂苷VIII;(2S,3R,4S,5S,6R)-2-(((2R,3R,4S,5S,6R)-4,5-二羥基-2-(((3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-羥基-4,4,8,10,14-五甲基-17-((S)-6-甲基-2-(((2S,3R,4S,5S,6R)-3,4,5-三羥基-6-(羥甲基)四氫-2H-吡喃-2-基)氧基)庚-5-烯-2-基)十六氫-1H-環(huán)戊烷[a]菲-3-基)氧基)-6-(羥甲基)四氫-2H-吡喃-3-基)氧基)-6-(羥甲基)四氫-2H-吡喃-3,4,5-三醇;絞股藍總皂甙

英文名稱:Ginsenoside Rd

英文別名:(3β,12β)-20-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside;Dammarane, β-D-glucopyranoside deriv.;3-O-β-D-Glucopyranosyl-(1→2)-β-D-glucopyranosyl-20-O-β-D-glucopyranosyldammar-24-ene-3β,12β,20S-triol;Chikusetsusaponin FK7;Ginsenoside Rd;Ginsenoside Rd1;Gypenoside VIII;

分子式:C48H82O18

分子量:947.15

CAS號:52705-93-8

純度:HPLC≥98%

熔點:204-206 °C

沸點:1015.6±65.0 °C | Condition: Press: 760 Torr

密度:1.38±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

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Related literature
Steamed Panax notoginseng attenuates renal anemia in an adenine-induced mouse model of chronic kidney disease
Source:SCI:JOURNAL OF ETHNOPHARMACOLOGY Author:Min Gao Notes:影響因子:4.36
Reference description

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.

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
Source:SCI:ANALYTICAL AND BIOANALYTICAL CHEMISTRY Author:Dong, Bangjian Notes:影響因子:4.157
Reference description

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).

Application of magnetically immobilized edible fungus for the biotransformation of panax notoginseng saponin Rb1 to Rd and Rg3
Source:SCI:JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES Author:Yuping Zang Notes:影響因子:2.603
Reference description

P. notoginseng were purchased from Wenshan County of Yunnan Province. P. notoginseng is dried by oven, powdered by a disintegrator (HX-200A, Tianjin Taisite Instrument Co., LTD, China) and sieved 40 mesh. The standard of saponins Rb1 (HPLC ≥ 98%), Rd (HPLC ≥ 98%) and Rg3 (HPLC ≥ 98%) were purchased from weikeqi-biotechnology limited company of Sichuan. Methanol and acetonitrile were of HPLC grade (J & K Chemical Ltd., China). Ethanol of analytical grade for extraction was bought from

Rapid characterization and determination of isoflavones and triterpenoid saponins in Fu-Zhu-Jiang-Tang tablets using UHPLC-Q-TOF/MS and HPLC-UV
Source:SCI:Analytical Methods Author:Yi Tao Notes:影響因子:1.915
Reference description

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.

Neuroprotective Effect of Ginsenoside Rd in Spinal Cord Injury Rats
Source:SCI:BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY Author:Lin Cong Notes:影響因子:4.084
Reference description

Penicillin (200,000 units) was intramuscularly injected every day to protect from post-operative infection. A twice-a-day manual bladder expression was performed until spontaneous voiding returned. Rats in the GS Rd groups received an intraperitoneal injection of GS Rd (purity: HPLC ≥98%, WKQ-00514; Sichuan Weikeqi Biological Technology Co., Ltd, Chengdu, China), and rats in the DEX group received an intraperitoneal injection of DEX (Tianjin Xinzheng, Tianjin, China) 1 hr before the surgery and once daily for 14 days. Rats in the sham and SCI groups received 0.9% NaCl only.

Discovery of triterpenoids as potent dual inhibitors of pancreatic lipase and human carboxylesterase 1
Source:SCI:JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY Author:Jing Zhang Notes:影響因子:5.051
Reference description

Oleanolic acid, maslinic acid, hederagenin, ursolic acid, corosolic acid, asiatic acid, β-boswellic acid, glycyrrhetic acid, celastrol, betulin, betulinicaldehyde, betulinic acid, pachymic acid, ganoderic acid B, polygalacic acid, glycyrrhizic acid, lupeol, ginsenosideol F1, ginsenoside Rg1, ginsenoside Rg2, were purchased from Dalian Meilun Company (Beijing, China), ginsenoside Rd, ginsenoside R1, Notoginsenoside R1 were purchased from Sichuan Weikeqi Biotechnology Co., Ltd. (Chengdu, China), ginsenoside Re, ginsenoside Rh1 were purchased from Chengdu Pfeid Biotech Technology Co., Ltd. (Chengdu, China), ginsenoside Ro, ginsenoside Rh4, and ginsenoside F4 were purchased from Chenguang Bio (Handan, 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
Source:SCI:JOURNAL OF ETHNOPHARMACOLOGY Author:Kewen Ding Notes:影響因子:4.36
Reference description

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
Source:SCI:Frontiers in Pharmacology Author:Yin Xiong, Notes:影響因子:4.225
Reference description

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)
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.

Optimisation of Ethanol-Reflux Extraction of Saponins from Steamed Panax notoginseng by Response Surface Methodology and Evaluation of Hematopoiesis Effect
Source:SCI:MOLECULES Author:Yupiao Hu Notes:影響因子:3.098
Reference description

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
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.

Ninjin’yoeito and ginseng extract prevent oxaliplatin-induced neurodegeneration in PC12 cells
Source:SCI:Journal of Natural Medicines Author:Suzuki, Toshiaki Notes:影響因子:1.593
Reference description

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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