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Review
. 2020 Jun 15;18(6):317.
doi: 10.3390/md18060317.

Chemical Diversity and Biological Activities of Meroterpenoids from Marine Derived-Fungi: A Comprehensive Update

Affiliations
Review

Chemical Diversity and Biological Activities of Meroterpenoids from Marine Derived-Fungi: A Comprehensive Update

Amr El-Demerdash et al. Mar Drugs. .

Abstract

Meroterpenoids are a class of hybrid natural products, partially derived from a mixed terpenoid pathway. They possess remarkable structural features and relevant biological and pharmacological activities. Marine-derived fungi are a rich source of meroterpenoids featuring structural diversity varying from simple to complex molecular architectures. A combination of a structural variability and their myriad of bioactivities makes meroterpenoids an interesting class of naturally occurring compounds for chemical and pharmacological investigation. In this review, a comprehensive literature survey covering the period of 2009-2019, with 86 references, is presented focusing on chemistry and biological activities of various classes of meroterpenoids isolated from fungi obtained from different marine hosts and environments.

Keywords: anti-inflammatory; antibacterial; biological activities; cytotoxicity; marine-derived fungi; meroterpenoids.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Chemical structures of acyclic merohemiterpenes 117.
Figure 2
Figure 2
Chemical structures of cyclic hemiterpenes 1828.
Figure 3
Figure 3
Chemical structures of meromonoterpenoids 2937.
Figure 4
Figure 4
Chemical structures of acyclic sesquiterpenes 3851.
Figure 5
Figure 5
Chemical structures of acyclic sesquiterpenes 5260.
Figure 6
Figure 6
Chemical structures of monocyclic sesquiterpenes 6169.
Figure 7
Figure 7
Chemical structures 7077.
Figure 8
Figure 8
Chemical structures of 7892.
Figure 9
Figure 9
Chemical structures of pyripyropenes 93103.
Figure 10
Figure 10
Chemical structures of 104 and 105.
Figure 11
Figure 11
Chemical structures of 106113.
Figure 12
Figure 12
Chemical structures of 114120.
Figure 13
Figure 13
Chemical structures of 121130.
Figure 14
Figure 14
Chemical structures of 131134.
Figure 15
Figure 15
Chemical structures of australides 135163.
Figure 16
Figure 16
Chemical structures of austinoids 164171.
Figure 17
Figure 17
Chemical structures dehydroaustinoid derivatives 172185.
Figure 18
Figure 18
Chemical structures isoaustinoids 186194.
Figure 19
Figure 19
Chemical structures of preaustinoids 195200, 202206 and 208213.
Figure 20
Figure 20
Chemical structures of preaustinoid derivatives 201, 207 and 214230.
Figure 21
Figure 21
Chemical structures of terretonin derivatives 231241.
Figure 22
Figure 22
Chemical structures of andrastin derivatives 242253.
Figure 23
Figure 23
Chemical structures of 254258.
Figure 24
Figure 24
Chemical structures of 259261.
Figure 25
Figure 25
Chemical structures 262268.
Figure 26
Figure 26
Chemical structures of 269288.
Figure 27
Figure 27
Chemical structures 289306.
Figure 28
Figure 28
Chemical structures of 307320.

References

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    1. Peng X., Qiu M. Meroterpenoids from Ganoderma species: A Review of Last Five Years. Nat. Prod. Bioprospect. 2018;8:137–149. doi: 10.1007/s13659-018-0164-z. - DOI - PMC - PubMed
    1. Menna M., Imperatore C., D’Aniello F., Aiello A. Meroterpenes from marine invertebrates: Structures, occurrence, and ecological implications. Mar. Drugs. 2013;11:1602–1643. doi: 10.3390/md11051602. - DOI - PMC - PubMed
    1. Geris R., Simpson T.J. Meroterpenoids produced by fungi. Nat. Prod. Rep. 2009;26:1063–1094. doi: 10.1039/b820413f. - DOI - PubMed
    1. Hu Y., Legako A.G., Espindola A.P.D.M., MacMillan J.B. Erythrolic acids A–E, meroterpenoids from a marine-derived Erythrobacter sp. J. Org. Chem. 2012;77:3401–3407. doi: 10.1021/jo300197z. - DOI - PMC - PubMed

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