Your browser doesn't support javascript.
loading
Tongalides, Halogenated Butenolides from an Antarctic Delisea sp. Rhodophyte.
Bracegirdle, Joe; Kennedy, Sarah J; Shan, Chuan; Wojtas, Lukasz; Shaw, Lindsey N; Amsler, Charles D; McClintock, James B; Baker, Bill J.
Affiliation
  • Bracegirdle J; Department of Chemistry, University of South Florida, 4202 E. Fowler Avenue, CHE205, Tampa, Florida 33620, United States.
  • Kennedy SJ; Department of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, 4202 E. Fowler Avenue, ISA2015, Tampa, Florida 33620, United States.
  • Shan C; Department of Chemistry, University of South Florida, 4202 E. Fowler Avenue, CHE205, Tampa, Florida 33620, United States.
  • Wojtas L; Department of Chemistry, University of South Florida, 4202 E. Fowler Avenue, CHE205, Tampa, Florida 33620, United States.
  • Shaw LN; Department of Cell Biology, Microbiology, and Molecular Biology, University of South Florida, 4202 E. Fowler Avenue, ISA2015, Tampa, Florida 33620, United States.
  • Amsler CD; Department of Biology, University of Alabama at Birmingham, 1300 University Boulevard, Birmingham, Alabama 35233, United States.
  • McClintock JB; Department of Biology, University of Alabama at Birmingham, 1300 University Boulevard, Birmingham, Alabama 35233, United States.
  • Baker BJ; Department of Chemistry, University of South Florida, 4202 E. Fowler Avenue, CHE205, Tampa, Florida 33620, United States.
J Nat Prod ; 85(7): 1886-1891, 2022 07 22.
Article in En | MEDLINE | ID: mdl-35771948
ABSTRACT
Six new halogenated butenolides, tongalides A-C (1-3) and their acetylated congeners (4-6), were isolated from an extract of the Antarctic rhodophyte Delisea sp. that displayed significant antibiotic activity. The structures of the compounds were determined by analysis of data acquired by spectroscopic and spectrometric techniques including NMR, HRESIMS, optical rotation, and X-ray diffraction studies. The newly isolated compounds were assayed for antibacterial activity, but exhibited no growth inhibition of ESKAPE pathogens. The extract bioactivity was attributed to the previously reported Z-acetoxyfimbrolide A also isolated from the extract, providing further evidence that the exocyclic double bond is essential to the antibacterial activity of the structurally related fimbrolide class of metabolite.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: 4-Butyrolactone / Anti-Bacterial Agents Language: En Journal: J Nat Prod Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: 4-Butyrolactone / Anti-Bacterial Agents Language: En Journal: J Nat Prod Year: 2022 Document type: Article Affiliation country: