Marine-Derived Penicillium Species as Producers of Cytotoxic Metabolites

Abstract

Since the discovery of penicillin, Penicillium has become one of the most attractive fungal genera for the production of bioactive molecules. Marine-derived Penicillium has provided numerous excellent pharmaceutical leads over the past decades. In this review, we focused on the cytotoxic metabolites * (* Cytotoxic potency was referred to five different levels in this review, extraordinary (IC₅₀/LD₅₀: <1 μM or 0.5 μg/mL); significant (IC₅₀/LD₅₀: 1~10 μM or 0.5~5 μg/mL); moderate (IC₅₀/LD₅₀: 10~30 μM or 5~15 μg/mL); mild (IC₅₀/LD₅₀: 30~50 μM or 15~25 μg/mL); weak (IC₅₀/LD₅₀: 50~100 μM or 25~50 μg/mL). The comparative potencies of positive controls were referred when they were available). produced by marine-derived Penicillium species, and on their cytotoxicity mechanisms, biosyntheses, and chemical syntheses.

1. Introduction

The oceans, which occupy more than 70% of the earth’s surface, undoubtedly support vast habitats and serve as prolific resources of various living organisms. Compared to terrestrial organisms, marine organisms often produce highly potent metabolites with unique structures to enable them to adapt to extremely challenging environments [1]. Developments and improvements made in biotechnology have led to a new era of bioprospecting for new marine products. Revolutionary target screening methods have improved the efficiency of drug discovery. In addition, leading edge genomics of biological symbiosis offer more opportunities to discover drug candidates and precursors. Marine endozoic microorganisms represent a new frontier in the discovery of pharmaceutical agents [2]. In particular, marine-derived fungi are excellent producers of biologically active secondary metabolites. Since the isolation of the broad-spectrum antibiotic, cephalosporin C from the marine-derived fungus Acremonium chrysogenum, thousands of bioactive metabolites have been discovered and evaluated [3].

Cancer is the second leading cause of death. Lung, prostate, colorectal, and digestive tract cancer are commonly encountered in males, whereas breast, lung, and cervical cancer are the major causes of female death. Marine microorganisms produce limited amounts of highly efficient toxic substances to protect their hosts from enemies, and these substances have been investigated as potential anticancer drug precursors. In particular, marine-derived Penicillium species represent a major source of cytotoxic metabolites. In this review, we list all cytotoxic or antitumor secondary metabolites isolated from marine-derived Penicillium species and classify them into distinct chemical groups. In addition, we summarize the cytotoxicity mechanisms and proposed biosyntheses of these metabolites. Overall, more than 200 natural products and their synthetic analogues are included in this review.

2. Alkaloids

Cytochalasan alkaloids, characterized by a highly substituted perhydoisoindol-1-one fused to a macrocyclic ring, have been shown to possess potential cytotoxicity against diverse tumor cell lines [4,5]. Penochalasins, chaetoglobosins, and cytoglobosins are common classes of cytochalasan alkaloids. A series of cytochalasans, penochalasins A–J (1–10), chaetoglobosins A, C, E–G, O (11–16), and cytoglobosin C (17) (Figure 1) were isolated from the mangrove endophytic fungus P. chrysogenum [6] and from the marine alga Enteromorpha intestinalis [7,8]. Penochalasins A–H (1–8) and chaetoglobosins A, F, O (11, 14, 16) exhibited significant cytotoxic activity (ED₅₀ = 0.4, 0.3, 0.5, 3.2, 2.1, 1.8, 1.9, 2.8, 0.6, 0.9, and 2.4 μg/mL, respectively) against P388 lymphocytic leukemia cells. Moreover, chaetoglobosin A (11) reportedly induced apoptosis of chronic lymphocytic leukemia (CLL) cells by targeting the cytoskeleton. The underlying mechanisms involve the induction of cell-cycle arrest and the inhibition of membrane ruffling and cell migration; therefore, it was proposed as a novel drug for CLL [9]. Penochalasin I (9) exhibited significant cytotoxic activities against MDA-MB-435 (human breast cancer cell line) and SGC-7901 (human gastric cancer cell line) with IC₅₀ values of ~7 μM. Cytoglobosin C (17) showed potential cytotoxicity against both SGC-7901 and A549 (human lung adenocarcinoma) with IC₅₀ values of 3–8 μM. Other cytochalasans, penochalasin J (10), chaetoglobosins C, E (12, 13), and chaetoglobosin G (15) showed moderate cytotoxicity against MDA-MB-435, SGC-7901, and A549 with IC₅₀ values in the range of 10–40 μM (epirubicin was used as a positive control with IC₅₀ values of 0.3~0.6 μM). A recent biosynthetic analysis showed that the fungal PKS-NRPS hybrid synthase, CheA, plays an essential role in cytochalasan formation [10].

Gliotoxin induces cellular immunosuppression and apoptosis [11], and its analogues are disulfur or polysulfur-containing mycotoxins that belong to a class of naturally occurring epipolythio piperazines (ETP). In 2012, the marine fungus Penicillium sp. JMF034, which was isolated from a deep sea sediment in Japan, was found to produce seven gliotoxin-related compounds, (bis(dethio)-10a-methylthio-3a-deoxy-3,3a-didehydrogliotoxin (18), 6-deoxy-5a,6-dide hydrogliotoxin (19), bis(dethio) bis(methylthio)gliotoxin (20), bis(dethio)bis(methylthio)-5a,6-dide hydrogliotoxin (21), 5a,6-dide hydrogliotoxin (22), gliotoxin (23), and gliotoxin G (24) (Figure 2) [12], which potently killed P388 murine leukemia cells (IC₅₀ = 3.4, 0.058, 0.11, 0.11, 0.056, 0.024, and 0.020 μM, respectively). Because of their extraordinary cytotoxicity, gliotoxin analogues are considered as antitumor leads [13]. Dimeric ETPs were reported to inhibit histone methyltransferase (HMT); in addition, compounds (22–24) with disulfide or tetrasulfide bonds showed significant inhibitory activities against HMT G9a (IC₅₀ = 2.6, 6.4, and 2.1 μM, respectively) rather than HMT SET7/9 (IC₅₀ > 100 μM). Gliotoxin G (24), isolated from the mangrove endophytic fungus P. brocae MA-231, was potently active against cisplatin-sensitive and resistant human ovarian cancer cell lines, A2780 and A2780 CisR, with IC₅₀ values of 664 and 661 nM, respectively (cisplatin was used as a positive control with IC₅₀ values of 1.67 and 12.63 μM, respectively) [14]. Compound 24 may be used as an anti-ovarian cancer agent, even in patients who are resistant to platinum compounds. Plausible hypotheses for the biosyntheses of ETPs have been previously reviewed [15].

Four new cytotoxic bisthiodiketopiperazines (brocazines A–F) (25–30) (Figure 3), which share molecular similarities with gliotoxin, were isolated from a fungal strain of P. brocae MA-231, collected from the marine mangrove Avicennia marina [16]. Their cytotoxicity was investigated in human prostate cancer (DU145), human cervical carcinoma (Hela), human hepatoma (HepG2), human breast carcinoma (MCF-7), human large-cell lung carcinoma (NCI-H460), SGC-790, human pancreatic cancer (SW1990), human colon carcinoma (SW480), and human glioma (U251) cell lines. Brocazines A, B, E, and F (25, 26, 29, and 30) exhibited significant cytotoxic effects against most of the cell lines tested with IC₅₀ values in the range of 0.89–9 μM (paclitaxel, cisplatin, cefitinib, doxorubicin, and gemcitabine were used as positive controls with IC₅₀ values of 1~11 μM). In contrast, brocazines C and D (27 and 28), which lack the α, β unsaturated ketone group, had much lower cytotoxicity (IC₅₀ > 20 μM), which suggests that the conjugated ketone system is crucial to the cytotoxic properties of bisthiodiketopiperazine analogues.

Two bisthiodiketopiperazines, pretrichodermamide C (31) and N-methylpretrichodermamide B (32) (also called adametizine B and A, respectively) (Figure 4), were isolated from a marine sponge-derived fungus (P. adametzioides AS-53) [17], a hyper saline lake-derived Penicillium sp. [18], and a marine algicolous fungus (Penicillium sp. KMM4672) [19]. All three studies showed that compound 32, which contains chlorine, exhibited significant cytotoxicity, wherein it reduced the viability of L5178Y mouse lymphoma cells, human prostate cancer 22Rv1 cells, PC-3 cells, LNCaP cells, and brine shrimps (IC₅₀ = 2, 0.51, 5.11, 1.76, and 4.8 μM, respectively; while kahalalide F, docetaxel, and colchicine were employed as positive controls with IC₅₀ values of 4.3, 0.013, 0.015, 0.004, and 8.1 μM, respectively). Furthermore, it was found active in hormone-resistant 22Rv1 cells at nanomolar concentrations. In contrast, metabolite 31 was completely inactive in all bioassays with IC₅₀ values > 100 μM. This remarkable difference in activity indicates that the halogen atom might improve the activity of the metabolite.

Roquefortine C (33) (Figure 5) is a potential neurotoxin that can activate P-glycoprotein and simultaneously inhibit P450-3A and other hemoproteins [20]. Roquefortine and meleagrin (38) analogues are considered biogenetically interrelated mycotoxins with promising cytotoxicity [21]. Recently, a series of roquefortine derivatives, roquefortines F–I (34–37), and meleagrin analogues, meleagrins B–E (39–42), were isolated from the deep ocean sediment-derived fungus Penicillium sp. [22], and most of these compounds (34, 35, and 39–42) were active against A549, HL-60 (human promyelocytic leukemia), BEL-7402 (human hepatoma), and MOLT-4 (human acute T lymphoblastic leukemia) cancer cell lines. Meleagrin B (39) was the most cytotoxic against these four cell lines with IC₅₀ values in the range of 1.5–7 μM; the other compounds had IC₅₀ values in the range of 4–50 μM. Meleagrin (38) was also isolated from a deep sea sediment-derived fungus, P. commune SD-118, and was found to be cytotoxic in HepG2, NCI-H460, Hela, MDA-MB-231 (human breast cancer cells), and DU145 human cancer cell lines (IC₅₀ = 12, 22, 20, 11, and 5 μg/mL, respectively; while fluorouracil was employed as a positive control with IC₅₀ values of 14, 1, 14, 8, and 0.4 μg/mL, respectively) [23].

Penicimutanins A,B (43–45) and fructigenine A (46) (Figure 6) are structurally similar to roquefortines, and were first isolated from diethyl sulfate- or gentamicin-induced mutants of the marine-derived fungus P. purpurogenum G59 [24,25]. Mutation-based approaches can activate silent fungal gene clusters and afford more potent metabolites with unique structures. Compounds 44 and 45 are mutant cytotoxic products that showed potent activities against five human cancer cell lines: K562 (human chronic myelogenous leukemia), HL-60, Hela, BGC-823 (human gastric adenocarcinoma), and MCF-7 (IC₅₀ values were 5–11 μM for 44 and 8–20 μM for 45). Compounds 43 and 46 also inhibited the proliferation of these cell lines (Inhibition Rate (IR)% = 22.6 and 20.8 (K562); 17.9 and 55.3 (HeLa); and 26.5 and 65.6% (MCF-7) at 100 μg/mL, respectively; while 5-fluorouracil was employed as a positive control with IR% of 48.5, 37.4, and 47.4 μg/mL at 100 μg/mL, respectively).

Since the isolation of (+)-chaetocin A (47) and (+)-verticillin A (48) (Figure 7) in 1970, dimeric epidithiodiketopiperazine alkaloids have received much attention owing to their diverse biological activities and complex molecular structures [26,27]. In 1999, two additional dimeric epidithiodiketopiperazine alkaloids, (+)-11,11′-dideoxyverticillin A (49) and (+)-11′-deoxyverticillin A (50), were isolated from a marine alga-derived fungus Penicillium sp. and were found to exhibit extraordinary cytotoxicity against HCT-116 cells (human colon cancer) with IC₅₀ of 30 ng/mL [28]. Chaetocin A (47) was the first compound reported to inhibit HMT, and to have specific effects on HMT SU(VAR)3-9 in vitro and in vivo [29]. (+)-11,11′-Dideoxyverticillin A (49), an alkaloid, exhibited diverse antitumor activities in vitro and in vivo [30]; in addition, it potently inhibited the phosphorylation of epidermal growth factor receptor in human breast cancer (MDA-MB-468) [31]. Movassaghi et al. used a concise enantioselective method for the total synthesis of (+)-11,11′-dideoxyverticillin A (49) in 2009 [32] based on mimicking the biosynthetic pathway; in addition, they used this approach to synthesize various dimeric epidithiodiketopiperazines [33].

Seven cytotoxic indole diterpene alkaloids, penitrems A,B (51–52), D–F (53–55), paspaline (58), and emindole SB (59) (Figure 8) were isolated from a marine Penicillium sp. KBr-induced mutation of this fungus produced two bromo-substituted indole alkaloids, 6-bromopenitrems B and E (56–57) [34]. Compounds (51–59) showed potent antiproliferative (IC₅₀ = 5–20 μM for MCF-7; 8–30 μM for MDA-MB-231), anti-migratory (IC₅₀ = 7–35 μM for MDA-MB-231) and anti-invasive properties (IR% = 10–75% at 15 μM) against human breast cancer cells. In addition, penitrems A, B, and E (51–52, 54) were evaluated in 60 human tumor cell lines as a part of the Development Therapeutics Program of the National Cancer Institute (NCI60). Penitrem B (52) exhibited the strongest mean growth inhibitory effect in the 60 human cancer cells (IR% = 41.05% at 10 μM) and was considered a potential selective inhibitory agent for leukemia cells. The nematode Caenorhabditis elegans was used to assess the brain’s Maxi-K (BK) channel inhibitory activity and toxicity in vivo [35,36]. Penitrem A (51) and 6-bromopenitrem E (57) displayed BK channel inhibition, comparable to that of a knockout strain. A pharmacophore study on the effects of the penitrem skeleton on the antiproliferative activity against MCF-7 cells indicated that less structural complexity of the penitrems, paspaline (58), and emindole SB (59) better maintained the molecular alignment and pharmacophoric features. Penitrem A (51) was also considered a neurotoxin that antagonizes BK channels [37].

Another large family of indole alkaloid mycotoxins, comprising communesins A–D (60–63) (Figure 9), was isolated from marine-derived Penicillium sp. from a marine alga [38], marine sponge [39], and marine sediment [40]. Communesin B (61) (also called nomofungin) was more cytotoxic to P388 lymphocytic leukemia cells (ED₅₀ = 0.45 μg/mL) than communesin A (60) (ED₅₀ = 3.5 μg/mL). The antiproliferative activity of communesins B–D (61–63) was further evaluated in six lymphocytic leukemia cell lines (U-937, THP-1, NAMALWA, L-428, MOLT-3, and SUP-B15). They steadily and effectively inhibited the proliferation of five of these cell lines with ED₅₀ values ranging from 7 to 16 μg/mL; however, they were inactive in L-428 cells. The total synthesis of communesin B (61) was previously reported [41].

Four new cytotoxic prenylated indole alkaloid derivatives, penioxamide (64) [42], 13-O-prenyl-26-hydroxyverruculogen (65) [43], and penipalines B and C (66–67) (Figure 10) [44], were isolated from marine mangrove-derived P. oxalicum EN-201, marine sediment-derived P. brefeldianum SD-273, and marine sediment-derived P. paneum SD-44, respectively. Metabolites 64–65 showed significant lethality in brine shrimps with LD₅₀ values of 5.6 and 9.4 μM, respectively (colchicine was employed as a positive control with an LD₅₀ value of 7.8 μM). Metabolites 66–67 induced moderate cytotoxicity against A549 (IC₅₀ = 20.44 and 21.54 μM, respectively) and HCT-116 cell lines (IC₅₀ = 14.88 and 18.54 μM, respectively).

In addition, three 1,4-diazepane derivatives, terretriones A, C, and D (68–70) (Figure 11), obtained from marine sponge-derived P. vinaceum [45] and marine tunicate-derived Penicillium sp. CYE-87 [46], moderately inhibited the migratory activity of MDA-MB-231 cells with IC₅₀ values of 17.7, 17.6, and 16.5 μM, respectively (Z-4-ethylthio-phenylmethylene hydantoin was used as a positive control with an IC₅₀ value of 43.4 μM). These findings indicate that terretriones might be potential anti-metastatic breast cancer candidates.

Six tetramic acid derivatives, penicillenols A1, A2, B1, B2, D1, and D2 (71–76) (Figure 12), were isolated from a marine sediment-derived fungus P. citrinum. Penicillenol B2 (74) exhibited the strongest cytotoxic activity against A-375 human malignant melanoma cell line (IC₅₀ = 0.97 μg/mL), whereas the IC₅₀ values of compounds 71–73 were 3.2, 13.8, and 2.8 μg/mL, respectively [47,48]. Penicillenols D1 and D2 (75–76) showed moderate cytotoxicity against A549 cells with IC₅₀ values of 17.2 and 12.1 μg/mL, respectively. However, penicillenols A1 and B1 (71, 73) showed significant cytotoxicity in HL-60 cells (IC₅₀ = 0.76 and 3.2 μM, respectively) [49]. A novel tetramic acid derivative, penicitrinine A (77), which contains a citrinin-like group, was isolated [50]. The combination of two cytotoxic fragments in this metabolite might contribute to its extensive antiproliferative activity in diverse tumor cell lines, particularly A-375 cells. Penicitrinine A (77) not only induced A-375 cell apoptosis by upregulating Bax and downregulating Bcl-2, but also inhibited A-375 cell metastatic activity by suppressing matrix metalloproteinase 9 (MMP-9) and promoting the expression of its specific inhibitor, tissue inhibitor of metalloproteinases-1 (TIMP-1). These findings suggest that penicitrinine A (77) is a potential lead compound.

Quinolinone and quinazolinone alkaloids have unique pharmacophores that allow their binding to multiple sites with high affinity; moreover, they possess various biological properties [51]. Some cytotoxic quinolinone (78–82) and quinazolinone alkaloids (83–85) (Figure 13) were isolated from marine-derived members of the Penicillium genus, such as P. janczewskii, Penicillium sp. ghq208, P. oxalicum 0312F1, P. chrysogenum EN-118, and P. commune SD-118 [23]. 2-quinolinone metabolites (78–79) exhibited IR% values of 50–60% at 10 μg/mL. Interestingly, compound 80, which has an additional prenyl chain, showed significant cytotoxicity against MDA-MB-231 and HT-29 (human colon carcinoma) cell lines with IR% values of 92–96% at 10 μg/mL [52]. In addition, a 4-quinolinone derivative (82) exhibited significant cytotoxicity against the human lung cancer cell line 95-D (IC₅₀ = 0.57 μg/mL). Both compounds 81 and 82 exhibited similar cytotoxicity (IC₅₀ = 11.3 and 13.2 μM, respectively) against HepG2 cells [53,54]. However quinazolinone derivatives (83–85) showed only moderate cytotoxicity (compound 83, IC₅₀ = 20 μg/mL in SW1990 cell line; compound 84, IC₅₀ = 8 μg/mL in DU145, A549, and Hela cell lines; and compound 85, IR% = 35–40 at 200 μg/mL in SGC-7901 and BEL-7404 cell lines) [55,56].

In an ongoing study that aims to produce new active metabolites from P. paneum SD-44 (a deep sea sediment-derived fungus) using culture variations, three amidine anthranilic acid analogues (86–88) and one triazole anthranilic acid derivative, penipanoid A (89) (Figure 14), were obtained after culture in malt and rice medium, respectively. Compounds 86 and 87 strongly inhibited RKO human colon cancer cell viability (IC₅₀ = 8.4 and 9.7 μM, respectively). In addition, compound 88 was cytotoxic to Hela cells (IC₅₀ = 6.6 μM) [57], whereas compound 89 with a triazole group only weakly inhibited SMMC-7721 cell viability (human hepatocarcinoma) (IC₅₀ = 54.2 μM) while fluorouracil was used as a positive control for three cell lines with IC₅₀ values of 25.0, 14.5, and 13.0 μM, respectively [58].

An azaphilone analogue, bis-sclerotioramin (90) (Figure 15), obtained from a marine mangrove endophytic fungus, Penicillium 303#, was found to possess moderate cytotoxicity against MDA-MB-435 cell line (IC₅₀ = 7.13 μg/mL), while epirubicin was used as a positive control with an IC₅₀ value of 0.325 μg/mL [59]. Another novel alkaloid, the sorbicilin-derived sorbicillactone A (91), was first isolated from a Mediterranean sponge-derived fungus, P. chrysogenum. Sorbicillactone A (91) exhibited a selective antileukemic activity in L5178Y cells (murine leukemic lymphoblast) with an IC₅₀ of 2.2 μg/mL, as well as in other tumor cell lines (IC₅₀ > 10 μg/mL). The biosynthesis of sorbicillactone A (91) was investigated using ¹³C-labeled precursor feeding experiments, which showed that the its skeleton was derived from acetate, alanine, and methionine [60]. Furthermore, a new strategy for the large-scale biotechnological production of sorbicilin-derived alkaloids was developed for preclinical screening and a structure-activity relationship (SAR) study [61]. In addition, a 4-oxoquinoline derivative, brocaeloid B (92), isolated from the mangrove endophytic fungus P. brocae, showed mild lethality against brine shrimps with an LD₅₀ of 36.7 μM, while colchicine was used as a positive control with an LD₅₀ value of 87.6 μM [62]. Li et al. cultured the marine mangrove fungus P. varibile with the DNA methyltransferase inhibitor 5-azacytidine to identify novel responsive molecules by gene silencing. A highly modified fatty acid amide, varitatin A (93), exhibited significant cytotoxicity against HCT-116 cells (IC₅₀ = 2.8 μM, while doxorubicin was used as a positive control with an IC₅₀ value of 0.2 μM) and potently inhibited protein tyrosine kinases, platelet-derived growth factor receptor-beta (PDGFR-β), and ErbB4 with IR% values of 50 and 40%, respectively, at a concentration of 1 μM [63]. In addition, a new pyridinyl-α-pyrone alkaloid, 18-hydroxydecaturin B (94), was isolated from an endophytic fungus, P. oxalicum EN-201, derived from the marine mangrove Rhizophora stylosa. Compound 94 showed significant lethality in brine shrimps (LD₅₀ = 2.3 μM, while colchicine was used as a positive control with an LD₅₀ value of 7.8 μM) [42]. A previous study showed that the metabolites of decaturin, a potent insecticide, were cytotoxic [64]. The isocyanide alkaloid, xantocillin X (95), which is a known antiviral and antibiotic agent [65], was first isolated from P. notatum in 1950 [66]. Recently, compound 95 was isolated from the deep sea sediment-derived fungus P. commune SD-118, and showed moderate cytotoxicity in six cancer cell lines (MCF-7, HepG2, NCI-H460, Hela, DU145, and MDA-MB-231) with IC₅₀ values of 12, 7, 10, 10, 8, and 8 μg/mL, respectively, while fluorouracil was used as a positive control with IC₅₀ values of 4, 14, 1, 14, 0.4, and 8 μg/mL, respectively [23]. A later pharmacological study on human HepG2 cells showed that compound 95 induced apoptosis and autophagy by inhibiting the MEK/EPK signaling pathway and activating the class III PI3K/Beclin 1 signaling pathway [67].

3. Terpenes, Meroterpenes, and Steroids

The genus Penicillium is a well-known producer of eremophilane-type sesquiterpenes with phytotoxic, mycotoxic, and phytohormonic activities [68,69]. Chemical investigation of an Antarctic deep sea-derived fungus, Penicillium sp. PR19 N-1, yielded three new cytotoxic eremophilane-type sesquiterpenes (96–98) (Figure 16), which were moderately cytotoxic to HL-60 (IC₅₀ = 45.8, 28.3, and 11.8 μM, respectively) and A549 (IC₅₀ = 82.8, 5.2, and 12.2 μM, respectively) cancer cell lines [70,71]. Three other eremophilane-type sesquiterpenes (99–101) were isolated from a sea mud-derived fungus, Penicillium sp. BL 27-2. Of these, compound 99 was the most cytotoxic to P388, A549, HL-60, and BEL-7402 cell lines (IC₅₀ = 0.073, 0.096, 0.065, and 4.59 μM, respectively), whereas compounds 100 and 101 had IC₅₀ values in the range of 3–12 μM [72]. These results suggest that the epoxide ring is essential for the cytotoxicity of eremophilane-type sesquiterpenes and that the presence of an acetyl group enhances the cytotoxicity. A new acorane sesquiterpene, adametacorenol B (102), isolated from a marine sponge-derived fungus, P. adametzioides AS-53, displayed selective cytotoxicity against NCI-H446 cell lines (IC₅₀ = 5 μM), compared to its cytotoxicity against the other 13 tumor cell lines tested (A549, DU145, HeLa, HepG2, Huh-7 (human hepatocarcinoma), L02 (human hepatocarcinoma), LM3 (murine breast cancer), MA (mouse Leydig tumor), MCF-7, SGC-7901, SW1990, SW480, and U251) (IC₅₀ > 10 μM) [17].

The deep sea sediment-derived fungus Penicillium sp. was reported to be a good source of cytotoxic diterpenes. Six tetracyclic diterpenes, conidiogenones B–G (103–108) (Figure 17), exhibited cytotoxicity against HL-60, A549, BEL-7402, and MOLT-4 cell lines. Conidiogenone C (104) was potently cytotoxic against HL-60 and BEL-7402 cells with IC₅₀ values of 0.038 and 0.97 μM, respectively; however, it was not cytotoxic against A549 and MOLT-4 cell lines at 50 μM. Other conidiogenones (103, 105–108) had moderate cytotoxicity with IC₅₀ values ranging from 1 to 50 μM [22]. The spiroditerpenes, breviones I and A (109–110) were also obtained from this fungus and showed cytotoxicity comparable to that of cisplatin (the positive control) against MCF-7 cells (IC₅₀ = 7.44 and 28.4 μM, respectively, versus 8.04 μM for cisplatin) [73].

Although several marine-derived steroids have been isolated, few have been found to be bioactive. A cytotoxic polyoxygenated steroid, penicisteroide A (111) (Figure 18), was isolated from a marine alga-derived fungus, P. chrysogenum QEN-24S. Penicisteroide A (111) displayed moderate cytotoxicity against Hela, SW1990, and NCI-H460 cell lines with IC₅₀ values of 15, 31, and 40 μg/mL, respectively [74]. Three other polyoxygenated steroids (112–114) and two epidioxygenated steroids (115–116) were isolated from the marine moss-derived fungus Penicillium sp. These steroids moderately inhibited HepG2 cell line growth (IC₅₀ values = 10.4, 15.6, 20.7, 16.8, and 21.3 μg/mL, respectively) [75]. In addition, an epidioxygenated steroid (117), produced by a sea squirt-derived fungus, P. stoloniferum QY2-10, was cytotoxic to P388 cells with an IC₅₀ of 4.07 μM [76]. Moreover, a marine Penicillium sp. fungus collected from the inner tissues of an unidentified sponge is reportedly the source of two epimeric steroids (118–119) and two cytotoxic steroids of a new class, dankasterone A (120) and B (121). Dankasterone A (120) was more effective than the positive control, adriamycin (IC₅₀ = 0.98 μM) against HL-60, Hela, and K562 cancer cell lines with IC₅₀ values of 0.78, 4.11, and 7.57 μM, respectively. Compounds 118–119 and 121 also significantly inhibited K562 cell growth (IC₅₀ = 4.38, 5.54, and 7.89 μM, respectively) [77].

Meroterpenes are widely distributed in the marine environment, particularly in brown algae and microorganisms. Terpene-quinone and -hydroquinone are the major bioactive members because they produce reactive oxygen species (ROS) [78]. Three quinone- and hydroquinone-type meroterpenes (122–124) (Figure 19) were isolated from a marine-derived Penicillium sp. Compounds 122 and 123 exhibited extensive cytotoxicity against five cancer cell lines (A549, SKOV-3 (human ovary adenocarcinoma), SKMEL-2 (human skin cancer), XF498 (human CNS cancer), and HCT15 (human colon cancer)) with IC₅₀ values in the range of 3–10 μg/mL, whereas compound 124 had IC₅₀ values ranging from 20 to 40 μg/mL (doxorubicin was used as a positive control with IC₅₀ values of 0.02~0.8 μg/mL). These results suggest that the quinone form tends to be less cytotoxic [79]. Penicillone A (125), isolated from marine-derived Penicillium sp. F11., contains a carboxylic acid group instead of the isoprenyl tail, which resulted in mild cytotoxicity against fibrosarcoma (HT1080) and human nasopharyngeal carcinoma (Cne2) cell lines (IC₅₀ = 45.8 and 46.2 μM, respectively) [80].

Two sesquiterpene α-pyrones, phenylpyropenes E and F (126–127) (Figure 20), were isolated from the marine-derived fungus P. concentricum ZLQ-69 and displayed moderate and selective cytotoxicity against MGC-803 cells (human gastric cancer) with IC₅₀ values of 19.1 and 13.6 μM, respectively (doxorubicin was used as a positive control with an IC₅₀ value of 0.37 μM) [81]. Furthermore, the marine sediment-derived fungus Penicillium sp. F446 yielded two new sesquiterpene γ-pyrone-type meroterpenes, penicillipyrone A and B (128–129), which were moderately cytotoxic against A549 cells (IC₅₀ = 15 and 17 μM, respectively, while doxorubicin was used as a positive control with an IC₅₀ value of 1.2 μM) [82]. Two polycyclic α-pyrone-type meroterpenes (130–131), isolated from the marine mangrove endophytic fungus Penicillium 303#, exhibited IC₅₀ values of 20–30 μg/mL in four cancer cell lines (MDA-MB-435, HepG2, HCT-116, and A549), while epirubicin was used as a positive control with IC₅₀ values of 0.2~0.6 μg/mL [59]. Fumagillin was first isolated from Aspergillus fumigatus in 1949, and has been used as an antimicrobial [83]. Recently, ligerin (132), a natural chlorinated merosesquiterpene related to fumagillin, was obtained from a marine-derived Penicillium sp., and showed selective in vitro antiproliferative activity against osteosarcoma cell lines (IC₅₀ = 117 nM against POS1 cells, which is 20 times greater than the IC₅₀ in other cancer cell lines), while doxorubicin was used as a positive control with IC₅₀ values of 0.04~2 μM [84]. Ligerin analogues were semi-synthesized in an SAR study, which showed that chlorohydrin and C6 substituents were crucial for cytotoxic activities. Furthermore, ligerin (132) exhibited stronger cytotoxicity against human osteosarcoma SaOS2 and MG63 cancer cell lines. However, its cytotoxicity was less than that of TNP470 (a positive control and fumagillin analogue) [85].

4. Polyketides

Chromone derivatives are abundantly present in nature and are considered potential immunomodulatory, anticancer, and anti-inflammatory agents. Chromone scaffolds were reported to possess outstanding pharmacological properties [86]. A Chinese research group recently isolated four dihydrothiophene-condensed chromones, oxalicumones D, E (133–134) and A, B (135–136) (Figure 21) from a marine gorgonian-derived fungus, P. oxalicum SCSGAF 0023. Similar to synthetic dihydrothiophene-condensed chromones (137–144), these four natural chromones (133–136) displayed significant cytotoxicity against eight carcinoma cell lines (human lung adenocarcinoma (H1975), human lymphoma (U937), K562, BGC823, MOLT-4. MCF-7, HL-60, and Huh-7) (IC₅₀ < 10 μM). Of these, oxalicumone A (135) was the most cytotoxic against MOLT-4 cell line (IC₅₀ = 0.30 μM). An SAR study showed that the 2,3-dihydrothiophene unit was crucial for activity and that the presence of 1-OH and absolute configuration at C-6 contributed to cytotoxicity [87,88]. Subsequent pharmacological studies showed that oxalicumone A (135) inhibited leukemia cell growth and induced apoptosis, in part, via the induction of the endoplasmic reticulum stress pathway by upregulating calnexin and Bax and activating unfolded protein response [89]. Another study found that oxalicumone A (135) could induce oxidative stress injury in the mitochondria, and thus promote human renal epithelial cell death [90]. Chromosulfine (145), a novel cyclopentachromone sulfide which is structurally similar to dihydrothiophene-condensed chromones, was isolated from a neomycin-resistant mutant of the marine-derived fungus P. purpurogenum G59, and showed selective cytotoxicity against HL-60 cancer cell line (IC₅₀ = 16.7 μM) [91]. Secalonic acid F (146), a chiral dimeric tetrahydroxanthone, was first isolated from Aspergillus sp. before discovering that the deep sea sediment-derived fungus Penicillium sp. F11 is a good source of this compound. Compound 146 induced HL-60 cell apoptosis by modulating the Rho GDP dissociation inhibitor 2 pathway [92]. Recent studies showed that secalonic acid F (146) could induce apoptosis by activating caspase 3 and 9 through the mitochondrial pathway in hepatocellular carcinoma, wherein it was found to be more effective than 5-fluorouracil [93]. Furthermore, a flavone, namely penimethavone A (147), obtained from a gorgonian-derived fungus, P. chrysogenum, exhibited selective cytotoxicity against Hela and rhabdomyosarcoma cell lines (IC₅₀ = 8.41 and 8.18 μM, respectively) while adriamycin was used as a positive control with IC₅₀ values of 0.43 and 0.09 μM, respectively [94].

Coumarin derivatives of the chromone isomers (148–150) (Figure 22) were also isolated from the deep sea sediment-derived fungus (P. chrysogenum SCSIO 41001), a marine sponge-derived fungus Penicillium sp., and a mangrove endophytic fungus (Penicillium sp. ZH16), respectively. The dimeric isocoumarin, bipenicillisorin (148), displayed significant cytotoxicity against K562, A549, and Huh-7 cell lines (IC₅₀ = 6.78, 6.94, and 2.59 μM, respectively), while taxol was used as a positive control with IC₅₀ values of 3.44, 2.61, and 14.70 nM, respectively [95]. The dihydroisocoumarin monocerin (149) exhibited significant cytotoxicity against L5178Y cells (a murine lymphoma cell line) with an IC₅₀ value of 8.4 μM (kahalalide F was used as a positive control with an IC₅₀ value of 4.3 μM) [96]. Moreover, furanocoumarin (150) showed moderate cytotoxicity against human nasopharyngeal carcinoma (KB and KBv200) cell lines (IC₅₀ = 5 and 10 μg/mL, respectively) [97].

Citrinin (151) (Figure 23), a typical azaphilone polyketide mycotoxin, was first found in P. citrinum in 1931 [98]. Compound 151 is strongly nephrotoxic because of its inhibition of respiration complex III [99]. The biosynthesis pathway of compound 151 was further investigated [100]. Interestingly, the marine sponge-derived fungus Penicillium sp. FF001 was found to be a good source of unique and potent citrinin derivatives [101]. Two new citrinin derivatives, penicitrinols L and M (152–153), isolated from the marine sediment-derived fungus P. citrinum, showed moderate cytotoxicity against a human Caucasian colon adenocarcinoma cell line (SW-620) (IC₅₀ = 25.6 and 20.9 μM, respectively) [48]. One penicitrinol analogue, berkelic acid (154), with a novel spiroketal structure, isolated from an acid mine lake fungal extremophile Penicillium sp., showed selective and extraordinary cytotoxicity against a human ovarian carcinoma cell line (OVCAR-3) at nanomolar concentrations (GI₅₀ = 91 nm) [102]. The total synthesis of (–)-berkelic acid (154) was previously described [103]. An alga-derived fungus, P. thomii, yielded a new citrinin analogue, sargassopenilline C (155), which possessed a unique 6,6-spiroketal skeleton and inhibited the transcription of oncogenic nuclear factor, AP-1 (IC₅₀ = 15 μM) [104]. Two phenalenone-skeleton citrinin analogues, sculezonones A and B (156–157), isolated from a marine sponge-derived fungus Penicillium sp., inhibited both DNA polymerases (α and β) [105]. Dicitrinone B (158), a marine sediment-derived fungal metabolite (P. citrinum) containing a rare carbon-bridge citrinin dimer, induced A-375 cell apoptosis by generating ROS via a caspase-related pathway [106]. In another study, two novel skeletal metabolites (159–160) possibly biogenetically derived from citrinin were found. Perinadine A (159), a scalusamide A-type pyrrolidine isolated from a fish gastrointestinal fungus, P. citrinum, exhibited mild cytotoxicity against a murine leukemia L1210 cell line (IC₅₀ = 20 μg/mL) [107]. However, herqueiazole (160), obtained from a marine sediment-derived fungus, Penicillium sp. F011, possessed a novel pyrrole-containing phenalenone moiety and demonstrated weak cytotoxicity against A549 cells (IC₅₀ = 67.3 μM), while doxorubicin was used as a positive control with an IC₅₀ value of 3.3 μM [108].

Other fungal azaphilone polyketides include comazaphilones D–F (161–163) (Figure 24), pinophilins A, B, and Sch 725680 (164–166), which were isolated from a marine sediment-derived fungus, P. commune QSD-17 (comazaphilones D–F), and a marine seaweed-derived P. pinophilum Hedgcok (pinophilins A-B and Sch 725680). Comazaphilones D–F (161–163) showed selective but weak cytotoxicity against SW1990 cell line (IC₅₀ = 51, 26, and 53 μM, respectively), while fluoruoracil was used as a positive control with an IC₅₀ value of 120 μM) [109]. Azaphilone derivatives (164–166) were suggested to suppress cancer cell proliferation by inhibiting DNA replication via the inhibition of mammalian DNA polymerases A, B, and Y [110].

Penicillium sp. strain OUPS-79, which is derived from the marine alga Enteromorpha intestinalis, yielded various cytotoxic polyketides, including penostatins A–C, E–I (167–169, 171–175) (Figure 25) [111,112]. They were found to be significantly cytotoxic to P388 lymphocytic leukemia cells (ED₅₀ = 0.8, 1.2, 1.0, 0.9, 1.4, 0.5, 0.8, and 1.2 μg/mL, respectively). However, penostatin D (170) exhibited moderate cytotoxicity (ED₅₀ = 11.0 μg/mL), which may be attributed to the absence of the cyclic conjugated enone system. Moreover, penostatin C (169) exhibited significant cytotoxicity in seven of the 36 cell lines tested with ED₅₀ values ranging from 1 to 2 μg/mL. Recent studies have shown that penostatins A–C (167–169) may be tyrosine phosphatase 1B (PTP1B) inhibitors, which can be used to treat type II diabetes and other associated metabolic diseases (IC₅₀ = 15.87, 33.65, and 0.37 μM, respectively), while sodium orthovanadate was used as a positive control with an IC₅₀ value of 0.65 μM [113]. The total synthesis of penostatins A, B, and F (167, 168, 172) was previously reported [114,115].

Fungal phenolic polyketides have diverse biological activities and unique structures [116]. A weak DNA topoisomerase Ι inhibitor, compound (176) (Figure 26), was obtained from the marine sediment-derived P. oxalicum HSY05 [117], whereas a racemic mixture (177–178) was obtained from the co-cultivation of marine mangrove-derived Penicillium sp. WC-29-5 and Streptomyces fradiae 007. Compounds 177–178 displayed significant cytotoxicity against H1975 cell lines (IC₅₀ = 3.97 and 5.73 μM, respectively). Moreover, compound 178 exhibited cytotoxicity against HL-60 cells (IC₅₀ = 3.73 μM) [118]. Using a bioinformatics tool, Marine Halogenated Compound Analysis (MeHaloCoA), three halogenated bioactive metabolites, (+)-5-chlorogriseofulvin (179) as well as griseophenones I and G (180–181), were isolated from a marine-derived P. canescens. They inhibited the growth of KB cells at a concentration of 0.6 μM (IR% = 49, 58, and 47%, respectively) [119]. Furthermore, one benzophenone, iso-monodictyphenone (182), and two diphenyl ether derivatives, penikellides A and B (183–184), were isolated from a mangrove endogenous fungus, Penicillium sp. MA-37. These three metabolites exhibited moderate brine shrimp lethality (LD₅₀ = 25.3, 14.2, and 39.2 μM, respectively), while colchicine was used as a positive control with an LD₅₀ value of 1.22 μM [120]. Penicillide (185), a multifunctional metabolite produced by a marine sediment-derived Penicillium sp. strain, was shown to be an acyl-CoA cholesterol acyltransferase (ACAT) [121], nonpeptide calpain inhibitor [122], and oxytocin antagonist [123]. Furthermore, compound 185 was found to exhibit cytotoxic, antibiotic, and plant growth inhibitory properties. Recently, two marine fungi, P. pinophilum (derived from a gorgonian) and Penicillium sp. ZLN29 (derived from a sediment), were found to produce penicillide (185) and penicillide derivatives (186–187) that exhibited potent cytotoxicity against HepG2 cell line (IC₅₀ = 9.7 and 9.9 μM for 185–186, respectively); moreover, compound 187 showed additional cytotoxicity against Hela cell line (IC₅₀ = 6.1 μM) [124,125]. Two anthraquinone derivatives, nidurufin (188) and averantin (189), isolated from a marine sediment-derived fungus, P. flavidorsum SHK1-27, were cytotoxic against K562 cell line (IC₅₀ = 12.6 and 27.7 μM, respectively), while adriamycin was used as a positive control with an IC₅₀ value of 1.5 μM. Nidurufin (188) was suggested to induce cell cycle arrest at the G2/M transition in a time-dependent manner [126]. The total synthesis of (±)-nidurufin (188), an aflatoxin precursor, was previously described [127].

Members of the sorbicillinoid family are hexaketide metabolites isolated from various fungi. In 2005, Zhu et al. found two sorbicillin analogues (benzoquinone (190–191)), two bisvertinolones (192–193), and three bridged bicyclic bisorbicillinoids (194–196) (Figure 27) in a marine sediment-derived fungus, P. terrestre. Dihydrobisvertinolone (192) and trichodimerol (196) demonstrated the strongest cytotoxic effects (IC₅₀ = 0.52 μM in A549, IC₅₀ = 0.33 μM in P388, respectively), while etoposide was used as a positive control with IC₅₀ values of 1.4 and 0.064 μM, respectively [128,129]. The preliminary SAR showed that an intact sorbyl side chain played a decisive role [130]. Further investigation of this strain yielded two additional chlorinated sorbicillinoids (197–198). Interestingly, the configuration at C-19 was found to largely determine the cytotoxicity, wherein chloctanspirone A (197) (R configuration) was 4-fold more active than chloctanspirone B (198) (S configuration) in HL-60 and A549 cancer cell lines [131].

Macrolides represent a well-known class of antibiotics, and curvularin (200) (Figure 28) is a heat shock protein (HSP90) inhibitor [132]. (10E, 15S)-10,11-Dehydrocurvularin (199) was isolated from marine sponge-derived Penicillium sp. DRF2 and Curvularia sp. It exhibited significant cytotoxicity with mean IC₅₀ values ranging from 0.28 to 6 μM in 14 different solid tumors (36 tumor cell lines) [133,134]. Penicillium fungi are also a good source of tanzawaic acid polyketides, which exhibit antibiotic resistance [135], as well as anti-inflammatory [136] and cytotoxic activities. Tanzawaic acid P (201), isolated from a marine-derived fungus, Penicillium sp. CF07370, was selectively toxic to U937 cancer cells via the activation of the mitochondrial apoptotic pathway [137]. Computational ligand-protein-DNA binding analysis revealed that tanzawaic acid D (202), isolated from P. steckii, effectively and selectively bound to the transcription factor, forkhead box O1 (FOXO1), which can regulate epidermal growth factor receptor (EFGR) signaling, suppress cell cycle progression, and stabilize the conformation of FOXO1-DNA [138].

5. Lipopeptides

Fellutamides A and B (210–211) (Figure 29) were the first cytotoxic lipopeptides isolated from fish-derived P. fellutanum [139]. Compounds 210 and 211 exhibited significant cytotoxicity against murine leukemia P388 (IC₅₀ = 0.2 and 0.1 μg/mL, respectively), L1210 (IC₅₀ = 0.8 and 0.7 μg/mL, respectively), and KB cells (IC₅₀ = 0.5 and 0.7 μg/mL, respectively). Recently, seven new similar lipopeptides, penicimutalides A–G (203–209) and fellutamides B and C (211–212) were isolated from a diethyl sulfate-induced mutant of the marine fungus, P. purpurogenum G59 [140]. They were cytotoxic against five human cancer cell lines (K562, HL-60, Hela, BGC-823, and MCF-7). Compounds 203–209 and 212 exhibited weak cytotoxicity (IR% = 10–50% at 100 μg/mL, while 5-fluoruoracil as a positive control with the IR% of 37~50% at 100 μg/mL). However, fellutamide B (211) with a C-terminal aldehyde group was more potent with IC₅₀ values that ranged from 20 to 80 μg/mL, which indicated that the C-terminal aldehyde group improves the cytotoxicity.

6. Miscellaneous Compounds

Polyphenol derivatives are the most abundant fungal secondary metabolites. Unsurprisingly, marine Penicillium sp. is a good source of polyphenol derivatives. Two trimeric peniphenylanes A, B (213–214) and three dimeric peniphenylanes D, F, G (215–217) (Figure 30) were isolated from the deep sea sediment-derived fungus, P. fellutanum HDN14-323. Peniphenylane D (215) displayed more potent and extensive cytotoxicity with IC₅₀ values in the range of 9–30 μM in three cancer cell lines (Hela, HL-60, and HCT-116), while doxorubicin was used as a positive control with the IC₅₀ values of 0.2, 0.6, and 0.2 μM, respectively [141]. The marine sediment-derived fungus, P. terrestre was found to produce several gentisyl alcohol derivatives, including trimeric terrestrol A (225) and dimeric terrestrols B–H (218–224), which were found to be cytotoxic against HL-60, MOLT-4, BEL-7402, and A549 cancer cell lines with IC₅₀ values in the range of 5–65 μM [142]. Interestingly, the marine mangrove endogenous P. expansum 091006 yielded four novel cytotoxic phenolic bisabolane sesquiterpenoids (expansols A–C; E (226–229)) with IC₅₀ values of 15.7, 5.4, 18.2, and 20.8 μM, respectively, in HL-60 cells. In addition, expansol B (227) showed significant cytotoxicity against A549 cells (IC₅₀ = 1.9 μM), while etoposide was used as a positive control with IC₅₀ values of 0.042 and 0.63 μM for two cell lines, respectively [143,144].

Patulin (230) (Figure 31) is a mycotoxin commonly found in rotting fruits, and is used as a potassium-uptake inhibitor or inducer of ion flux across cell membranes. An alga-derived Penicillium sp. was found to produce patulin (230) along with (+)-epiepoxydon (231), both of which exhibited extraordinary cytotoxic effects in P388 cells (IC₅₀ = 0.06 and 0.2 μg/mL, respectively). Furthermore, (+)-epiepoxydon (231) had significant cytotoxicity against seven other cancer cell lines with IC₅₀ values in the range of 0.3–1.5 μg/mL [111]. The isobenzofurannone derivative (232) isolated from a mangrove endophytic Penicillium sp. displayed moderate cytotoxicity against KB and KBV200 cells (IC₅₀ = 6 and 10 μg/mL, respectively) [145], whereas the penicillic acid (233), isolated from marine-derived Penicillium strain, exhibited moderate cytotoxicity against POS1, AT6-1(murine prostatic carcinoma), and L929 (murine fibroblasts) cell lines (IC₅₀ = 7.8, 29.4, and 12.9 μM, respectively) while doxorubicin was used as a positive control with IC₅₀ values of 0.04~2 μM [84].

7. Conclusions

The rapid development of marine biotechnology and ever increasing needs of industrial applications resulted in the emergence of marine natural products as alternative drug sources in the early 1990s [146]. Marine-associated microorganisms are sensitive to culture conditions; therefore, strains living in extremely competitive environments tend to provide high potency leads (compound 154 in this review inhibited OVCAR-3 cell line at nanomolar concentrations). Furthermore, the activation of silent gene clusters may activate new biosynthetic pathways that produce compounds with novel structure, which provide equally valid leads (compounds 44 and 45, which have unique skeletons, had cytotoxic effects in the five cancer cell lines with IC₅₀ values of ~10 μM). Interestingly, the halogenation of compound 31, which was completely inactive, produces compound 32, which exhibited a much greater potency (compound 32 had significant cytotoxicity in 22Rv1 cells at nanomolar levels) [147].

The genus Penicillium has been explored for antitumor leads in recent years [148]. However, the marine ecological diversity of this genus offers more opportunities for drug discovery. This review includes more than 200 cytotoxic or antitumor compounds isolated from marine Penicillium fungus and chemically synthesized analogues. Of these, the major metabolites are alkaloids, particularly diketopiperazine alkaloids and indole alkaloids (Appendix A,

Table A1. Secondary metabolites from Penicillium strain of marine origin. Items are listed according to the metabolite numbers used in this review.

Metabolites	Producing Stain	Environment Source	Type	Cell Lines/Brine Shrimp	IC50, LD50, or IR (%)	Target	Reference
Penochalasin A (1)	Penicillium sp.	Marine alga	Indole alkaloid	P388	0.4 μg/mL		[8]
Penochalasin B (2)	Penicillium sp.	Marine alga	Indole alkaloid	P388	0.3 μg/mL		[8]
Penochalasin C (3)	Penicillium sp.	Marine alga	Indole alkaloid	P388	0.5 μg/mL		[8]
Penochalasin D (4)	Penicillium sp.	Marine alga	Indole alkaloid	P388	3.2 μg/mL		[7]
Penochalasin E (5)	Penicillium sp.	Marine alga	Indole alkaloid	P388	2.1 μg/mL		[7]
Penochalasin F (6)	Penicillium sp.	Marine alga	Indole alkaloid	P388	1.8 μg/mL		[7]
Penochalasin G (7)	Penicillium sp.	Marine alga	Indole alkaloid	P388	1.9 μg/mL		[7]
Penochalasin H (8)	Penicillium sp.	Marine alga	Indole alkaloid	P388	2.8 μg/mL		[7]
Penochalasin I (9)	P. chrysogenum V11	Mangrove	Indole alkaloid	MDA-MB-435, SGC-7901, A549	(7.55, 7.32, 16.13) μM		[6]
Penochalasin J (10)	P. chrysogenum V11	Mangrove	Indole alkaloid	MDA-MB-435, SGC-7901, A549	(36.68, 37.70, 35.93) μM		[6]
Chaetoglobosin A (11)	P. chrysogenum V11	Mangrove	Indole alkaloid	P388, MDA-MB-435, SGC-7901, A549	0.6 μg/mL (37.56, 7.84, 6.56) μM	Cell-cycle arrest induction, membrane ruffling inhibition, and cell migration	[6,8,9]
Chaetoglobosin C (12)	P. chrysogenum V11	Mangrove	Indole alkaloid	MDA-MB-435, SGC-7901, A549	(19.97, 15.36, 17.82) μM		[6]
Chaetoglobosin E (13)	P. chrysogenum V11	Mangrove	Indole alkaloid	A549	36.63 μM		[6]
Chaetoglobosin F (14)	P. chrysogenum V11	Mangrove	Indole alkaloid	P388, MDA-MB-435, SGC-7901, A549	0.9 μg/mL, (37.77, 26.53, 27.72) μM		[6,8]
Chaetoglobosin G (15)	P. chrysogenum V11	Mangrove	Indole alkaloid	MDA-MB-435, SGC-7901, A549	(38.77, 25.86, 27.63) μM		[6]
Chaetoglobosin O (16)	Penicillium sp.	Marine alga	Indole alkaloid	P388	2.4 μg/mL		[7]
Cytoglobosin C (17)	P. chrysogenum V11	Mangrove	Indole alkaloid	MDA-MB-435, SGC-7901, A549	(12.58, 8.15, 3.35) μM		[6]
18	Penicillium sp. JMF034	Deep sea sediment	Diketopiperazine	P388	3.4 μM		[12]
19	Penicillium sp. JMF034	Deep sea sediment	Diketopiperazine	P388	0.058 μM	HMT G9a (IC50 = 55 μM)	[12]
20	Penicillium sp. JMF034	Deep sea sediment	Diketopiperazine	P388	0.11 μM		[12]
21	Penicillium sp. JMF034	Deep sea sediment	Diketopiperazine	P388	0.11 μM	HMT G9a (IC50 = 58 μM)	[12]
22	Penicillium sp. JMF034	Deep sea sediment	Diketopiperazine	P388	0.056 μM	HMT G9a (IC50 = 2.6 μM)	[12]
Gliotoxin (23)	Penicillium sp. JMF034	Deep sea sediment	Diketopiperazine	P388	0.024 μM	HMT G9a (IC50 = 6.4 μM) Dual inhibitor of farnesyltransferase and geranylgeranyltransferase I	[12,13]
Gliotoxin G (24)	Penicillium sp. JMF034 P. brocae MA-231	Deep sea sediment Mangrove	Diketopiperazine	P388 A2780, A2780 CisR	0.02 μM (0.664, 0.661) μM	HMT G9a (IC50 = 2.1 μM)	[12] [14]
Brozazine A (25)	P. brocae MA-231	Mangrove	Diketopiperazine	Du145, Hela, HepG2, MCF-7, NCI-H460, SGC-7901, SW1990, SW480, U251	(4.2, 6.8, 6.4, 5.5, 4.9, 2.6, 6.0, 2.0, 5.2) μM		[16]
Brozazine B (26)	P. brocae MA-231	Mangrove	Diketopiperazine	Du145, Hela, HepG2, MCF-7, NCI-H460, SGC-7901, SW1990, SW480, U251	(3.6, 5.3, 5.5, 6.1, 4.0, 2.4, 6.4, 1.2, 3.5) μM		[16]
Brozazine E (29)	P. brocae MA-231	Mangrove	Diketopiperazine	Du145, Hela, HepG2, MCF-7, NCI-H460, SGC-7901, SW1990, U251	(11.2, 4.3, 5.6, 9.0, 12.4, 3.3, 2.1, 6.1) μM		[16]
Brozazine F (30)	P. brocae MA-231	Mangrove	Diketopiperazine	Du145, Hela, HepG2, MCF-7, NCI-H460, SGC-7901, SW1990, U251	(1.7, 6.9, 2.9, 3.0, 0.89, 8.0, 5.9, 5.3) μM		[16]
N-methylpretrichodermam ide B/adametizines A (32)	P. adametzioides AS-53 Penicillium sp.	Marine sponge/sediment/alga	Diketopiperazine	Artemia salina	4.8 μM		[17,18,19]
				L5178Y, 22Rv1, PC-3, LNCaP	(2, 0.51, 5.11, 1.76) μM
Roquefortine C (33)	Penicillium sp.	Deep sea sediment	Diketopiperazine			Activate P-glycoprotein and inhibit P450-3A and other haemoproteins	[20,22]
Roquefortine F (34)	Penicillium sp.	Deep sea sediment	Diketopiperazine	A549, HL-60, BEL-7402, MOLT-4	(14.0, 33.6, 13.0, 21.2) μM		[22]
Roquefortine G (35)	Penicillium sp.	Deep sea sediment	Diketopiperazine	A549, HL-60	(42.5, 36.6) μM		[22]
Meleagrin (38)	Penicillium sp. P. commune SD-118	Deep sea sediment	Indole alkaloid	A549, HL-60 HepG2, NCI-H460, Hela, DU145, MDA-MB-231,	(19.9, 7.4) μM (12.0, 22.0, 20.0, 11.0, 5.0) μg/mL	Arrest the cell cycle through G2/M phase Inhibitor of tubulin polymerization	[21,22,23]
Meleagrin B (39)	Penicillium sp.	Deep sea sediment	Indole alkaloid	A549, HL-60, BEL-7402, MOLT-4	(2.7, 6.7, 1.8, 2.9) μM		[21,22]
Meleagrin C (40)	Penicillium sp.	Deep sea sediment	Indole alkaloid	A549, BEL-7402, MOLT-4	(9.9, 10.0, 4.7) μM		[22]
Meleagrin D (41)	Penicillium sp.	Deep sea sediment	Indole alkaloid	A549	32.2 μM		[21]
Meleagrin E (42)	Penicillium sp.	Deep sea sediment	Indole alkaloid	A549	55.9 μM		[21]
Penicimutanin (43)	Mutant P. purpurogenum G59	Marine soil	Diketopiperazine	K562, Hela, MCF-7	IR% (100 μg/mL): 22.6%, 17.9%, 26.5%		[24]
Penicimutanin A (44)	Mutant P. purpurogenum G59	Marine soil	Diketopiperazine	K562, HL-60, Hela, BGC-823, MCF-7	(11.4, 5.4, 9.5, 8.0, 5.4) μM		[24]
Penicimutanin B (45)	Mutant P. purpurogenum G59	Marine soil	Diketopiperazine	K562, HL-60, Hela, BGC-823, MCF-7	(19.9, 12.1, 17.7, 16.6, 8.0) μM		[24]
Fructigenine A (46)	Mutant P. purpurogenum G59	Marine soil	Diketopiperazine	K562, Hela, MCF-7, BGC-823	IR% (100μg/mL): 20.8%, 55.3%, 65.6%, 34.8%		[24,25]
11,11′-dideoxyverticillin A (49)	Penicillium sp.	Marine alga	Diketopiperazine	HCT-116	30 ng/mL	Induce G2/M arrest through p38 MAPK pathway; Epidermal growth factor receptor tyrosine kinase inhibitor	[28,30,31]
11′-deoxyverticillin A (50)	Penicillium sp.	Marine alga	Diketopiperazine	HCT-116	30 ng/mL		[28]
Penitrem A (51)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory) MDA-MB-231 (anti-invasion)	(11.9, 9.8) μM 8.7 μM IR% (15 μM)> 75%	BK channel inhibitor	[34]
Penitrem B (52)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF-7, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory)	(5.5, 13.7) μM 10.3 μM		[34]
Penitrem D (53)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF-7, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory)	(8.3, 29.7) μM 9.2 μM		[34]
Penitrem E (54)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF-7, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory)	(17.5, 25.4) μM 20.3 μM		[34]
Penitrem F (55)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF-7, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory)	(15.0, 13.8) μM 35.0 μM		[34]
6-bromopenitrem B (56)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF-7, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory) MDA-MB-231 (anti-invasion)	(19.3, 18.8) μM 30.3 μM IR%(15 μM) > 40%		[34]
6-bromopenitrem E (57)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF-7, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory)	(16.7, 8.5) μM 9.6 μM	BK channel inhibitor	[34]
Paspaline (58)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF-7, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory)	(12.8, 12.4) μM 7.6 μM		[34]
Emnidole SB (59)	P. commune isolate GS20	Sponge/Sediment	Indole alkaloid	MCF-7, MDA-MB-231 (antiproliferative) MDA-MB-231 (antimigratory)	(10.1, 21.3) μM 19.0 μM		[34,37]
Communesin A (60)	Penicillium sp.	Marine alga/Sediment	Indole alkaloid	P388	3.5 μg/mL		[38,40]
Communesin B (61)	Penicillium sp.	Marine alga/Sponge/Sediment	Indole alkaloid	P388, U-937, THP-1, NAMALWA, MOLT-3, SUP-B15	(0.45, 10.4, 11.4, 9.9, 8.1, 7.2) μg/mL		[38,39,40]
Communesin C (62)	Penicillium sp.	Marine sponge	Indole alkaloid	U-937, THP-1, NAMALWA, MOLT-3, SUP-B15	(11.3, 13.1, 8.2, 8.6, 10.8) μg/mL		[39]
Communesin D (63)	Penicillium sp.	Marine sponge	Indole alkaloid	U-937, THP-1, NAMALWA, MOLT-3, SUP-B15	(13.1, 16.2, 14.6, 9.9, 9.0) μg/mL		[39]
Penioxamide (64)	P. oxalicum EN-201	Mangrove	Indole alkaloid	A. salina	5.6 μM		[42]
65	P. brefeldianum SD-273	Marine sediment	Indole alkaloid	A. salina	9.4 μM		[43]
Penipaline B (66)	P. paneum SD-44	Marine sediment	Indole alkaloid	A549, HCT-116	(20.44, 14.88) μM		[44]
Penipaline C (67)	P. paneum SD-44	Marine sediment	Indole alkaloid	A549, HCT-116	(21.54, 18.54) μM		[44]
Terretrione A (68)	P. vinaceum	Marine sponge	1,4-diazepane alkaloid	MDA-MB-231	17.7 μM		[45]
Terretrione C (69)	Penicillium sp.CYE-87	Marine tunicate	1,4-diazepane alkaloid	MDA-MB-231	17.6 μM		[46]
Terretrione D (70)	Penicillium sp.CYE-87	Marine tunicate	1,4-diazepane alkaloid	MDA-MB-231	16.5 μM		[46]
Penicillenol A1 (71)	Penicillium sp. GQ-7/P. citrinum	Mangrove/Marine sediment	Pyrrolidinone alkaloid	A-375, HL-60, A549, BEL-7402, P388	3.2 μg/mL (0.76, 23.8, 13.03, 8.85) μM		[47,49]
Penicillenol A2 (72)	Penicillium sp. GQ-7/P. citrinum	Mangrove/Marine sediment	Pyrrolidinone alkaloid	A-375 HL-60	13.8 μg/mL 16.26 μM		[47,49]
Penicillenol B1 (73)	Penicillium sp. GQ-7/P. citrinum	Mangrove/Marine sediment	Pyrrolidinone alkaloid	A-375 HL-60	2.8 μg/mL 3.2 μM		[47,49]
Penicillenol B2 (74)	Penicillium sp. GQ-7/P. citrinum	Mangrove/Marine sediment	Pyrrolidinone alkaloid	A-375 HL-60	0.97 μg/mL 7.65 μM		[47,49]
Penicillenol D1 (75)	P. citrinum	Marine sediment	Pyrrolidinone alkaloid	A549, HL-60	(17.2, 18.5) μg/mL		[48]
Penicillenol D2 (76)	P. citrinum	Marine sediment	Pyrrolidinone alkaloid	A549, HL-60	(12.1, 14.5) μg/mL		[48]
Penitrinine A (77)	P. citrinum	Marine sediment	Pyrrolidinone alkaloid	A-375, SPC-A1, HGC-27	(20.12, 28.67, 29.49) μM	Upregulate Bax, downregulate Bcl-2, suppress MMP-9 and TIMP-1	[50]
78	P. janczewskii	Sea water	Quinolinone	MDA-MB-231, DU-145, SKOV-3, HT-29, A549, CAKI-1, SK-MEL-2, K562	IR % (10 μg/mL) = 20~50%		[52]
79	P. janczewskii	Sea water	Quinolinone	MDA-MB-231, DU-145, SKOV-3, HT-29, A549, CAKI-1, SK-MEL-2, K562	IR % (10 μg/mL) = 30~90%		[52]
80	P. janczewskii	Sea water	Quinolinone	MDA-MB-231, DU-145, SKOV-3, HT-29	IR % (10 μg/mL) = 91.6%, 69.2%, 79.8%, 96.0%		[52]
81	Penicillium sp. ghq208/Penicillium sp.	Marine sediment/Mangrove	Quinolinone	95-D, HepG2	(0.57, 6.5) μg/mL		[53,54]
82	Penicillium sp. ghq208	Marine sediment	Quinolinone	HepG2	13.2 μM		[53]
83	P. commune SD-118	Deep sea sediment	Quinazolinone	SW1990	20 μg/mL		[23]
84	P. chrysogenum EN-118	Marine alga	Quinazolinone	DU145, A549, Hela	8 μg/mL		[56]
85	P. oxalicum 0312F1	Marine (not clear)	Quinazolinone	SGC-7901, BEL-7404	IR % (200 μg/mL) = 30~40%		[55]
Penipacid A (86)	P. paneum SD-44	Deep sea sediment	Amidine alkaloid	RKO	8.4 μM		[57]
Penipacid E (87)	P. paneum SD-44	Deep sea sediment	Amidine alkaloid	RKO	9.7 μM		[57]
88	P. paneum SD-44	Deep sea sediment	Imine alkaloid	Hela	6.6 μM		[57]
Penipanoid A (89)	P. paneum SD-44	Deep sea sediment	Triazole alkaloid	SMMC-7721	54.2 μM		[58]
Bis-sclerotioramin (90)	Penicillium 303#	Mangrove	Azaphilone alkaloid	MDA-MB-231	7.13 μM		[59]
Sorbicillactone (91)	P. chrysogenum	Marine sponge	Miscellaneous Alkaloid	L5178Y	2.2 μg/mL	Selective anti-leukemic	[60]
Brocaeloid B (92)	P. brocae	Mangrove	Miscellaneous Alkaloid	A. salina	36.7 μM		[62]
Varitatin (93)	Mutant P. varibile	Mangrove	Amide alkaloid	HCT-116	2.8 μM	IR%(1μM) = 50% and 40% (PDGFR-βand ErbB4)	[63]
18-hydroxydecaturin B (94)	P. oxalicum EN-201	Mangrove	Pyridinyl-α-pyrone alkaloid	A. salina	2.3 μM		[42]
Xantocillin X (95)	P. commune SD-118	Deep sea sediment	Isocyanide alkaloid	MCF-7, HepG2, NCI-H460, Hela, DU145, MDA-MB-231	(12, 7, 10, 10, 8, 8) μg/mL	Inhibit MEK/EPK pathway and activate class III PI3K/Beclin 1 pathway	[23,67]
96	Penicillium sp. PR19 N-1	Marine sludge	Sesquiterpene	HL-60, A549	(45.8, 82.8) μM		[70]
97	Penicillium sp. PR19 N-1	Marine sludge	Sesquiterpene	HL-60, A549	(28.3, 5.2) μM		[70]
98	Penicillium sp. PR19 N-1	Marine sludge	Sesquiterpene	HL-60, A549	(11.8, 12.2) μM		[71]
99	Penicillium sp. BL 27-2	Sea mud	Sesquiterpene	P388, A549, HL-60, BEL-7402	(0.073, 0.096, 0.065, 4.59) μM		[72]
Sporogen-AO 1 (100)	Penicillium sp. BL 27-2	Sea mud	Sesquiterpene	P388, A549, HL-60, BEL-7402	(10.1, 8.81, 10.4, 5.7) μM		[72]
101	Penicillium sp. BL 27-2	Sea mud	Sesquiterpene	P388, A549, HL-60, BEL-7402	(8.71, 3.51, 7.75, 11.8) μM		[72]
Adametacorenol B (102)	P. adametzioides AS-53	Marine sponge	Diterpene	NCI-H446	5.0 μM		[17]
Conidiogenone B (103)	Penicillium sp.	Deep sea sediment	Diterpene	A549, HL-60	(40.3, 28.2) μM		[22]
Conidiogenone C (104)	Penicillium sp.	Deep sea sediment	Diterpene	HL-60, BEL-7402	(0.038, 0.97) μM		[22]
Conidiogenone D (105)	Penicillium sp.	Deep sea sediment	Diterpene	A549, HL-60, BEL-7402, MOLT-4	(9.3, 5.3, 11.7, 21.1) μM		[22]
Conidiogenone E (106)	Penicillium sp.	Deep sea sediment	Diterpene	A549, HL-60, MOLT-4	(15.1, 8.5, 25.8) μM		[22]
Conidiogenone F (107)	Penicillium sp.	Deep sea sediment	Diterpene	A549, HL-60, BEL-7402	(42.2,17.8, 17.1) μM		[22]
Conidiogenone G (108)	Penicillium sp.	Deep sea sediment	Diterpene	A549, HL-60, BEL-7402, MOLT-4	(8.3, 1.1, 43.2, 4.7) μM		[22]
Brevione I (109)	Penicillium sp.	Deep sea sediment	Diterpene	MCF-7	7.44 μM		[73]
Brevione A (110)	Penicillium sp.	Deep sea sediment	Diterpene	MCF-7	28.4 μM		[73]
Penicisteroid A (111)	P. chrysogenum QEN-24S	Marine alga	Steroid	Hela, SW1990, NCI-H460	(15, 31, 40) μg/mL		[74]
112	Penicillium sp.	Marine moss	Steroid	HepG2	10.4 μg/mL		[75]
113	Penicillium sp.	Marine moss	Steroid	HepG2	15.6 μg/mL		[75]
114	Penicillium sp.	Marine moss	Steroid	HepG2	20.7 μg/mL		[75]
115	Penicillium sp.	Marine moss	Steroid	HepG2	16.8 μg/mL		[75]
116	Penicillium sp.	Marine moss	Steroid	HepG2	21.3 μg/mL		[75]
117	P. stoloniferum QY2-10	Sea squirt	Steroid	P388	4.07 μM		[76]
118	Penicillium sp.	Marine sponge	Steroid	K562	5.54 μM		[77]
119	Penicillium sp.	Marine sponge	Steroid	K562	4.38 μM		[77]
Dankasterone A (120)	Penicillium sp.	Marine sponge	Steroid	HL-60, Hela, K562	(0.78, 4.11, 7.57) μM		[77]
Dankasterone B (121)	Penicillium sp.	Marine sponge	Steroid	HL-60, Hela, K562	(3.25, 4.74, 7.89) μM		[77]
7-deacetoxyyanuthone (122)	Penicillium sp.	Marine (not clear)	Meroterpene	A549, SKOV-3, SKMEL-2, XF498, HCT-15	(7.74, 6.35, 3.86, 10.04, 10.07) μg/mL		[79]
Farnesylbenzenediol (123)	Penicillium sp.	Marine (not clear)	Meroterpene	A549, SKOV-3, SKMEL-2, XF498, HCT-15	(4.73, 5.31, 4.80, 5.94, 6.11) μg/mL		[79]
Farnesylquinone (124)	Penicillium sp.	Marine (not clear)	Meroterpene	A549, SKOV-3, SKMEL-2, XF498, HCT-15	(25.44, 37.29, 18.41, 38.07, 42.56) μg/mL		[79]
Penicillone A (125)	Penicillium sp. F11	Marine (not clear)	Meroterpene	HT1080, Cne2	(45.8, 46.2) μM		[80]
Phenylpyropene E (126)	P. concentricum ZLQ-69	Sea water	Sesquiterpene	MGC-803	19.1 μM		[81]
Phenylpyropene F (127)	P. concentricum ZLQ-69	Sea water	Sesquiterpene	MGC-803	13.6 μM		[81]
Penicillipyrone A (128)	Penicillium sp. F446	Marine sediment	Sesquiterpene	K562, A549	(28, 15) μM		[82]
Penicillipyrone B (129)	Penicillium sp. F446	Marine sediment	Sesquiterpene	K562, A549	(50, 17) μM		[82]
130	Penicillium 303#	Mangrove	Meroterpene	MDA-MB-435, HepG2, HCT-116, A549	(34.25, 24.56, 33.72, 37.82) μg/mL		[59]
131	Penicillium 303#	Mangrove	Meroterpene	MDA-MB-435, HepG2, HCT-116, A549	(31.32, 23.87, 29.19, 34.06) μg/mL		[59]
Ligerin (132)	Penicillium sp.	Sea water	Merosesquiterpene	POS1, SaOS2, MG63	(117/78, 137, 1459) nM		[84,85]
Oxalicumone D (133)	P. oxalicum SCSGAF 0023	Marine gorgonian	Chromone	BGC823, MOLT-4	(10.10, 5.74) μM		[87]
Oxalicumone E (134)	P. oxalicum SCSGAF 0023	Marine gorgonian	Chromone	H1975, U937, K5652, BGC823, MOLT-4, MCF-7, HL-60, Huh-7	(5.45, 4.16, 8.80, 1.96, 1.36, 4.32, 2.96, 6.33) μM		[87]
Oxalicumone A (135)	P. oxalicum SCSGAF 0023	Marine gorgonian	Chromone	H1975, U937, K5652, BGC823, MOLT-4, MCF-7, HL-60, Huh-7, A375, A549, Hela, HepG2, SW-620, L-02	(10.38, 2.35, 4.53, 4.89, 0.30, 11.30, 2.55, 9.49, 11.7, 41.9, 46.2, 77.8, 22.6, 99.0) μM		[87,88]
Oxalicumone B (136)	P. oxalicum SCSGAF 0023	Marine gorgonian	Chromone	U937, MOLT-4, HL-60, A375, Hela, SW-620	(5.00, 2.30, 6.41, 27.8, 60.9, 40.6) μM		[87,88]
Chromosulfine (145)	Mutant P. purpurogenum G59	Marine (not clear)	Chromone	K562, HL-60, BGC-823, Hela, MCF-7	(60.8, 16.7, 73.8, 75.4, 59.2) μM		[91]
Secalonic acid F (146)	Penicillium sp.	Deep sea sediment	Xanthone	HL-60		Modulate Rho GDP dissociation inhibitor 2 Activate caspase 3 and caspase 9	[92,93]
Penimethavone A (147)	P. chrysogenum	Marine gorgonian	Flavone	Hela, rhabdomyosarcoma	(8.41, 8.18) μM		[94]
Bipenicillisorin (148)	P. chrysogenum SCSIO 41001	Deep sea sediment	Coumarin	K562, A549, Huh-7	(6.78, 6.94, 2.59) μM		[95]
Monocerin (149)	Penicillium sp.	Marine sponge	Coumarin	L5178Y	8.4 μM		[96]
150	Penicillium sp. ZH16	Mangrove	Coumarin	KB, KBv200	(5, 10) μg/mL		[97]
Citrinin (151)	Penicillium sp FF001	Marine sponge	Azaphilone polyketide			Inhibit respiration complex III	[99,101]
Penicitrinol L (152)	P. citrinum	Marine sediment	Azaphilone polyketide	SW-620	25.6 μM		[48]
Penicitrinol M (153)	P. citrinum	Marine sediment	Azaphilone polyketide	SW-620	20.9 μM		[48]
Berkelic acid (154)	Penicillium sp.	Acid mine lake	Azaphilone polyketide	OVCAR-3 (in NCI60)	91 nM	Inhibit MMP-3 (GI50 = 1.87 μM) Inhibit caspase 1 (GI50 = 98 μM)	[102]
Sargassopenilline C (155)	P. thomii	Marine alga	Azaphilone polyketide			Inhibit the oncogenic nuclear factor AP-1 (IC50 = 15 μM)	[104]
Sculezonone A (156)	Penicillium sp.	Marine sponge	Azaphilone polyketide			Inhibit both DNA polymerases (α and β)	[105]
Sculezonone B (157)	Penicillium sp.	Marine sponge	Azaphilone polyketide			Inhibit both DNA polymerases (α and β)	[105]
Dicitrinone B (158)	P. citrinum	Marine sediment	Azaphilone polyketide			Induce apoptosis through ROS-related caspase pathway	[106]
Perinadine A (159)	P. citrinum	Marine fish	Azaphilone polyketide	L1210	20 μg/mL		[107]
Herqueiazole (160)	Penicillium sp F011	Marine sediment	Azaphilone polyketide	A549	67.3 μM		[108]
Comazaphilone D (161)	P. commune QSD-17	Marine sediment	Azaphilone polyketide	SW1990	51 μM		[109]
Comazaphilone E (162)	P. commune QSD-17	Marine sediment	Azaphilone polyketide	SW1990	26 μM		[109]
Comazaphilone F (163)	P. commune QSD-17	Marine sediment	Azaphilone polyketide	SW1990	53 μM		[109]
Pinophilin A (164)	P. pinophilum Hedgcok	Marine seaweed	Azaphilone polyketide	A549, BALL-1, HCT-116, Hela, NUGC-3	(52.5, 50.2, 51.3, 55.6, 54.7) μM	Inhibit the mammalian DNA polymerases A, B, Y family	[110]
Pinophilin B (165)	P. pinophilum Hedgcok	Marine seaweed	Azaphilone polyketide	A549, BALL-1, HCT-116, Hela, NUGC-3	(93.1, 90.4, 92.5, 99.0, 96.8) μM	Inhibit the mammalian DNA polymerases A, B, Y family	[110]
Sch 725680 (166)	P. pinophilum Hedgcok	Marine seaweed	Azaphilone polyketide	A549, BALL-1, HCT-116, Hela, NUGC-3	(65.7, 62.0, 64.6, 68.8, 66.4) μM	Inhibit the mammalian DNA polymerases A, B, Y family	[110]
Penostatin A (167)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388	0.8 μg/mL	PTP1B inhibitor (IC50 = 15.87 μM)	[111,113]
Penostatin B (168)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388	1.2 μg/mL	PTP1B inhibitor (IC50 = 33.65 μM)	[111,113]
Penostatin C (169)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388, BSY-1, MCF-7, HCC2998, NCI-H522, DMS114, OVCAR-3, MKN1	(1.0, 2.0, 1.6, 2.0, 2.5, 1.9, 2.4, 1.7) μg/mL	PTP1B inhibitor (IC50 = 0.37 μM)	[111,113]
Penostatin D (170)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388	11.0 μg/mL		[111]
Penostatin E (171)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388	0.9 μg/mL		[111]
Penostatin F (172)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388	1.4 μg/mL		[112]
Penostatin G (173)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388	0.5 μg/mL		[112]
Penostatin H (174)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388	0.8 μg/mL		[112]
Penostatin I (175)	Penicillium sp. OUPS-79	Marine alga	Polyketide	P388	1.2 μg/mL		[112]
176	P. oxalicum HSY05	Marine sediment	Phenolic polyketide			DNA topoisomerase I inhibitor	[117]
177	Co-cultured Penicillium sp. WC-29-5	Mangrove	Phenolic polyketide	H1975	3.97 μM		[118]
178	Co-cultured Penicillium sp. WC-29-5	Mangrove	Phenolic polyketide	H1975, HL-60	(5.73, 3.73) μM		[118]
(+)-5-chlorogriseofulvin (179)	P. canescens MMS460	Sea water	Phenolic polyketide	KB	IR% (0.6 μM) = 49%		[119]
Griseophenone I (180)	P. canescens MMS460	Sea water	Phenolic polyketide	KB	IR% (0.6 μM) = 58%		[119]
Griseophenone G (181)	P. canescens MMS460	Sea water	Phenolic polyketide	KB	IR% (0.6 μM) = 47%		[119]
Iso-monodictyphenone (182)	Penicillium sp. MA-37	Mangrove	Phenolic polyketide	A. salina	25.3 μM		[120]
Penikellide A (183)	Penicillium sp. MA-37	Mangrove	Phenolic polyketide	A. salina	14.2 μM		[120]
Penikellide B (184)	Penicillium sp. MA-37	Mangrove	Phenolic polyketide	A. salina	39.2 μM		[120]
Penicillide (185)	Penicillium sp. ZLN29	Marine sediment	Phenolic polyketide	HepG2	(6.7/9.7, 7.8) μM	ACAT and nonpeptide calpain inhibitor	[121,122,124,125]
Prepenicillide (186)	Penicillium sp. ZLN29	Marine sediment	Phenolic polyketide	HepG2, RD	9.9 μM		[124]
Hydroxypenicillide (187)	P. pinophilum	Marine gorgonian	Phenolic polyketide	Hela	6.1 μM		[125]
Nidurufin (188)	P. flavidorsum SHK1-27	Marine sediment	Anthraquinone	K562	12.6 μM	Induce cell cycle arrest at G2/M transition	[126]
Averantin (189)	P. flavidorsum SHK1-27	Marine sediment	Anthraquinone	K562	12.6 μM		[126]
190	P. terrestre	Marine sediment	Polyketide	A549, P388	(5.3, 15.7) μM		[128]
191	P. terrestre	Marine sediment	Polyketide	A549, P388	(7.6, 10.5) μM		[128]
Dihydrobisvertinolone (192)	P. terrestre	Marine sediment	Polyketide	A549, P388	(0.52, 1.7) μM		[128]
193	P. terrestre	Marine sediment	Polyketide	A549	1.4 μM		[128]
194	P. terrestre	Marine sediment	Polyketide	A549, P388	(2.1, 2.8) μM		[129]
195	P. terrestre	Marine sediment	Polyketide	A549, P388	(4.3, 8.8) μM		[129]
Trichodimerol (196)	P. terrestre	Marine sediment	Polyketide	A549, P388	(4.7, 0.33) μM		[129]
Chloctanspirone A (197)	P. terrestre	Marine sediment	Polyketide	HL-60, A549	(9.2, 39.7) μM		[131]
Chloctanspirone B (198)	P. terrestre	Marine sediment	Polyketide	HL-60	37.8 μM		[131]
(10E,15S)-10,11-Dehydrocurvularin (199)	Penicillium sp. DRF2	Marine sponge	Macrolide	36 tumor cell lines	0.28~6 μM		[133,134]
Curvularin (200)	Penicillium sp. DRF2	Marine sponge	Macrolide			HSP90 inhibitor	[132]
Tanzawaic acid P (201)	Penicillium sp. CF07370	Marine sediment	Polyketide	Jurkat, K562, Raji	(28.6, 30.2, 20.3) μM	Active the mitochondrial apoptotic pathway	[137]
Tanzawaic acid D (202)	P. steckii	Marine (not clear)	Polyketide			Bind to the FOXO1 which regulates EFGR signaling and stabilizes the FOXO1-DNA conformation	[138]
Penicimutamide A (203)	Mutant P. purpurogenum G59	Marine soil	Lipopepetide	K562, HL-60, Hela, BGC-823, MCF-7	IR% (100 μg/mL) = 10~40%		[140]
Penicimutamide B (204)	Mutant P. purpurogenum G59	Marine soil	Lipopepetide	K562, HL-60, Hela, BGC-823, MCF-7	IR% (100 μg/mL) = 25~40%		[140]
Penicimutamide C (205)	Mutant P. purpurogenum G59	Marine soil	Lipopepetide	K562, HL-60, Hela, BGC-823, MCF-7	IR% (100 μg/mL) = 10~40%		[140]
Penicimutamide D (206)	Mutant P. purpurogenum G59	Marine soil	Lipopepetide	K562, HL-60, Hela, BGC-823, MCF-7	IR% (100 μg/mL) = 20~40%		[140]
Penicimutamide E (207)	Mutant P. purpurogenum G59	Marine soil	Lipopepetide	K562, HL-60, Hela, BGC-823, MCF-7	IR% (100 μg/mL) = 10~45%		[140]
Penicimutamide F (208)	Mutant P. purpurogenum G59	Marine soil	Lipopepetide	K562, HL-60, Hela, BGC-823, MCF-7	IR% (100 μg/mL) = 10~50%		[140]
Penicimutamide G (209)	Mutant P. purpurogenum G59	Marine soil	Lipopepetide	K562, HL-60, Hela, BGC-823, MCF-7	IR% (100 μg/mL) = 10~20%		[140]
Fellutamide A (210)	P. fellutanum	Marine fish	Lipopepetide	P388, L1210	(0.2, 0.8) μg/mL		[139]
Fellutamide B (211)	P. fellutanum	Marine fish	Lipopepetide	P388, L1210	(0.1, 0.7) μg/mL		[139]
Fellutamide C (212)	Mutant P. purpurogenum G59	Marine soil	Lipopepetide	K562, HL-60, Hela, BGC-823, MCF-7	IR% (100 μg/mL) = 30~50%		[140]
Peniphenylane A (213)	P. fellutanum HDN14-323	Deep sea sediment	Polyphenol	Hela	14.5 μM		[141]
Peniphenylane B (214)	P. fellutanum HDN14-323	Deep sea sediment	Polyphenol	Hela, HCT-116	(11.4, 15.8) μM		[141]
Peniphenylane D (215)	P. fellutanum HDN14-323	Deep sea sediment	Polyphenol	Hela, HL-60, HCT-116	(9.3, 18.2, 31.7) μM		[141]
Peniphenylane F (216)	P. fellutanum HDN14-323	Deep sea sediment	Polyphenol	Hela	29.3 μM		[141]
Peniphenylane G (217)	P. fellutanum HDN14-323	Deep sea sediment	Polyphenol	Hela, HL-60, HCT-116	(16.6, 23.2, 24.7) μM		[141]
Terrestol B (218)	P. terrestre	Marine sediment	Polyphenol	HL-60, MOLT-4, A549, BEL-7402	(6.1, 5.8, 18.3, 62.3) μM		[142]
Terrestol C (219)	P. terrestre	Marine sediment	Polyphenol	HL-60, MOLT-4, A549, BEL-7402	(5.5, 5.6, 18.2, 57.3) μM		[142]
Terrestol D (220)	P. terrestre	Marine sediment	Polyphenol	HL-60, MOLT-4, A549, BEL-7402	(5.3, 5.5, 14.3, 38.5) μM		[142]
Terrestol E (221)	P. terrestre	Marine sediment	Polyphenol	HL-60, MOLT-4, A549, BEL-7402	(54.7, 6.4, 9.6, 59.0) μM		[142]
Terrestol F (222)	P. terrestre	Marine sediment	Polyphenol	HL-60, MOLT-4, A549, BEL-7402	(55.0, 58.1, 13.8, 63.2) μM		[142]
Terrestol G (223)	P. terrestre	Marine sediment	Polyphenol	HL-60, MOLT-4, A549, BEL-7402	(5.1, 6.5, 5.7, 6.0) μM		[142]
Terrestol H (224)	P. terrestre	Marine sediment	Polyphenol	HL-60, MOLT-4, A549, BEL-7402	(6.3, 5.8, 33.8, 61.9) μM		[142]
Terrestol A (225)	P. terrestre	Marine sediment	Polyphenol	HL-60, MOLT-4, A549, BEL-7402	(33.3, 5.5, 23.5, 57.0) μM		[142]
Expansol A (226)	P. expansum 091006	Mangrove	Polyphenol	HL-60	15.7 μM		[143]
Expansol B (227)	P. expansum 091006	Mangrove	Polyphenol	HL-60, A549	(5.4, 1.9) μM		[143,144]
Expansol C (228)	P. expansum 091006	Mangrove	Polyphenol	HL-60	18.2 μM		[143]
Expansol E (229)	P. expansum 091006	Mangrove	Polyphenol	HL-60	20.8 μM		[143]
Patulin (230)	Penicillium sp.	Marine alga	Other	P388, BSY-1, MCF-7, HCC2998, NCI-H522, DMS114, OVCAR-3, MKN1	(0.06, 0.34, 0.65, 1.54, 0.30, 0.57, 0.37, 0.39) μg/mL	Potassium-uptake inhibitor Ion flux across cell membranes inducer	[111]
(+)-Epiepoxydon (231)	Penicillium sp.	Marine alga	Other	P388	0.2 μg/mL		[111]
232	Penicillium sp.	Mangrove	Other	KB, KBv200	(6, 10) μg/mL		[145]
Penicillic acid (233)	Penicillium sp.	Sea water	Other	POS1, AT6-1, L299	(7.8, 29.4, 12.9) μM		[84]

). Cytochalasan alkaloids, which are indole alkaloids, constitute a large class of mycotoxins that exhibit significant cytotoxicity against P388 cells (IC₅₀ < 1 μg/mL). Furthermore, a series of diketopiperazine alkaloids, gliotoxin analogues, and roquefortine analogues with remarkable cytotoxicity at nanomolar levels are potential anticancer leads. Terpenoid metabolites appear to be more effective against cancer cell lines than steroids; in particular, compounds 99, 104, and 132 were effective at nanomolar levels. Furthermore, citrinins (chromone analogues) and their derivatives, which are polyketide mycotoxins, possess excellent cytotoxic activities. Penostatins (cytotoxic polyketides) are cytotoxic to P388 cells with IC₅₀ values of ~1 μg/mL. With the exception of 210 and 211, lipopeptides exhibited moderate cytotoxicity. In addition, the Penicillium genus can produce polyphenolic compounds (terrestrols) with pronounced cytotoxicity.

Although our review includes most of the cytotoxic metabolites described in the literature, more compounds are yet to be identified in marine Penicillium sp. Different marine hosts and environments can also affect the biosynthesis of metabolites by endozoic fungi. Notably, over 99% of the symbiotic microorganisms cannot be cultured. Further investigations may utilize metagenome libraries of the host organisms to identify more metabolites produced by symbiotic microorganisms [149]. Additionally, further studies are needed to explore the functional mechanisms of the bioactive compounds and to optimize their production.