Affiliations 

  • 1 Center of Chemical Innovation for Sustainability (CIS) and School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand
  • 2 Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand
  • 3 School of Biosciences, Faculty of Health and Medical Sciences, Taylor's University, Lakeside Campus, 47500 Subang Jaya, Selangor, Malaysia
  • 4 School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand
  • 5 Medicinal Plant Innovation Center of Mae Fah Luang University and School of Integrative Medicine, Mae Fah Luang University, Chiang Rai 57100, Thailand
  • 6 Chanae, Narathiwat 96220, Thailand
  • 7 Departments of Chemistry and Earth, Ocean & Atmospheric Sciences, University of British Columbia, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
J Nat Prod, 2024 Jun 28;87(6):1611-1617.
PMID: 38805684 DOI: 10.1021/acs.jnatprod.4c00248

Abstract

The first phytochemical investigation of the twig extract of Uvaria leptopoda resulted in the isolation and identification of three new tetrahydroxanthene-1,3(2H)-diones, uvarialeptones A-C, two new oxidized hexadiene derivatives, uvarialeptols A and B, together with ten known compounds. Their structures were elucidated by spectroscopic techniques and mass spectrometry. Uvarialeptones A and B were unprecedented tetrahydroxanthene-1,3(2H)-dione dimers which exhibited a cyclobutane ring via [2 + 2] cycloaddition from uvarialeptone C and 9a-O-methyloxymitrone, respectively. The structure of uvarialeptone A was confirmed by X-ray diffraction analysis using Mo Kα radiation. Compound 3 inhibited NO production at an IC50 value of 6.7 ± 0.1 μM.

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