Search results for "Biomolecular"

showing 10 items of 507 documents

Chemical Composition and Antimicrobial Activity of the Essential Oil from Flowers of Eryngium triquetrum (Apiaceae) Collected Wild in Sicily

2016

The chemical composition of the essential oil from flowers of Eringium triquetrum Vahl. collected in Sicily was evaluated by GC and GC-MS. The main components were pulegone (50.6%), piperitenone (30.5%) and menthone (7.0%). Comparison of this oil with other studied oils of Eringium species is discussed. The oil showed good antibacterial and antifungal activities against some microorganisms that infest historical art works.

EryngiumFlowersPlant Science01 natural scienceslaw.inventionchemistry.chemical_compoundAnti-Infective AgentslawPulegoneVolatile componentDrug DiscoveryBotanyOils VolatilePlant OilsEryngium triquetrumPiperitenoneSettore BIO/15 - Biologia FarmaceuticaSicilyChemical compositionEssential oilPharmacologyApiaceaeBacteriabiology010405 organic chemistryMenthone.Drug Discovery3003 Pharmaceutical ScienceFungiSettore CHIM/06 - Chimica OrganicaGeneral MedicineComplementary and Alternative Medicine2708 Dermatologybiology.organism_classificationAntimicrobialEryngium triquetrumMenthone0104 chemical sciences010404 medicinal & biomolecular chemistryComplementary and alternative medicinechemistryTriquetrumPulegoneApiaceaeNatural Product Communications
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Two new biologically active triterpenoidal saponins acylated with salicylic acid from Albizia adianthifolia

2003

International audience; Two new oleanane-type triterpene saponins, adianthifoliosides A (1) and B (2), were isolated from a 95% ethanolic extract of roots of Albizia adianthifolia. Their structures were elucidated mainly by using a combination of 600 MHz 1D and 2D NMR techniques (COSY, NOESY, TOCSY, HSQC, and HMBC) and by FABMS and HRESIMS. Compounds 1 and 2 were characterized as glycosides of acacic acid acylated by an o-hydroxybenzoyl unit. The crude saponin mixture (CSM), compounds 1 and 2 together with 3 and 4 (prosapogenins obtained from the mild alkaline hydrolysate of the CSM), were evaluated for immunomodulatory activity on the Jurkat T cell line and for hemolytic property against s…

ErythrocytesStereochemistrySaponinPharmaceutical ScienceAlbizziaPharmacognosy01 natural sciencesHemolysisPlant Roots[ CHIM ] Chemical SciencesHydrolysateAnalytical Chemistry[ SDV.EE ] Life Sciences [q-bio]/Ecology environmentJurkat CellsTriterpeneAdjuvants ImmunologicDrug DiscoveryAnimalsHumans[CHIM]Chemical SciencesOleanolic AcidNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classification[SDV.EE]Life Sciences [q-bio]/Ecology environmentPlants MedicinalSheepbiologyDose-Response Relationship DrugMolecular Structure010405 organic chemistryOrganic ChemistryGlycosideBiological activityAcetylationSaponinsbiology.organism_classificationAntineoplastic Agents PhytogenicTerpenoidTriterpenes0104 chemical sciences010404 medicinal & biomolecular chemistryCote d'IvoireComplementary and alternative medicinechemistryMolecular MedicineSalicylic AcidAlbizia adianthifolia
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Caffeate and piperidine-3-ol derivatives from the stem bark of Cassia sieberiana

2019

A new caffeate derivative from the ethanol extract of the stem bark of Cassia sieberiana DC. is described herein along with the known secondary metabolites spectaline (2), iso-6-cassine (3), 3-O-methyl-chiro-inositol (4), monobehenin (5), octyl nonadecyloate (6), β-sitosterol (7), stigmasterol (8) and sitosterol 3-O-β-D-glucopyranoside (9). The chemical structures were elucidated by means of various spectroscopic and spectrometric techniques. Extract and isolated compounds were devoid of inhibitory action against the herein selected bacterial strains (MICs > 256 μg/mL) but showed capacities to reduce 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical (EC50 < 3 μg/mL) considerably better than the …

EthanolStigmasterolbiology010405 organic chemistryDPPHOrganic ChemistryPlant Sciencebiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistry010404 medicinal & biomolecular chemistrychemistry.chemical_compoundCassia sieberianachemistryPiperidineTroloxAntibacterial activityNuclear chemistryEC50Natural Product Research
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Hastifolins A-G, antefeedant neo-clerodane diterpenoids from Scutellaria hastifolia

2010

From the aerial parts of Scutellaria hastifolia, family Lamiaceae (Labiatae), seven neo-clerodane diterpenoids (hastifolins A-G) were isolated. The products are similar to the known scuteparvin and are characterized by being trans-cinnamoyl derivatives. Structures and stereochemistry were determined by intensive NMR investigation. Six of the products form three pairs of epimers at C-13. Hastifolins A-C showed significant antifeedant activity.

Family LamiaceaeStereochemistryScutellariaChemical structurePlant ScienceHorticultureSpodopteraBiochemistryDiterpenes Clerodanechemistry.chemical_compoundFeeding behaviorAnimalsMolecular BiologyNuclear Magnetic Resonance BiomolecularbiologyMolecular StructureGeneral MedicineFeeding BehaviorSettore CHIM/06 - Chimica Organicabiology.organism_classificationTerpenoidchemistryLarvaScutellariaLamiaceaeEpimerDiterpeneScutellaria hastifolia Lamiaceae diterpenes neo-clerodanes epimers antifeedant
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Chemical composition of the essential oil from different vegetative parts of Foeniculum vulgare subsp. piperitum (Ucria) Coutinho (Umbelliferae) grow…

2021

In the present study, the chemical compositions of the essential oils from roots, stems, leaves and fruits of Foeniculum vulgare subsp. piperitum collected in Sicily were evaluated by GC and GC-MS. The main components of the roots were terpinolene (33.15%), gamma-terpinene (12.18%) and fenchyl acetate (11.23%). Stems and leaves were very rich in alpha-phellandrene (36.85% and 41.59%, respectively) and beta-phellandrene (19.68% and 25.79%, respectively), whereas the main components of fruits were terpinolene (20.10%) and limonene (17.84%)These results were compared with those of the EOs of the same vegetative parts of Foeniculum vulgare subsp. vulgare, collected in the same station and in th…

FoeniculumPlant ScienceFoeniculum vulgare subsp. vulgareBiologySubspecies01 natural sciencesBiochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawβ phellandreneChemical compositionEssential oilLimoneneterpinoleneApiaceae010405 organic chemistryOrganic Chemistrybiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistryHorticultureFoeniculum vulgare subsp. piperitumchemistryvolatile componentsβ-phellandreneα-phellandreneEstragoleApiaceaeNatural Product Research
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Chemical and spectroscopic characteristics of the wood of Vitis vinifera cv. Sangiovese affected by esca disease.

2009

Chemical and spectroscopic analyses ((13)C cross-polarization-magic angle spinning NMR and attenuated total reflection Fourier transform infrared spectroscopies) were carried out on the wood of Vitis vinifera cv. Sangiovese with brown-red discoloration and black streaks caused by esca disease. The analyses of the brown-red wood revealed the destruction of hemicelluloses and noncrystalline cellulose as well as modifications in the pectic and ligninic wood fractions. The pectic fraction consisted of carbohydrates associated with polyphenols. The lignin fraction exhibited only a few changes in the aromatic systems and a partial demethylation, and it appeared to be associated with condensed phe…

Fomitiporia mediterraneaSettore AGR/13 - Chimica AgrariaPhaeomoniella chlamydosporaChemical Fractionationcomplex mixturesesca diseasechemistry.chemical_compoundSpectroscopy Fourier Transform InfraredLigninOrganic chemistryVitisCelluloseCelluloseChemical compositionNuclear Magnetic Resonance BiomolecularPlant Diseasesbiologybiology.plant_disease_causetechnology industry and agriculturegrapevine woodfood and beveragesGeneral Chemistry13C CP-MAS NMRSerial ExtractionWoodPhaeoacremonium aleophilumchemistryPolyphenolAttenuated total reflectionVitis viniferaGeneral Agricultural and Biological SciencesNuclear chemistryJournal of agricultural and food chemistry
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Computing Metal-Binding Proteins for Therapeutic Benefit

2021

Over one third of biomolecules rely on metal ions to exert their cellular functions. Metal ions can play a structural role by stabilizing the structure of biomolecules, a functional role by promoting a wide variety of biochemical reactions, and a regulatory role by acting as messengers upon binding to proteins regulating cellular metal-homeostasis. These diverse roles in biology ascribe critical implications to metal-binding proteins in the onset of many diseases. Hence, it is of utmost importance to exhaustively unlock the different mechanistic facets of metal-binding proteins and to harness this knowledge to rationally devise novel therapeutic strategies to prevent or cure pathological st…

Functional roleModels MolecularMetalloenzymesCellular functionsMetallo enzymeMolecular ConformationComputational biologyMolecular Dynamics01 natural sciencesBiochemistryQM/MMDockingMetals HeavyDrug DiscoveryBiochemical reactionsMetal transportersGeneral Pharmacology Toxicology and PharmaceuticsPharmacology010405 organic chemistryOrganic ChemistryComputational BiologyMetal binding proteins0104 chemical sciences010404 medicinal & biomolecular chemistryDocking (molecular)Settore CHIM/03 - Chimica Generale E InorganicaMolecular MedicineCarrier Proteins
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Isolactarane and Sterpurane Sesquiterpenoids from the Basidiomycete Phlebia uda

2012

Three new sesquiterpenoids, named udasterpurenol A, udalactarane A, and udalactarane B, as well as the known compounds hyphodontal and sterpuric acid have been isolated from the basidiomycete Phlebia uda. These compounds represent the first natural products described from this species. The structures were elucidated by NMR spectroscopy and mass spectrometry. Udalactaranes A and B were isolated as mixtures with their respective epimeric acetals. These mixtures inhibited the spore germination of the plant pathogenic fungus Fusarium graminearum at 10 and 5 μg/mL, respectively, and were active against Jurkat cells with IC(50) values of 101 and 42 μM, respectively.

FusariumStereochemistryPharmaceutical ScienceMicrobial Sensitivity TestsMass spectrometryAnalytical ChemistryInhibitory Concentration 50Jurkat CellsFusariumDrug DiscoveryIc50 valuesSpore germinationHumansNuclear Magnetic Resonance BiomolecularPharmacologyMolecular StructurebiologyBasidiomycotaOrganic ChemistryBasidiomycotaNuclear magnetic resonance spectroscopyPathogenic fungusbiology.organism_classificationPhlebia udaComplementary and alternative medicineMolecular MedicineSesquiterpenesJournal of Natural Products
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Comparison of the Fungistatic Activity of Selected Essential Oils Relative to Fusarium graminearum Isolates

2019

The aim of the study was to determine the chemical composition of lemon, rosewood, geranium and rosemary oils, and compare their effect on the sensitivity of Fusarium graminearum ZALF 24 and Fusarium graminearum ZALF 339 isolated from infected cereals. The tested oils were added to Potato Dextrose Agar (PDA) medium at concentrations of 0.125%, 0.25%, 0.5%, 1.0% and 2.0%. The activity of the oils on inhibition of the linear growth of mycelium was evaluated by measuring the growth of fungal colonies (growth index), while the fungistatic activity was evaluated on the basis of the percentage growth inhibition of a fungal colony and calculated according to Abbott&rsquo

Fusariumlemon oilPharmaceutical Science01 natural sciencesAnalytical Chemistrylcsh:QD241-44103 medical and health scienceschemistry.chemical_compoundlcsh:Organic chemistrygeranium oilDrug Discoveryrosemary oilFood sciencePhysical and Theoretical ChemistryROSEMARY OILessential oilsMycelium<i>Fusarium graminearum</i>030304 developmental biology0303 health sciencesbiologyOrganic Chemistryrosewood oilfood and beveragesbiology.organism_classificationRosewood0104 chemical sciencesRosewood oil010404 medicinal & biomolecular chemistryFusarium graminearumchemistryChemistry (miscellaneous)GeraniumMolecular MedicinePotato dextrose agarGrowth inhibitionMolecules
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Molecular recognition of nucleotides in water by scorpiand-type receptors based on nucleobase discrimination.

2014

Abstract: The detection of nucleotides is of crucial impor-tance because they are the basic building blocks of nucleicacids. Scorpiand-based polyamine receptors functionalizedwith pyridine or anthracene units are able to form stablecomplexes with nucleotides in water, based on coulombic,p–p stacking, and hydrogen-bonding interactions. This be-havior has been rationalized by means of an explorationwith NMR spectroscopy and DFT calculations. Binding con-stants were determined by potentiometry. Fluorescencespectroscopy studies have revealed the potential of these re-ceptors as sensors to effectively and selectively distinguishguanosine-5’-triphosphate (GTP) from adenosine-5’-triphos-phate (ATP…

GTP'StereochemistryStackingSupramolecular chemistrysensorsCatalysissupramolecular chemistryNucleobaseMolecular recognitionAdenosine TriphosphateMoleculeNucleotidescorpiandsNuclear Magnetic Resonance Biomolecularchemistry.chemical_classificationMolecular StructureNucleotidesOrganic ChemistryWaterHydrogen BondingGeneral ChemistryNuclear magnetic resonance spectroscopyModels TheoreticalSpectrometry Fluorescencechemistrymolecular recognitionGuanosine TriphosphateChemistry (Weinheim an der Bergstrasse, Germany)
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