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Antineuroinflammatory and Antiproliferative Activities of Constituents from Tilia amurensis

Authors
Kim, KH[Kim, Ki Hyun]Moon, E[Moon, Eunjung]Cha, SM[Cha, Joon Min]Lee, S[Lee, Seulah]Yu, JS[Yu, Jae Sik]Kim, CS[Kim, Chung Sub]Kim, SY[Kim, Sun Yeou]Choi, SU[Choi, Sang Un]Lee, KR[Lee, Kang Ro]
Issue Date
Oct-2015
Publisher
PHARMACEUTICAL SOC JAPAN
Keywords
Tilia amurensis; Tiliaceae; isoflavonoid glycoside; nitric oxide; antineuroinflammation; antiproliferation
Citation
CHEMICAL & PHARMACEUTICAL BULLETIN, v.63, no.10, pp.837 - 842
Indexed
SCIE
SCOPUS
Journal Title
CHEMICAL & PHARMACEUTICAL BULLETIN
Volume
63
Number
10
Start Page
837
End Page
842
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/42914
ISSN
0009-2363
Abstract
As part of our ongoing search for bioactive constituents of natural Korean medicinal resources, we found in a preliminary study that the methanol (MeOH) extract from the trunks of Tilia amurensis RUPR. showed an inhibitory effect on nitric oxide (NO) production in an activated murine microglial cell line. A bioassay-guided fractionation and chemical investigation of the MeOH extract resulted in the isolation and identification of a new isoflavonoid glycoside, orobol 4'-O-beta-D-apiofuranosyl-(1-->6)-beta-D-glucopyranoside (1) and 16 known compounds (2-17). The structure of the new compound was determined by spectroscopic methods, i.e., one-dimensional (1D) and two-dimensional (2D)-NMR techniques and high resolution (HR)-MS, and chemical methods. The antineuroinflammatory activities of the isolated compounds were determined by measuring NO levels in the medium using murine microglial BV-2 cells. Among them, 12 compounds, including compound 1 (most active with an IC50 value of 23.42 mu M), inhibited NO production in lipopolysaccharide-stimulated BV-2 cells. Moreover, compounds 1-4 showed moderate antiproliferative activities against the SK-MEL-2 cell line, with IC50 values ranging from 12.31 to 19.67 mu M.
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