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Dendrillic Acids A and B: Nitrogenous, Rearranged Spongian Nor-Diterpenes from a Dendrilla sp. Marine Sponge.
Sala, Samuele; James, Patrick J C; Nealon, Gareth L; Fromont, Jane; Gomez, Oliver; Vuong, Daniel; Lacey, Ernest; Flematti, Gavin R.
Afiliação
  • Sala S; School of Molecular Sciences, The University of Western Australia, Crawley, WA 6009, Australia.
  • James PJC; Australian National Phenome Centre and Centre for Computational and Systems Medicine, Health Futures Institute, Murdoch University, Harry Perkins Building, Perth, WA 6150, Australia.
  • Nealon GL; School of Molecular Sciences, The University of Western Australia, Crawley, WA 6009, Australia.
  • Fromont J; School of Molecular Sciences, The University of Western Australia, Crawley, WA 6009, Australia.
  • Gomez O; Collection and Research, Western Australian Museum, Welshpool, WA 6106, Australia.
  • Vuong D; Collection and Research, Western Australian Museum, Welshpool, WA 6106, Australia.
  • Lacey E; Microbial Screening Technologies Pty. Ltd., Smithfield, NSW 2164, Australia.
  • Flematti GR; Microbial Screening Technologies Pty. Ltd., Smithfield, NSW 2164, Australia.
J Nat Prod ; 86(3): 482-489, 2023 03 24.
Article em En | MEDLINE | ID: mdl-36926864
Two nitrogenous rearranged spongian nor-diterpenoids, dendrillic acids A and B, were isolated from a marine sponge Dendrilla sp. (order: Dendroceratida; family: Darwinellidae). The structures of the metabolites were elucidated on the basis of spectroscopic analysis as well as density functional theory prediction of NMR chemical shifts and application of the DP4+ algorithm. The absolute configuration of the metabolites was established via comparison of experimental and time-dependent density functional theory predicted electronic circular dichroism data. An unusual epimerization reaction was observed leading to the interconversion of the metabolites upon storage in dimethyl sulfoxide solution, which is proposed to proceed via an anionic pathway as probed via isotopic incorporation experiments. Evaluation against a panel of micro-organisms and cell lines revealed that the compounds were devoid of any significant biological activity against all organisms tested, with the exception of mild antiprotozoal activity displayed by dendrillic acid B (2) against Giardia duodenalis.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poríferos / Diterpenos Limite: Animals Idioma: En Revista: J Nat Prod Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poríferos / Diterpenos Limite: Animals Idioma: En Revista: J Nat Prod Ano de publicação: 2023 Tipo de documento: Article