Results 161 to 170 of about 40,113 (187)
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Phenylethanoid glycoside from Veronica undulata

Phytochemistry, 1994
From a water extract of whole plants of Veronica undulata, a new phenylethanoid triglycoside and five known glycosides were isolated. The structure of the new compound was elucidated from chemical and spectroscopic evidence.
H, Aoshima, T, Miyase, A, Ueno
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Phenylethanoid Glycosides and Phenolic Glycosides From Stem Bark of Magnolia officinalis

Phytochemistry, 2016
An investigation of the hydrophilic constituents of the stem bark of Magnolia officinalis was performed and which led to isolation and identification of twenty-one previously unreported glycosides. These included eleven phenylethanoid glycosides, magnolosides F-P, and ten phenolic glycosides, magnolosides Q-Z, along with eight known compounds.
Xue Zhenzhen
exaly   +3 more sources

Phenylethanoid Glycosides From Plantago depressa

Phytochemistry, 1993
Abstract The five known phenylethanoid glycosides, cistanoside F, β-hydroxyacteoside, campenoside I, acteoside and orobanchoside, and a new phenylethanoid ...
Sansei Nishibe
exaly   +2 more sources

Phenylethanoid Glycosides from Callicarpa nudiflora

Chemistry of Natural Compounds, 2020
A new phenylethanoid glycoside, named cis-alyssonoside (1), was isolated from the leaves of Callicarpa nudiflora, along with four known phenylethanoid glycosides (2–5). Their structures were determined on the basis of extensive spectroscopic analysis and comparison with literature data. The inhibitory effects on lipopolysaccharide induced nitric oxide (
Xiao-Jie Yan   +6 more
openaire   +1 more source

Biodiversity of Phenylethanoid Glycosides

2002
Phenylethanoid glycosides are a group of natural products widely distributed in the plant kingdom, most of which have been isolated from medicinal plants, and their patterns of distrubition have been suggested to be valuable taxonomic markers. The most widely studied families are Scrophulariaceae, Oleaceae, Plantaginaceae, Lamiaceae and Orobanchaceae1 ...
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Phenylethanoid glycosides from Plantago asiatica

Phytochemistry, 1991
Abstract Six new phenylethanoid glycosides, plantainosides A–F, were isolated from a water extract of the whole plants of Plantago asiatica together with eight known phenylethanoid glycosides. Their structures were determined on the basis of chemical and spectral evidence.
Toshio Miyase   +5 more
openaire   +1 more source

Phenylethanoid glycosides from Michelia champaca leaves

Phytochemistry
Chemical investigation on the leaves of Michelia champaca L. (Magnoliaceae) led to the isolation of five previously undescribed phenylethanoid glycosides (PhGs), 4-O-β-d-glucopyranosyl-acteoside (1), 4‴-O-(6-O-E-caffeoyl)-β-d-glucopyranosyl-acteoside (2), 4‴-O-(6-O-E-caffeoyl)-β-d-glucopyranosyl-isoacteoside (3), 6""-O-E-feruloyl-echinacoside (4), and ...
Meihong, Liu, Haibo, Tan, Haihui, Xie
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Concise Total Synthesis of Phenylethanoid Glycoside Acteoside

Chemistry – An Asian Journal
Abstract Acteoside is a prominent phenylethanoid glycoside (PhG) with diverse pharmacological activities. However, its chemical synthesis has been challenging due to the reliance on extensive protection/deprotection strategies, leading to lengthy routes and low overall yields.
Duc Thinh Khong   +2 more
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Phenylethanoid glycosides from Prostanthera melissifolia

Phytochemistry, 1999
Abstract Six phenylethanoid glycosides were isolated from aerial parts of Prostanthera melissifolia, together with apigenin and ursolic acid. The glycosides were characterized by spectral methods as martynoside, isomartynoside, verbascoside, isoverbascoside, betonyoside F and isobetonyoside F, the latter being a new natural product.
W KISIEL, F PIOZZI
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Synthetic phenylethanoid glycoside derivatives as potent neuroprotective agents

European Journal of Medicinal Chemistry, 2015
Several phenylethanoid glycoside derivatives were designed and synthesized. Most of the synthetic compounds showed significant neuroprotective effects, including antioxidative and anti-apoptotic properties. Specifically, target compounds displayed potent effects against various toxicities such as H2O2 and 6-hydroxydopamine (6-OHDA) in PC12 cells. Among
Ying-Guo, Liu   +5 more
openaire   +2 more sources

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