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Phenylpropanoids from Myristica fragrans Houtt  

Song, Myoung-Chong (Biotechnology Graduate School & Plant Metabolism Research Center)
Ahn, Eun-Mi (Biotechnology Graduate School & Plant Metabolism Research Center)
Bang, Myun-Ho (Biotechnology Graduate School & Plant Metabolism Research Center)
Kim, Se-Young (Department of Oriental Medicinal Materials.Processing & Oriental Medicinal Materials.Processing Center, KyungHee University)
Rho, Yeong-Deok (Department of Oriental Medicinal Materials.Processing & Oriental Medicinal Materials.Processing Center, KyungHee University)
Kwon, Byuong-Mog (Korea Research Institute of Bioscience & Biotechnology)
Lee, Hyun-Sun (Korea Research Institute of Bioscience & Biotechnology)
Baek, Nam-In (Biotechnology Graduate School & Plant Metabolism Research Center)
Publication Information
Applied Biological Chemistry / v.47, no.3, 2004 , pp. 366-369 More about this Journal
Abstract
Myristica fragrans Houtt were extracted in 80% aq. MeOH and solvent fractionated sing $CHCl_3$, EtOAc, n-BuOH and water, successively. The n-BuOH fraction gave three phenylpropanoids through application of silica gel column chromatographies. The chemical structures of the phenylpropanoids were determined by the interpretation of several spectral data, including NMR and MS as meso-dihydroguaiaretic acid (1), nectandrin B (2) and syringin methyl ether (3). Compound 1, which was first isolated from this plant by authors, showed inhibitory activities with $60.0{\pm}2.1%\;(100\;{\mu}g/ml),\;42.6{\pm}0.9%\;(140\;{\mu}g/ml)\;and\;12.2{\pm}0.2%\;(200\;{\mu}g/ml)$ on ACAT(acyl-CoA:Cholesterol Acyltransferase), chitin synthase III and HMG-CoA reductase (3-hydroxy-3-methylglutaryl coenzyme A reductase), respectively. Compound 3 showed inhibitory activities with $27.2{\pm}0.9%\;(100\;{\mu}g/ml),\;45.5{\pm}0.8%\;(200\;{\mu}g/ml)$ on ACAT and chitin synthase III.
Keywords
Myristica fragrans Houtt; meso-dihydroguaiaretic acid; nectandrin B; syringin methyl ether; chitin synthase III; HMG-CoA reductase; ACAT;
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