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Review
. 2020 Jan 17;25(2):395.
doi: 10.3390/molecules25020395.

Naturally Occurring Isocoumarins Derivatives from Endophytic Fungi: Sources, Isolation, Structural Characterization, Biosynthesis, and Biological Activities

Affiliations
Review

Naturally Occurring Isocoumarins Derivatives from Endophytic Fungi: Sources, Isolation, Structural Characterization, Biosynthesis, and Biological Activities

Ahmad Omar Noor et al. Molecules. .

Abstract

Recently, the metabolites separated from endophytes have attracted significant attention, as many of them have a unique structure and appealing pharmacological and biological potentials. Isocoumarins represent one of the most interesting classes of metabolites, which are coumarins isomers with a reversed lactone moiety. They are produced by plants, microbes, marine organisms, bacteria, insects, liverworts, and fungi and possessed a wide array of bioactivities. This review gives an overview of isocoumarins derivatives from endophytic fungi and their source, isolation, structural characterization, biosynthesis, and bioactivities, concentrating on the period from 2000 to 2019. Overall, 307 metabolites and more than 120 references are conferred. This is the first review on these multi-facetted metabolites from endophytic fungi.

Keywords: biological activities; biosynthesis; dihydroisocoumarins; endophytes; isocoumarins.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Isocoumarin, 3,4-dihydroisocoumarin, coumarin, and isochroman skeletons.
Figure 2
Figure 2
Distribution of isocoumarin derivatives in different fungal genus.
Figure 3
Figure 3
Structures of isocoumarin derivatives 116.
Figure 4
Figure 4
Structures of isocoumarin derivatives 1733.
Figure 5
Figure 5
Structures of isocoumarin derivatives 3444.
Figure 6
Figure 6
Structures of isocoumarin derivatives 4553.
Figure 7
Figure 7
Structures of isocoumarin derivatives 5466.
Figure 8
Figure 8
Structures of isocoumarin derivatives 6782.
Figure 9
Figure 9
Structures of isocoumarin derivatives 8396.
Figure 10
Figure 10
Structures of isocoumarin derivatives 97105.
Figure 11
Figure 11
Structures of isocoumarin derivatives 106113.
Figure 12
Figure 12
Structures of isocoumarin derivatives 114123.
Figure 13
Figure 13
Structures of isocoumarin derivatives 124136.
Figure 14
Figure 14
Structures of isocoumarin derivatives 137149.
Figure 15
Figure 15
Structure of isocoumarin derivatives 150159.
Figure 16
Figure 16
Structures of isocoumarin derivatives 160164.
Figure 17
Figure 17
Structures of isocoumarin derivatives 165174.
Figure 18
Figure 18
Structures of isocoumarin derivatives 175182.
Figure 19
Figure 19
Structures of isocoumarin derivatives 183187.
Figure 20
Figure 20
Structures of isocoumarin derivatives 188200.
Figure 21
Figure 21
Structures of isocoumarin derivatives 201211.
Figure 22
Figure 22
Structures of isocoumarin derivatives 212228.
Figure 23
Figure 23
Structures of isocoumarin derivatives 229239.
Figure 24
Figure 24
Structures of isocoumarin derivatives 240250.
Figure 25
Figure 25
Structures of isocoumarin derivatives 251264.
Figure 26
Figure 26
Structures of isocoumarin derivatives 265272.
Figure 27
Figure 27
Structures of isocoumarin derivatives 273279.
Figure 28
Figure 28
Structures of isocoumarin derivatives 280294.
Figure 29
Figure 29
Structures of isocoumarin derivatives 295300.
Figure 30
Figure 30
Structures of isocoumarin derivatives 301307.
Figure 31
Figure 31
Proposed biosynthetic pathway of 11, 35, 88, 90, and 165 [21,23,24,25,26].
Figure 32
Figure 32
Proposed biosynthetic pathway of 56 and 125 [27].
Figure 33
Figure 33
Proposed biosynthetic pathway of 273 [28].
Figure 34
Figure 34
Proposed biosynthetic pathway of 70, 71, 138, 179, and 180 [22].
Figure 35
Figure 35
Proposed biosynthetic pathway of 235, 236, and 296 [29].

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References

    1. Ibrahim S.R., Abdallah H.M., Mohamed G.A., Ross S.A. Integracides HJ: New tetracyclic triterpenoids from the endophytic fungus Fusarium sp. Fitoterapia. 2016;112:161–167. doi: 10.1016/j.fitote.2016.06.002. - DOI - PubMed
    1. Ibrahim S.R., Mohamed G.A., Khedr A.I. γ-Butyrolactones from Aspergillus species: Structures, biosynthesis, and biological activities. Nat. Prod. Commun. 2017;12:791–800. doi: 10.1177/1934578X1701200526. - DOI - PubMed
    1. Ibrahim S.R., Elkhayat E.S., Mohamed G.A., Khedr A.I., Fouad M.A., Kotb M.H., Ross S.A. Aspernolides F and G, new butyrolactones from the endophytic fungus Aspergillus terreus. Phytochem. Lett. 2015;14:84–90. doi: 10.1016/j.phytol.2015.09.006. - DOI
    1. Ibrahim S.R., Mohamed G.A., Moharram A.M., Youssef D.T. Aegyptolidines A and B: New pyrrolidine alkaloids from the fungus Aspergillus aegyptiacus. Phytochem. Lett. 2015;12:90–93. doi: 10.1016/j.phytol.2015.03.001. - DOI
    1. Ibrahim S.R., Mohamed G.A., Al Haidari R.A., El-Kholy A.A., Zayed M.F. Potential anti-malarial agents from endophytic fungi: A review. Mini Rev. Med. Chem. 2018;18:1110–1132. doi: 10.2174/1389557518666180305163151. - DOI - PubMed