Secondary metabolites of fungi from marine habitats

Rateb, Mostafa E.; Ebel, Rainer

doi:10.1039/c0np00061b

Cited by 573 publications

(441 citation statements)

References 458 publications

(527 reference statements)

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“…Due to the frequent rediscovery of the known fungal metabolites from common habitats, fungi from special ecological niches have attracted much attention of natural product researchers (Bugni & Ireland 2004;Rateb & Ebel 2011;Lin et al 2012;Zhou 2014). Marine fungi produce unique and biologically active secondary metabolites (Zhao et al 2010;Deng et al 2013;Suciati et al 2013).…”

Section: Introductionmentioning

confidence: 99%

A new naphthalene glycoside from the sponge-derived fungus Arthrinium sp. ZSDS1-F3

Wang

et al. 2014

Natural Product Research

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(2014) A new naphthalene glycoside from the sponge-derived fungus Arthrinium sp. ZSDS1-F3, Natural Product Research: Formerly Natural Product Letters, 28:14, 1070-1074, DOI: 10.1080/14786419.2014 To link to this article: http://dx.doi.org/10.1080/14786419.2014.905935 PLEASE SCROLL DOWN FOR ARTICLETaylor & Francis makes every effort to ensure the accuracy of all the information (the "Content") contained in the publications on our platform. However, Taylor & Francis, our agents, and our licensors make no representations or warranties whatsoever as to the accuracy, completeness, or suitability for any purpose of the Content. Any opinions and views expressed in this publication are the opinions and views of the authors, and are not the views of or endorsed by Taylor & Francis. The accuracy of the Content should not be relied upon and should be independently verified with primary sources of information. Taylor and Francis shall not be liable for any losses, actions, claims, proceedings, demands, costs, expenses, damages, and other liabilities whatsoever or howsoever caused arising directly or indirectly in connection with, in relation to or arising out of the use of the Content.This One new naphthalene derivative, 1,8-dihydroxynaphthol-1-O-a-L-rhamnopyranoside (1), together with one known a-dibenzopyrone, alternariol (2), and five xanthones (3 -7) were isolated from the sponge-derived fungus Arthrinium sp. ZSDS1-F3. All the isolated compounds (1 -7) were established by comprehensive analysis of the spectral data, especially 1D and 2D NMR (HMQC and HMBC) spectra. In the primary bioassays, compound 3 exhibited moderate COX-2 inhibition, with IC 50 values of 12.2 mM.article may be used for research, teaching, and private study purposes. Any substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing, systematic supply, or distribution in any form to anyone is

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Section: Introductionmentioning

confidence: 99%

A new naphthalene glycoside from the sponge-derived fungus Arthrinium sp. ZSDS1-F3

Wang

et al. 2014

Natural Product Research

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“…This information coupled with the key HMBC correlations from H-2, H-13 and H-17 to C-11 and from H-14 and H-16 to C-18 enabled us to establish the structure of (2) as shown in Figure 2. We proposal that chorismate acid may be a biogenetic precursor for (2).…”

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confidence: 89%

“…1,2 The genus Aspergillus (Moniliaceae), with over 180 species, has attracted considerable attention as a rich source of alkaloids, terpenoids, xanthones, polyketides and etc, some of which showed antifungal, antibacterial, anti-HIV and cytotoxic activities. [3][4][5] In order to obtain new bioactive metabolites from marine fungi, we investigated on the marine fungal strain Aspergillus sydowii SCSIO 00305 isolated from a healthy tissue of Verrucella umbraculum.…”

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confidence: 99%

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Indole alkaloids from marine-derived fungus Aspergillus sydowii SCSIO 00305

Sun

Liu

et al. 2011

J Antibiot

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“…Secondary metabolites of marine-derived fungi have attracted a great attention for natural product research since the end of last century, which afforded more than 1000 new compounds so far (Rateb & Ebel 2011). Among them, over 20% were obtained from marine algicolous fungi, including endophytic and epiphytic strains (Rateb & Ebel 2011).…”

Section: Introductionmentioning

confidence: 99%