4.3 Article

Structure characterization and biological activity of 2-arylbenzofurans from an Indonesian plant, Sesbania grandiflora (L.) Pers

期刊

PHYTOCHEMISTRY LETTERS
卷 35, 期 -, 页码 211-215

出版社

ELSEVIER
DOI: 10.1016/j.phytol.2019.12.008

关键词

Herbal medicine; Natural product; 2-arylbenzofuran; Sesbagrandiflorain; Sesbania grandiflora

资金

  1. Directorate of Research and Community Services, The Ministry of Research, Technology and Higher Education, Republic of Indonesia [393/UN26.21/PN/2018, 123.44/D2.3/KP/2018]
  2. Oregon State University NMR Facility - National Institutes of Health, HEI Grant [1S10OD018518]
  3. M. J. Murdock Charitable Trust grant [2014162]

向作者/读者索取更多资源

A new 2-arylbenzofuran, sesbagrandiflorain C (1), together with four known compounds, 2-(3,4-dihydroxy-2-methoxyphenyl)-4-hydroxy-6-methoxybenzofuran-3-carbaldehyde (2), 2-(4-hydroxy-2-methoxyphenyl)-5,6-dimethoxybenzofuran-3-carboxaldehyde (3), sesbagrandiflorain A (4) and sesbagrandiflorain B (5), have been isolated from the stem bark of an Indonesian plant, Sesbania grandiflora (L.) Pers. The chemical structure of compound 1 was elucidated by UV, IR, MS, and NMR spectroscopic techniques. The proton and carbon NMR resonances of 1 were also compared with the predicted chemical shifts obtained from DFT quantum mechanical calculations with Gaussian. None of the compounds showed antibacterial activity against Bacillus subtilis, Escherichia coli, Mycobacterium smegmatis, Pseudomonas aeruginosa, and Staphylococcus aureus in an agar diffusion assay. However, sesbagrandiflorains A (4) and B (5) exhibited moderate activity against Mycobacterium tuberculosis H37Rv. In addition, compounds 1 - 5 have moderate cytotoxicity against HeLa, HepG2, and MCF-7 cancer cell lines.

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