英文名稱 | Ginsenoside Rc |
---|---|
中文名稱 | 人參皂苷Rc/人參皂甙Rc |
CAS號 | 11021-14-0 |
分子式 | C53H90O22 |
分子量 | 1079.27 |
外觀 | HPLC-ELSD≥98 白色粉末 |
熔點 | 193-196 °C |
沸點 | 1128.3±65.0 °C | Condition: Press: 760 Torr |
酸度系數(shù)pKa | 12.85±0.70 | Condition: Most Acidic Temp: 25 °C |
英文名稱 | Ginsenoside Rc |
---|---|
中文名稱 | 人參皂苷Rc/人參皂甙Rc |
CAS號 | 11021-14-0 |
分子式 | C53H90O22 |
分子量 | 1079.27 |
外觀 | HPLC-ELSD≥98 白色粉末 |
熔點 | 193-196 °C |
沸點 | 1128.3±65.0 °C | Condition: Press: 760 Torr |
酸度系數(shù)pKa | 12.85±0.70 | Condition: Most Acidic Temp: 25 °C |
WKQ-0000466
中文名稱:人參皂苷Rc
中文別名:人參皂甙Rc
英文名稱:Ginsenoside Rc
英文別名:(3β,12β)-20-[(6-O-α-L-Arabinofuranosyl-β-D-glucopyranosyl)oxy]-12-hydroxydammar-24-en-3-yl 2-O-β-D-glucopyranosyl-β-D-glucopyranoside;Dammarane, β-D-glucopyranoside deriv.;Ginsenoside Rc;NSC 310104;Panaxoside Rc;
分子式:C53H90O22
分子量:1079.27
CAS號:11021-14-0
純度:HPLC-UV≥98%
熔點:193-196 °C
沸點:1128.3±65.0 °C | Condition: Press: 760 Torr
密度:1.42±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
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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. |
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). |
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. |