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Jin-Yu Li

Researcher at Chinese Academy of Sciences

Publications -  17
Citations -  203

Jin-Yu Li is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Dendrobium & Mangostin. The author has an hindex of 7, co-authored 17 publications receiving 97 citations.

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Structural characterization and hypoglycemic effect via stimulating glucagon-like peptide-1 secretion of two polysaccharides from Dendrobium officinale.

TL;DR: In vivo assays showed that D. officinale polysaccharides (DOPs) exerted significant hypoglycemic effects accompanying increased serum insulin and glucagon-like peptide-1 levels in streptozotocin-induced diabetic rats, and in vitro experiments indicated that DOPs may decrease fasting blood sugar levels by stimulating GLP-1 secretion and that intracellular DOP-induced GLPs involved the Ca2+/calmodulin/CaMKII and
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Stilbenes with anti-inflammatory and cytotoxic activity from the rhizomes of Bletilla ochracea Schltr.

TL;DR: Four new dihydrophenanthrenofuran, bleochranols A-D, along with 21 known compounds including phenanthrenes and bibenzyls were isolated and elucidated from the rhizomes of Bletilla ochracea, showing remarkable cytotoxic activity against HL-60, A-549, and MCF-7 and anti-inflammatory activity against NO production in LPS-stimulated RAW 264.
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Phenolic Constituents with Antioxidative, Tyrosinase Inhibitory and Anti-aging Activities from Dendrobium loddigesii Rolfe.

TL;DR: Results suggest that phenolic constituents from D. loddigesii may be candidate antioxidants, skin-whitening and/or anti-aging agents.
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Poly p-hydroxybenzyl substituted bibenzyls and phenanthrenes from Bletilla ochracea Schltr with anti-inflammatory and cytotoxic activity

TL;DR: Ten previously undescribed stilbenoids, including six bibenzyls (bleochrins A-F, 1-6), three phenanthrenes derivatives (bleechrins G-J, 7-10) along with eleven known compounds were isolated from the rhizomes of Bletilla ochracea Schltr.
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Design, synthesis and structure–activity relationships of mangostin analogs as cytotoxic agents

TL;DR: Structural–activity relationship analysis indicates that the maintenance of the isopentene group at C-8 is essential for the cytotoxic activity of mangostin.