29 results match your criteria: "Vietnam National University - Hochiminh[Affiliation]"
Molecules
January 2015
Department of Biology, University of Taynguyen, 567 Le Duan, Dac Lac City 630000, Vietnam.
An HPLC-DAD method for the quality control of wild and cultivated Ganoderma lucidum (Linhzhi) and related species samples was developed and validated. The quantitative determination of G. lucidum and its related species using 14 triterpene constituents, including nine ganoderma acids (compounds 4-12), four alcohols (compounds 13-16), and one sterol (ergosterol, 17) were reported.
View Article and Find Full Text PDFMolecules
November 2014
Research Center of Ginseng and Medicinal Materials, 41 Dinh Tien Hoang, District 1, Ho Chi Minh City 700-00, Vietnam.
A series of Lycopodium alkaloids, namely lycosquarosine A (1), acetylaposerratinine (2), huperzine A (3), huperzine B (4), 8α-hydrophlemariurine B (5), and huperzinine (6), has been isolated from Vietnamese Huperzia squarrosa. Among them, lycosquarosine A (1) is the new metabolite of the natural source. Lycosquarosine A completely inhibited AChE activity in a dose dependent manner with an IC50 value of 54.
View Article and Find Full Text PDFJ Phys Condens Matter
May 2014
Computational Physics Lab, Institute of Technology, Vietnam National University-HochiMinh City, 268 Ly Thuong Kiet Street, District 10, HochiMinh City, Vietnam.
We present molecular dynamics (MD) simulations of the formation of 2D materials with a honeycomb structure from 2D simple monatomic liquids with honeycomb interaction potential (Rechtsman et al 2005 Phys. Rev. Lett.
View Article and Find Full Text PDFJ Nat Prod
November 2012
Faculty of Chemistry, University of Science, Vietnam National University-HoChiMinh City, 227 Nguyen Van Cu Street, District 5, HoChiMinh City, Vietnam.
From the methanolic-soluble extract of the wood of Artocarpus heterophyllus, four new flavones, artocarmins A-D (1-4), and three new chalcones, artocarmitins A-C (5-7), have been isolated together with 13 known compounds. Their structures were determined on the basis of the spectroscopic data. Compounds 1-4, 6, 7, 9-16, and 20 displayed significant tyrosinase inhibitory activity.
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