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Sesquiterpenes from the Brazilian red alga Laurencia dendroidea J. Agardh.

Molecules (Basel, Switzerland)2014da Silva Machado FL, Ventura TL, Gestinari LM, et al.
Study designOther primary literature
SubjectAnimal

Abstract

Two new chamigrane sesquiterpenes 1-2 and three known compounds 3-5 were isolated from a lipophilic extract of the red alga Laurencia dendroidea collected from the Southeastern Brazilian coast. Dendroidone (1) and dendroidiol (2) were isolated from samples collected at Biscaia Inlet, Angra dos Reis, Rio de Janeiro and at Manguinhos Beach, Serra, Espírito Santo, respectively. Debromoelatol (3), obtusane (4) and (1S*,2S*,3S*,5S*,8S*,9S*)-2,3,5,9-tetramethyltricyclo[6.3.0.0¹·⁵]undecan-2-ol (5) were obtained from specimens collected at Vermelha Beach, Parati, Rio de Janeiro. The structures of new compounds were elucidated by extensive NMR (¹H-, ¹³C-, COSY, HSQC, HMBC and NOESY) and high resolution mass spectrometry analysis. Additionally, the absolute configuration of compound 2 was assigned by X-ray analysis. Full spectroscopic data is described for the first time for compound 3. Anti-inflammatory and antimycobacterial activities of compounds 2-5 were evaluated. Compounds 3-5 inhibited the release of inflammatory mediator NO while TNF-α levels were only affected by 3. All compounds tested displayed moderate antimycobacterial action.

MeSH

AnimalsCell LineInhibitory Concentration 50LaurenciaMacrophagesMiceNitric OxideNuclear Magnetic Resonance, BiomolecularPlant ExtractsSesquiterpenesTumor Necrosis Factor-alpha

DOI 10.3390/molecules19033181

PMID 24642907

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