2,6-Cyclo-xenicanes from the brown algae Dilophus fasciola and Dilophus spiralis

Iοannou, Efstathia; Zervou, Maria; Ismail, Amel; Ktari, L.; Vagias, Constantinos; Roussis, Vassilios

doi:10.1016/j.tet.2009.10.081

Cited by 15 publications

(16 citation statements)

References 17 publications

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“…352 In a study of a Mediterranean Dictyota sp. 357 A brassinosteroid-related compound 322 was isolated from Cystoseira myrica (Fayed, Egypt) in an investigation centered on the cytotoxic activity of the extract against two human cancer cell lines. A study was carried out on the antifouling properties of the more abundant of this series against Pseudoalteromonas sp.…”

Section: Brown Algaementioning

confidence: 99%

Marine natural products

et al. 2011

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Section: Brown Algaementioning

confidence: 99%

Marine natural products

et al. 2011

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“…New diterpenes featuring the 2,6-cyclo-xenicane skeleton (31) were isolated from Dilophus fasciola (Roth) J. V. Lamouroux and Dilophus spiralis (Montagne) G. Hamel (Ioannou et al, 2009). New brominated selinane (32) and cadinane (33) sesquiterpenes were reported from the genus Dictyopteris Lamouroux Qiao et al, 2009;Wen et al, 2009).…”

Section: Brown Algaementioning

confidence: 99%

Marine natural products: chemical and biological potential of seaweeds and their endophytic fungi

Oliveira¹,

Felício²,

Debonsi³

2012

Rev. bras. farmacogn.

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Marine natural products have currently been recognized as the most promising source of bioactive substances for drug discovery research. In this review, extraordinary metabolites from marine algae species are illustrated, as well as approaches for their isolation and determination of their biological properties and pharmaceutical potential. Furthermore, marine endophytic microorganisms (from marine algae) are presented as a new subject for extensive investigation to find novel natural products, which make them a potentially rich and innovative source for new drug candidates.

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“…ligulatus ). Previously, we described the isolation and structural characterization of five new dolastanes, one new 2,6- cyclo -xenicane, twenty new dolabellanes, two diterpenes featuring novel carbon skeletons, and several known compounds [3,4,5,6,7]. Herein, we report the isolation and structure elucidation of three new dolastanes ( 1 – 3 ) and five known perhydroazulene diterpenes.…”

Section: Introductionmentioning

confidence: 98%

Isolation and Structure Elucidation of Three New Dolastanes from the Brown Alga Dilophus spiralis

Iοannou¹,

Vagias²,

Roussis³

2013

Marine Drugs

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Three new dolastane diterpenes (1–3) and five previously reported perhydroazulenes were isolated from the organic extracts of the brown alga Dilophus spiralis. The structure elucidation and the assignment of the relative configurations of the isolated natural products were based on extensive analyses of their spectroscopic data, whereas the absolute configuration of metabolite 2 was determined through its chemical conversion to a previously isolated compound of known configuration.

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2,6-Cyclo-xenicanes from the brown algae Dilophus fasciola and Dilophus spiralis

Cited by 15 publications

References 17 publications

Marine natural products

Marine natural products

Marine natural products: chemical and biological potential of seaweeds and their endophytic fungi

Isolation and Structure Elucidation of Three New Dolastanes from the Brown Alga Dilophus spiralis

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