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. 2015 Jul 22;13(7):4520–4538. doi: 10.3390/md13074520

Table 1.

Antiviral activities of marine fungi and their mechanism of action.

Virus Antiviral Agent Source Chemical Class Effect/Mechanism Reference
EV71 Stachybogrisephenone B (1) Stachybotrys sp. Xanthone IC50: 30.1 µM [34]
Grisephenone A (2) Stachybotrys sp Xanthone IC50: 50.0 µM [34]
3,6,8-Trihydroxy-1-methylxanthone (3) Stachybotrys sp Xanthone IC50: 40.3 µM [34]
HSV Halovirs A–E (48) Scytalidium sp. Peptide direct inactivation [36]
11a-dehydroxyisoterreulactone A (9) Aspergillus terreus SCSGAF0162 Lactone IC50: 33.38 μM [37]
Arisugacin A (10) Aspergillus terreus SCSGAF0162 Lactone IC50: 12.76 μM [37]
Isobutyrolactone II (11) Aspergillus terreus SCSGAF0162 Lactone IC50: 62.08 μM [37]
Aspernolide A (12) Aspergillus terreus SCSGAF0162 Lactone IC50: 68.16 μM [37]
Balticolid (13) Ascomycetous strain 222 Macrolide IC50: 0.45 μM [38]
HIV Equisetin (14) Fusarium heterosporum Tetramic acid IC50: 15 µM [39]
Phomasetin (15) Phoma sp. Tetramic acid IC50: 10 µM [39]
Integric acid (16) Xylaria sp. Acylated eremophilane sesquiterpenoid IC50: 10 µM [40]
IFV Stachyflin (17) Stachybotrys sp. RF-7260 Sesquiterpenoidal alkaloid inhibition of fusion between the viral envelope and the endosome [41,42]
Oxoglyantrypine (18) Cladosporium sp. Indole alkaloid IC50: 85 µM [43]
Norquinadoline A (19) Cladosporium sp. Indole alkaloid IC50: 82 µM [43]
Deoxynortryptoquivaline (20) Cladosporium sp. Alkaloid IC50: 87 µM [43]
Deoxytryptoquivaline (21) Cladosporium sp. Alkaloid IC50: 85 µM [43]
Tryptoquivaline (22) Cladosporium sp. Alkaloid IC50: 89 µM [43]
Quinadoline B (23) Cladosporium sp. Alkaloid IC50: 82 µM [43]
Cladosin C (24) Cladosporium sphaerospermum 2005-01-E3 Hybrid polyketide IC50: 276 μM [44]
(Z)-5-(Hydroxymenthyl)-2-(6′)-methylhept-2′-en-2′-yl)-phenol (25) A. sydowii ZSDS1-F6 Bisabolane-type sesquiterpenoid IC50: 57.4 µM [45]
Diorcinol (26) A. sydowii ZSDS1-F6 Prenylated diphenyl ether IC50: 66.5 µM [45]
Cordyol C (27) A. sydowii ZSDS1-F6 Diphenyl ether IC50: 78.5 µM [45]
Rubrolide S (28) A. terreus OUCMDZ-1925 Rubrolide IC50: 87.1 µM [46]
Asperterrestide A (29) A.terreus SCSGAF0162 Cyclic tetrapeptide H1N1 IC50: 15 µM; H3N2 IC50: 8.1 µM [47]
Isoaspulvinone E (30) A.terreus Gwq-48 Butenolide IC50: 101.23 µM [48]
Aspulvinone E (31) A.terreus Gwq-48 Butenolide IC50: 192.05 µM [48]
Pulvic acid (32) A.terreus Gwq-48 Butenolide IC50: 94.42 µM [48]
Emerimidine A (33) Emericella sp. (HK-ZJ) Isoindolone IC50: 201.1 µM [49]
Emerimidine B (34) Emericella sp. (HK-ZJ) Isoindolone IC50: 296.62 µM [49]
Purpurquinone B (35) P. purpurogenum JS03-21 Azaphilone IC50: 61.3 μM [50]
Purpurquinone C (36) P. purpurogenum JS03-21 Azaphilone IC50: 64.0 μM [50]
Purpuresters A (37) P. purpurogenum JS03-21 Benzofuran IC50: 85.3 μM [50]
TAN-931 (38) P. purpurogenum JS03-21 Nonsteroidal aromatase IC50: 58.6 μM [50]
Sorbicatechol A (39) P. chrysogenum PJX-17 Sorbicillinoids IC50: 85 μM [51]
Sorbicatechol B (40) P. chrysogenum PJX-17 Sorbicillinoids IC50: 113 µM [51]
PRRS Tetrahydroaltersolanol C (41) Alternaria sp. ZJ-2008003 Anthraquinone derivatives IC50: 65 µM [52]
Alterporriol Q (42) Alternaria sp. ZJ-2008003 Isoindolone derivatives IC50: 39 µM [52]
MCV Sansalvamide A (43) Fusarium sp. Pentadepsipeptide inhibition of topoisomerase [53]
RSV 22- O-(N-Me-l-valyl)-21-epi-aflaquinolone B (44) Aspergillus sp. XS-20090B15 Prenylated dihydroquinolone derivatives IC50: 42 nM [54]
TMV 2-(4-hydroxybenzyl) quinazolin-4(3H)-one (45) P. oxalicum 0312F1 Alkaloid EC50: 399.57 µM [55,56]
2-(4-hydroxybenzoyl) quinazolin-4(3H)-one (46) P. oxalicum 0312F1 Alkaloid EC50 not tested [55,56]
Methyl 4-hydroxyphenylacetate (47) P. oxalicum 0312F1 Ester EC50: 829.15 µM [55,56]
AGI-B4 (48) Neosartorya fischeri 1008F1 Dihydroxanthenone IC50: 260 µM [57]
3,4-dihydroxybenzoic acid (49) Neosartorya fischeri 1008F1 Polyphenol IC50: 630 µM [57]