Antimicrobial activity of essential oils and their components against the three major pathogens of the cultivated button mushroom, Agaricus bisporus

Essential oils of Matricaria chamommilla, Mentha piperita, M. spicata, Lavandula angusti folia, Ocimum basilicum, Thymus vulgaris, Origanum vulgare, Salvia officinalis, Citrus limon and C. aurantium and their components; linalyl acetate, linalool, limonene, α-pinene, β-pinene, 1,8-cineole, camphor, carvacrol, thymol and menthol were assayed for inhibitory activity against the three major pathogens of the button mushroom, Agaricus bisporus, i.e. the fungi Verticillium fungicola and Trichoderma harzianum and the bacterium Pseudomonas tolaasii. The highest and broadest activity was shown by the Origanum vulgare oil. Carvacrol possessed the highest antifungal activity among the components tested.     

Structure–activity relationships of eugenol derivatives against Aedes aegypti (Diptera: Culicidae) larvae

BACKGROUND: Dengue fever is a severe public health problem for several countries. In order to find effective larvicides to aid control programs, the structure‐activity relationships of eugenol derivatives against Aedes aegypti (Diptera: Culicidae) larvae were evaluated. Additionally, the composition and larvicidal activity of Syzygium aromaticum essential oil was assessed. RESULTS: Four compounds representing 99.05% of S. aromaticum essential oil have been identified. The essential oil was active against Ae. aegypti larvae (LC₅₀ = 62.3 and 77.0 ppm, field‐collected and Rockefeller larvae respectively). The larvicidal activity of eugenol, the major compound of the essential oil, was further evaluated (LC₅₀ = 93.3 and 71.9 ppm, field‐collected and Rockefeller larvae respectively). The larvicidal activity and structure‐activity relationships of synthetic derivatives of eugenol were also assessed. The larvicidal activity of the derivatives varied between 62.3 and 1614.9 ppm. Oxidation of eugenol allylic bond to a primary alcohol and removal of the phenolic proton resulted in decreased potency. However, oxidation of the same double bond in 1‐benzoate‐2‐methoxy‐4‐(2‐propen‐1‐yl)‐phenol resulted in increased potency. CONCLUSION: Structural characteristics were identified that may contribute to the understanding of the larvicidal activity of phenylpropanoids. The present approach may help future work in the search for larvicidal compounds. Copyright © 2012 Society of Chemical Industry     

Synergistic and antagonistic interactions of terpenes against Meloidogyne incognita and the nematicidal activity of essential oils from seven plants indigenous to Greece

BACKGROUND: Biorational means for phytonematode control were studied within the context of an increasingly ecofriendly pest management global approach. The nematicidal activity and the chemical composition of essential oils (EOs) isolated from seven plants grown in Greece and ten selected compounds extracted from them against second‐stage juveniles (J2) of Meloidogyne incognita (Kof. & White) Chitwood were evaluated using juvenile paralysis experiments. Additionally, synergistic and antagonistic interactions between nematicidal terpenes were studied using an effect addition model, with the comparison made at one concentration level. RESULTS: The 96 h EC₅₀ values of Foeniculum vulgare Mill., Pimpinella anisum L., Eucalyptus meliodora A Cunn ex Schauer and Pistacia terebinthus L. were 231, 269, 807 and 1116 µg mL^?1, respectively, in an immersion bioassay. Benzaldehyde (9 µg mL^?1) was the most toxic compound, followed by γ‐eudesmol (50 µg mL^?1) and estragole (180 µg mL^?1), based on 96 h EC₅₀ values. The most potent terpene pairs between which synergistic actions were found, in decreasing order, were: trans‐anethole/geraniol, trans‐anethole/eugenol, carvacrol/eugenol and geraniol/carvacrol. CONCLUSION: This is the first report on the activity of F. vulgare, P. anisum, E. meliodora and P. terebinthus, and additionally on synergistic/antagonistic nematicidal terpene interactions, against M. incognita, providing alternative methods for nematode control. Copyright © 2010 Society of Chemical Industry     

Functional Analysis of ABC Transporter Genes From Botrytis cinerea Identifies BcatrB as a Transporter of Eugenol

The role of multiple ATP-binding cassette (ABC) and major facilitator superfamily (MFS) transporter genes from the plant pathogenic fungus Botrytis cinerea in protection against natural fungitoxic compounds was studied by expression analysis and phenotyping of gene-replacement mutants. The expression of 11 ABC (BcatrA–BcatrK) and three MFS genes (Bcmfs1, Bcmfs2 and Bcmfs4) was studied. All genes showed a low basal level of expression, but were differentially induced by treatment with cycloheximide and the plant defence compounds camptothecin, eugenol, psoralen, resveratrol and rishitin. The latter compounds induced expression of BcatrB at a high level. Eugenol was more toxic to BcatrB gene-replacement mutants than to the control isolates. Eugenol also caused an instantaneous increase in mycelial accumulation of the fungicide fludioxonil, a known substrate of BcatrB. However, there was no difference in virulence between the wild-type and BcatrB gene-replacement mutants on Ocimum basilicum, a plant known to contain eugenol. The results indicate that BcatrB is a transporter of lipophilic compounds, such as eugenol, but its role in virulence remains uncertain.     

Nematicidal activity of some essential plant oils from tropical West Africa

Abstract

Plant parasitic nematodes are among the most destructive plant pathogens worldwide and their control is very challenging. Plant essential oils (EOs) have showed a great potential in nematode control. In this work, EOs from 10 aromatic plants acclimatized in Togo were assessed in vitro for their nematicidal activity on the root-knot nematode Meloidogyne incognita. EOs were subsequently analyzed by GC-MS and compounds were tested individually on nematodes. The most potent EOs were: Ocimum sanctum L., Cymbopogon schoenanthus (L.) Spreng and Cinnamomum zeylanicum Blume with EC_50/72h values of 282?±?53, 288?±?30 and 355?±?126?mg/L, respectively. The EC_50/48h values of tested compounds were 81?±?14, 117?±?33, 128?±?42, 141?±?47, 168?±?40, 216?±?86 and 235?±?43?mg/L for cinnamyl acetate, methyl eugenol, cinnamyl alcohol, acetyl eugenol, isoeugenol, eugenol and benzyl benzoate, respectively. Furthermore, we found a synergistic nematicidal activity when we combined phenylpropanoids compounds with carvone. EOs and their constituents described herein merit further studies, especially in pot experiments before serving as nematicides.     

Repellancy and contact toxicity of clove bud oil and its constituents against German cockroaches,Blatella germanica (Dictyoptera: Blattellidae), under laboratory conditions

Abstract

The German cockroach, Blattella germanica L. (Dictyoptera: Blattellidae), an invasive pest of human habitats, is distributed throughout the world, except in Antarctica. They have developed resistance against chemical pesticides used for the management of their populations. Numerous essential oils and their constituents have been tested; however, the insecticidal activities of clove bud powder, oil, and their constituents have not yet been tested against the German cockroaches. Thus, in this study, clove bud powder, oil, and their major constituents, eugenol and eugenol acetate, were evaluated for their contact toxicity and repellancy against adult German cockroaches under laboratory conditions. The clove bud powder applied at 30?mg/cm² killed 92% of German cockroaches at 6?hours after treatment (HAT). Similarly, clove bud oil, eugenol and eugenol acetate applied at 4.00?ml/cm² provided 95%, 85%, and 87% German cockroach mortality at 24, 6, and 24 HAT, respectively. At 2.0?ml/cm², clove bud oil repelled 80% of German cockroaches within 30?min. In contrast, eugenol and eugenol acetate repelled 85% at 1.0?ml/cm² and 2.5?ml/cm², respectively, at 0.5 HAT. Based on this study, clove bud powder, oil, eugenol, and eugenol acetate could be environmentally friendly tools for the management of German cockroaches.     

丁香酚对烟草抗烟草花叶病毒的诱导作用初探

为探讨植物源化合物丁香酚对烟草抗烟草花叶病毒(TMV)的诱导作用,初步研究了丁香酚对接种TMV的烟草叶片中叶绿素和丙二醛(MDA)含量,防御酶苯丙氨酸解氨酶(PAL)、过氧化物酶(POD)和超氧化物岐化酶(SOD)活性,以及病程相关蛋白基因 PR-1 、PR-3 、PR-5 表达的影响。结果表明:丁香酚处理可促进叶绿素的合成,减轻烟草体内MDA的积累,提高PAL、POD和SOD的活性,增强 PR-1 、PR-3 、PR-5 基因的表达。表明丁香酚可提高植物的诱导抗病性,进而减轻TMV对烟草的危害。     

Bioactivity against Tribolium castaneum Herbst (Coleoptera: Tenebrionidae) of Cymbopogon citratus and Eucalyptus citriodora essential oils grown in Colombia

BACKGROUND: Essential oils isolated from Cymbopogon citratus (DC) Stapf. and Eucalyptus citriodora Hook grown in Colombia were analysed by gas chromatography–mass spectrometry (GC‐MS) and tested for repellent activity and contact toxicity against Tribolium castaneum (Herbst.) (Coleoptera: Tenebrionidae). RESULTS: The main components of C. citratus oil were geranial (34.4%), neral (28.4%) and geraniol (11.5%), whereas those of E. citriodora were citronellal (40%), isopulegol (14.6%) and citronellol (13%). The mean repellent doses after 4 h exposure were 0.021 and 0.084 mL L^?1 for C. citratus and E. citriodora oils respectively—values lower than that observed for the commercial product IR3535 (0.686 mL L^?1). CONCLUSION: These studies showed the composition and repellent activity of essential oils of C. citratus and E. citriodora, suggesting that these are potential candidates as insect repellents. Copyright © 2010 Society of Chemical Industry     

Control of phytopathogenic fungi by the essential oil and methanolic extracts of <Emphasis Type="Italic">Erigeron ramosus</Emphasis> (Walt.) B.S.P.

The efficacy of the essential oil and methanolic extracts of Erigeron ramosus (Walt.) B.S.P. was evaluated for controlling the growth of some important phytopathogenic fungi. The hydrodistilled essential oil was analysed by GC-MS. Thirty one compounds representing 95.3% of the total oil were identified, of which β-caryophyllene (24.0%), α-humulene (14.5%), 1,8-cineole (9.0%), eugenol (7.2%), globulol (7.1%), caryophyllene oxide (5.2%), δ-cadinene (5.0%), α-copaene (4.9%) and widdrol (2.0%) were the major compounds. Thus, the monoterpenes and sesquiterpenes were the predominant portions of the oil. Essential oil and methanol extract of E. ramosus and the derived fractions of hexane, chloroform and ethyl acetate were tested for anti-fungal activity, which was determined by disc diffusion and minimum inhibitory concentration (MIC) determination methods. The oil (1,000 ppm) and methanolic extracts (1,500 ppm) displayed great potential of anti-fungal activity as a mycelial growth inhibition against the tested phytopathogenic fungi such as Fusarium oxysporum (KACC 41083), Phytophthora capsici (KACC 40157), Colletotricum capsici (KACC 410978), Fusarium solani (KACC 41092), Rhizoctonia solani (KACC 40111), Sclerotinia sclerotiorum (KACC 41065) and Botrytis cinerea (KACC 40573), in the range of 49.3–70.3% and minimum inhibitory concentration ranging from 125–500 μg ml^-1. The results obtained from this study may contribute to the development of new anti-fungal agents to protect the crops from fungal diseases.     

Larvicidal and oviposition‐altering activity of monoterpenoids,trans‐anithole and rosemary oil to the yellow fever mosquito Aedes aegypti (Diptera: Culicidae)

BACKGROUND: Aedes aegypti L. is the major vector of dengue fever and dengue hemorrhagic fever. In an effort to find effective tools for control programs to reduce mosquito populations, the authors assessed the acute toxicities of 14 monoterpenoids, trans‐anithole and the essential oil of rosemary against different larval stages of Ae. aegypti. The potential for piperonyl butoxide (PBO) to act as a synergist for these compounds to increase larvicidal activity was also examined, and the oviposition response of gravid Ae. aegypti females to substrates containing these compounds was evaluated in behavioral bioassays. RESULTS: Pulegone, thymol, eugenol, trans‐anithole, rosemary oil and citronellal showed high larvicidal activity against all larval stages of Ae. aegypti (LC₅₀ values 10.3–40.8 mg L^?1). The addition of PBO significantly increased the larvicidal activity of all test compounds (3–250‐fold). Eugenol, citronellal, thymol, pulegone, rosemary oil and cymene showed oviposition deterrent and/or repellent activities, while the presence of borneol, camphor and β‐pinene increased the number of eggs laid in test containers. CONCLUSIONS: This study quantified the lethal and sublethal effects of several phytochemical compounds against all larval stages of Aedes aegypti, providing information that ultimately may have potential in mosquito control programs through acute toxicity and/or the ability to alter reproductive behaviors. Copyright © 2008 Society of Chemical Industry     

Virulence and efficacy of different entomopathogenic nematode species against western flower thrips (Frankliniella occidentalis)

Virulence and efficacy of five species and strains of the entomopathogenic nematodes of the families Steinernematidae and Heterorhabditidae:Steinernema riobravis, Steinernema feltiae strains Ger. and UK, andHeterorhabditis bacteriophora strains HP88 and IS5, against the prepupal and pupal stages of the western flower thrips (WFT),Frankliniella occidentalis (Pergande) (Thysanoptera: Thripidae), were investigated in the laboratory. Although all these nematodes controlled WFT to some extent, they differed in efficiency. The heterorhabditid nematodeH. bacteriophora strain HP88 was more specific to the soil-inhabiting WFT stages (36–49% thrips mortality). The steinernematid nematodesS. riobravis andS. feltiae strains Ger. and UK had only a slight effect (10% mortality) on prepupal and pupal populations of WFT, andH. bacteriophora strain IS5 had the least effect of all. A possible reason for such species variation is suggested and discussed.     

Fumigant toxicity of volatile natural products from Korean spices and medicinal plants towards the rice weevil,Sitophilus oryzae (L)

The fumigant toxicity of various volatile constituents of essential oils extracted from sixteen Korean spices and medicinal plants towards the rice weevil, Sitophilus oryzae L (Coleoptera: Curculionidae), was determined. The most potent toxicity was found in the essential oil from Mentha arvensis L var piperascens (LC₅₀ = 45.5 µl litre^?1 air). GC–MS analysis of essential oil from M arvensis showed it to be rich in menthol (63.2%), menthone (13.1%) and limonene (1.5%), followed in abundance by β‐pinene (0.7%), α‐pinene (0.6%) and linalool (0.2%). Treatment of S oryzae with each of these terpenes showed menthone to be most active (LC₅₀ = 12.7 µl litre^?1 air) followed by linalool (LC₅₀ = 39.2 µl litre^?1 air) and α‐pinene (LC₅₀ = 54.9 µl litre^?1 air). Studies on inhibition of acetylcholinesterase activity of S oryzae showed menthone to have a nine‐fold lower inhibitory effect than menthol, despite menthone being 8.1‐fold more toxic than menthol to the rice weevil. Different modes of toxicity of these monoterpenes towards S oryzae are discussed. © 2001 Society of Chemical Industry     

Selection forMeloidogyne incognita virulence against resistance genes from tomato and pepper and specificity of the virulence/resistance determinants

Experiments were designed to analyze the relationships between the root-knot nematodeMeloidogyne incognita and resistant tomato and pepper genotypes. From a natural avirulent isolate, near-isogenic nematode lineages were selected with virulence either against the tomatoMi resistance gene or the pepperMe3 resistance gene. Despite the drastic selection pressure used, nematodes appeared unable to overcome the pepperMe1 gene, therefore suggesting some differences in the resistance conferred byMe1 andMe3 in this species. Nematodes virulent onMi-resistant tomatoes were not able to reproduce onMe1-resistant nor onMe3-resistant peppers, and nematodes virulent onMe3-resistant peppers were not able to reproduce onMi-resistant tomatoes nor onMe1-resistant peppers. These results clearly demonstrate the specificity ofM. incognita virulence against resistance genes from both tomato and pepper, and indirectly suggest that gene-for-gene relationships could occur between these two solanaceous crops and the nematode.     

Effect of Glomus mosseae on concentrations of rosmarinic and caffeic acids and essential oil compounds in basil inoculated with Fusarium oxysporum f.sp. basilici

This study investigated the potential of the arbuscular mycorrhizal (AM) fungus Glomus mosseae to protect basil (Ocimum basilicum) against Fusarium oxysporum f.sp. basilici (Fob). It was hypothesised that G. mosseae could confer a bioprotective effect against Fob as a result of increases in leaf rosmarinic (RA) and caffeic acids (CA) or essential oil concentrations. Glomus mosseae conferred a bioprotective effect against Fob by reducing plant mortality to 20% compared to 33% in non‐mycorrhizal (NM) plants. This bioprotective effect was not related to improved phosphorus (P) nutrition, as AM and NM plants treated with Fob had similar shoot P concentrations (6 and 8 mg g^?1 dry weight (DW), respectively). Both AM and NM plants treated with Fob had similar leaf and root RA and CA concentrations. Furthermore, phenolic (40–70 mg CA g^?1 DW) or essential oil concentrations (0·1–0·6 mg g^?1 DW) were not increased in plants treated with the AM fungus and Fob. Therefore, the bioprotective effect conferred by G. mosseae was not a result of increases in the phytochemicals tested in this study. However, under the AM symbiosis, basil plants treated with Fob had lower methyleugenol concentrations in their leaves (0·1 mg g^?1 DW) than NM plants treated with the pathogen (0·6 mg g^?1 DW).     

Polygalacturonase inhibiting proteins fromAllium porrumL. and their role in plant tissue against fungal endo-polygalacturonases

Five endo-polygalacturonases (PGs), three produced in culture filtrate byFusarium moniliforme, Sclerotium cepivorumandBotrytis aclada,respectively, and two (one acidic and one basic isoform) obtained fromSclerotinia sclerotiorumsoybean infected hypocotyls, were purified in order to characterize the activity of polygalacturonase inhibitor(s) (PGIP(s)) from leek stalk tissue (Allium porrumL.). Three apparently different PGIPs (PGIP-I, PGIP-II and PGIP-III) were purified from the leek tissue. The two more abundant PGIPs (PGIP-I and PGIP-III), although possessing similar pIs of about 6.5, differed in chromatographic behaviour, their molecular mass (39 and 42 kDa, respectively), and specific activity when assayed with the fungal endo-PGs. In addition, PGIP-I was solubilized from tissue homogenate with a low-salt buffer whilst PGIP-III needed a high-salt buffer for extraction (behaving as an ionically wall-bound protein). PGIP-II had very similar properties to PGIP-I, but was extracted using the high-salt buffer. The purified PGIPs and the crude leek extract showed similar inhibition activity patterns against the five fungal endo-PGs. The maximum inhibition activity was observed against the basic endo-PG fromS. sclerotiorum,followed by the acidic endo-PG ofS. sclerotiorumand the endo-PG fromB. aclada.In contrast, no inhibition of endo-PGs fromS. cepivorumandF. moniliformewas observed. Four different concentrations of the five fungal endo-PGs were incubated separately with slices of leek stalk, and the galacturonides released in the incubation mixture were measured. At every level used the endo-PGs ofF. moniliformeandS. cepivorumshowed the maximum activity in uronide releasing. The endo-PGs ofS. sclerotiorum(acidic PG) andB. acladawere active only when high levels were used while the basic endo-PG ofS. sclerotiorumwas not active in combustion with any level of PGIP. These results indicate that a close relationship exists between PGIP activityin vitroand the ability of PGIP to protect leek tissue from endo-PG degradation.     

Insecticidal and repellent properties of nine volatile constituents of essential oils against the American cockroach,Periplaneta americana (L.)

The toxic and repellent properties of nine major constituents of essential oils, comprising benzene derivatives and terpenes, were evaluated against Periplaneta americana (L.). Contact and fumigant toxicities to adult females and repellency to nymphs were determined. The decreasing order of knockdown activity via contact was methyl-eugenol>isosafrole=eugenol>safrole. The killing effect via contact was in the order eugenol=methyl-eugenol=isosafrole>safrole. Fumigant toxicity was only observed for safrole and isosafrole, with safrole being the more potent. Isoeugenol and the tested terpenes had neither contact nor fumigant toxic effect. The decreasing order of repellency to nymphs was safrole>isosafrole>methyl-eugenol=α-pinene> eugenol>isoeugenol. The benzene derivatives were generally more toxic and repellent to P. americana than the terpenes. The distance of the side chain double bond from the aromatic ring and the substitution of a methoxy group to these compounds appeared to be important determinants of their toxicity and repellency. © 1998 Society of Chemical Industry     

Fumigant and contact toxicity of Myrtaceae plant essential oils and blends of their constituents against adults of German cockroach (Blattella germanica) and their acetylcholinesterase inhibitory activity

Fumigant and contact toxicities of 11 Myrtaceae plant essential oils and their constituents against adult male and female Blattella germanica were evaluated. Of 11 Myrtaceae plant essential oils, Eucalyptus polybractea, Eucalyptussmithii, Eucalyptusradiata, Eucalyptusdives, Eucalyptusglobulus, and Melaleuca uncinata, showed 100% fumigant toxicity against adult male German cockroaches at a concentration of 7.5 mg/liter air concentration. In contact toxicity tests, E. polybractea, E. smithii, E. radiata, E. dives, E. globulus, Melaleucadissitiflora, and M. uncinata produced strong insecticidal activity against adult male and female German cockroaches. Of the essential oil constituents, terpinolene, α-terpinene, and terpinen-4-ol demonstrated strong fumigant toxicity against adult male and female B. germanica. Eugenol, isoeugenol, methyl eugenol, and terpinen-4-ol showed strong contact toxicity against adult male B. germanica. The toxicity of the constituent blends identified from M. dissitiflora essential oils indicated that terpinen-4-ol were major contributor to the fumigant activity or contact toxicity of the artificial blend. Only isoeugenol exhibited inhibition activity against male acetylcholinesterase. IC₅₀ values of isoeugenol were 0.22 mg/mL against male acetylcholinesterase.     

Potential of zimtaldehyde, 4-allyl-anisol, linalool, terpineol and other phytochemicals for the control of the confused flour beetle (Tribolium confusum J. d. V.) (Col., Tenebrionidae)

Toxicity and repellency effects of several pure compounds (of plant origin) against the confused flour beetle (Tribolium confusum) were investigated in a filter paper test. The compounds were α-pinen, β-pinen, 4-allyl-anisol, camphor, 1,8-cineol, eugenol, linalool, menthol, piperin, terpineol, thymol and zimtaldehyde. Five compounds (4-allyl-anisol, linalood, terpineol, thymol and zimtaldehyde) caused enough mortality of this insect to allow the determination of LD₅₀ and LD₉₅ values. Zimtaldehyde and 4-allyl-anisol showed the strongest toxicity effects with LD₅₀ values of 0.04–0.05 μl/cm² within an exposure period of 24 h. When the isolated fumigant effects were tested by separating the insects from the filter paper, the toxicity of zimtaldehyde (LD₅₀=0.29 μl/cm²) was much lower than that of 4-allyl-anisol (LD₅₀=0.10μl/cm²).     

Potential of zimtaldehyde, 4-allyl-anisol, linalool, terpineol and other phytochemicals for the control of the confused flour beetle (Tribolium confusum J. d. V.) (Col., Tenebrionidae)

Toxicity and repellency effects of several pure compounds (of plant origin) against the confused flour beetle (Tribolium confusum) were investigated in a filter paper test. The compounds were α-pinen, β-pinen, 4-allyl-anisol, camphor, 1,8-cineol, eugenol, linalool, menthol, piperin, terpineol, thymol and zimtaldehyde. Five compounds (4-allyl-anisol, linalood, terpineol, thymol and zimtaldehyde) caused enough mortality of this insect to allow the determination of LD₅₀ and LD₉₅ values. Zimtaldehyde and 4-allyl-anisol showed the strongest toxicity effects with LD₅₀ values of 0.04–0.05 μl/cm² within an exposure period of 24 h. When the isolated fumigant effects were tested by separating the insects from the filter paper, the toxicity of zimtaldehyde (LD₅₀=0.29 μl/cm²) was much lower than that of 4-allyl-anisol (LD₅₀=0.10μl/cm²).     

基于丁香酚的异(口恶)唑啉类化合物的设计合成及抑菌活性

为了探索新型异齅唑啉类化合物作为杀菌剂候选化合物开发的潜力,本研究以廉价易得的芳香醛类化合物为原料制备了32个氯代肟类化合物,通过其与天然产物丁香酚的1,3-偶极环加成反应和后期官能团化反应,制备了35个异齅唑啉类化合物 ( D1 ~ D32 , E1 ~ E3 ),其中34个为新化合物。所有化合物的结构均经过液相色谱-电喷雾质谱 (LC-ESI-MS)、核磁共振氢谱 (1H NMR) 及元素分析确认。初步抑菌活性测试结果表明:多数目标化合物对油菜菌核病菌、水稻纹枯病菌、番茄早疫病菌和辣椒疫霉病菌具有较好的抑菌活性,其中化合物 D26 对油菜菌核病菌的活性最高,有效抑制中浓度 (EC₅₀) 为14.3 mg/L,具有进一步研究的价值。