Résumé
In the present study, three compounds were isolated from Argyreia acuta, among them, compounds 1 and 2 were new and Compounds 1 and 3 were isomers. They were separated by several types of columns, such as normal phase, RP, size exclusion and preparative HPLC, and their structures were elucidated by several spectroscopic methods, such as 1D- and 2D-NMR and HR-TOF-MS.
Sujets)
Convolvulaceae , Chimie , Médicaments issus de plantes chinoises , Chimie , Hétérosides , Chimie , Isomérie , Spectrométrie de masse , Structure moléculaire , Résonance magnétique nucléaire biomoléculaire , Parties aériennes de plante , Chimie , Résines végétales , Chimie , SpectrophotométrieRésumé
In the present study, three compounds were isolated from Argyreia acuta, among them, compounds 1 and 2 were new and Compounds 1 and 3 were isomers. They were separated by several types of columns, such as normal phase, RP, size exclusion and preparative HPLC, and their structures were elucidated by several spectroscopic methods, such as 1D- and 2D-NMR and HR-TOF-MS.
Sujets)
Convolvulaceae , Chimie , Médicaments issus de plantes chinoises , Chimie , Hétérosides , Chimie , Isomérie , Spectrométrie de masse , Structure moléculaire , Résonance magnétique nucléaire biomoléculaire , Parties aériennes de plante , Chimie , Résines végétales , Chimie , SpectrophotométrieRésumé
In the present study, two new compounds from Ipomoea cairica were identified and demonstrated to have α-glucosidase inhibitory activity. They were isolated by column chromatography on silica gel and sephadex LH-20 and finally purified by prep-HPLC, with their structures being elucidated by spectroscopic methods, such as 1D- and 2D-NMR and HR-TOF-MS, and chemical methods. Compounds 1 and 2, named cairicoside A and cairicoside B, were evaluated for α-glucosidase inhibitory activity by the MTT method, with the IC50 values being 25.3 ± 1.6 and 28.5 ± 3.3 μmol·L(-1), respectively.