INTRODUCTION: Astragalus anthylloides, A. dipsaceus, A. karamasicus, A. lycius, A. sigmoideus and A. xylobasis var. angustus are an endemic and generally grow in the Irano-Turanian phytogeographic region of Turkey. Astragalus species contain saponins, polysaccharides, and phenolics, while the toxic compounds include imidazoline alkaloids, nitro toxins, and selenium derivatives. OBJECTIVES: To apply a combined metabolomic fingerprinting approach by nuclear magnetic resonance (NMR) and gas chromatography-mass spectrometry (GC-MS) of endemic six Astragalus species extract. METHODOLOGY: The whole plant collected in Turkey of six endemic Astragalus subsp. were dried and then extracted with hexane, chloroform, ethylacetate, n-butanol and methanol solvents, respectively. The hexane extracts were analyzed by GC-MS. Carbon-13 (13 C)-NMR analyzes of all extracts were performed. In both analyses, a biomarker was obtained. RESULTS: The hexane extracts were determined as palmitic acid, arachidic acid, behenic acid, and linolenic acid as the main components. As a result of 13 C-NMR analyzes, in hexane, chloroform, and ethylacetate the extracts detected were palmitic acid, arachidic acid, behenic acid, and linolenic acid. d-Pinitol was obtained using 13 C-NMR analyzes with n-butanol and methanol extracts. CONCLUSION: This study demonstrated that d-pinitol is a biomarker for the endemic six Astragalus subsp.
INTRODUCTION:Astragalus anthylloides, A. dipsaceus, A. karamasicus, A. lycius, A. sigmoideus and A. xylobasis var. angustus are an endemic and generally grow in the Irano-Turanian phytogeographic region of Turkey. Astragalus species contain saponins, polysaccharides, and phenolics, while the toxic compounds include imidazoline alkaloids, nitro toxins, and selenium derivatives. OBJECTIVES: To apply a combined metabolomic fingerprinting approach by nuclear magnetic resonance (NMR) and gas chromatography-mass spectrometry (GC-MS) of endemic six Astragalus species extract. METHODOLOGY: The whole plant collected in Turkey of six endemic Astragalus subsp. were dried and then extracted with hexane, chloroform, ethylacetate, n-butanol and methanol solvents, respectively. The hexane extracts were analyzed by GC-MS. Carbon-13 (13 C)-NMR analyzes of all extracts were performed. In both analyses, a biomarker was obtained. RESULTS: The hexane extracts were determined as palmitic acid, arachidic acid, behenic acid, and linolenic acid as the main components. As a result of 13 C-NMR analyzes, in hexane, chloroform, and ethylacetate the extracts detected were palmitic acid, arachidic acid, behenic acid, and linolenic acid. d-Pinitol was obtained using 13 C-NMR analyzes with n-butanol and methanol extracts. CONCLUSION: This study demonstrated that d-pinitol is a biomarker for the endemic six Astragalus subsp.
Authors: Haidy A Gad; Nilufar Z Mamadalieva; Stefan Böhmdorfer; Thomas Rosenau; Gokhan Zengin; Rano Z Mamadalieva; Nawal M Al Musayeib; Mohamed L Ashour Journal: Plants (Basel) Date: 2021-01-08