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Ai‐Xue Zuo Yong Shen Zhi‐Yong Jiang Xue‐Mei Zhang Jun Zhou Jun Lü Ji‐Jun Chen 《Helvetica chimica acta》2010,93(3):504-510
Three new phenolic glucosides named orcinosides A, B, and C ( 1, 2 , and 3 , resp.) were isolated in low yields (4.0×10−6, 11.5×10−6, 4.5×10−6%, resp.) from the rhizomes of Curculigo orchioides. Their structures were elucidated by comprehensive spectroscopic analyses including FAB‐MS, HR‐ESI‐MS, IR, and 1D‐ and 2D‐NMR (HSQC, HMBC) data. Compounds 1 – 3 contained two orcinol‐glucoside moieties linked through a CH2 group. 相似文献
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Xue Song Feng Yang Qu Zhao Hua Wu Lei Xu Dong Song Zhang Hui Yuan Gao Li Jun Wu 《中国化学快报》2009,20(6):702-705
Chemical investigation of Syringa velutinai Kom. led to the isolation of two new secoiridoid glucosides. Their structures were identified as 6'-O-(6, 7-dihyrofoliamenthoyl)-8-epi-kingisidic acid (syrveoside A, 1) and 6'-O-menthiafoloyl-8-epi-kingisidic acid (syrveoside B, 2) on the basis of chemical and physicochemical evidence. 相似文献
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Ren‐Qiang Mei Qing Lu Yan‐Fen Hu Hai‐Yang Liu Fu‐Kai Bao Yu Zhang Yong‐Xian Cheng 《Helvetica chimica acta》2008,91(1):90-96
Three new linear C14 polyyne (=polyacetylene) glucosides, cordifolioidynes A–C ( 1 – 3 ), together with two known polyynes, lobetyol ( 4 ) and lobetyolin ( 5 ), and five known phenylpropanoids, i.e., sinapinaldehyde ( 6 ), coniferaldehyde ( 7 ), coniferoside ( 8 ), sachaliside ( 9 ), and isoconiferin ( 10 ), were isolated from the roots of Codonopsis cordifolioidea. The structures of 1 – 3 were established from spectral evidences and by characterization of their hydrolysis products. Acid hydrolysis of 1 afforded the aglycone 1a , while hydrolysis of 2 and 3 gave the cyclization products 2a and 3a , respectively. Compounds 4 – 10 were isolated from this plant for the first time. The antibacterial activity of compounds 1 – 5 were assessed against eight microbial strains by the agar dilution method, none of them exhibited antibacterial effects at concentrations up to 100 μg/ml. 相似文献
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Zong‐Yun Li Hui‐Min Gao Jian Sun Liang‐Mian Chen Zhi‐Min Wang Qi‐Wei Zhang 《Helvetica chimica acta》2012,95(7):1144-1151
The new secoiridoid sulfonates 1 – 3 were isolated from the 50% EtOH/H2O extract of the sulfiting‐processed Lonicera japonica Flos (LJF) by semi‐prep. HPLC, and their structures were identified on the basis of mass spectrometry and NMR spectroscopy. HPLC and LC‐DAD‐MS/MS analyses of the different samples of LJF obtained by various process techniques suggested that the sulfur fumigation led to the decrease of secologanic acid ( 4 ) and the formation of secologanic acid‐derived sulfonate 1 and its derivatives 2, 2a , and 3 in the crude materials, which revealed that sulfur fumigation, the traditional process technique, could alter the phytochemical profiles of some Chinese herbal medicines. 相似文献
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Guangyin Wang Junzeng Zhang Marianna Kulka Fujiang Guo Yiming Li 《Helvetica chimica acta》2014,97(7):985-991
Three new eremophilane glucosides, namely, petasitosides A–C, and seven known eremophilane‐type sesquiterpenoids were isolated from the roots of Petasites japonicus. Their structures were elucidated by spectroscopic techniques including 1D‐ and 2D‐NMR spectroscopy and mass spectrometry. This is the first report on eremophilane glycosides from the genus Petasites. 相似文献
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Hyun-Jung Lee Oh-Kyu Lee Yeong-Han Kwon Don-Ha Choi Ha-Young Kang Hyeon-Yong Lee Ki-Hyon Paik Hak-Ju Lee 《Chemistry of Natural Compounds》2006,42(4):415-418
Four known isoflavone glucosides have been isolated from the bark of Amorpha fruticosa, which is a traditional remedy plant,
for the first time. They were elucidated as 3′-hydroxy-4′-methoxyisoflavone-7-O-β-D-glucopyranoside (1), 4′,6-dimethoxyisoflavone-7-O-β-D-glucopyranoside (2), 4′-methoxyisoflavone-7-O-β-D-glucopyranoside (3), and 3′,5-dihydroxy-4′-methoxyisoflavone-7-O-β-D-glucopyranoside (4), based on the UV, FT-IR, EIMS, FABMS, HREIMS, and NMR (1H and 13C, DEPT, COSY, NOESY, HMQC, and HMBC) data.
Published in Khimiya Prirodnykh Soedinenii, No. 4, pp. 336–338, July–August, 2006. 相似文献
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Shuai Wang Xiaopo Zhang Xin Li Qibing Liu Yue Zhou Peng Guo 《Natural product research》2019,33(6):893-896
The phenylpropanoid glucosides from Tadehagi triquetrum were found to be beneficial to glucose and lipid metabolism in vitro. Herein, we investigated the effects of these compounds on oxidised low-density lipoprotein (oxLDL)-induced foam cell formation in RAW264.7 macrophages, aiming to evaluate their potential utility in prevention of atherosclerosis. Our results showed that three out of seven phenylpropanoid glucosides significantly inhibited oxLDL-evoked foam cell formation. These three compounds remarkably inhibited cholesterol influx and enhanced cholesterol efflux. Treatment with compounds 3, 4 and 7 significantly down-regulated the expression of scavenge receptors 1 (SR-1) and cluster of differentiation 36 (CD36) and increased the expression ATP-binding cassette transporters A1 and G1 (ABCA1 and ABCG1). Analyses of structure–activity relationships revealed that cinnamyl group was the most pivotal group for their activities. This work provided phenomenon that these phenylpropanoid glucosides are effective regulator of cholesterol influx/efflux and may be useful in leading for development of anti-atherosclerotic agents. 相似文献
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N. F. Samoshina M. V. Denisenko V. A. Denisenko N. I. Uvarova 《Chemistry of Natural Compounds》2003,39(6):575-582
A preparative synthesis of glucosides of the lupane-type triterpene acids betulinic, dihydrobetulinic, betulonic, dihydrobetulonic, and 3,20-dioxo-30-norlupan-28-oic was proposed. Glycosylation of 3-hydroxyacids by -acetobromoglucose (ABG) with Ag2O was performed in pyridine (Py)to formglycosides at C-28, repeated glycosylation of which by these same reagents but in CH2Cl2 generated a glycoside bond at C-3 to form bisglucosides. 28-Glucosides of ketoacids were formed in high yields in both Py and CH2Cl2. 相似文献