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Noralashinols D-F, New Norlignans from Syringa pinnatifolia and its Anti-Inflammation in BV2 Cells.
Liang, Yana; Wuken, Shana; Chen, Panlong; Huang, Zhiqiang; Liu, Changxin; Wang, Jiatong; Chen, Hongying; Zhang, Ye; Chai, Xingyun.
Afiliación
  • Liang Y; Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 102448, P. R. China.
  • Wuken S; Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 102448, P. R. China.
  • Chen P; Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 102448, P. R. China.
  • Huang Z; Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 102448, P. R. China.
  • Liu C; College of Pharmacy, Inner Mongolia Medical University, Hohhot, Inner Mongolia, 010110, P. R. China.
  • Wang J; Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 102448, P. R. China.
  • Chen H; Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 102448, P. R. China.
  • Zhang Y; Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 102448, P. R. China.
  • Chai X; College of Pharmacy, Inner Mongolia Medical University, Hohhot, Inner Mongolia, 010110, P. R. China.
Chem Biodivers ; : e202401567, 2024 Aug 08.
Article en En | MEDLINE | ID: mdl-39117598
ABSTRACT
Four new norlignans, noralashinols D-F (1a/b-3), and two known analogues (4 and 5) were isolated from the peeled stems of Syringa pinnatifolia Hemsl. The structures were elucidated by analysis of spectroscopic data, such as IR, HR-ESI-MS, 1D and 2D NMR, and ECD. All compounds were evaluated for anti-inflammatory activities against NO production induced by LPS in BV2 microglia cells. Compounds 1b and 2 exhibited moderate activities with IC50 values of 32.39±9.1 and 47.83±10.44 µM, respectively, compared with positive control indomethacin (IC50=21.62 µM). It is worth to note that 1, 3, and 4 have a distinctive woody fragrance.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chem Biodivers Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Chem Biodivers Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2024 Tipo del documento: Article