Isolation and Structural Elucidation of a Novel Heptaoxygenated Xanthone from Securidaca longepedunculata Fresen. with Potential Antimicrobial Properties

Authors

  • Akpemi Audu Musa Department of Chemistry, Federal University of Education, Zaria-Nigeria Author
  • Adebayo Ojo Oyewale Department of Chemistry, Ahmadu Bello University, Zaria, Nigeria Author
  • George Iloegbulam Ndukwe Department of Chemistry, Ahmadu Bello University, Zaria, Nigeria Author
  • Sabo E. Yakubu Department of Microbiology, Ahmadu Bello University, Zaria-Nigeria Author

DOI:

https://doi.org/10.33003/chemclass-2025-0902/198

Keywords:

1, 6-Dihydroxyl-2, 3, 5, 7, 8-pentamethoxyxanthone, Securidaca longepedunculata, xanthone , drug resistance, Antimicrobial agents

Abstract

In the search for novel antimicrobial agents to combat drug-resistant pathogens, we isolated and 
characterized a new heptaoxygenated xanthone, 1,6-dihydroxy-2,3,5,7,8-pentamethoxyxanthone (1), from 
Securidaca longepedunculata. The structure was elucidated using comprehensive spectroscopic techniques 
(IR, UV, EIMS, and 1D/2D NMR), revealing a unique substitution pattern. Additionally, the known 
benzophenone (4-methoxybenzo[1,3]dioxol-5-yl)-phenylmethanone (2) was identified. Compound 1’s 
structural features suggest potential antimicrobial activity, warranting further biological evaluation. This 
study underscores the plant’s role as a source of bioactive xanthones for addressing antimicrobial resistance.

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Published

2025-07-17