Search results for "antifungal activity"

showing 10 items of 41 documents

Bioactivity of essential oils in phytopathogenic and post-harvest fungi control

2017

[EN] Commercial thyme and lavender essential oils were analysed by GC/MS. Sixty-six compounds accounting for 98.6¿99.6% of total essential oil were identified. Thymol (52.14 ± 0.21%), followed by pcymene (32.24 ± 0.16%), carvacrol (3.71 ± 0.01%) and ¿-terpinene (3.34 ± 0.02%), were the main compounds in thyme essential oil, while large amounts of oxygenated monoterpenes linalool acetate (37.07 ± 0.24%) and linalool (30.16 ± 0.06%) were found in lavender one. In vitro antifungal activity of the essential oils was evaluated at 200 and 300 ¿g/mL against 10 phytopathogenic and post-harvest fungi, which significantly affect agriculture. Micelial growth inhibition was calculated for each tested f…

AntifungalLavendermedicine.drug_classAcyclic MonoterpenesBOTANICAPlant ScienceFungusCyclohexane MonoterpenesMicrobial Sensitivity Tests01 natural sciencesBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionThymus Plantchemistry.chemical_compoundLinaloollawLavenderBotanymedicineOils VolatilePlant OilsCarvacrolFood scienceAntifungal activityThymolEssential oilBIOLOGIA VEGETALbiology010405 organic chemistryOrganic ChemistryFungiThymebiology.organism_classificationThymol0104 chemical sciencesFungicides Industrial010404 medicinal & biomolecular chemistryLavandulachemistryEssential oilsMonoterpenesCymenesGrowth inhibition
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Synthesis and structural elucidation of novel antifungal N-(fluorophenyl)piperazinyl benzoxaboroles and their analogues

2019

Abstract Series of novel N-(fluorophenyl)piperazine derivatives of phenylboronic compounds including benzoxaboroles, phenylboronic acids and phenylboronic methyl monoester have been obtained by facile synthetic methods starting from 2-formylphenylboronic acid. Molecular and crystal structures of those novel derivatives have been investigated by single crystal X-ray diffraction method. The Bond Valence Vector Model was used to describe strains in the boron coordination sphere. Microbiological activity of novel benzoxaboroles as well as their corresponding acid analogues against: A. niger, A. terreus, P. ochrochloron, C. tenuis and F. dimerum has been evaluated. The presence of heterocyclic b…

AntifungalorganoboronValence (chemistry)Coordination sphere010405 organic chemistryChemistrymedicine.drug_classphenylboronic acidantifungal activityOrganic ChemistrybenzoxaboroleCrystal structurepiperazine010402 general chemistry01 natural sciencesCombinatorial chemistryfluorophenyl0104 chemical sciencesAnalytical ChemistryInorganic Chemistrychemistry.chemical_compoundPiperazinemedicinePhenylboronic acidSpectroscopyJournal of Molecular Structure
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Aceites esenciales: productos antimicrobianos y antioxidantes naturales en la industria agroalimentaria

2020

[ES] Los consumidores son conscientes del peligro derivado del uso de antioxidantes y antimicrobianos sintéticos en la industria agroalimentaria, demandando alternativas más seguras y ecológicas. En este estudio, se ha determinado la actividad antioxidante de aceites esenciales comerciales mediante el método DPPH y su efecto antimicrobiano frente a la bacteria Pseudomonas syringae y el hongo fitopatógeno Fusarium oxysporum a través del empleo del método estandarizado de disco. Los aceites esenciales de clavo, ajedrea, canela y orégano, así como carvacrol, mostraron la máxima actividad antioxidante, comparable a antioxidantes establecidos. El aceite esencial de gaulteria fue el más potente i…

AntioxidantDPPHActividad antifúngicamedicine.medical_treatmentAntioxidantesAntioxidantslaw.inventionchemistry.chemical_compoundAntioxidant activitylawFusarium oxysporum2302.10 Aceites EsencialesIndustria agroalimentariamedicineBIOQUIMICA Y BIOLOGIA MOLECULARCarvacrolAntifungal activityReference standardsAgri-food industryEssential oilAntifungalsbiologyTraditional medicinebiology.organism_classificationAntimicrobialAntibacterialchemistryEssential oilsAceites esencialesWinter savoryActividad antibacterianaAntibacterial activityActividad antioxidanteAntifúngicosAntibacterianoAgrifood industry
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Antibacterial and antifungal activities of Otanthus maritimus (L.) Hoffmanns.Link essential oil from Sicily.

2013

The chemical composition of the essential oil obtained from the flowers of Otanthus maritimus L., a perennial plant growing wild in maritime sands in the Mediterranean region, was investigated by GC and GC-MS analyses. Totally 66 were identified. The oil was dominated by the high content of monoterpene compounds, especially oxygenated monoterpenes which accounted for 73.1%. The most abundant components were yomogi alcohol (20.8%), camphor (15.8%), artemisyl acetate (15.3%) and artemisia alcohol (13.7%). The oil was tested against two Gram (+) and six Gram (-) bacterial strains, both American Type Culture Collection standard strains and clinically isolated (CI), one potentially pathogenic ye…

Artemisyl acetateAntifungal AgentsMonoterpenePlant ScienceFlowersMicrobial Sensitivity TestsAsteraceaeGram-Positive BacteriaBiochemistryYomogi alcoholGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionRhizoctonia solaniCamphorchemistry.chemical_compoundlawBotanyCandida albicansGram-Negative BacteriaOils VolatileAntifungal activitySettore BIO/15 - Biologia FarmaceuticaSicilyEssential oilBotrytis cinereabiologyOrganic Chemistryfood and beveragesSettore CHIM/06 - Chimica Organicabiology.organism_classificationCamphorAnti-Bacterial AgentsOtanthuschemistryMonoterpenesArtemisiaAntibacterial activityOtanthus maritimuAntibacterial activityNatural product research
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Synthesis and in vitro antimicrobial activities of new (cyano-NNO-azoxy) pyrazole derivatives

2011

The antibacterial and antifungal activity of a series of products, in which the 1,5-dimethyl-4-(cyano- NNO-azoxy)pyrazol-3-yl and 1,3-dimethyl-4-(cyano-NNO-azoxy)pyrazol-5-yl moieties were linked to pyridine, pyrazole, isoxazole, thiophene and the furan ring, were examined. No molecule displayed activity against the Gram-negative bacteria tested. Conversely, some compounds displayed activity against two Staphylococcus aureus strains, including the methicillin resistant strain. All compounds displayed interesting antifungal activity, the most active compound of the series being the thiophene derivative 7a. This compound’s activity against Candida krusei and Candida glabrata (MIC = 0.25 and 0…

AzoxyStaphylococcus aureusAntifungal AgentsStereochemistryClinical BiochemistryPharmaceutical ScienceMicrobial Sensitivity TestsPyrazoleBiochemistryChemical synthesisAntifungal activity Pyrazole Azole sistance Cyano-NNO-azoxy Thiophenechemistry.chemical_compoundAnti-Infective AgentsThiopheneCandida kruseiNitrilesDrug DiscoveryThiopheneAntifungal activityIsoxazoleAntifungal activity; Pyrazole; Azole resistance; Cyano-NNO-azoxy; Thiophene.Molecular BiologyCandidaMolecular StructurebiologyCandida glabrataOrganic ChemistryBiological activitybiology.organism_classificationSettore CHIM/08 - Chimica FarmaceuticachemistryCyano-NNO-azoxyPyrazoleAzole resistancePyrazolesMolecular MedicineAzo Compounds
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Aktywność biologiczna Bacillus amyloliquefaciens wobec Fusarium spp. wyizolowanych z pędów szparaga (Asparagus officinalis L.)

2016

Patogeny roślin, takie jak Fusarium spp. to najważniejsze czynniki, które co roku powodują znaczne straty i/lub uszkodzenia produktów rolnych. Celem przeprowadzonych badań była ocena in vitro właściwości biologicznych B. amyloliquefaciens wobec F. proliferatum i F. oxysporum wyizolowanych z pędów bielonego szparaga odmiany Grolim. W badaniach uwzględniono: gęstość i wiek hodowli bakterii, rodzaj podłoża oraz wpływ płynu pohodowlanego. Ocenę właściwości antagonistycznych hodowli bakterii 6, 12, 24 i 48- godzinnych przeprowadzono w oparciu o wskaźniki: zdolność kiełkowania zarodników, tempo wzrostu liniowego i indeks tempa wzrostu grzybów z zastosowaniem podłoży PDA oraz szparagowego. Najwięk…

B. amyloliquefaciensaktywność przeciwgrzybowaasparagusantifungal activityszparagiFusarium spp.
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The influence of fluorine position on the properties of fluorobenzoxaboroles

2015

5-Fluoro-2,1-benzoxaborol-1(3H)-ol, a potent antifungal drug also known as Tavaborole or AN2690, has been compared with its three isomers in terms of its activity against several fungi as well as pKa and multinuclear NMR characterization. The molecular and crystal structure of 6-fluoro-2,1-benzoxaborol-1(3H)-ol was determined and compared with that of AN2690.

Boron CompoundsModels Molecularcrystal structureAntifungal AgentsMagnetic Resonance SpectroscopyHalogenationStereochemistryAntifungal drugchemistry.chemical_elementCrystal structureCrystallography X-RayBiochemistrybenzoxaborolesIsomerismDrug DiscoveryHumansMolecular BiologytavaboroleTavaboroleChemistryOrganic Chemistryantifungal activityFungiFluorineBridged Bicyclo Compounds HeterocyclicMycosesFluorineBioorganic Chemistry
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Bacillus subtilis BS-2 and Peppermint Oil as Biocontrol Agents Against Botrytis cinerea

2019

The purpose of this study was to assess the activity of Bacillus subtilis BS-2 and peppermint oil against Botrytis cinerea. In this study parameters such as the age and the density of the bacterial culture and the incubation temperature were taken into consideration. Furthermore, the cellulolytic activity of the bacterium was determined. The effect of peppermint oil was evaluated at a concentration range of 0.5-4.0 %. The research was conducted with a dual culture plate method. The influence of B. subtilis BS-2 and peppermint oil on the growth of B. cinerea was evaluated based on the growth rate index. It was noted that the bacterial culture occurred at an initial density of OD560 = 1.0, cu…

CMCase activityBotrytis cinereapeppermint oilBacillus subtilis BS-2antifungal activityEcological Chemistry and Engineering S-Chemia I Inzynieria Ekologiczna S
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Assessment of the antifungal properties of nettle extracts against Fusarium proliferatum = Ocena właściwości przeciwgrzybowych pokrzywy zwyczajnej wo…

2015

Celem przeprowadzonych badań była ocena właściwości przeciwgrzybowych ekstraktów z liści i korzenia pokrzywy zwyczajnej wobec Fusarium proliferatum. Ocenę właściwości antagonistycznych ekstraktów w stężeniach 2,5, 5,0, 10, 20 i 40% przeprowadzono metodą hodowlano-płytkową z zastosowaniem podłoży PDA pomidorowego. Hodowlę prowadzono w temp. 26ºC przez 9 dni, dokonując pomiarów co 1-2 dni. Kontrolę pozytywną stanowił Topsin M 500 S.C, a kontrolę negatywną woda destylowana. Określono indeks kiełkowania zarodników, indeks tempa wzrostu oraz stopień redukcji liniowego wzrostu Fusarium sp. Uzyskane wyniki badań wykazały zahamowanie kiełkowania zarodników przez wszystkie zastosowane stężenia ekstr…

Fusarium proliferatumaktywność przeciwgrzybowaantifungal activitypokrzywa zwyczajnastinging nettleProceedings of ECOpole
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Antifungal effects of the bioactive compounds enniatins A, A1, B, B1

2010

To produce enniatin (ENs), Fusarium tricinctum CECT 20150 was grown in a liquid medium of potato (PDB), being mycotoxin purified by high performance liquid chromatography (HPLC) with a reverse phase semipreparative column using a mobile phase of acetonitrile/water using gradient condition. The purity of the ENs fractions was verified by analytical HPLC and LC/MS-MS. The pure fractions of ENs were utilized to study the biological activity on several mycotoxigenic moulds as Fusarium verticilloides, Fusarium sporotrichioides, Fusarium tricinctum, Fusarium poae, Fusarium oxysporum, Fusarium proliferatum, Beauveria bassiana, Trichoderma harzianum, Aspergillus flavus, Aspergillus parasiticus, Asp…

FusariumAntifungal AgentsChromatographybiologyantifungal activityTrichoderma harzianumFusarium proliferatumhplcMicrobial Sensitivity TestsToxicologybiology.organism_classificationFusarium sporotrichioidesAspergillus parasiticusMicrobiologyTandem Mass SpectrometryDepsipeptidesFusarium oxysporumenniatinEnniatinAspergillus ochraceusChromatography High Pressure LiquidToxicon
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