| Product Name | Nuciferine |
|---|---|
| CAS | 475-83-2 |
| Formula | C19H21NO2 |
| MW | 295.38 |
| Appearance | 白色粉末 類白色結晶 |
| Melting point | 162.5-163.5 °C |
| Boiling point | 430.7±45.0 °C | Condition: Press: 760 Torr |
| PKa | 7.87±0.20 | Condition: Most Basic Temp: 25 °C |
| Product Name | Nuciferine |
|---|---|
| CAS | 475-83-2 |
| Formula | C19H21NO2 |
| MW | 295.38 |
| Appearance | 白色粉末 類白色結晶 |
| Melting point | 162.5-163.5 °C |
| Boiling point | 430.7±45.0 °C | Condition: Press: 760 Torr |
| PKa | 7.87±0.20 | Condition: Most Basic Temp: 25 °C |
| An eco-friendly extraction and purification method of nuciferine from Folium nelumbinis with p-sulfonatocalix[6]arenes | ||
| Source:SCI:PHYTOCHEMICAL ANALYSIS | Author:Xuan Yu | Notes:影響因子:Xuan Yu |
| Reference description | ||
Nuciferine (batch number 141113, purity > 98%) and Rhodamine 6G(Rh6G, batch number 160713, purity > 95%) were purchasedfrom Weikeqi Biotechnology Co., Ltd. (Sichuan, China). Quercetin(batch number H-009-170,426, purity > 98%), rutin (batch numberL-001-160,520, purity > 98%) and kaempferol (batch numberS-014-160,708, purity > 98%) were bought from Chengdu HerbpurifyCo., Ltd. (Sichuan, China). | ||
| Nuciferine administration in C57BL/6J mice with gestational diabetes mellitus induced by high-fat diet: the improvement of glycolipid disorders and intestinal dysbacteriosis | ||
| Source:SCI:Food & Function | Author:Zhuohong Tang | Notes:影響因子:5.396 |
| Reference description | ||
Nuciferine (chemical structure is presented in Fig. S1A?), with a purity of more than 98%, was purchased from Weikeqi Biological Technology Co. Ltd (Chengdu, China), and its structure was identified by 1H-NMR (Fig. S1B?) and 13C-NMR (Fig. S1C?) spectroscopy. | ||
| Comparative Analysis of Chemical Constituents in Different Parts of Lotus by UPLC and QToF-MS | ||
| Source:SCI:MOLECULES | Author:Haotian Pei | Notes:影響因子:4.412 |
| Reference description | ||
Five standard compounds, including rutin, quercetin, kaempferol, caffeic acid, and luteolin 7-glucoside, were purchased from the China National Institutes for Food and Drug Control. Six standard compounds, including isoquercitrin, isorhamnetin, catechin, epicatechin, nuciferine, and chlorogenic acid, were purchased from Sichuan Weikeqi Biological Technology Co., Ltd. (Sichuan, China). The purity of all the regents was HPLC ≥ 98%. | ||
| Untargeted Metabolomic Analysis of the Effects and Mechanism of Nuciferine Treatment on Rats With Nonalcoholic Fatty Liver Disease | ||
| Source:SCI:Frontiers in Pharmacology | Author:Cui Huantian | Notes:影響因子:4.225 |
| Reference description | ||
Nuciferine (C19H21NO2; molecular weight, 295.38 Da; purity ≥ 98%) was purchased from Sichuan Weikeqi Biological Technology Co., Ltd. (Sichuan, China). HFD (17.7% sucrose, 17.7% fructose, 19.4% protein, and 40% fat) was obtained from Beijing Huafukang Bioscience Co., Ltd. (Beijing, China). | ||
| Metabolism profiles of nuciferine in rats using ultrafast liquid chromatography with tandem mass spectrometry | ||
| Source:SCI:BIOMEDICAL CHROMATOGRAPHY | Author:Lin-Hu Ye | Notes:影響因子:1.729 |
| Reference description | ||
NF (98.0%, Fig. 1) was purchased from Weikeqi Biological TechnologyCo. Ltd. (Chengdu, Sichuan province, China).N-Nornuciferine(N-NF, 97.8%) and 2-hydroxy-1-methoxyaporphine (HMA, 98.3%)were isolated from lotus leaves | ||