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Review

Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi

by
Xiaohan Wang
,
Yuying Li
,
Xuping Zhang
,
Daowan Lai
and
Ligang Zhou
*
Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China
*
Author to whom correspondence should be addressed.
Molecules 2017, 22(12), 2026; https://doi.org/10.3390/molecules22122026
Submission received: 4 October 2017 / Revised: 22 November 2017 / Accepted: 15 November 2017 / Published: 23 November 2017
(This article belongs to the Section Natural Products Chemistry)
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Versions Notes

Abstract

:
Cyclodipeptides, called 2,5-diketopiperazines (2,5-DKPs), are obtained by the condensation of two amino acids. Fungi have been considered to be a rich source of novel and bioactive cyclodipeptides. This review highlights the occurrence, structures and biological activities of the fungal cyclodipeptides with the literature covered up to July 2017. A total of 635 fungal cyclodipeptides belonging to the groups of tryptophan-proline, tryptophan-tryptophan, tryptophan–Xaa, proline–Xaa, non-tryptophan–non-proline, and thio-analogs have been discussed and reviewed. They were mainly isolated from the genera of Aspergillus and Penicillium. More and more cyclodipeptides have been isolated from marine-derived and plant endophytic fungi. Some of them were screened to have cytotoxic, phytotoxic, antimicrobial, insecticidal, vasodilator, radical scavenging, antioxidant, brine shrimp lethal, antiviral, nematicidal, antituberculosis, and enzyme-inhibitory activities to show their potential applications in agriculture, medicinal, and food industry.

1. Introduction

Cyclodipeptides (or cyclic dipeptides) are usually called 2,5-diketopiperazines (2,5-DKPs) or dioxopiperazines, and result from the condensation of two amino acids such as tryptophan, proline, alanine, histidine, leucine, isoleucine, phenylalanine, serine, and tyrosine [1]. They are the smallest cyclopeptides, and are distributed in many organisms including fungi, bacteria, plants and animals [1,2,3]. Since the first report in 1924, a large number of bioactive cyclodipeptides has been discovered to show cytotoxic, antitumor, antiviral, antifungal, antibacterial, antiprion, antioxidant, antihyperglycemic as well as biofilm and glycosidase inhibitory activities [2,3,4]. Some cyclodipeptides (e.g., tryprostatin A (103), tryprostatin B (104), FR106969 (590), and phenylahistin (392)) showed their potential applications [1].
Among the organisms, fungi have been considered as the most important sources of novel and bioactive cyclodipeptides. More and more cyclodipeptides with interesting biological activities have been isolated and characterized from fungi. However, no detailed and comprehensive summary of the fungal cyclodipeptides on their occurrence, structures and biological activities has been reported though chemistry and biology of the cyclodipeptides from either all organisms or a certain class of cyclodipeptides have been documented [3,5,6]. In this review, we aim to describe the diversity of chemical structures and biological activities of the fungal cyclodipeptides and their analogs. A total of 635 fungal cyclodipeptides have been discussed and reviewed with literature covered up to July 2017. According to their biosynthetic origins and structural characters, these cyclodipeptides are classified as tryptophan–proline, tryptophan–tryptophan, tryptophan–Xaa (Xaa is indicated as an unspecified amino acid), proline–Xaa, non-tryptophan–non-proline, and thio analogs. Some special cyclodipeptides (e.g., gunnilactams A–C (378–380)), which did not belong to 2,5-DKPs, were also included in the group of non-tryptophan-non-proline analogs.

2. Tryptophan–Proline Cyclodipeptides

Tryptophan and proline are simultaneously incorporated into the cyclodipeptides in fungi. The proline residue adopts a cis-conformation about the Xaa–Pro tertiary amide bond and hence makes the Xaa–Pro sequence prone to cyclodipeptide formation. The tryptophan-proline cyclo(l-Trp–l-Pro) core was derived from condensation of tryptophan and proline residues, and this was often further modified by heterocyclization and isoprenyl addition [6]. The occurrence and biological activities of the tryptophan-proline cyclodipeptides from fungi are listed in Table 1, and their structures are provided in Figure 1.
About 116 tryptophan-proline cyclodipeptides have been isolated from fungi so far. They are mainly distributed in the genera Aspergillus and Penicillium, and are also distributed in other genera such as Alternaria, Paecilomyces, and Pseudallescheria.
(+)-Austamide (4) and (+)-deoxyisoaustamide (28) were isolated from the maize meal cultures of the toxigenic fungus Aspergillus ustus, and (+)-austamide (4) caused acute toxicosis in day-old ducklings [7].
Fumitremorgin C (40) and its derivatives (38, 39) were identified in Aspergillus fumigatus from the holothurian Stichopus alternata. They displayed significant cytotoxic activity against MOLT-4 (human acute lymphoblastic leukemia cells), A-549 (human lung adenocarcinoma epithelial cells), and HL-60 (human promyelocytic leukemia cells), which speculated that this cytotoxic activity may be linked to hydroxyl groups in the side chains of the molecules [8]. Demethoxyfumitremorgin C (26) from marine-derived Aspergillus fumigatus showed inhibitory activity in the mouse cell cycle against tsFT210, and also inhibited tumor cell cycle arrest at G2/M with a minimum inhibitory concentration (MIC) value of 0.45 μM [9].
18-Oxotryprostatin A (77) was isolated from the marine-derived fungus Aspergillus sydowi and found to exhibit weak cytotoxic activity against A-549 cells with a median inhibitory concentration (IC50) value of 1.28 μM [10]. This compound was also obtained from the endophytic fungus Aspergillus fumigatus from Melia azedarach to display plant growth inhibitory activity [11].
Spirotryprostatins (87–94) were isolated from Aspergillus fumigatus. These compounds showed cytotoxic activity by inhibiting mammalian cell cycle at G2/M phase [8,12,13].
Stephacidin B (98) was isolated from Aspergillus ochraceus. This compound exhibited potent cytotoxic activity against LNCaP (a testosterone-dependent prostate cancer cell line), with IC50 values from 91 to 621 nM [14].
Both tryprostatins A (103) and B (104), which are prenylated, were isolated from the fermentation broth of the marine-derived fungus Aspergillus fumigatus [15]. Tryprostatin A (103) was an inhibitor of the multidrug-resistance breast cancer protein (BCRP) that mediated resistance to chemotherapeutics in breast cancer treatment [16], whereas tryprostatin B (104) was a mammalian cell-cycle inhibitor, attractive as a potential anticancer agent [17]. Furthermore, tryprostatin A (103) exhibited inhibitory activity on the elongation of lettuce shoots [11].

3. Tryptophan–Tryptophan Cyclodipeptides

The ditryptophan cyclodipeptides, which have two tryptophan units, are widely distributed in filamentous fungi, especially in the genera Penicillium and Aspergillus. Their occurrence and biological activities are listed in Table 2, and the structures are provided in Figure 2.
Amauromine (117) from Amauroascus sp. [54] was identical with nigrifortine (117) from Penicillium nigricans. It is a diannulated DKP analog which shows hypotensive vasodilating activity [55]. This compound was later isolated from Auxarthron reticulatum, and identified as a selective cannabinoid CB1 receptor antagonist [56].
Epiamauromine (120) and N-methylepiamauromine (127) were isolated from the sclerotia of Aspergillus ochraceus. They caused moderate reduction in weight gain against the corn earworm Helicoverpa zea [57].
Fellutanines A–D (121, 123–125), the analogs of cyclo(l-Trp–d-Trp), were isolated from the cultures of Penicillium fellutanum. Among them, only fellutanine D (125) was diannulated and displayed cytotoxic activity against K-562 (human myeloid leukemia cells), L-929 (mouse fibroblastic cell), and HeLa (human epitheloid cervix carcinoma cells) with IC50 values of 9.5, 11.6 and 19.7 μg/mL, respectively [58].
Novoamauromine (128) was obtained from Aspergillus novofumitatus CBS117520. This compound had inhibitory activity on the cell proliferation of A549, HeLa, LNCap (human prostate carcinoma cells) [59].
Okaramines A–U (129–149) have been isolated from Aspergillus aculeatus [60], Aspergillus taichungensis [61], and Penicillium simplicissimum [62,63,64,65]. Structure–activity studies indicated the importance of the azetidine and azocine rings to okaramine insecticidal activity [66]. The action of okaramine B (130) on silkworm larval neurons using patch-clamp electrophysiology revealed that this compound activated the l-glutamate-gated chloride channel (GluCl) [67].

4. Tryptophan–Xaa Cyclodipeptides

Apart from Trp–Pro and Trp–Trp cyclodipeptides, other tryptophan cyclodipeptides are also abundant in fungi and represent a structurally diverse group of natural products. Their occurrence and biological activities are shown in Table 3, and their structures are provided in Figure 3.
Aspertryptanthrins A–C (156–158) were obtained from a terrestrial-derived fungus Aspergillus sp. These compounds all contain an anthranilate unit and a tryptophan residue. In addition, aspertryptanthrin C (158) contains a rare 16-membered ring [74].
The cyclodipeptides brevicompanine C (163), cyclo(l-Trp–d-Ile) (182) and cyclo(l-Trp–d-Leu) (183) from Penicillium brevi-compactum [75], as well as cyclo(l-Trp–l-Phe) (187) from Penicillium sp. [76] accelerated the root growth of the lettuce seedlings in proportion to their concentrations from 1 to 100 mg/L.
Brevicompanines D–H (164–168) were isolated from a deep ocean sediment derived fungus Penicillium sp. [77]. Both brevicompanines E (165) and H (168) inhibited lipopolysaccharide (LPS)-induced nitric oxide production in BV2 microglial cells. Further studies showed that brevicompanine E (165) reduced lipopolysaccharide-induced production of pro-inflammatory cytokines and enzymes in microglia by inhibiting activation of activator protein-1 and nuclear factor κB and, hence, may be potentially useful for modulating neuroinflammation [78].
Cycloechinulin (190) was isolated from the sclerotia of Aspergillus ochraceus, and it showed moderate insecticidal activity against the lepidopteran crop pest Helicoverpa zea [57].
Echinulin (206) is one of the simplest classes of isoprenylated tryptophan cyclodipeptides. It was toxic to rabbits, producing a significant degree of damage to lung and liver [79].
Fructigenines A (211) and B (212) are annulated derivatives of cyclo(l-Trp–l-Phe) (187), and were isolated from Penicillium fructigenum. Only fructigenine A (211) inhibited growth of Avena coleoptiles and L-5178Y (mouse lymphoma cells), and was subsequently found to have more potent anti-inflammatory activity than indomethacin in the mouse ear edema model [80]. Fructigenine A (211) was also named rugulosuvine B (211) in Penicillium rugulosum, and showed potent anti-inflammatory and antitumor activities in vitro [81].
Neoechinulin A (234) had scavenging, neurotrophic factor-like and antiapoptotic activities. The protective properties of neoechinulin A (234) against SIN-1-induced neuronal cell death suggested that neoechinulin A (234) could protect against neuronal cell death in neurodegenerative diseases [82].
The valine analog polanrazine A (250) was isolated from the blackleg fungus Phoma lingam (teleomorph: Leptosphaeria maculans). This compound was toxic to canola (Brassica napus and B. rapa) [83].
Rubrumlines A–O (267–281) were isolated from the marine-derived fungus Eurototium rubrum. Among them, rubrumlines D (270), F (272), G (273), J (276), M (279), N (280), and O (281) showed inhibitory activity against influenza A/WSN/33 virus. Further analysis of the structure–activity relationship revealed that the analogs with an isoprenyl unit in indole ring displayed stronger cytotoxic effects than those linked by an oxygenated isoprenyl unit. Neoechinulin B (235) was also isolated from Eurototium rubrum. This compound was efficient in inhibiting influenza A/WSN/33 virus propagation even after the fifth passage. In addition, it exerted potent inhibition against H1N1 virus infected in MDCK cells, and was able to inhibit a panel of influenza virus strains including amantadine- and oseltamivir-resistant clinical isolates. The high potency and broad-spectrum activities against influenza viruses with less drug resistance made neoechinulin B (235) a new lead for the development of potential inhibitor of influenza viruses [84].
The prenylated pyranoindole derivatives talathermophilins A (284) and B (285) were isolated from a thermophilic fungus Talaromyces thermophilus strain YM1-3. Both talathermophilins A (284) and B (285) showed nematicidal activity toward the worms of the free-living nematode Panagrellus redivevus [85].
Variecolorins A–L (293–304) were isolated from halotolerant fungus Aspergillus variecolor [80], and variecolorins M–O (305–307) from deep ocean sediment-derived fungus Penicillium griseofulvum [86]. They all showed weak radical scavenging activity against DPPH [86,87].

5. Proline–Xaa Cyclodipeptides

Except Trp–Pro cyclodipeptides, other proline containing cyclodipeptides (Pro–Xaa) are also abundantly distributed in fungi. Their occurrence and biological activities are shown in Table 4, and their structures are provided in Figure 4.
Cyclo(l-Pro–l-Ala) (318) was isolated from Alternaria alternata [149] and the phytopathogenic fungus Colletotrichum gloesporoides [150]. This compound inhibited aflatoxin production in aflatoxigenic fungi without affecting fungal growth. Further investigation on the mode of action suggested that this cyclodipeptide inhibited aflatoxin biosynthesis by affecting glutathione S-transferase (GST) function in Aspergillus flavus to show its potency as the biocontrol agent [151].
Cyclo(l-Pro–l-Phe) (334) and cyclo(l-Pro–l-Tyr) (337), which were also called maculosin-2 (334) and maculosin-1 (337), were host-specific fungal phytotoxins produced by Alternaria alternata on spotted knapweed (Centaurea maculosa) to show their protential as the bioherbicides [149].
The dechlorinated cyclodipeptide, cyclo(13,15-dichloro-l-Pro–l-Tyr) (338), isolated from the fungus Leptoxyphium sp. is considered as an inhibitor of monocyte chemotactic protein-1 (CCL2)-induced chemotaxis and was 10- to 20-fold more active than the nonchlorinated from maculosin-1 (337). In addition, no cellular toxicity was observed when cyclo(13,15-dichloro-l-Pro–l-Tyr) (338) at 100 μM was in contact with human monocyte culture for 24 h, suggesting its potential as a lead structure for the future development of anti-inflammatory compounds [152].

6. Non-Tryptophan–Non-Proline Cyclodipeptides

Non-tryptophan–non-proline cyclodipeptides mean neither tryptophan nor proline is incorporated into this group of cyclodipeptides in the fungi. Their occurrence and biological activities are shown in Table 5, and the structures are provided in Figure 5.
3-Acetamino-6-isobutyl-2,5-dioxopiperazine (346) and 3-isopropyl-6-isobutyl-2,5-dioxopiperazine (383), belonging to the aliphatic isoleucine cyclodipeptide, were isolated from Cordyceps sinensis. Only 3-acetamino-6-isobutyl-2,5-dioxopiperazine (346) had cytotoxic activity against L-929, A375, and HeLa cells [169].
Azonazine (350) was isolated from a Hawaiian marine sediment-derived fungus Aspergillus insulicola, and exhibited anti-inflammatory activity by inhibiting NF-κB luciferase (IC50, 8.37 μM) and nitrate production (IC50, 13.7 μM) [170].
Cyclo(l-Phe–l-Phe) (357) originally isolated from Penicillium nigricans was also isolated from a marine mangrove endophytic fungus [171], and exhibited good anthelmintic activity against Hymenolepis nata and Schistosoma mansoni in mice [172].
Cyclic phenylalanyl serine cyclo(Phe–Ser) (358) was isolated from the insect pathogenic fungus Verticillium hemipterigenum. It exhibited concentration-dependent atypical intestinal absorption in the small intestine of rats, which consisted of passive transport, carrier-mediated absorptive transport by PEPT1, and carrier-mediated excretive transport. It also exhibited weak inhibition of several cancer cell lines and selected microorganisms [173,174].
The tyrosine analog cyclo(l-Tyr–l-Tyr) (360) isolated from the culture broth of Cordyceps sinensis reversibly blocked voltage-dependent L-type calcium channels [169].
Diatretol (365) from the fungus Clitocybe diatreta exhibited a weak antibacterial activity. A single-crystal X-ray analysis showed that diatretol (365) has a nearly planar boat conformation in the solid state [175].
Dimerumic acid (368) has been isolated from the fungus Monascus anka, traditionally used for fermentation of food, and shown to be an antioxidant with hepatoprotective actions against chemically induced liver injuries [176], as well as protecting against oxidative stress-induced cytotoxicity in the isolated rat hepatocytes [177].
Gliocladride (374) isolated from marine fungus Gliocladium sp. showed a cytotoxic effect with an IC50 value of 3.86 mg/mL against human A375-S2 melanoma cell line [178].
Gliocladrides A (375) and B (376) as well as deoxymycelianamide (363) were isolated from the marine fungus Gliocladium sp. to show cytotoxic activity against the three cell lines (HL-60, U937 and T47D) with IC50 values 11.6–52.8 μg/mL, while deoxymycelianamide (363) showed the strongest cytotoxic activity against U937 cell line with an IC50 value of 0.8 μg/mL [179].
Golmaenone (377) from the culture broth of the marine-derived fungus Aspergillus sp. exhibited a significant radical scavenging activity against 1,1-diphenyl-2-picrylhydrazyl (DPPH) and showed UV-A (320–390 nm) protecting activity which was more active than oxybenzone currently used as a sunscreen [103].
The marine-derived fungus Aspergillus sp. yielded mactanamide (386) containing an R-2,6-dihydroxyphenylalanine, which showed fungistatic activity to Candida albicans at nontoxic concentration [180].
Three siderophores NBRI16716A (388), NBRI16716B (389), and NBRI16716C (390) were isolated from the fungus Perisporiopsis melioloides Mer-f16716. Compounds NBRI16716A (388) and NBRI16716B (389) inhibited the growth of human prostate cancer DU-145 cells in the coculture with human prostate stromal cells (PrSCs) more strongly than that of DU-145 cells alone. Furthermore, both compounds showed antitumor effect against xenograft models of DU-145 cells and PrSCs in vivo [181].
Phenylahistin (392) from the culture broth of Aspergillus ustus NSC-F038 exhibited a strong growth inhibition on various tumor cell lines for its microtubule binding function to show its potency as the tubulin depolymerizing agent [182].

7. Thio-Cyclodipeptides

The thio-cyclodipeptides are 2,5-diketopiperazines containing thio functionality in bridged or open form, and their occurrence and activities have been reviewed in 2006 and 2014 [1,207]. According to the positions of the sulfur linkages, we divide thio cyclodipeptides into four subgroups: 1,4-bridged epipolythioxopiperazines (ETPs), derivatives with sulfur-bridge outside 2,5-DKP ring, nonbridged dimethylthio derivatives, and other sulfur-containing cyclodipeptides. About 232 thio-cyclodipeptides have been isolated from fungi.

7.1. 1,4-Bridged Epiplythiodioxopiperazine Analogs

The sulfur-bridged cyclodipeptides are a class of metabolites mainly dominated by the epipolythiodioxopiperazines (ETPs) [1]. The toxicity of ETPs is due to the presence of a sulfide bridge, which can inactivate proteins via reaction with thiol groups and by generation of reactive oxygen species by redox cycling [5]. The ETPs are known for their cytotoxic effect on cancer cell lines, and it has been shown mechanistically that ETPs were transcriptional antagonists that block the interaction of the p300/CBP coactivator with the hypoxia-inducible transcription factor HIF-1α by a zinc ejection mechanism, which resulted in rapid down regulation of hypoxia-inducible genes critical for cancer progression [208]. The occurrence and biological activities of 1,4-bridged epiplythiodioxopiperazine analogs from fungi are shown in Table 6, and their structures are provided in Figure 6.
The dimeric ETP chaetocin (420) was isolated from the fungus Chaetomium minutum, and, in addition to its antibacterial and cytostatic activity, was reported to have inhibitory activity against lysine-specific histone methyltransferases (HMTs), which are key enzymes in the epigenetic control of gene expression [209]. Chaetocins B (421) and C (422) from a Chaetomium sp. fermentation broth were potent inhibitors of Staphylococcus aureus, and exhibited potent cytotoxic activity against HeLa cells with IC50 values of 0.03 and 0.02 μg/mL, respectively [210].
Chaetocochins B (423) and C (424), which were isolated from Chaetomium cochliodes, showed cytotoxic activity to the cells of Bre-04 (breast cancer cells), Lu-04 (big cell lung cells), and N-04 (glioma cells) [211].
Three ETPs deoxyapoaranotin (432), acetylaranotin (408) and acetylapoaranotin (407) were isolated from Aspergillus sp. KMD 901 found in the marine sediment obtained from the East Sea of Korea. They had directly cytotoxic and apoptosis inducing effects toward HCT116 colon cancer cell lines [212].
Emethallicins A–F (444–449) were obtained from Emericella heterothallica. These compunds all displayed inhibitory activity on histamine release from mast cells [213,214,215].
The best known ETP was the small lipid-soluble gliotoxin (461), which exerted toxic effects on phagocytic cells and T-lymphocytes at low concentrations in vitro. This compound was the first ETP to be obtained from fungi. It has been isolated from a variety of fungi including species in the genera of Penicillium, Aspergillus, Gliocladium, Thermoascus, and Candida [2]. High levels of gliotoxin (461) were produced by Aspergillus fumigatus in vivo, and it appeared to be a virulence factor associated with invasive aspergillosis of immunocompromised patients [216]. Gliotoxin (461) was also a dual inhibitor of farnesyltransferase and geranylgeranyltransferase I with antitumor activity against breast cancer in vivo [217].
Two bridged disulfides epicoccin T (450) and rostratin A (493) were isolated from the endophytic fungus Epicoccum nigrum obtained from the leaves of Lysidice rhodostegia. However, they did not show detectable cytotoxic activities toward six tumor cell lines in the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay [188]. In contrast, the rostratins A–D (493–496), which were extracted from Exserohilum rostratum, were found to be modestly cytotoxic against human colon carcinoma HCT-116 [218]. Similarly, the unsaturated analogs epicorazines A (452), B (453), and C (454) isolated from the culture broth of the basidiomycete Stereum hirsutum HKI 0195 were highly cytotoxic against HeLa cells and also exhibited antiproliferative effects against several mouse fibroblast and cancer cell lines [219].
The antifungal macrolide MPC1001 (438) possessing an ETP ring was isolated from the fungus Cladorrhinum sp. KY4922, which was found in a soil sample collected in Indonesia. It possessed antiproliferative activity against the human prostate cancer cell line (DU145) with an IC50 of 9.3 nM, and had antibacterial activity against Gram-positive bacteria [220].
Secoemestrin D (500) was obtained from the endophytic fungus Emericella sp. AST0036 isolated from a healthy leaf tissue of Astragalus lentiginosus. This compound showd cytotoxic activity with IC50 values ranging from 0.06 to 0.24 μM on tumor cell lines [221].
Verticillin A (515) was obtained from Gliocladium roseum derived from submerged wood. It showed antinematodal activity against Panagrellus redivivus and Caenorhabditis elegans, and cytotoxic activity against HeLa cells with an IC50 value of 0.2 μg/mL [222]. Verticillins B (516) and C (517) were isolated from Verticillium sp. [223]. Verticillin D (518), which was isolated from Bionectria byssicola [222] and Gliocladium catenulatum [224], showed antibacterial activity against Staphylococcus aureus. Verticillins E (519) and F (520) from Gliocladium catenulatum showed antibacterial activity [224]. Verticillin G (521) from Bionectra byssicola showed antibacterial activity against Staphylococcus aureus including methicillin-resistant and quinolone-resistant varieties with minimum inhibitory concentrations (MICs) of 3–10 μg/mL [225].

7.2. Analogs with Sulfur-Bridge outside 2,5-DKP Ring

There are a group of sulfur-bridged cyclodipeptides where the sulfur linkage is outside the 2,5-diketoperazine ring. The occurrence and biological activities of fungal analogs with sulfur-bridges outside 2,5-DKP ring are shown in Table 7, and their structures are provided in Figure 7.
Both aspirochlorine (524) and tetrathioaspirochlorine (551) were isolated from Aspergillus flavus and were potent antifungals that inhibited azole-resistant Candida albicans [107]. Aspirochlorine (524) was a rather potent and selective inhibitor of fungal protein synthesis that did not inhibit bacterial or mammalian protein synthesis [267].
Epicoccins are diannulated 2,5-DKPs containing mono- or bis-cross ring sulfide/disulfide bridges. Epicoccins A–F (528–533) have been isolated from the solid-substrate fermentation culture of the Cordyceps-colonizing fungus Epicoccum nigrum [194,268]. Epicoccin A (528) showed modest antimicrobial activity against Bacillus subtilis [268].
The dimeric 2,5-DKPs vertihemiptellides A (553) and B (554) were isolated from the insect pathogenic fungus Verticillium hemipterigenum, and exhibited growth inhibitory activity against Mycobacterium tuberculosis H37Ra, and also showed moderate cytotoxic activity [174].

7.3. Nonbridged Methylthio-Containing Cyclodipeptide Analogs

Nonbridged methylthio-containing analogs were often isolated from fungi as co-metabolites with their sulfur-bridge 2,5-DKP parents. They had a related biosynthetic pathway [275]. The occurrence and biological activities of this group of fungal metabolites are shown in Table 8, and their corresponding structures are provided in Figure 8.
Alternarosin A (555) from Alternaria raphanin, a halotolerant marine fungus obtained from the sediment of the Hongdao sea salt field, showed very weak antimicrobial activity against Escherichia coli, Bacillus subtilis, and Candida albicans with MIC values ranging from 200 to 400 μM [276].
Three 2,5-DKPs, bilains A–C (558–560) and cis-bis(methylthio)silvatin (480) were isolated from the marine-derived fungus Penicillium bilaii collected in Tasmania. However, only cis-bis(methylthio)silvatin (569) showed weak cytotoxicity against NS-1 cells [161]. Both cis-bis(methylthio)silvatin (569) and its enantiomer Sch 54794 (524) were previously isolated from the fungus Fusarium chlamydosporum OUPS-N124 obtained from the marine alga Carpopeltis affinis. They exhibited weak cytotoxic activity against P388 lymphocytic leukemia cells [277].
Bis-N-norgliovictin (570) was first isolated from Gliocladium virens [233]. It was also isolated from three marine-derived fungi Aspergillus fumigatus [278], Neosartorya pseudosidcheri [136], and Dichotomomyces sp. L-8 [113]. Bis-N-norgliovictin (570) significantly inhibited lipopolysaccharide (LPS)-induced inflammation in macrophages and improved survival in sepsis, and it should be a therapeutic candidate for the treatment of sepsis and other inflammatory diseases [279].
Dehydroxybisdethiobis(methylthio)gliotoxin (577) has been isolated from the broth of a marine-derived fungus Pseudallescheria sp. and exhibited weak antibacterial activity against methicillin-resistant and multidrug-resistant Staphylococcus aureus with MIC values of 31.2 μg/mL [280].
Ent-epicoccin G (582) from the endophytic fungus Epicoccum nigrum showed potent in vitro activity (IC50, 3.07 μM) against the release of β-glucuronidase in rat polymorphonuclear leukocytes induced by platelet-activating factor [188].
The bis(methylthio)-2,5-DKP FR106969 (590) isolated from Penicillium citrinum showed high inhibitory activity against the platelet activating factor (PAF)-induced rabbit platelet aggregation to have its potency as the anti-inflammatory inhibitor [281].
The indole derivatives gliocladins A (594) and B (595) as well as glioperazine (597) have been obtained from a marine-derived fungus Gliocladium roseum PS-N132 isolated from the sea hare Aplysia qkurodai. All three 2,5-DKPs exhibited cytotoxicity against murine P388 lymphocytic leukemia cells [125].
Both haematocin (600) and mycoediketopiperazine (607) were dimethylthio 2,5-DKPs. Haematocin (600) was isolated from the phytopathogenic fungus Nectria haematococca and had inhibitory activity on the spore germination and germ-tube elongation of Magnarporte oryzae [282]. Mycoediketopiperazine (607) from the fungus Papularia sp. exhibited potent cytotoxic activity on KB cells with an IC50 value of 120 μg/mL [283].
Plectosphaeroic acids A (620) and B (621) were obtained from marine-derived fungus Plectosphaerella cucumerina. They were inhibitors of indoeamine 2,3-dioxygenase (IDO), which existed in primary tumor cells. IDO has been considered as an important molecular target for cancer therapy [254].

7.4. Other Sulfur-Containing Cyclodipeptide Analogs

Other sulfur-containing cyclodipeptide analogs included MPC1001G (633), silvathione (634) and taichunamide D (635) with their structures shown in Figure 9. MPC1001G (633) was isolated from Cladorrhinum sp. KY4922 [236], silvathione (634) from Aspergillus silvaticus [235], and taichunamide D (635) from Aspergillus taichungensis IBT 19404 [53]. Their biological activities have not been reported.

8. Conclusions and Future Perspectives

A large number of cyclodipeptides have been identified in fungi, and many have received attention not only as challenging synthetic targets but also because some of these compounds displayed diverse and interesting biological activities. Since then, interest has increased in the biosynthesis, genetics, total synthesis, biological activities, and medicinal properties of this class of natural products. Some cyclodipeptides such as tryprostatins A (103) and B (104), cyclo(l-Pro–l-Ala) (318), cyclo(l-Pro–l-Phe) (334), cyclo(l-Pro–l-Tyr) (337), phenylahistin (392), and FR106969 (590) have displayed their potential applications in agriculture and medicinal industry [16,17,149,151,182,281].
The fungal cyclodipeptides are mainly distributed in the genera of Aspergillus and Penicillium. However, the cyclodipeptides in the remaining genera seem to be less explored. Further identification and exploration of the cyclodipeptides from all of the fungal genera are needed. In recent years, more and more cyclodipeptides have been isolated from marine-derived and plant endophytic fungi [297,298,299,300]. These fungi inhabiting particular environments could be rich sources of biologically active cyclodipeptides that are indispensable for medicinal and agricultural applications.
The biological activities (shown in Table 1, Table 2, Table 3, Table 4, Table 5, Table 6, Table 7 and Table 8) of the cyclodipeptides reported by each investigator were random and limited. Systematical screening of biological activities for each cyclodipeptide should be necessary. In most cases, the biological activities as well as the mode of action of fungal cyclodipeptides have been investigated based on in vitro studies or animal modes. Few studies have been performed at the level of clinical trials in patients. Effective research and development methods for these compounds should be explored to maximize their usefulness in the drug discovery and development processes [6]. For the diverse biological activities, the cyclodipeptides from fungi are expected to inspire medicinal chemists in their search for better agents such as antitumors, antifungals, and antibacterials than existing ones [297].
It is very important to understand biosynthetic mechanisms of the cyclodipeptides in fungi. These need to combine their biochemical and genetic approaches. More and more designed biologically active cyclodipeptides will be expected to be produced by genetic manipulation. With a good understanding of the biosynthetic pathways of bioactive cyclodipeptides, we can not only increase outputs of the beneficial cyclodipeptides but also block biosynthesis of some harmful cyclodipeptides by specific interferences [6].

Acknowledgments

This work was co-financed by the grants from the National Key R&D Program of China (2017YFD0201105), and the National Natural Science Foundation of China (31271996).

Author Contributions

Xiaohan Wang performed bibliographic research, and drafted and corrected the manuscript. Yuying Li and Xuping Zhang retrieved literature, participated in the discussions and supported manuscript corrections. Daowan Lai reviewed the manuscript and helped to revise it. Ligang Zhou conceived the idea, designed the review structure, supervised manuscript drafting, and revised the manuscript. All authors read and approved the final manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Molecules 22 02026 g001a 550Molecules 22 02026 g001b 550Molecules 22 02026 g001c 550Molecules 22 02026 g001d 550Molecules 22 02026 g001e 550Molecules 22 02026 g001f 550Molecules 22 02026 g001g 550
Figure 1. Structures of the tryptophan-proline cyclodipeptide analogs isolated from fungi.
Figure 1. Structures of the tryptophan-proline cyclodipeptide analogs isolated from fungi.
Molecules 22 02026 g001aMolecules 22 02026 g001bMolecules 22 02026 g001cMolecules 22 02026 g001dMolecules 22 02026 g001eMolecules 22 02026 g001fMolecules 22 02026 g001g
Molecules 22 02026 g002a 550Molecules 22 02026 g002b 550
Figure 2. Structures of the tryptophan-tryptophan cyclodipeptide analogs isolated from fungi.
Figure 2. Structures of the tryptophan-tryptophan cyclodipeptide analogs isolated from fungi.
Molecules 22 02026 g002aMolecules 22 02026 g002b
Molecules 22 02026 g003a 550Molecules 22 02026 g003b 550Molecules 22 02026 g003c 550Molecules 22 02026 g003d 550Molecules 22 02026 g003e 550Molecules 22 02026 g003f 550Molecules 22 02026 g003g 550Molecules 22 02026 g003h 550Molecules 22 02026 g003i 550Molecules 22 02026 g003j 550
Figure 3. Structures of the tryptophan-Xaa cyclodipeptide analogs isolated from fungi.
Figure 3. Structures of the tryptophan-Xaa cyclodipeptide analogs isolated from fungi.
Molecules 22 02026 g003aMolecules 22 02026 g003bMolecules 22 02026 g003cMolecules 22 02026 g003dMolecules 22 02026 g003eMolecules 22 02026 g003fMolecules 22 02026 g003gMolecules 22 02026 g003hMolecules 22 02026 g003iMolecules 22 02026 g003j
Molecules 22 02026 g004a 550Molecules 22 02026 g004b 550
Figure 4. Structures of the proline-Xaa cyclodipeptide analogs isolated from fungi.
Figure 4. Structures of the proline-Xaa cyclodipeptide analogs isolated from fungi.
Molecules 22 02026 g004aMolecules 22 02026 g004b
Molecules 22 02026 g005a 550Molecules 22 02026 g005b 550Molecules 22 02026 g005c 550
Figure 5. Structures of the non-tryptophan-non-proline cyclodipeptide analogs isolated from fungi.
Figure 5. Structures of the non-tryptophan-non-proline cyclodipeptide analogs isolated from fungi.
Molecules 22 02026 g005aMolecules 22 02026 g005bMolecules 22 02026 g005c
Molecules 22 02026 g006a 550Molecules 22 02026 g006b 550Molecules 22 02026 g006c 550Molecules 22 02026 g006d 550Molecules 22 02026 g006e 550
Figure 6. Structures of the 1,4-bridged epiplythiodioxopiperazine cyclodipeptide analogs isolated from fungi.
Figure 6. Structures of the 1,4-bridged epiplythiodioxopiperazine cyclodipeptide analogs isolated from fungi.
Molecules 22 02026 g006aMolecules 22 02026 g006bMolecules 22 02026 g006cMolecules 22 02026 g006dMolecules 22 02026 g006e
Molecules 22 02026 g007a 550Molecules 22 02026 g007b 550Molecules 22 02026 g007c 550
Figure 7. Structures of the analogs with sulfur-bridge outside 2,5-DKP ring isolated from fungi.
Figure 7. Structures of the analogs with sulfur-bridge outside 2,5-DKP ring isolated from fungi.
Molecules 22 02026 g007aMolecules 22 02026 g007bMolecules 22 02026 g007c
Molecules 22 02026 g008a 550Molecules 22 02026 g008b 550Molecules 22 02026 g008c 550Molecules 22 02026 g008d 550Molecules 22 02026 g008e 550
Figure 8. Structures of the nonbridged methylthio-containing cyclodipeptide analogs isolated from fungi.
Figure 8. Structures of the nonbridged methylthio-containing cyclodipeptide analogs isolated from fungi.
Molecules 22 02026 g008aMolecules 22 02026 g008bMolecules 22 02026 g008cMolecules 22 02026 g008dMolecules 22 02026 g008e
Molecules 22 02026 g009 550
Figure 9. Structures of the other sulfur-containing cyclodipeptide analogs isolated from fungi.
Figure 9. Structures of the other sulfur-containing cyclodipeptide analogs isolated from fungi.
Molecules 22 02026 g009
Table
Table 1. Fungal tryptophan-proline cyclodipeptide analogs and their biological activities.
Table 1. Fungal tryptophan-proline cyclodipeptide analogs and their biological activities.
NameFungus and Its OriginBiological ActivityRef.
Aspergamide A (1)Aspergillus ochraceus-[5]
Aspergamide B (2)Aspergillus ochraceus-[5]
Aspergilazine A (3)Marine-derived Aspergillus taichungensis ZHN-7-07Weak activity against influenza A (H1N1) virus[18]
(+)-Austamide (4)Aspergillus ustusAcute toxicosis in day-old ducklings[7]
6-epi-Avrainvillamide (5)Aspergillus taichungensis-[19]
Brevianamide E (6)Deep sea derived Aspergillus versicolor CXCTD-06-6aModerate radical scavenging activity against DPPH[20]
Brevianamide F = Cyclo(l-Trp–l-Pro) (7)Endophytic Aspergillus fumigatus-[21]
Endophytic Aspergillus fumigatus from Melia azedarachPlant growth inhibitory activity[11]
Marine-derived Aspergillus taichungensis ZHN-7-07-[18]
Marine-derived Penicillium vinaceumAntimicrobial activity[22]
Marine-derived Pseudallescheria sp. isolated from the surface of the drift woodAntibacterial activity against Staphylococcus aureus[23]
Brevianamide J (8)Aspergillus versicolor-[24]
Brevianamide K (9)Aspergillus versicolor-[24]
Marine-derived Aspergillus versicolor from the sediment collected from the Bohai Sea of China-[25]
Aspergillus versicolor from the marine brown alga Sargassum thunbergii-[26]
Deep sea derived Aspergillus versicolor CXCTD-06-6aModerate radical scavenging activity against DPPH[20]
Brevianamide Q (10)Aspergillus versicolor-[27]
Deep sea derived Aspergillus versicolor CXCTD-06-6aModerate radical scavenging activity against DPPH[20]
Brevianamide R (11)Aspergillus versicolor-[27]
Deep sea derived Aspergillus versicolor CXCTD-06-6aModerate radical scavenging activity against DPPH[20]
Brevianamide S (12)Marine-derived Aspergillus versicolor from the sediment collected from the Bohai Sea of ChinaSelective antibacterial activity[25]
Brevianamide T (13)Marine-derived Aspergillus versicolor from the sediment collected from the Bohai Sea of China-[25]
Brevianamide U (14)Marine-derived Aspergillus versicolor from the sediment collected from the Bohai Sea of China-[25]
Brevianamide V (15)Marine-derived Aspergillus versicolor from the sediment collected from the Bohai Sea of China-[25]
Deep sea derived Aspergillus versicolor CXCTD-06-6aModerate radical scavenging activity against DPPH[20]
Brevianamide W (16)Deep sea derived Aspergillus versicolor CXCTD-06-6aModerate radical scavenging activity against DPPH[20]
5-Chlorosclerotiamide (17)Deep sea derived Aspergillus westerdijkiae-[28]
Cyclo(d-Trp–l-Pro) (18)Marine-derived Penicillium vinaceumAntimicrobial activity[22]
Cyclo(N-benzyl-Trp–Pro) (19)Endophytic Aspergillus tamari from Ficus carica-[29]
Cyclo(N’-prenyl-l-Trp–l-Pro) (20)Endophytic Aspergillus fumigatus-[21]
Cyclotryprostatin A (21)Endophytic Aspergillus fumigatus from Melia azedarach-[11]
Aspergillus fumigatusInhibitory activity at G2/M-phase of the mammalian cell cycle[30]
Endophytic Aspergillus tamari from Ficus carica-[29]
Cyclotryprostatin B (22)Endophytic Aspergillus fumigatus from Melia azedarachPlant shoot elongation inhibitory activity[11]
Aspergillus fumigatusInhibitory activity at G2/M-phase of the mammalian cell cycle[30]
Endophytic Aspergillus tamari from Ficus carica-[29]
Cyclotryprostatin C (23)Aspergillus fumigatusInhibitory activity at G2/M-phase of the mammalian cell cycle[30]
Endophytic Aspergillus tamari from Ficus carica-[29]
Cyclotryprostatin D (24)Aspergillus fumigatusInhibitory activity at G2/M-phase of the mammalian cell cycle[30]
Endophytic Aspergillus tamari from Ficus carica-[29]
12,13-Dehydroprolyltryptopha-nyldiketopiperazine (25)Penicillium piscarium-[31]
Demethoxyfumitremorgin C (26)Aspergillus fumigatusCytotoxic activity[9]
Deoxybrevianamide E (27)Aspergillus sp.-[32]
Marine-derived Aspergillus versicolor from the sediment collected from the Bohai Sea of China-[25]
(+)-Deoxyisoaustamide (28)Aspergillus ustus-[7]
Dihydrocarneamide A (29)Marine-derived Paecilomyces variotiiWeak cytotoxic activity[33]
8,9-Dihydroxyfumitremorgin C = 12,13-Dihydroxyfumitremorgin C (30)Endophytic Aspergillus fumigatus-[21]
Marine-derived Aspergillus sydowi from a driftwood sample-[10]
Marine-derived Aspergillus sp.Cytotoxic activity[34]
Deep-sea derived Aspergillus sp. SCSIO Ind09F01Anti-tuberculosis and cytotoxic activity[35]
Marine-derived Pseudallescheria sp. isolated from the surface of the drift woodAntibacterial activity against Staphylococcus aureus[23]
rel-(8S)-19,20-Dihydro-9,20-dihydroxy-8-methoxy-9,18-di-epi-fumitremorgin C (31)Endophytic Aspergillus fumigatus-[21]
rel-(8S,19S)-19,20-Dihydro-,19,20-trihydroxy-8-methoxy-9-epi-fumitremorgin C (32)Endophytic Aspergillus fumigatus-[21]
(3S,8S,9S,18S)-8,9-Dihydroxyspirotryprostatin A (33)Endophytic Aspergillus fumigatus-[21]
9ξ-O-2(2,3-Dimethylbut-3-enyl) brevianamide Q (34)Aspergillus versicolor from the marine brown alga Sargassum thunbergii-[26]
(-)-Enamide (35)Marine-derived Aspergillus versicolor-[36]
Fumitremorgin A (36)Marine sediment-derived Penicillium brefeldianum SD-273-[37]
Fumitremorgin B (37)Endophytic Aspergillus tamari from Ficus carica-[29]
Endophytic Aspergillus fumigatus from Melia azedarachPlant shoot elongation inhibitory activity[11]
Aspergillus fumigatus-[8]
Endophytic Alternaria sp. FL25 from Ficus caricaAntiphytopathogenic fungal activity[38]
Derivative of fumitremorgin B (24R) (38)Aspergillus fumigatusCytotoxic activity[8]
Derivative of fumitremorgin B (24S) (39)Aspergillus fumigatusCytotoxic activity[8]
Fumitremorgin C (40)Endophytic Aspergillus fumigatus-[21]
Marine-derived Aspergillus sydowi from a driftwood sample-[10]
Endophytic Aspergillus tamari from Ficus carica-[29]
Marine-derived Aspergillus sp.Cytotoxic activity[34]
Marine-derived Pseudallescheria sp. from the surface of driftwoodAntibacterial activity against Staphylococcus aureus[23]
Endophytic Alternaria sp. FL25 from Ficus caricaAntiphytopathogenic fungi activity[38]
Endophytic Aspergillus fumigatus from Melia azedarachPlant shoot elongation inhibitory activity[11]
rel-(8R)-9-Hydroxy-8-methoxy-18-epi-fumitremorgin C (41)Endophytic Aspergillus fumigatus-[21]
12β-Hydroxy-13α-methoxyverruculogen TR-2 (42)Endophytic Aspergillus fumigatus from Melia azedarachPlant shoot elongation inhibitory activity[11]
N-Hydroxy-6-epi-stephacidin (43)Aspergillus taichungensis-[19]
21-Hydroxystephacidin A (44)Marine-derived Aspergillus ostianus-[39]
12β-Hydroxyverruculogen TR-2 (45)Endophytic Aspergillus fumigatus from Melia azedarach-[11]
24-Hydroxyverruculogen (46)Marine sediment-derived Penicillium brefeldianum SD-273-[37]
26-Hydroxyverruculogen (47)Marine sediment-derived Penicillium brefeldianum SD-273-[37]
6-Methoxyspirotryprostatin B (48)Marine-derived Aspergillus sydowi from a driftwood sampleWeak cytotoxicity against HL-60 cells and A-549 cells[10]
Endophytic Aspergillus fumigatus from Melia azedarachInhibition on elongation of lettuce shoots[11]
Endophytic Aspergillus fumigatus from the stem of Erythrophloeum fordii-[40]
Notoamide A (49)Marine-derived Aspergillus sp.Moderate cytotoxicity on Hela and L1210 cells[32]
Notoamide B (50)Marine-derived Aspergillus sp.Moderate cytotoxicity on Hela and L1210 cells[32]
(-)-Notoamide B (51)Aspergillus protuberus MF297-2-[32]
(+)-Notoamide B (52)Aspergillus versicolor NRRL 35600-[41]
iso-Notoamide B (53)Marine-derived Paecilomyces variotiiWeak cytotoxic activity[33]
Notoamide C (54)Marine-derived Aspergillus sp.-[32]
3-epi-Notoamide C (55)Marine-derived Aspergillus sp.-[42]
Notoamide D (56)Marine-derived Aspergillus sp.-[32]
Notoamide E (57)Aspergillus versicolor NRRL 35600-[43]
Notoamide E2 (58)Marine-derived Aspergillus sp.-[42]
Notoamide E3 (59)Marine-derived Aspergillus sp.-[42]
Notoamide F (60)Marine-derived Aspergillus sp.-[44]
Marine-derived Aspergillus ostianus-[39]
Notoamide G (61)Marine-derived Aspergillus sp.-[44]
Notoamide H (62)Marine-derived Aspergillus sp.-[44]
Notoamide I (63)Marine-derived Aspergillus sp.Weak cytotoxicity on HeLa cells[44]
Notoamide J (64)Marine-derived Aspergillus sp.-[44]
Notoamide K (65)Marine-derived Aspergillus sp.-[44]
Notoamide L (66)Marine-derived Aspergillus sp.-[45]
Notoamide M (67)Marine-derived Aspergillus sp.-[45]
Notoamide N (68)Marine-derived Aspergillus sp.-[45]
Notoamide O (69)Marine-derived Aspergillus sp.-[46]
Notoamide P (70)Marine-derived Aspergillus sp.-[46]
Notoamide Q (71)Marine-derived Aspergillus sp.-[46]
Notoamide R (72)Aspergillus ostianus-[39]
Marine-derived Aspergillus sp.-[46]
Notoamide S (73)Aspergillus amoenus-[47]
Notoamide T (74)Marine-derived Aspergillus sp.-[48]
6-epi-Notoamide T (75)Marine-derived Aspergillus sp.-[48]
13-Oxofumitremorgin B (76)Endophytic Aspergillus tamari from Ficus carica-[29]
18-Oxotryprostatin A (77)Marine-derived Aspergillus sydowi from a driftwood sampleWeak cytotoxicity against A-549 cells[10]
Endophytic Aspergillus fumigatus-[21]
Endophytic Aspergillus fumigatus from Melia azedarachPlant growth inhibitory activity[11]
13-Oxoverruculogen (78)Aspergillus fumigatusModerate cytotoxic activity on four cancer cell lines[8]
Piscarinine A (79)Penicillium piscarium VKM F-691Cytotoxic and antimicrobial activities[49]
Piscarinine B (80)Penicillium piscarium VKM F-691Cytotoxic and antimicrobial activities[49]
13-O-Prenyl-26-hydroxyverruculogen (81)Marine sediment-derived Penicillium brefeldianum SD-273Lethal activity against brine shrimp[37]
Sclerotiamide (82)Aspergillus sclerotiorumAntiinsectan activity against the earworm Helicoverpa zea[50]
10-epi-Sclerotiamide (83)Deep-sea-derived Aspergillus westerdijkiae-[28]
Speramide A (84)Freshwater-derived Aspergillus ochraceus KM007Moderate activity against Pseudomonas aeruginosa[51]
Speramide B (85)Freshwater-derived Aspergillus ochraceus KM007-[51]
Spiro[5H,10H-dipyrrolo-[1,2-a:1’2’-d]pyrazine-2(3H),2’-[2H]-indol]-3’,5,10(1’H) trione (86)Endophytic Aspergillus fumigatus from the stem of Erythrophloeum fordii-[40]
Spirotryprostatin A (87)Aspergillus fumigatusInhibitory activity on mammalian cell cycle at G2/M phase[12]
Endophytic Aspergillus fumigatus from Melia azedarachThe elongation of lettuce shoots inhibitory activity[11]
Marine-derived Aspergillus sydowi from a driftwood sample-[10]
Spirotryprostatin B (88)Aspergillus fumigatusInhibitory activity on mammalian cell cycle at G2/M phase[12]
Spirotryprostatin C (89)Holothurian-derived Aspergillus fumigatus from Stichopus japonicusCytotoxic activity[8]
Spirotryprostatin D (90)Holothurian-derived Aspergillus fumigatus from Stichopus japonicusCytotoxic activity[8]
Spirotryprostatin E (91)Holothurian-derived Aspergillus fumigatus from Stichopus japonicusCytotoxic activity[8]
Spirotryprostatin Fa (92)Marine-derived Aspergillus fumigatus from soft coral Sinularia sp.Stimulating action on the growth of sprout roots of soy, buckwheat and corn[52]
Spirotryprostatin Fb (93)Plant endophytic Penicillium brefeldianum from the rhizome of Pinellia ternataCytotoxic activity against HepG2 and MDA-MB-231 cells[13]
Spirotryprostatin K (94)Endophytic Aspergillus fumigatus from the stem of Erythrophloeum fordii-[40]
(-)-Stephacidin A (95)Aspergillus amoenus (formerly A. versicolor) NRRL 35600-[41]
(+)-Stephacidin A (96)Aspergillus protuberus MF297-2-[32]
6-epi-Stephacidin A (97)Aspergillus taichungensis-[19]
Stephacidin B (98)Aspergillus ochraceusCytotoxic activity[14]
Taichunamide C (99)Aspergillus taichungensis (IBT 19404)-[53]
Taichunamide E (100)Aspergillus taichungensis (IBT 19404)-[53]
Taichunamide F (101)Aspergillus taichungensis (IBT 19404)-[53]
Taichunamide G (102)Aspergillus taichungensis (IBT 19404)-[53]
Tryprostatin A (103)Endophytic Aspergillus fumigatus from Melia azedarachInhibitory activities on elongation of lettuce shoots, and on multidrug-resistance protein[11,16]
Endophytic Aspergillus tamari from Ficus carica-[29]
Tryprostatin B (104)Endophytic Aspergillus fumigatus-[21]
Endophytic Aspergillus tamari from Ficus carica-[29]
-Inhibitory activity on mammalian cell-cycle[17]
Verruculogen (105)Endophytic Aspergillus fumigatus from Melia azedarachThe elongation of lettuce shoots inhibitory activity[11]
Endophytic Aspergillus tamari from Ficus carica-[29]
Marine sediment-derived fungus Penicillium brefeldianum SD-273-[37]
Verruculogen TR-2 = TR-2 (106)Endophytic Aspergillus fumigatus from Melia azedarachInhibitory activity on elongation of lettuce shoots[11]
Marine sediment-derived Penicillium brefeldianum SD-273-[37]
Versicamide A (107)Marine-derived Aspergillus versicolor-[36]
Versicamide B (108)Marine-derived Aspergillus versicolor-[36]
Versicamide C (109)Marine-derived Aspergillus versicolor-[36]
Versicamide D (110)Marine-derived Aspergillus versicolor-[36]
Versicamide E (111)Marine-derived Aspergillus versicolor-[36]
Versicamide F (112)Marine-derived Aspergillus versicolor-[36]
Versicamide G (113)Marine-derived Aspergillus versicolor-[36]
(−)-Versicolamide B (114)Aspergillus sp.-[45]
(+)-Versicolamide B (115)Aspergillus versicolor NRRL 35600-[41]
(−)-Versicolamide C (116)Aspergillus taichungensis-[19]
Table
Table 2. Fungal tryptophan-tryptophan cyclodipeptide analogs and their biological activities.
Table 2. Fungal tryptophan-tryptophan cyclodipeptide analogs and their biological activities.
NameFungus and its OriginBiological ActivityRef.
Amauromine = Nigriforine (117)Amauroascus sp.Hypotensive vasodilating activity[54]
Penicillium nigricans-[55]
Auxarthron reticulatumSelective cannabinoid CB1 receptor antagonist[56]
Amauromine B (118)Aspergillus terreus 3.05358Inhibitory activity on α-glucosidase[68]
Cyclo(l-Trp–l-Trp) (119)Endophytic Aspergillus niger from the liverwort Heteroscyphus tener-[69]
Epiamauromine (120)Aspergillus ochraceusModerate reduction in weight gain activity against the corn earworm[57]
Fellutanine A (121)Penicillium fellutanum-[58]
Marine sponge-derived Neosartorya glabra KUFA 0702-[70]
Fellutanine A 2’S,3’S-epoxide (122)Marine sponge-derived Neosartorya glabra KUFA 0702-[70]
Fellutanine B (123)Penicillium fellutanum-[58]
Fellutanine C (124)Penicillium fellutanum-[58]
Fellutanine D (125)Penicillium fellutanumCytotoxic activity[58]
Gypsetin (126)Nannizzia gypsea var. incurvataInhibitory activity on acyl-CoA:cholesterol acyltransferase[71]
N-Methylepiamauromine (127)Aspergillus ochraceusModerate reduction in weight gain activity against the corn earworm[57]
Novoamauromine (128)Aspergillus novofumigatusInhibitory activity on the cell proliferation of A549, Hela, and LNCap cells[59]
Okaramine A (129)Penicillium simplicissimum AK-40Insecticidal activity[62]
Okaramine B (130)Penicillium simplicissimum AK-40Insecticidal activity[62]
Okaramine C (131)Penicillium simplicissimum-[65]
Penicillium simplicissimumOral insecticide activity against silkworms[72]
Okaramine D (132)Penicillium simplicissimumInsecticidal activity[63]
Okaramine E (133)Penicillium simplicissimum-[63]
Okaramine F (134)Penicillium simplicissimum-[63]
Okaramine G (135)Penicillium simplicissimumInsecticidal activity[73]
Okaramine H (136)Aspergillus aculeatus-[60]
Okaramine I (137)Aspergillus aculeatus-[60]
Okaramine J (138)Penicillium simplicissimum-[64]
Okaramine K (139)Penicillium simplicissimum-[64]
Okaramine L (140)Penicillium simplicissimum-[64]
Okaramine M (141)Penicillium simplicissimum-[64]
Okaramine N (142)Penicillium simplicissimum-[65]
Okaramine O (143)Penicillium simplicissimum-[65]
Okaramine P (144)Penicillium simplicissimum-[65]
Okaramine Q (145)Penicillium simplicissimum-[65]
Okaramine R (146)Penicillium simplicissimum-[65]
Okaramine S (147)Aspergillus taichungensis ZHN-7-07Cytotoxic activity against HL-60 cells with IC50 value of 0.78 μM[61]
Okaramine T (148)Aspergillus taichungensis ZHN-7-07-[61]
Okaramine U (149)Aspergillus taichungensis ZHN-7-07-[61]
Note: IC50, median inhibitory concentration.
Table
Table 3. Fungal tryptophan-Xaa cyclodipeptide analogs and their biological activities.
Table 3. Fungal tryptophan-Xaa cyclodipeptide analogs and their biological activities.
NameFungus and its OriginBiological ActivityRef.
Acyl aszonalenin (150)Aspergillus flavipesSubstance P inhibitory activity[88]
Alkaloid E-7 (151)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Mangrove-derived Eurotium rubrum from Hibiscus tiliaceusCytotoxic activity[89]
Marine-derived Eurotium rubrum MPUC136Inhibitory activity against melanin synthesis[90]
Arestrictin A (152)Aspergillus restrictus-[91]
Arestrictin B (153)Aspergillus restrictus-[91]
Aspergillus penicilloides-[91]
Asperazine (154)Marine-derived Aspergillus nigerCytotoxic activity[92]
Endophytic Aspergillus niger from the liverwort Heteroscyphus tenerWeak cytotoxic activity[69]
Endophytic Aspergillus sp. KJ-9 from Melia azedarachAntifungal and antibacterial activity[93]
Plant fungal pathogen Pestalotiopsis theaeInhibitory effect on HIV-1 replication in C8166 cells[94]
Asperazine A (155)Endophytic Aspergillus niger from the liverwort Heteroscyphus tenerWeak cytotoxic activity[69]
Aspertryptanthrin A (156)Endophytic Aspergillus sp. from the stem bark of Melia azedarach-[74]
Aspertryptanthrin B (157)Endophytic Aspergillus sp. from the stem bark of Melia azedarach-[74]
Aspertryptanthrin C (158)Endophytic Aspergillus sp. from the stem bark of Melia azedarach-[74]
Benzodiazepinedione (159)Aspergillus flavipes-[88]
Brevicompanine A (160)Penicillium brevicompactumAcceleration of the root growth of the lettuce seedlings[95]
Brevicompanine B (161)Penicillium brevicompactumAcceleration of the root growth of the lettuce seedlings[95]
Aspergillus janusInhibitory activity against the malaria parasite Plasmodium falciparum 3D7[96]
allo-Brevicompanine B (162)Deep ocean sediment derived fungus Penicillium sp.-[77]
Brevicompanine C (163)Penicillium brevi-compactumAcceleration of the root growth of the lettuce seedlings[75]
Brevicompanine D (164)Deep ocean sediment derived Penicillium sp.-[77]
Brevicompanine E (165)Deep ocean sediment derived Penicillium sp.Inhibitory activity on lipopolysaccharide-induced nitric oxide production in BV2 microglial cells[77,78]
Brevicompanine F (166)Deep ocean sediment derived Penicillium sp.-[77]
Brevicompanine G (167)Deep ocean sediment derived Penicillium sp.-[77]
Brevicompanine H (168)Deep ocean sediment derived Penicillium sp.Inhibitory activity on lipopolysaccharide-induced nitric oxide production in BV2 microglial cells[77]
Citreoindole (169)Penicillium citreovirideCytotoxicity against HeLa cells[97]
Cristatin A (170)Aspergillus penicilloides-[91]
Cristatumin A (171)Mangrove-derived endophytic Eurotium cristatum EN-220Antibacterial activity against Escherichia coli and Staphyloccocus aureus[98]
Cristatumin B (172)Mangrove-derived endophytic Eurotium cristatum EN-220Moderate lethal activity against brine shrimp[98]
Cristatumin C (173)Mangrove-derived endophytic Eurotium cristatum EN-220-[98]
Cristatumin E (174)Algal-derived Eurotium herbariorum HT-2Cytotoxic activity on K562 tumor cell line and antibacterial activity on Enterobacter aerogenes and Escherichia coli[99]
Cristatumin F (175)Eurotium cristatum isolated from Fuzhuan brick teaModest radical scavenging activity against DPPH radicals, and marginal attenuation of 3T3L1 pre-adipocytes[100]
Cryptoechinuline C (176)Marine-derived Eurotium rubrum-[84]
Cryptoechinuline D (177)Mangrove rhizosphere soil-derived Aspergillus effuses H1-1Cytotoxic activity[101]
Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceusRadical scavenging activity against DPPH[102]
Cryptoechinuline G (178)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against 1,1‘-diphenyl-1-picryhydrazyl (DPPH)[87]
Marine-derived Eurotium rubrum MPUC136Inhibitory activityagainst melanin synthesis[90]
Mangrove-derived Eurotium rubrum from Hibiscus tiliaceus-[89]
Cyclo(l-Trp–l-Ala) (179)Marine-derived Eurotium rubrumWeak antiviral effects[84]
Marine-derived Aspergillus sp.-[103]
Eurotium rubrum MA-150 obtained from mangrove-derived rhizospheric soilModest lethal activity on brine shrimp[104]
Cyclo(Trp–Gly) (180)Thermophilic Talaromyces thermophilus YM3-4 collected in Tengchong hot spring, Yunnan of China-[105]
Cyclo(l-Trp–dehydro-His) (181)Endophytic Penicillium sp. HS-3 from the stems of Huperzia serrata-[106]
Cyclo(l-Trp–d-Ile) (182)Penicillium brevi-compactumAcceleration of root growth of lettuce seedlings[75]
Cyclo(l-Trp–d-Leu) (183)Penicillium brevi-compactumAcceleration of root growth of lettuce seedlings[75]
Cyclo(N-methyl-Trp–Leu) (184)Endophytic Aspergillus tamari from Ficus carica-[29]
Cyclo(l-Trp-d-N-methyl-Leu) (185)Aspergillus flavus-[107]
Cyclo(l-Trp–d-Phe) (186)Endophytic Aspergillus niger from the liverwort Heteroscyphus tener-[69]
Cyclo(l-Trp–l-Phe) (187)Aspergillus syndowi-[108]
Penicillium sp.Acceleration of root growth of lettuce seedlings[76]
Cyclo(Trp–Tyr) (188)Terrestrial Aspergillus oryzae-[109]
Cyclo(l-N-isopropyl-Trp–l-Val) (189)An unidentified marine derived fungus M-3 from laver (Porphyra yezoensis)Antifungal activity against the rice pathogen Pyricularia oryzae with MIC 0.36 μM[110]
Cycloechinulin (190)Aspergillus ochraceusInsecticidal activity against the lepidopteran crop pest Helicoverpa zea[57]
ent-Cycloechinulin (191)Aspergillus novofumigatus CBS117520Antifungal activity against Aspergillus fumigatus, A. Niger, Candida albicans, and Cryptococcus neoformans[59]
Dehydroechinulin (192)Eurotium cristatum isolated from Fuzhuan brick tea-[100]
Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceus-[102]
Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Lethal activity on brine shrimp[104]
Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
Dehydrovariecolorin L (193)Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceus-[102]
12-Demethyl-12-oxo-eurotechinulin B (194)Mangrove-derived Eurotium rubrum from Hibiscus tiliaceusCytotoxic activity[89]
Dichotocejpin B (195)Dichotomomyces cejpii FS110-[112]
Dichotocejpin C (196)Dichotomomyces cejpii FS110-[112]
Marine-derived Dichotomomyces sp. L-8-[113]
Didehydroechinulin = Didehydroechinulin B (197)Deep ocean sediment-derived Penicillium griseofulvum-[86]
Mangrove rhizosphere soil-derived Aspergillus effuses H1-1Cytotoxic activity[101]
Dihydrocryptoechinulin D (198)Mangrove rhizosphere soil-derived Aspergillus effuses H1-1Cytotoxic activity against P388 cells[114]
Dihydroneochinulin B (199)Mangrove rhizosphere soil-derived Aspergillus effuses H1-1Weak cytotoxic activity against BEL-7402 and A-549 cell lines[101]
3,12-Dihydroroquefortine (200)Permafrost sediment derived Penicillium aurantiogrieum-[115]
7,9-Dihydroxy-3-(1H-indol--ylmethyl)-8-methoxy-2,3,11,11a-tetrahydro-6H-pyrazino[1,2-b]isoquinoline-1,4-dione (201)Terrestrial Aspergillus oryzae-[109]
Dihydroxyisoechinulin A (202)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceus-[102]
Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Modest brine shrimp lethal and antibacterial activities[104]
11,14-Dihydroxylneoechinulin E (203)Mushroom Psilocybe merdaria from suburban district of Haikou of China-[116]
Dipodazine (204)Penicillium dipodomyis-[117]
Ditryptophenaline (205)Aspergillus flavus-[118]
Aspergillus flavusWeak substance-P inhibitor activity[119]
Marine-derived Aspergillus flavus C-F-3-[120]
Terrestrial Aspergillus oryzae-[109]
Echinulin (206)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of China-[87]
Aspergillus chevalieri in rabbitsToxic activity to rabbits by producing a significant degree of damage to lung and liver[79]
Soil-derived Chaetomium globosum-[121]
Eurotium cristatum isolated from Fuzhuan brick tea-[100]
Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceus-[102]
Marine-derived Eurotium rubrumWeak antiviral effect[84]
Marine-derived Eurotium rubrum MPUC136Inhibitory activity against melanin synthesis[90]
Deep ocean sediment-derived Penicillium griseofulvum-[86]
Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Modest lethal activity on brine shrimp[104]
Effusin A (207)Mangrove rhizosphere soil-derived Aspergillus effuses H1-1-[114]
Epoxyisoechinulin A (208)Marine-derived Aspergillus ruber 1017 from a crinoid Himerometra magnipinna-[122]
Eurocristatine (209)Sponge-associated Eurotium cristatum KUFC 7356-[123]
Eurotechinulin B (210)Mangrove-derived Eurotium rubrum from Hibiscus tiliaceus-[89]
Fructigenine A = Rugulosuvine B (211)Penicillium fructigenumInhibitory activity on the growth of Avena coleoptiles and L-5178Y cells[80]
Penicillium rugulosumModerate cytotoxic activity[81]
Fructigenine B = Verrucofortine (212)Deep ocean sediment derived Penicillium sp.-[77]
Penicillium verrucosum var. cyclopium-[124]
Penicillium fructigenum-[80]
Gliocladin C (213)Gliocladium roseum PS-N132Significant cytotoxicity against murine P388 lymphocytic leukemia cells[125]
Glioperazine C (214)Bionectra byssicola F120-[126]
Haenamindole (215)Marine-derived Penicillium sp. KCB12F005-[127]
3-((1-Hydroxy-3-(2-methylbut- 3-en-2-yl)-2-oxoindilin- 3-yl)methyl)-1-methyl-3,4-dihydrobenzo[1,4] diazepine-2,5-dione (216)Sponge-derived Aspergillus sp. from the Mediterranean sponge Tethya auranthiumAntibacteria activity on a few marine-derived Vibrio species[128]
16-Hydroxyroquefortine C (217)Endophytic Penicillium sp. HS-3 from the stems of Huperzia serrata-[106]
14-Hydroxyterezine D (218)Marine-derived Aspergillus sydowi from a driftwood sampleWeak cytotoxic activity against A-549 cells[10]
(E)-3-(1H-Imidazole-4-yimethylene)-6-(1H-indl-3-ylmethyl)-2,5-piperazinediol (219)Antarctic soil-derived Penicillium sp. SCSIO 05705-[129]
3-[(1H-Indol-3-yl)methyl]-6-benzylpiperazine-2,5-dione (220)Marine-derived Aspergillus flavus C-F-3-[120]
(3S, 11aS)-3- [(1H-Indol-3-yl) methyl]-7,9- dihydroxy-8-methoxy- 2,3,11,11a-tetrahydro- 6H- pyrazino [1,2-b] isoquinoline-1,4-dione (221)Algicolous Aspergillus flavusWeak cytotoxicity against HL-60 cells[130]
Isoechinulin A (222)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceus-[102]
Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Modest lethal activity on brine shrimp[104]
Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
Marine-derived Eurotium rubrumInhibitory activity against influenza A/WSN/33 virus[84]
Isoechinulin B (223)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Marine-derived Eurotium rubrum MPUC136Inhibitory activity against melanin synthesis[90]
Marine-derived Eurotium rubrum-[84]
Mangrove-derived Eurotium rubrum from Hibiscus tiliaceus-[89]
Deep ocean sediment-derived Penicillium griseofulvum-[86]
Isoechinulin C (224)Marine-derived Eurotium rubrum MPUC136-[90]
Isoechinulin D (225)Marine-derived Eurotium rubrum MPUC136-[90]
Isopenilline A (226)Antarctic soil-derived Penicillium sp. SCSIO 05705-[129]
7-Isopentenylcryptoechinuline D (227)Mangrove-derived Eurotium rubrum from Hibiscus tiliaceus-[89]
Leptosin S (228)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[131]
Lumpidin (229)Penicillium nordicum-[132]
3-Methyl-6-[[(1-(3-methyl-2-butenyl)-1H-indol-3-yl)methyl)-2,5-piperazinediione (230)Marine-derived Eurotium rubrumWeak antiviral effect[84]
7-O-Methylvariecolortide A (231)Mangrove derived endophytic Eurotium rubrum from the inner tissue of the stems of Hibiscus tilliaceus-[133]
Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of ChinaInhibitory activity on caspase-3[111]
(+)-(R)-7-O-Methylvariecolortide A (232)Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
(−)-(S)-7-O-Methylvariecolortide A (233)Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
Neoechinulin A (234)Aspergillus spp.Scavenging, neurotrophic factor-like and antiapoptotic activities[82]
Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Marine-derived Aspergillus sp.Ultraviolet-A (320-390 nm) protecting activity with IC50 value of 170 μM.[103]
Marine mudflat sediment derived Chaetomium cristatum collected at Suncheon Bay of KoreaRadical-scavenging activity against DPPH with IC50 value of 24 μM[134]
Eurotium cristatum from Fuzhuan brick tea-[100]
Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceus-[102]
Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Modest brine shrimp lethal activity[104]
Marine-derived Eurotium rubrum MPUC136-[90]
Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
Deep ocean sediment-derived Penicillium griseofulvum-[86]
Mushroom Psilocybe merdaria from suburban district of Haikou of China-[116]
Marine-derived Eurotium rubrum-[84]
Neoechinulin B (235)Mangrove rhizosphere soil-derived Aspergillus effuses H1-1-[101]
Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Marine-derived Eurotium rubrumInhibition against H1N1 virus infected in MDCK cells, and a panel of influenza virus strains[84]
Deep ocean sediment-derived Penicillium griseofulvum-[86]
Neoechinulin C (236)Marine-derived Eurotium rubrumInhibitory activity against influenza A/WSN/33 virus[84]
Neoechinulin D (237)Aspergillus amstelodami-[135]
Neoechinulin E (238)Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceusDPPH radical scavenging activity[102]
Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Lethal activity on brine shrimp[104]
Neosartin A (239)Marine-derived Neosartorya pseudofischeri from the inner tissue of starfish Acanthaster planci-[136]
Neosartin B (240)Marine-derived Neosartorya pseudofischeri from the inner tissue of starfish Acanthaster planci-[136]
Oidioperazine B (241)Antarctic psychrophilic fungus Oidiodendron truncatum-[137]
Oidioperazine C (242)Antarctic psychrophilic fungus Oidiodendron truncatum-[137]
Oidioperazine D (243)Antarctic psychrophilic fungus Oidiodendron truncatum-[137]
Penilline A (244)Antarctic soil-derived Penicillium sp. SCSIO 05705-[129]
Penilline B (245)Antarctic soil-derived Penicillium sp. SCSIO 05705-[129]
Penilloid A (246)Antarctic soil-derived Penicillium sp. SCSIO 05705-[129]
Pestalazine A (247)Plant pathogen Pestalotiopsis theaeInhibitory activity on HIV-1 replication in C8166 cells[94]
Pestalazine B (248)Plant pathogen Pestalotiopsis theae-[94]
1’-(2-Phenyl-ethylene)- ditryptophenaline (249)Aspergillus flavusWeak substance-P inhibitor activity[119]
Polanrazine A = Cyclo(l-Trp–l-Val) (250)Plant pathogen Phoma lingamPhytotoxic activity[83]
Polanranine E (251)Plant pathogen Phoma lingamModerate and selective phytotoxicity by causing necrotic and chlorotic lesions[138]
Polanranine F (252)Plant pathogen Phoma lingam-[138]
Preechinulin (253)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of China-[87]
Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceus-[102]
Marine-derived Eurotium rubrumWeak antiviral effect[84]
Deep ocean sediment-derived Penicillium griseofulvum-[86]
Protubonine A (254)Marine-derived Aspergillus sp. SF-5044 from an intertidal sediment sample-[139]
Protubonine B (255)Marine-derived Aspergillus sp. SF-5044 from an intertidal sediment sample-[139]
Rhinocladin A (256)Endophytic Rhinocladiella sp. lgt-3 from Tripterygium wilfordiiWeak inhibitory activity on monoamine oxidase[140]
Rhinocladin B (257)Endophytic Rhinocladiella sp. lgt-3 from Tripterygium wilfordiiWeak inhibitory activity on monoamine oxidase[140]
Roquefortine C = Roquefortine (258)Permafrost sediment derived Penicillium aurantiogriseum-[115]
Penicillium roqueforti from soil-[141]
Endophytic Penicillium sp. HS-3 from the stems of Huperzia serrata-[106]
Roquefortine E (259)Gymnoascus reessiiWeak cytotoxic activity to mammalian cells[142]
Roquefortine F (260)Marine-derived Penicillium sp.-[143]
Roquefortine G (261)Marine-derived Penicillium sp.-[143]
Roquefortine H (262)Deep ocean sediment-derived Penicillium sp.-[144]
Roquefortine I (263)Deep ocean sediment-derived Penicillium sp.-[144]
Rubrumazine A (264)Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Modest brine shrimp lethal activity[104]
Rubrumazine B (265)Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Brine shrimp lethal activity[104]
Rubrumazine C (266)Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Modest brine shrimp lethal activity[104]
Rubrumline A (267)Marine-derived Eurotium rubrum-[84]
Marine-derived Eurotium rubrum MPUC136-[90]
Rubrumline B (268)Marine-derived Eurotium rubrum-[84]
Rubrumline C (269)Marine-derived Eurotium rubrum-[84]
Rubrumline D (270)Marine-derived Eurotium rubrumInhibitory activity against influenza A/WSN/33 virus[84]
Marine-derived Eurotium rubrum MPUC136-[90]
Rubrumline E (271)Marine-derived Eurotium rubrum-[84]
Rubrumline F (272)Marine-derived Eurotium rubrumWeak antiviral effect[84]
Rubrumline G (273)Marine-derived Eurotium rubrumWeak antiviral effect[84]
Rubrumline H (274)Marine-derived Eurotium rubrum-[84]
Rubrumline I (275)Marine-derived Eurotium rubrum-[84]
Rubrumline J (276)Marine-derived Eurotium rubrumWeak antiviral effect[84]
Rubrumline K (277)Marine-derived Eurotium rubrum-[84]
Rubrumline L (278)Marine-derived Eurotium rubrum-[84]
Rubrumline M (279)Marine-derived Eurotium rubrumWeak antiviral effect[84]
Rubrumline N (280)Marine-derived Eurotium rubrumWeak antiviral effect[84]
Rubrumline O (281)Marine-derived Eurotium rubrumWeak antiviral effect[84]
Rugulosuvine A (282)Penicillium rugulosumModerate cytotoxic activity[81]
SF5280-415 (283)Marine-derived Aspergillus sp. SF-5280-[145]
Talathermophilin A (284)Thermophilic Talaromyces thermophilus YM1-3Nematicidal toxicity[85]
Thermophilic Talaromyces thermophilus YM3-4 collected in Tengchong hot spring, Yunnan of China-[105]
Talathermophilin B (285)Thermophilic Talaromyces thermophilus YM1-3Nematicidal toxicity[85]
Thermophilic Talaromyces thermophilus YM3-4 collected in Tengchong hot spring, Yunnan of China-[105]
Talathermophilin C (286)Thermophilic Talaromyces thermophilus YM3-4 collected in Tengchong hot spring, Yunnan of China-[105]
Talathermophilin D (287)Thermophilic Talaromyces thermophilus YM3-4 collected in Tengchong hot spring, Yunnan of China-[105]
Talathermophilin E (288)Thermophilic Talaromyces thermophilus YM3-4 collected in Tengchong hot spring, Yunnan of China-[105]
Tardioxopiperazine A (289)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of China-[87]
Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Modest lethal activity on brine shrimp[104]
Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
Microascus tardifaciensModerate inhibition on con A and LPS mediated T cell proliferation[146]
Deep ocean sediment-derived Penicillium griseofulvum-[86]
Tardioxopiperaine B (290)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of China-[87]
Microascus tardifaciensWeak inhibition on con A and LPS mediated T cell proliferation[146]
Terezine D (291)Marine-derived Aspergillus sydowi from a driftwood sample-[10]
Tryhistatin (292)Endophytic fungus Penicillium sp. HS-3 from the stems of Huperzia serrata-[106]
Variecolorin A (293)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Variecolorin B (294)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Variecolorin C (295)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Variecolorin D (296)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Variecolorin E (297)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Eurotium rubrum MA-150 obtained from mangrove-derived rhizospheric soilModest lethal activity on brine shrimp[104]
Variecolorin F (298)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Variecolorin G (299)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Mangrove-derived Eurotium rubrum from Hibiscus tiliaceusCytotoxic activity[89]
Eurotium rubrum MA-150 obtained from mangrove-derived rhizospheric soilModest lethal activity on brine shrimp[104]
Variecolorin H (300)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Deep ocean sediment-derived fungus Penicillium griseofulvum-[86]
Variecolorin I (301)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Variecolorin J (302)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Mangrove-derived Eurotium rubrum from Hibiscus tiliaceus-[89]
Variecolorin K (303)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of ChinaWeak radical scavenging activity against DPPH[87]
Variecolorin L (304)Halotolerant Aspergillus variecolor from sediments collected in the Jilantai salt field of China-[87]
Mangrove-derived Eurotium rubrum from the inner tissue of stems of Hibiscus tiliaceus-[102]
Mangrove rhizosphere soil-derived Eurotium rubrum MA-150Modest lethal activity on brine shrimp[104]
Variecolorin M (305)Deep ocean sediment-derived Penicillium griseofulvumWeak radical scavenging activity against DPPH[86]
Variecolorin N (306)Deep ocean sediment-derived Penicillium griseofulvumWeak radical scavenging activity against DPPH[86]
Variecolorin O (307)Eurotium cristatum isolated from Fuzhuan brick tea-[100]
Deep ocean sediment-derived Penicillium griseofulvumWeak radical scavenging activity against DPPH[86]
Variecolortide A (308)Halotolerant fungus Aspergillus variecolor B-17Weak cytotoxic and antioxidant activities[147]
Variecolortide B (309)Halotolerant Aspergillus variecolor B-17Weak cytotoxic and antioxidant activities[147]
(−)-(S)-Variecolortide B (310)Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
(+)-(R)-Variecolortide B (311)Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
Variecolortide C (312)Halotolerant fungus Aspergillus variecolor B-17Weak cytotoxic and antioxidant activities[147]
(−)-(S)-Variecolortide C (313)Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
(+)-(R)-Variecolortide C (314)Lichen-derived Eurotium sp. No. 17-11-8-1 from Cladina grisea collected in Changbaishan Mountain of China-[111]
WIN 64745 (315)Aspergillus sp. SC319-[148]
WIN 64821 (316)Aspergillus sp. SC319-[148]
Note: IC50, median inhibitory concentration; MIC, minimum inhibitory concentration.
Table
Table 4. Proline-Xaa cyclodipeptide analogs and their biological activities.
Table 4. Proline-Xaa cyclodipeptide analogs and their biological activities.
NameFungus and its OriginBiological ActivityRef.
Amoenamide A (317)Aspergillus amoenus NRRL 35600-[153]
Cyclo(l-Pro–l-Ala) (318)Alternaria alternata-[149]
Phytopathogenic Colletotrichum gloesporoidesInhibition of aflatoxin production in Aspergillus flavus[150,151]
Cyclo(trans-4-hydroxy-l-Pro–l-Ala) (319)Endophytic Alternaria alternata from grapevineAntifungal activity on Plasmopara viticola[154]
Cyclo(l-Pro–l-Gly) (320)Phytopathogenic Colletotrichum gloesporoides-[150]
Cyclo(2-hydroxy-Pro–Gly) (321)Simplicillium sp. YZ-11-[155]
Cyclo(l-Pro–l-Ile) (322)Endophytic fungus Alternaria tenuissima from the bark of Erythrophleum fordii-[156]
Endophytic Aspergillus fumigatus-[21]
Rhizoctonia solani-[157]
Cyclo(l-Pro–d-Leu) (323)Marine-derived Chromocleista sp. from a deep-water sediment sample collected in the Gulf of Mexico-[158]
Cyclo(l-Pro–l-Leu) (324)Endophytic Aspergillus fumigatusWeak inhibitory activity of β-glucuronidase release[21]
Phytopathogenic Colletotrichum gloesporoidesPhytotoxic, antitumoral and fungicide activity[150]
Rhizoctonia solani-[157]
Endophytic Alternaria tenuissima from the bark of Erythrophleum fordii-[156]
Cyclo(Pro–Homoleucine) (325)Alternaria alternata-[149]
Cyclo(4-hydroxy-R-Pro–S-Leu) = Cyclo(cis-4-hydroxy-d-Pro–l-Leu) (326)Marine-sponge derived yeast Aureobasidium pullulans at Okinawa of Japan-[159]
Mangrove-derived endophytic Pestalotiopsis vaccinii from a branch of Kandelia candel-[160]
Cyclo(trans-4-hydroxy-l-Pro–l-Leu) (327)Endophytic Alternaria alternata from grapevineAntifungal activity on Plasmopara viticola[154]
Endophytic Alternaria tenuissima from the bark of Erythrophleum fordii-[156]
Cyclo(d-Pro–d-Phe) (328)Endophytic Alternaria tenuissima from the bark of Erythrophleum fordii-[156]
Cyclo(l-Pro–d-Phe) (329)Alternaria alternata-[149]
Marine-derived Chromocleista sp. from a deep-water sediment sample collected in the Gulf of Mexico-[158]
Marine-derived Penicillium bilaii-[161]
Cyclo(6,7-en-Pro–l-Phe) (330)Marine-derived Chromocleista sp. from a deep-water sediment sample collected in the Gulf of Mexico-[158]
Cyclo(4-Hydroxy-R-Pro–S-Phe) = Cyclo-(cis-4-Hydroxy-d-Pro–l-Phe) (331)Marine-sponge derived yeast Aureobasidium pullulans at Okinawa of Japan-[159]
Cyclo(d-6-Hydroxy-Pro–l-Phe) = Cyclo(d-6-Hyp–l-Phe) (332)Marine-derived Chromocleista sp. from a deep-water sediment sample collected in the Gulf of Mexico-[158]
Marine-derived Chromocleista sp.-[162]
Cyclo(6-Hydroxy-l-Pro–l-Phe) = Cyclo(l-6-Hyp–l-Phe) (333)Marine-derived Chromocleista sp. from a deep-water sediment sample collected in the Gulf of Mexico-[158]
Marine-derived Chromocleista sp.-[162]
Cyclo(l-Pro–l-Phe) = Maculosin-2 (334)Alternaria alternata from spotted knapweed (Centaurea maculosa)Phytotoxic activity[149,163]
Cyclo(trans-4-hydroxy-l-Pro–l-Phe) (335)Endophytic Alternaria alternata from grapevineAntifungal activity on Plasmopara viticola[154]
Cyclo(l-Pro–l-Pro) (336)Endophytic Alternaria tenuissima from the bark of Erythrophleum fordii-[156]
Endophytic fungus Stagonosporopsis oculihominis from Dendrobium huoshanense-[164]
Cyclo(l-Pro–l-Tyr) = Maculosin-1 (337)Alternaria alternata from spotted knapweed (Centaurea maculosa)Phytotoxic activity[149,163]
Marine-derived Chromocleista sp. from a deep-water sediment sample collected in the Gulf of Mexico-[158]
Marine-derived Penicillium bilaii-[161]
Cyclo(13,15-dichloro-l-Pro–l-Tyr) (338)Leptoxyphium sp.Inhibitory activity on CCL2-induced chemotaxis[152]
Cyclo(l-Pro–d-Val) (339)Alternaria alternata-[149]
Endophytic Alternaria tenuissima from the bark of Erythrophleum fordii-[156]
Cyclo(d-Pro–l-Val) (340)Aspergillus sp. F70609Inhibitory activity on β-glucosidase[165]
Cyclo(l-Pro–l-Val) (341)Marine-derived Chromocleista sp. from a deep-water sediment sample collected in the Gulf of Mexico-[158]
Phytopathogenic Colletotrichum gloesporoidesPhytotoxic and antibiotic activities[150]
Phytopathogenic Fusarium oxysporum-[166]
Marine-derived Penicillium bilaii-[161]
Rhizoctonia solani-[157]
(R)-2-(2-(Furan-2-yl)-oxoethyl- octahydropyrrolo[1,2-a] pyranine-1,4-dione (342)Edible and medicinal Armillaria mellea-[167]
Macrophominol (343)Phytopathogenic Macrophomina phaseolina-[168]
Taichunamide A (344)Aspergillus taichungensis (IBT 19404)-[53]
Taichunamide B (345)Aspergillus taichungensis (IBT 19404)-[53]
Table
Table 5. Non-tryptophan–non-proline cyclodipeptide analogs and their biological activities.
Table 5. Non-tryptophan–non-proline cyclodipeptide analogs and their biological activities.
NameFungus and its OriginBiological ActivityRef.
3-Acetamino-6-isobutyl-2,5-dioxopiperazine (346)Cordyceps sinensisCytotoxic activity[169]
Altenarizine A (347)Endophytic Alternaria alternata from the root of Ceratostigma griffithii-[183]
Altenarizine B (348)Endophytic Alternaria alternata from the root of Ceratostigma griffithii-[183]
Aurantiamine (349)Penicillium aurantiogriseum var. aurantiogriseum-[184]
Azonazine (350)Aspergillus insulicolaAnti-inflammatory activity[170]
(3S)-6-Benzyl-3-isopropyl-1-methylpiperazine-2,5-dione (351)Entomogenous Paecilomyces tenuipesModerate cytotoxicity against prostate cancer cells 22RV1 and DU-145[185]
Cordycedipeptide A (352)Cordyceps sinensisCytotoxic activity[169]
Cyclo(Gly–Phe) (353)Unidentified fungus from Kandelia candel leaf-[186]
Cyclo(Leu–Leu) (354)Unidentified fungus from Kandelia candel leaf-[186]
Cyclo(Leu–Tyr) (355)Unidentified fungus from Kandelia candel leaf-[186]
Cyclo(l-Leu–l-Val) (356)Endophytic Aspergillus fumigatus from the stem of Erythrophleum fordii-[187]
Cyclo(l-Phe–l-Phe) (357)Penicillium nigricansAnthelmintic activity against Hymenolepis nana and Schistosoma mansoni in mice[171,172]
Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Cyclo(Phe–Ser) (358)Endophytic Alternaria sp. FL25 from Ficus caricaAntiphytopathogenic fungal activity[38]
Insect pathogenic Verticillium hemipterigenumCytotoxic and antimicrobial activity[173,174]
Cyclo(l-Phe-N-methyl-l-Tyr) (359)Geotrichum candidumInhibitory activity against Peronophythora litchii[189]
Cyclo(l-Tyr–l-Tyr) (360)Cordyceps sinensis-[169]
Cyclopenin (361)Penicillium verrucosum var. cyclopium-[124]
Cyclopenol (362)Penicillium verrucosum var. cyclopium-[124]
Mangrove endophytic Penicillium sclerotiorum from Bruguiera gymnorrhiza-[190]
Deoxymycelianamide (363)Marine-derived Gliocladium sp.Strong cytotoxic activity[179]
Desferricoprogen (364)Mud dauber wasp-derived Talaromyces sp. CMB-W045-[191]
Diatretol (365)Clitocybe diatretaWeak antibacterial activity[175]
(6S)-3-(1,3-Dihydroxypropyl)-6-(2-methylpropyl)piperzaine-2,5-dione (366)Plant endophytic Trichosporum sp. from the seeds of Trigonella foenum-graecumAntileishmanial activity against Leishmania donovani with IC50 value of 96.3 μg/mL[192]
(6R)-3-(1,3-Dihydroxypropyl)-6-(2-methylpropyl)piperzaine-2,5-dione (367)Plant endophytic Trichosporum sp. from the seeds of Trigonella foenum-graecumAntileishmanial activity against Leishmania donovani with IC50 value of 82.5 μg/mL[192]
Dimerumic acid (368)Monascus ankaAntioxidant activity[176,177]
Mud dauber wasp-derived Talaromyces sp. CMB-W045Demonstratinghigh affinity for Fe(III)[191]
Monascus ankaAntioxidant activity by inhibition on lipid peroxidation and hemeprotein-mediated oxidation[193]
Diphenylalazine A (369)Epicoccum nigrum colonizing on Cordyceps sinensisInhibitory effects on HIV-1 replication in C8166 cells[194]
Diphenylalazine B (370)Epicoccum nigrum colonizing on Cordyceps sinensis-[194]
Diphenylalazine C (371)Tin mine tailings-derived Schizophyllum communeWeak antibacterial and cytotoxic activities[195]
Eleutherazine B (372)Mud dauber wasp-derived Talaromyces sp. CMB-W045-[191]
Fusaperazine C (373)Endophytic Fusarium sp. from Viguiera arenaria-[196]
Gliocladride (374)Marine-derived Gliocladium sp.Cytotoxic activity[178]
Gliocladride A (375)Marine-derived Gliocladium sp.Moderate cytotoxic activity[179]
Gliocladride B (376)Marine-derived Gliocladium sp.Moderate cytotoxic activity[179]
Golmaenone (377)Marine-derived Aspergillus sp.Radical scavenging activity against DPPH, UV-A protecting activity[103]
Marine mudflat sediment derived Chaetomium cristatum collected at Suncheon Bay of KoreaRadical-scavenging activity against DPPH with IC50 value of 20 μM[134]
Gunnilactam A (378)Entomogenous Paecilomyces gunniiCytotoxic activity against human prostate cancer C42B cells[197]
Gunnilactam B (379)Entomogenous Paecilomyces gunnii-[197]
Gunnilactam C (380)Entomogenous Paecilomyces gunnii-[197]
14-Hydroxy-cyclopeptine (381)Aspergillus sp. SCSIOW2Inhibition of nitric oxide production with IC50 value of 40.3 μg/mL in a lipopolysaccharide and recombinant mouse interferon-γ-activated macrophage-like cell line[198]
Hypocreasin (382)Hypocrea spp.-[199]
3-Isopropyl-6-isobutyl-2,5-dioxopiperazine (383)Cordyceps sinensis-[169]
JBIR-74 (384)Marine-derived Aspergillus sp. fS14 from the unidentified marine sponge-[200]
JBIR-75 (385)Marine-derived Aspergillus sp. fS14 from the unidentified marine sponge-[200]
Mactanamide (386)Marine-derived Aspergillus sp.Fungistatic activity to Candida albicans[180]
MPC1001H (387)Podospora australis-[201]
NBRI16716A (388)Perisporiopsis melioloides Mer-f16716Cytotoxic activity[181]
NBRI16716B (389)Perisporiopsis melioloides Mer-f16716Cytotoxic activity[181]
NBRI16716C (390)Perisporiopsis melioloides Mer-f16716-[181]
Penicillivinacine (391)Marine-derived Penicillium vinaceumAntimigratory activity[22]
Phenylahistin (392)Aspergillus ustus NSC-F038Growth inhibition of various tumor cell lines[182]
PJ147 (393)Marine-derived Gliocladium sp. YUP08 from soilCytotoxic activity on A375-S2, Hela, P388, A-549, HL-60, and BEL-7420 cell lines[202,203]
PJ157 (394)Marine-derived Gliocladium sp. YUP08 from soil-[202]
Pre-aurantiamine (395)Marine-derived Aspergillus aculeatus CRI322-03 from the sponge Stylissa flabeliformis-[204]
Spirobrocazine C (396)Mangrove-derived Penicillium brocae MA-231 from Avicennia marinaModerate cytotoxic and antibacterial activities[205]
Talarazine A (397)Mud dauber wasp-derived Talaromyces sp. CMB-W045-[191]
Talarazine B (398)Mud dauber wasp-derived Talaromyces sp. CMB-W045-[191]
Talarazine C (399)Mud dauber wasp-derived Talaromyces sp. CMB-W045-[191]
Talarazine D (400)Mud dauber wasp-derived Talaromyces sp. CMB-W045-[191]
Talarazine E (401)Mud dauber wasp-derived Talaromyces sp. CMB-W045-[191]
Terretrione A (402)Marine-derived Penicillium vinaceumAntimigratory activity[22]
Waspergillamide A (403)Aspergillus sp. CMB-W031-[206]
Note: IC50, median inhibitory concentration.
Table
Table 6. Fungal 1,4-bridged epiplythiodioxopiperazine analogs and their biological activities.
Table 6. Fungal 1,4-bridged epiplythiodioxopiperazine analogs and their biological activities.
NameFungus and its OriginBiological ActivityRef.
3822-A (404)Stereum hirsutum HKI 0195 -[219]
A26771A (405)Penicillium turbatumAntiviral and antibacterial activity[226]
A26771 C (406)Penicillium turbatumAntiviral and antibacterial activity[226]
Acetylapoaranotin (407)Marine-derived Aspergillus sp. KMD 901Directly cytotoxic and apoptosis inducing effects on HCT116 colon cancer cell lines[212]
Acetylaranotin (408)Marine-derived Aspergillus sp. KMD 901Directly cytotoxic and apoptosis inducing effects on HCT116 colon cancer cell lines[212]
Apoaranotin (409)Arachniotus aureus-[227]
Aranotin (410)Arachniotus aureus-[227]
Bionectin A (411)Bionectra byssicola F120Anti-MRSA activity[228]
Bionectin B (412)Bionectra byssicola F120Anti-MRSA activity[228]
Brocazine A (413)Endophytic Penicillium brocae MA-231 from mangrove Avicennia marinaCytotoxic activity[229]
Brocazine B (414)Endophytic Penicillium brocae MA-231 from mangrove Avicennia marinaCytotoxic activity[229]
Brocazine C (415)Endophytic Penicillium brocae MA-231 from mangrove Avicennia marina-[229]
Brocazine D (416)Endophytic Penicillium brocae MA-231 from mangrove Avicennia marina-[229]
Brocazine E (417)Endophytic Penicillium brocae MA-231 from mangrove Avicennia marinaCytotoxic activity[229]
Brocazine F (418)Endophytic Penicillium brocae MA-231 from mangrove Avicennia marinaCytotoxic activity[229]
Brocazine G (419)Marine-derived Penicillium brocae MA-231 from the mangrove Avicennia marinaCytotoxicity against both sensitive and cisplatin-resistant human ovrian cancer cells and strong antimicrobial activity on pathogenic Staphylococcus aureus[205]
Chaetocin = Chaetocin A (420)Chaetomium minutumAntibacterial, cytostatic, inhibitory activity on lysine-specific histone methyltransferases[209]
Chaetocin B (421)Chaetomium sp.Cytotoxic activity[210]
Chaetocin C (422)Chaetomium sp.Cytotoxic activity[210]
Chaetocochin B (423)Chaetomium cochliodesCytotoxic activity[211]
Chaetocochin C (424)Chaetomium cochliodesCytotoxic activity[211]
Chetomin (425)Marine mudflat sediment derived Chaetomium cristatum collected at Suncheon Bay of KoreaRadical-scavenging activity against DPPH with an IC50 value of 15 μM[134]
Chetoseminudin A (426)Chaetomium globosumAntibacterial activity[230]
Chaetomium seminudumImmunomodulatory activity[231]
Chetracin A (427)Chaetomium spp.Cytotoxic activity[210]
Chetracin B (428)Antarctic psychrophilic fungus Oidiodendron truncatumCytotoxic activity[137]
Chetracin C (429)Antarctic psychrophilic fungus Oidiodendron truncatumCytotoxic activity[137]
Cristazine (430)Mudflat-sediment-derived Chaetomium cristatumRadical-scavenging activity, cytotoxic activity against human cervical carcinoma (HeLa) cells[134]
Dehydrogliotoxin (431)Gliocladium flavofuscumAntituberculosis activity[232]
Gliocladium virensAntituberculosis activity[233]
Deoxyapoaranotin (432)Marine-derived Aspergillus sp. KMD 901Directly cytotoxic and apoptosis inducing effects on HCT116 colon cancer cell lines[212]
11‘-Dexoyverticillin A (433)Gliocladium roseum from submerged woodAntinematodal activity[222]
11,11‘-Dihydroxychaetocin (434)Verticillium tenerumAntibacterial and antimitotic activities[234]
Dithiosilvatin (435)Aspergillus silvaticus-[235]
Emestrin (436)Cladorrhinum sp. KY4922Antiproliferative activity[236]
Emestrin B (437)Emericella striataAntifungal activity[237]
Emestrin C = MPC1001 (438)Podospora australisAntifungal activity[201]
Cladorrhinum sp. KY4922Antiproliferative activity[236]
Cladorrhinum sp. KY4922Antitumor and antibacterial activity[220]
Emestrin D = MPC1001D (439)Podospora australisAntifungal activity[201]
Cladorrhinum sp. KY4922Antiproliferative activity[236]
Emestrin E (440)Podospora australisAntifungal activity[201]
Emestrin F (441)Armillaria tabescensAntifungal activity[238]
Emestrin G (442)Armillaria tabescens-[238]
Emestrin J (443)Podospora australis-[201]
Emethallicin A (444)Emericella heterothallicaInhibitory activity on histamine release from mast cells[213]
Emethallicin B (445)Emericella heterothallicaInhibitory activity on histamine release from mast cells[214]
Emethallicin C (446)Emericella heterothallicaInhibitory activity on histamine release from mast cells[214]
Emethallicin D (447)Emericella heterothallicaInhibitory activity on histamine release from mast cells[214]
Emethallicin E (448)Emericella heterothallicaInhibitory activity on histamine release from mast cells[215]
Emethallicin F (449)Emericella heterothallicaInhibitory activity on histamine release mast cells[215]
Epicoccin T (450)Endophytic fungus Epicoccum nigrum from the leaves Lysidice rhodostegia-[188]
Epicoccin U (451)Tin mie tailings-derived Schizophyllum communeWeak antibacterial and cytotoxic activities[195]
Epicorazine A (452)Capnodium sp. from palm leaf litter collected in Quetzalito, Guatemala-[239]
Epicoccum purpurascens-[240]
Marine-derived Penicillium brocae MA-231 from the mangrove plant Avicennia marina-[229]
Marine-derived Phoma sp. OUCMDZ-1847 from the mangrove plant Kandelia candelCytotoxic activity[241]
Podaxis pistillarisAntibacterial and cytotoxic activities[242]
Basidiomycete Stereum hirsutum HKI 0195Cytotoxic activity against HeLa cells and antiproliferative effects against several mouse fibrobalst and cancer cell lines[219]
Epicorazine B (453)Epicoccum purpurascens-[240]
Marine-derived Phoma sp. OUCMDZ-1847 from the mangrove Kandelia candelCytotoxic activity[241]
Podaxis pistillarisAntibacterial and cytotoxic activities[242]
Basidiomycete Stereum hirsutum HKI 0195Cytotoxic activity against HeLa cells and antiproliferative effects against several mouse fibroblast and cancer cell lines[219]
Epicorazine C (454)Marine-derived Phoma sp. OUCMDZ-1847 from the mangrove plant Kandelia candelCytotoxic activity[241]
Podaxis pistillarisAntibacterial activity[242]
Stereum hirsutum HKI 0195 Antibacterial, antifungal, antiproliferative and cytotoxic activities[219]
Gliocladine A (455)Gliocladium roseum from submerged woodAtinematodal activity[222]
Gliocladine B (456)Gliocladium roseum from submerged woodAtinematodal activity[222]
Gliocladine C (457)Gliocladium roseum from submerged woodAtinematodal activity[222]
Gliocladine D (458)Gliocladium roseum from submerged woodAtinematodal activity[222]
Gliocladine E (459)Gliocladium roseum from submerged woodAtinematodal activity[222]
Glionitrin A (460)Coculture of the fungus Aspergillus fumigatus KMC-901 and the bacterium Sphingomonas sp. KMK-001Antibacerial and cytotoxic activities[243]
Gliotoxin (461)Aspergillus fumigatusCytotoxic activity[217]
Gliocladium flavofuscum-[232]
Deep-sea derived Aspergillus sp. SCSIO Ind09F01Anti-tuberculosis and cytotoxic activities[35]
Hyalodendrin (462)Marine-derived Asteromyces cruciatusis 763 from an unidentified decaying green alga-[244]
Hyalodendrin-S3 (463)Unidentified fungus NRRL 3888-[245]
Hyalodendrin-S4 (464)Hyalodendron sp.-[246]
Leptosin A (465)Leptosphaeria sp. from a marine algaCytotoxicity[247]
Leptosin B (466)Leptosphaeria sp. from a marine alga-[247]
Leptosin C (467)Leptosphaeria sp. from a marine algaCytotoxicity[247]
Leptosin D (468)Leptosphaeria sp. from a marine alga-[247]
Leptosin E (469)Leptosphaeria sp. from a marine alga-[247]
Leptosin F (470)Leptosphaeria sp. from a marine alga-[247]
Leptosin G (471)Leptosphaeria sp. from a marine algaCytotoxicity[248]
Leptosin G1 (472)Leptosphaeria sp. from a marine algaCytotoxicity[248]
Leptosin G2 (473)Leptosphaeria sp. from a marine algaCytotoxicity[248]
Leptosin H (474)Leptosphaeria sp. from a marine algaCytotoxicity[248]
Leptosin I (475)Leptosphaeria sp. from a marine algaCytotoxicity[249]
Leptosin J (476)Leptosphaeria sp. from a marine algaCytotoxicity[249]
Leptosin K (477)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[250]
Leptosin K1 (478)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[250]
Leptosin K2 (479)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[250]
Leptosin M (480)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells; Inhibition on two protein kinases, PTK and CaMKIII, and human topoisomerase II[251]
Leptosin M1 (481)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[251]
Leptosin N (482)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[251]
Leptosin N1 (483)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[251]
Melinacidin II (484)Acrostalagmus cinnabarinus var. melinacidinusAntibacterial activity[252]
Melinacidin III (485)Acrostalagmus cinnabarinus var. melinacidinusAntibacterial activity[252]
Melinacidin IV (486)Acrostalagmus cinnabarinus var. melinacidinusAntibacterial activity[252]
Antarctic psychrophilic fungus Oidiodendron truncatumCytotoxic activity[137]
MPC1001B (487)Cladorrhinum sp. KY4922Antiproliferative activity[236]
MPC1001C (488)Cladorrhinum sp. KY4922Antiproliferative activity[236]
Podospora australisAntifungal activity[201]
MPC1001E (489)Cladorrhinum sp. KY4922Antiproliferative activity[236]
Phomalirazine (490)Leptosphaeria maculansPhytotoxic activity[253]
Phomazine C (491)Marine-derived Phoma sp. OUCMDZ-1847 from the mangrove plant Kandelia candel-[241]
Plectosphaeroic acid C (492)Marine-derived Plectosphaerella cucumerinaInhibtion of indoleamine 2,3-dioxygenase[254]
Rostratin A (493)Endophytic Epicoccum nigrum from the leaves Lysidice rhodostegia-[188]
Exserohilum rostratumModerate cytotoxicity[218]
Rostratin B (494)Exserohilum rostratumModerate cytotoxicity[218]
Rostratin C (495)Exserohilum rostratumModerate cytotoxicity[218]
Rostratin D (496)Exserohilum rostratumModerate cytotoxicity[218]
Sch52900 (497)Gliocladium roseum from submerged woodAntinematodal activity[222]
Sch52901 (498)Gliocladium roseum from submerged woodAntinematodal activity[222]
Secoemestrin C (499)Emericella foveolata-[255]
Secoemestrin D (500)Podospora australis-[201]
Endophytic fungus Emericella sp. AST0036 from healthy leaf tissue of Astragalus lentiginosusCytotoxic activity[221]
Sirodesmin A (501)Sirodesmium diversumAntiviral activity[256]
Sirodesmin B (502)Leptosphaeria maculansPhytotoxic activity[257]
Sirodesmium diversumAntiviral activity[256]
Sirodesmin C (503)Leptosphaeria maculansPhytotoxic activity[257]
Sirodesmium diversumAntiviral activity[256]
Sirodesmin G = Sirodesmin PL (504)Leptosphaeria maculansPhytotoxic activity[257,258]
Sirodesmium diversumAntiviral activity[256]
Sirodesmin H (505)Leptosphaeria maculansPhytotoxic activity[257]
Sporidesmin A = Sporidesmin (506)Pithomyces chartarumImmunoregulatory activity[259,260]
Delitschia corticolaAntibacterial and antifungal activities[261]
Sporidesmin B (507)Pithomyces chartarum-[259]
Sporidesmin C (508)Pithomyces chartarum-[262]
Sporidesmin E (509)Penicillium terlikowskii-[263]
Sporidesmin G (510)Pithomyces chartarumAntiproliferative, cytotoxic, immunomodulatory, antiviral, antibacterial, antifungal activities[264]
Sporidesmin H (511)Pithomyces chartarumAntiproliferative, cytotoxic, immunomodulatory, antiviral, antibacterial, antifungal activities[265]
Sporidesmin J (512)Pithomyces chartarumAntiproliferative, cytotoxic, immunomodulatory, antiviral, antibacterial, antifungal activities[265]
T988 A (513)Tilachidium sp.Cytotoxic activity[266]
Antarctic psychrophilic fungus Oidiodendron truncatumCytotoxic activity[211]
T988 C (514)Tilachidium sp.Cytotoxic activity[266]
Antarctic psychrophilic fungus Oidiodendron truncatumCytotoxic activity[211]
Verticillin A (515)Gliocladium roseum from submerged woodAntinematodal and cytotoxic activities[222]
Verticillium sp.-[223]
Verticillin B (516)Verticillium sp.-[223]
Verticillin C (517)Verticillium sp.-[223]
Verticillin D (518)Bionectria byssicolaAntibacterial activity[225]
Gliocladium catenulatumAntibacterial activity[224]
Verticillin E (519)Gliocladium catenulatumAntibacterial activity[224]
Verticillin F (520)Gliocladium catenulatumAntibacterial activity[224]
Verticillin G (521)Bionectra byssicolaAntibacterial activity[225]
Note: IC50, median inhibitory concentration.
Table
Table 7. Fungal analogs with sulfur-bridge outside 2,5-DKP ring and their biological activities.
Table 7. Fungal analogs with sulfur-bridge outside 2,5-DKP ring and their biological activities.
NameFungus and Its OriginBiological ActivityRef.
Adametizine A = N-methyl pretrichodermamide B (522)Marine sponge-derived Penicillium adametzioides AS-53Lethal activity against brine shrimp and antibacterial activity[269]
Adametizine B = Pretrichodermamide C (523)Marine sponge-derived Penicillium adametzioides AS-53-[269]
Aspirochlorine (524)Aspergillus flavusAntifungal activity on azole-resitant Candida albicans[107]
Chlorotrithiobrevamide (525)Trichoderma cf. brevicompactumCytotoxic effects against Jurkat cells with IC50 values of 16 µM[270]
DC1149B (526)Trichoderma cf. brevicompactumCytotoxic effect against Jurkat cells with IC50 values of 5.1 µM[270,271]
DC1149R(527)Trichoderma cf. brevicompactum-[271]
Epicoccin A (528)Cordyceps-colonizing Epicoccum nigrumModerate antimicrobial activity[268]
Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin B (529)Cordyceps-colonizing Epicoccum nigrum-[268]
Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin C (530)Cordyceps-colonizing Epicoccum nigrum-[268]
Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin D (531)Cordyceps-colonizing Epicoccum nigrum-[268]
Epicoccin E (532)Cordyceps-colonizing Epicoccum nigrum-[194]
Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin F (533)Cordyceps-colonizing Epicoccum nigrum-[194]
Epicoccin I (534)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin M (535)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin N (536)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin O (537)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin P (538)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin Q (539)Endophytic Epicoccum nigrum from the leaves of Lysidice rhodostegia-[188]
Epicoccin R (540)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin S (541)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Gliovirin (542)Trichoderma cf. brevicompactum-[270,271]
Iododithiobrevamide (543)Trichoderma cf. brevicompactum-[271]
Outovrin A (544)Endophytic Penicillium raciborskii from Rhododendron tomentosum-[272]
Outovirin B (545)Endophytivc Penicillium raciborskii from Rhododendron tomentosum-[272]
Outovirin C (546)Endophytic Penicillium raciborskii from Rhododendron tomentosumAntifungal activity[272]
Penicisulfuranol A (547)Mangrove-derived Penicillium janthinellum HDN13-309 from the roots of Sonneratia caseolarisCytotoxic activity on the cell lines HeLa and HL-60[273]
Penicisulfuranol B (548)Mangrove-derived Penicillium janthinellum HDN13-309 from the roots of Sonneratia caseolarisCytotoxic activity on the cell lines HeLa and HL-60[273]
Penicisulfuranol C (549)Mangrove-derived Penicillium janthinellum HDN13-309 from the roots of Sonneratia caseolarisCytotoxic activity on the cell lines HeLa and HL-60[273]
Pretrichodermamide A (550)Trichoderma cf. brevicompactum-[270,271]
Trichoderma sp. BCC 5926Activity against Mycobacterium tuberculosis H37Ra with an MIC value of 12.5 µg/mL[274]
Tetrathioaspirochlorine (551)Aspergillus flavusAntifungal activity on azole-resitant Candida albicans[107]
Trithioaspirochlorine (552)Aspergillus flavus-[107]
Vertihemiptellide A (553)Insect pathogenic Verticillium hemipterigenum BBC 1449Inhibitory activity against Mycobacterium tuberculosis H37Ra, moderate cytotoxic activity[174]
Vertihemiptellide B (554)Insect pathogenic Verticillium hemipterigenum BBC 1449Inhibitory activity against Mycobacterium tuberculosis H37Ra, moderate cytotoxic activity[174]
Note: IC50, median inhibitory concentration; MIC, minimum inhibitory concentration.
Table
Table 8. Nonbridged methylthio-containing cyclodipeptide analogs from fungi and their biological activities.
Table 8. Nonbridged methylthio-containing cyclodipeptide analogs from fungi and their biological activities.
NameFungus and its OriginBiological ActivityRef.
Alternarosin A (555)Marine-derived Alternaria raphaniWeak antimicrobial activity[276]
Asteroxepin (556)Aspergillus terreus-[284]
(Z)-6-Benzylidene-3-hydroxymethyl-1,4-dimethyl-3-methylsulfanylpiperazine-2,5-dione (557)Marine-derived unidentified strain CRIF2 of the order PleosporalesWeak cytotoxic activity[285]
Bilain A (558)Marine-derived Penicillium bilaii-[161]
Bilain B (559)Marine-derived Penicillium bilaii-[161]
Bilain C (560)Marine-derived Penicillium bilaii-[161]
Bionectin C (561)Bionectra byssicola F120Anti-MRSA activity[228]
Bisdethiobis(methylsulfanyl)acetylapoaranotin (562)Aspergillus terreus BCC 4651-[286]
Bisdethiobis(methylsulfanyl)acetylaranotin = Bisdethiodi(methylthio)-acetylaranotin (563)Aspergillus terreus BCC 4651-[286]
Bisdethiobis(methylsulfanyl)apoaranotin = Bisdethiodi(methylthio)-acetylapoaranotin (564)Aspergillus terreus BCC 4651Weak antimycobacterial activity[286]
Bisdethiobis(methylsulfanyl)aranotin (565)Aspergillus terreus BCC 4651-[286]
Bisdethiobis(methylthio) gliotoxin (566)Marine-derived Aspergillus fumigatus-[278]
Aspergillus fumigatus from saltwaterModerate trypanocidal activity[287]
Endophytic Colletotrichum gloeosporioides from Viguiera robustaSpecific inhibitor of the platelet activating factor and antibacterial activity[196]
Marine-derived fungus Pseudallescheria sp.Antibacterial activity[280]
Bisdethiodi(methylthio)-1-demethylhyalodendrin (567)Insect pathogenic Verticillium hemipterigenum BCC 1449Inhibitory activity against Mycobacterium tuberculosis H37Ra; moderate cytotoxic activity[174]
(3R,6R)-Bisdethiodi(methylthio)-hyalodendrin (568)Marine-derived unidentified strain CRIF2 of the order PleosporalesWeak cytotoxic activity[285]
Cordyceps-colonizing fungus Isaria farinosa-[288]
cis-Bis(methylthio)silvatin = cis-Bisdethiodi(methylthio) silvatin (569)Fusarium chlamydosporum from the marine alga Carpopeltis affinisWeak cytotoxic activity against P388 lymphocytic leukemia cells[277]
Marine-derived Penicillium bilaiiWeak cytotoxicity against NS-1 cells[161]
Plant endophytic Penicillium sp.Antibacterial activity against Staphylococcus aureus with an MIC value of 43.4 μg/mL[289]
Bis-N-norgliovictin (570)Gliocladium virens-[233]
Marine-derived Aspergillus fumigatus-[278]
Marine-derived fungus Neosartorya pseudofischeri-[136]
Marine-derived Dichotomomyces sp. L-8-[113]
-Inhibitory activity on LPS-induced inflammation in macrophages[279]
Chaetocochin A (571)Chaetomium cochliodesCytotoxic activity[211]
Chetoseminudin B (572)Nectria inventaTrypanocidal activity in the whole cell assay of Trypanosoma brucei[287]
Chetoseminudin C (573)Antarctic psychrophilic fungus Oidiodendron truncatum-[137]
Chaetomium seminudum-[231]
Chetoseminudin E (574)Endophytic fungus Chaetomium sp. 88194-[290]
Chetracin D (575)Antarctic psychrophilic fungus Oidiodendron truncatumCytotoxic activity[137]
Colletopiperazine (576)Endophytic Colletotrichum gloeosporioides from Viguiera robusta-[196]
Dehydroxybisdethiobis(methylthio) gliotoxin (577)Marine-derived Pseudallescheria sp.Antibacterial activity[280]
Dethio-tetra(methylthio)chetomin (578)Chaetomium cochliodesCytotoxic activity[211]
Dichotocejpin A (579)Dichotomomyces cejpii FS110Inhibitory activity against α-glucosidase[112]
Didehydrobisdethiobis (methylthio) gliotoxins (580)Marine-derived Aspergillus sydowi from a driftwood sample-[10]
Epicoccin G (581)Cordyceps-colonizing Epicoccum nigrumInhibitory effect on HIV-1 replication in C8166 cells[194]
ent-Epicoccin G (582)Endophytic Epicoccum nigrum from Lysidice rhodostegiaInhibitory activity against the release of β-glucuronidase in rat polymorphonuclear leukocytes induced by platelet-activating factor[188]
Epicoccin H (583)Cordyceps-colonizing Epicoccum nigrumInhibitory effect on HIV-1 replication in C8166 cells[194]
Epicoccin J (584)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin K (585)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Epicoccin L (586)Endophytic Epicoccum nigrum from Lysidice rhodostegia-[188]
Emestrin H (587)Podospora australis-[201]
Emestrin I (588)Podospora australis-[201]
Emestrin K (589)Podospora australis-[201]
FR106969 (590)Penicillium citrinumInhibitory activity against PAF-induced rabbit platelet aggregation[281]
Fusaperazine A (591)Fusarium chlamydosporum OUPS-N124 from the marine alga Carpopeltis affinisWeak cytotoxic activity[277]
Fusaperazine B (592)Fusarium chlamydosporum OUPS-N124 from the marine alga Carpopeltis affinis-[277]
Fusaperazine E (593)Endophytic Penicillium crustosum from Viguiera robusta-[196]
Gliocladin A (594)Gliocladium roseum PS-N132Cytotoxicity against murine P388 lymphocytic leukemia cells[125]
Gliocladin B (595)Gliocladium roseum PS-N132Cytotoxicity against murine P388 lymphocytic leukemia cells[125]
Glionitrin B (596)Coculture of the fungus Aspergillus fumigatus KMC-901 and the bacterium Sphingomonas sp. KMK-001Suppression of DU145 cell invasion[291]
Glioperazine (597)Gliocladium roseum PS-N132Cytotoxic activity[125]
Bionectra byssicola F120-[126]
Glioperazine B (598)Bionectra byssicola F120Weak antibacterial activity[126]
Gliovictin = (−)-Gliovictin = A26771E (599)Marine-derived Asteromyces cruciatusis 763 from an unidentified decaying green alga-[244]
Marine-derived Asteromyces cruciatus-[292]
Haematocin (600)Phytopathogenic Nectria haematococcaAntifungal activity by inhibiting spore-germination and germ-tube elongation[282]
3-[(4-Hydroxyphenyl)-methyl]-1,4-dimethyl-3,6-bis(methylthio)-2,5-piperazinedione (601)Fusarium chlamydosporum OUPS-N124 from the marine alga Carpopeltis affinis-[277]
Leptosin O (602)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[131]
Leptosin P (603)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[131]
Leptosin Q (604)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[131]
Leptosin R (605)Leptosphaeria sp. from a marine algaCytotoxicity on P388 cells[131]
MPC1001F (606)Cladorrhinum sp. KY4922Antifungal activity[236]
Podospora australis-[201]
Mycoediketopiperazine (607)Papularia sp.Cytotoxicity on KB cells[283]
1N-Norgliovictin (608)Marine-derived Asteromyces cruciatusis 763 from an unidentified decaying green alga-[244]
Oidioperazine A (609)Antarctic psychrophilic fungus Oidiodendron truncatum-[137]
Penicibrocazine A (610)Marine-derived Penicillium brocae MA-231 from the mangrove plant Avicennia marina-[293]
Penicibrocazine B (611)Marine-derived Penicillium brocae MA-231 from the mangrove plant Avicennia marinaAntimicrobial activity[293]
Penicibrocazine C (612)Marine-derived Penicillium brocae MA-231 from the mangrove plant Avicennia marinaAntimicrobial activity[293]
Penicibrocazine D (613)Marine-derived Penicillium brocae MA-231 from the mangrove plant Avicennia marinaAntimicrobial activity[293]
Penicibrocazine E (614)Marine-derived Penicillium brocae MA-231 from the mangrove plant Avicennia marinaAntimicrobial activity[293]
Penicisulfuranol D (615)Mangrove-derived Penicillium janthinellum HDN13-309 from the roots of Sonneratia caseolaris-[273]
Penicisulfuranol E (616)Mangrove-derived Penicillium janthinellum HDN13-309 from the roots of Sonneratia caseolaris-[273]
Penicisulfuranol F (617)Mangrove-derived Penicillium janthinellum HDN13-309 from the roots of Sonneratia caseolaris-[273]
Phomazine A (618)Marine-derived Phoma sp. OUCMDZ-1847 from the mangrove plant Kandelia candel-[241]
Phomazine B (619)Marine-derived Phoma sp. OUCMDZ-1847 from the mangrove plant Kandelia candelCytotoxic activity[241]
Marine-derived Penicillium brocae MA-231 from the mangrove plant Avicennia marinaAntimicrobial activity[293]
Plectosphaeroic acid A (620)Marine-derived Plectosphaerella cucumerinaInhibition of indoleamine 2,3-dioxygenase[254]
Plectosphaeroic acid B (621)Marine-derived Plectosphaerella cucumerinaInhibition of indoleamine 2,3-dioxygenase[254]
Polanrazine B (622)Plant pathogen Phoma lingamPhytotoxic activity[138]
Polanrazine C (623)Plant pathogen Phoma lingamModerate and selective phytotoxicity by causing necrotic and chlorotic lesions[138]
Polanrazine D (624)Plant pathogen Phoma lingam-[138]
Pseudellone D (625)Marine-derived Pseudallescheria ellipsoidea F42-3 associated with the soft coral Lobophytum crassum-[294]
Sch 54794 (626)Fusarium chlamydosporum OUPS-N124 from the marine alga Carpopeltis affinisWeak cytotoxic activity against P388 lymphocytic leukemia cells[277]
Sch 54796 (627)Fusarium chlamydosporum OUPS-N124 from the marine alga Carpopeltis affinis-[277]
Spirobrocazine A (628)Mangrove-derived Penicillium brocae MA-231 from Avicennia marinaModerate antibacterial activity[205]
Spirobrocazine B (629)Mangrove-derived Penicillium brocae MA-231 from Avicennia marina-[205]
Sporidesmin D (630)Pithomyces chartarum-[295]
Sporidesmin F (631)Pithomyces chartarum-[296]
T988 B (632)Tilachidium sp.Cytotoxic activity[225]
Antarctic psychrophilic fungus Oidiodendron truncatum-[211]
Note: MIC, minimum inhibitory concentration.

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Wang, X.; Li, Y.; Zhang, X.; Lai, D.; Zhou, L. Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi. Molecules 2017, 22, 2026. https://doi.org/10.3390/molecules22122026

AMA Style

Wang X, Li Y, Zhang X, Lai D, Zhou L. Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi. Molecules. 2017; 22(12):2026. https://doi.org/10.3390/molecules22122026

Chicago/Turabian Style

Wang, Xiaohan, Yuying Li, Xuping Zhang, Daowan Lai, and Ligang Zhou. 2017. "Structural Diversity and Biological Activities of the Cyclodipeptides from Fungi" Molecules 22, no. 12: 2026. https://doi.org/10.3390/molecules22122026

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