Affiliations 

  • 1 Department of Chemistry, Faculty of Mathematics and Natural Sciences, University of Lampung, Bandar Lampung 35145, Lampung, Indonesia
  • 2 Department of Pharmaceutical Sciences, Oregon State University, Corvallis, Oregon 97331-3507, USA
  • 3 Institute of Innovative Research, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152-8550, Japan
  • 4 Department of Pharmacognosy and Phytochemistry, Faculty of Pharmacy, University of Airlangga, Surabaya 60286, Indonesia
  • 5 School of Biological Sciences, Universiti Sains Malaysia, Minden 11800, Penang, Malaysia
  • 6 Department of Chemistry, Oregon State University, Corvallis, Oregon 97331-3507, USA
Phytochem Lett, 2020 Feb;35:211-215.
PMID: 32863985 DOI: 10.1016/j.phytol.2019.12.008

Abstract

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.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.