Product Name | Nuciferine |
---|---|
CAS | 475-83-2 |
Formula | C19H21NO2 |
MW | 295.38 |
Appearance | 白色粉末 类白色结晶 |
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 类白色结晶 |
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 |
WKQ-0000249
中文名称:荷叶碱
中文别名:(R)-1,2-二甲氧基-6-甲基-5,6,6a,7-四氢-4H-二苯并de,g喹啉;1,2-二甲氧基-6-甲基-5,6,6A,7-四氢-4H-二苯并DE,G喹啉;达泊西汀
英文名称:Nuciferine
英文别名:4H-Dibenzo[de,g]quinoline, 5,6,6a,7-tetrahydro-1,2-dimethoxy-6-methyl-, (R)-;6aβ-Aporphine, 1,2-dimethoxy- (8CI);Nuciferine (6CI,7CI);(6aR)-5,6,6a,7-Tetrahydro-1,2-dimethoxy-6-methyl-4H-dibenzo[de,g]quinoline;(-)-Nuciferine;(6AR)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline;(R)-1,2-Dimethoxyaporphine;(R)-Nuciferine;1,2-Dimethoxy-6aβ-aporphine;D-(-)-Nuciferine;Nuciferin;Sanjoinine E;VLT 049;l-Nuciferine;
分子式:C19H21NO2
分子量:295.38
CAS号:475-83-2
纯度:HPLC≥98%
熔点:162.5-163.5 °C
沸点:430.7±45.0 °C | Condition: Press: 760 Torr
密度:1.150±0.06 g/cm3 | Condition: Temp: 20 °C Press: 760 Torr
酸系度数:7.87±0.20 | Condition: Most Basic Temp: 25 °C
储存条件:-20℃,干燥、避光、密封
规格:5mg10mg20mg50mg100mg500mg1g2g等应客户需求包装
供应单位:四川省维克奇生物科技有限公司
供应电话:028-81700200/4008005713
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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:影响因子: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:影响因子: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:影响因子: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:影响因子: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:影响因子: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 |