One-step isolation of carnosic acid and carnosol from rosemary by centrifugal partition chromatography

2017 ◽  
Vol 40 (5) ◽  
pp. 1057-1062 ◽  
Author(s):  
Mary H. Grace ◽  
Yin Qiang ◽  
Shengmin Sang ◽  
Mary Ann Lila
Planta Medica ◽  
2016 ◽  
Vol 81 (S 01) ◽  
pp. S1-S381
Author(s):  
AA Abdelgadir ◽  
L Boudesocque-Delaye ◽  
I Thery-Koné ◽  
A Gueiffier ◽  
EM Ahmed ◽  
...  

2019 ◽  
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Birgit Waltenberger ◽  
Stefan Schwaiger ◽  
Loi Huynh ◽  
Hung Tran ◽  
...  

2015 ◽  
Vol 156 ◽  
pp. 444-449 ◽  
Author(s):  
Abdelgadir A. Abdelgadir ◽  
Leslie Boudesocque-Delaye ◽  
Isabelle Thery-Koné ◽  
Alain Gueiffier ◽  
Elhadi M. Ahmed ◽  
...  

2007 ◽  
Vol 30 (16) ◽  
pp. 2693-2697 ◽  
Author(s):  
Chul Young Kim ◽  
Hee Ju Lee ◽  
Mi Kyeong Lee ◽  
Mi-Jeong Ahn ◽  
Jinwoong Kim

Metabolites ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 309
Author(s):  
Diana Isabel Correa ◽  
Edgar Pastene-Navarrete ◽  
Luis Bustamante ◽  
Marcelo Baeza ◽  
Julio Alarcón-Enos

Preparative separation of three lycorine type alkaloids from Rhodolirum speciosum (Amaryllidaceae) was successfully carried out using pH-zone-refinement centrifugal partition chromatography (CPC) using the solvent system methyl-tert-butyl ether/acetonitrile/water (4:1:5, v/v/v) in descending mode. Using this system, Alkaloid 1 (165.7 mg, 88.2%, purity), 2 (60.1 mg, 97.7% purity) and 3 (12.3 mg, 84.4% purity) were obtained in one step. For structure elucidation, the pure alkaloids were subjected to spectroscopy analysis using nuclear magnetic resonance experiments (1H-NMR, 13C-NMR) and gas chromatography coupled with mass spectrometry (GC-MS). Alkaloids 1, 2, and 3 were identified as 1-O-acetyl-5,6-dehydrolycorine, 1-O-acetyl-lycorine, and 1,2-O-diacetyl-5,6-dehydrolycorine, respectively. The acetylcholinesterase inhibitory activity of these alkaloids was IC50 151.1 μg/mL, IC50 203.5 μg/mL, IC50 470.0 μg/mL, and IC50 17.1 μg/mL, respectively.


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