A New Neolignan Glycoside from the Leaves of Acer truncatum
Autor: | Jun-Zhu Li, Wei Ni, Lang-Ping Dong, Chang-Xiang Chen, Hai-Yang Liu, Jin-Yang Dong |
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Jazyk: | angličtina |
Rok vydání: | 2006 |
Předmět: |
Magnetic Resonance Spectroscopy
Stereochemistry Pharmaceutical Science Acer Microbial Sensitivity Tests Acer truncatum Lignans Analytical Chemistry lcsh:QD241-441 chemistry.chemical_compound antibacterial activity lcsh:Organic chemistry Chlorogenic acid Drug Discovery Glycosides Physical and Theoretical Chemistry chemistry.chemical_classification Carbon Isotopes Neochlorogenic acid Schizandriside biology Bacteria Aceraceae Communication Organic Chemistry Absolute configuration neolignan glycosides Glycoside biology.organism_classification Anti-Bacterial Agents Plant Leaves chemistry Chemistry (miscellaneous) Molecular Medicine Protons Antibacterial activity |
Zdroj: | Molecules, Vol 11, Iss 12, Pp 1009-1014 (2006) |
Popis: | A new neolignan glycoside, (7R,8R)-7,8-dihydro-9′-hydroxyl-3′-methoxyl- 8-hydroxymethyl-7-(4-hydroxy-3-methoxyphenyl)-1′-benzofuranpropanol 9′-O-β-D- glucopyranoside (1) was isolated from the leaves of Acer truncatum along with (7R,8R)-7,8-dihydro-9′-hydroxyl-3′-methoxyl-8-hydroxymethyl-7-(4-O-α-L-rhamno- pyranosyloxy-3-methoxyphenyl)-1′-benzofuranpropanol (2), schizandriside (3), lyoniresinol (4), berchemol (5), (-)-pinoresinol-4-O-β-D-glucopyranoside (6), hecogenin (7), chlorogenic acid (8) and neochlorogenic acid (9). Their structures were elucidated on the basis of extensive spectroscopic data. The absolute configuration of compounds 1 was established by its CD spectrum. The antibacterial activities of compounds 1-7 were evaluated. |
Databáze: | OpenAIRE |
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