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Byung Sun Min

Researcher at The Catholic University of America

Publications -  403
Citations -  8937

Byung Sun Min is an academic researcher from The Catholic University of America. The author has contributed to research in topics: Chemistry & Antioxidant. The author has an hindex of 43, co-authored 385 publications receiving 7465 citations. Previous affiliations of Byung Sun Min include Catholic University of Daegu & Korea Research Institute of Bioscience and Biotechnology.

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Inhibitory activity of coumarins from Artemisia capillaris against advanced glycation endproduct formation.

TL;DR: Five key AGE inhibitors, including 4,5-di-Ocaffeoylquinic acid, umbelliferone, esculetin, esculin, and scopoletin were identified as potential candidates for use as therapeutic or preventive agents for diabetic complications and oxidative stress-related diseases.
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Iridoid glycosides from Gardeniae Fructus for treatment of ankle sprain.

TL;DR: The structures and relative stereochemistries of the metabolites were elucidated on the basis of 1D- and 2D-NMR spectroscopic techniques, high-resolution mass spectrometry, and chemical evidence to indicate the potential effect of geniposide for the treatment of disorders such as ankle sprain.
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Anti-human immunodeficiency virus-type 1 activity of constituents from Juglans mandshurica

TL;DR: Three naphthalene glycosides, flavonoids, and galloyl tannins were isolated from the stem-bark of Juglans mandshurica and showed the most potent HIV-induced cytopethic activity against MT-4 cells and maximum cytotoxic concentration of above 100 μg/ml.
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Lanostane triterpenes from the fruiting bodies of Ganoderma lucidum and their inhibitory effects on adipocyte differentiation in 3T3-L1 cells.

TL;DR: Four new lanostane triterpenes were isolated from the fruiting bodies of Ganoderma lucidum together with 14 known compounds and the inhibitory effect of isolated compounds on adipocyte differentiation in 3T3-L1 cells was examined.
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Compounds from the heartwood of Caesalpinia sappan and their anti-inflammatory activity.

TL;DR: Two new phenolics, (3S,4R)-3,7,2',3'-tetrahydroxy-3,4-dihydro-9H-indeno[6,5-c]chromene (caesalpiniaphenol E and F), together with eleven known compounds, were isolated from the heartwood of Caesalpinia sappan and showed strong inhibitory activities toward the LPS-induced NO production in mac