Search results for "Farmaceutica"

showing 10 items of 582 documents

Le farmacie tra mercato e contratto: alcune riflessioni sugli strumenti civilistici di trasferimento intergenerazionale

2012

farmacie trust donazione modale legislazione farmaceuticaSettore IUS/01 - Diritto Privato
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Biofilm capability of staphylococcus strains isolated from food and the anti-biofilm activity of a chemically synthesized pyrrolomycin

2018


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food isolatespyrrolomycinSettore BIO/19 - Microbiologia GeneraleSettore CHIM/08 - Chimica FarmaceuticaAntibiofilm
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HSV-1 Glycoprotein D and Its Surface Receptors: Evaluation of Protein–Protein Interaction and Targeting by Triazole-Based Compounds through In Silico…

2023

Protein–protein interactions (PPI) represent attractive targets for drug design. Thus, aiming at a deeper insight into the HSV-1 envelope glycoprotein D (gD), protein–protein docking and dynamic simulations of gD-HVEM and gD-Nectin-1 complexes were performed. The most stable complexes and the pivotal key residues useful for gD to anchor human receptors were identified and used as starting points for a structure-based virtual screening on a library of both synthetic and designed 1,2,3-triazole-based compounds. Their binding properties versus gD interface with HVEM and Nectin-1 along with their structure-activity relationships (SARs) were evaluated. Four [1,2,3]triazolo[4,5-b]pyridines were i…

glycoprotein DOrganic Chemistrymolecular dynamics simulationsGeneral MedicineHSV-1Settore CHIM/08 - Chimica FarmaceuticaCatalysisComputer Science ApplicationsInorganic Chemistryprotein–protein interactionprotein–protein interaction; HSV-1; 123-triazoles; docking; molecular dynamics simulations; glycoprotein Ddocking123-triazolesPhysical and Theoretical ChemistryMolecular BiologySpectroscopyInternational Journal of Molecular Sciences
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COUPLING ELECTROCHEMISTRY TO ELECTROSPRAY: A NOVEL PREPARATION OF GOLD NANOSTRUCTURES

2013

nanoparticles on ITO (Indium tin oxide) coated glass using the electrospray (ESI) method Method:The starting point of this study is that the ESI/MS spectrum (Figure 1) of an ethanolic solution of HAuCl 4 shows a reduction process of Au (III) strongly dependent on the Cone Voltage (CV) values (20, 80, 150 V), affording to the ion at m/z 197 (Au+). Further, the decrease of the abundance of this ion at the highest cone voltage suggests the subsequent its reduction with the formation of Au 0 . Figure 1: ESI/MS spectra of an ethanolic solution of HAuCl4 at various cone voltages: Conclusion: Such experimental evidence leads us to use electrospray technique as a preparative tool to obtain the form…

gold nanoparticles electrospray S.E.M.Settore CHIM/01 - Chimica AnaliticaSettore CHIM/08 - Chimica FarmaceuticaSettore CHIM/02 - Chimica Fisica
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Editorial: Emerging heterocycles as bioactive compounds

2023

Heterocycles represent a privileged scaffold due to their ability to interact with biological systems via heteroatoms. It is no coincidence that every year the Food and Drug Administration approves numerous new drugs that contain at least one heterocyclic system as active pharmacophoric part in their structure. Many heterocyclic compounds with therapeutic properties, including anticancer, antimicrobial, anti-inflammatory and so on, come from natural sources such as plants and animals, and medicinal chemists very often use them to study their chemical space and improve their biological activity. In fact, several efficient approaches for the formation of aromatic heterocyclic compounds and th…

heterocycles new chemical entities natural products purine nucleoside phosphorylase pantetheinase sulfhydrylase activity quinazolineGeneral ChemistrySettore CHIM/08 - Chimica FarmaceuticaFrontiers in Chemistry
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The Role of 1,3-Dipolar Cycloaddition Reactions in the Design and Synthesis of Complex Heterocyclic Scaffolds with Anti-tumor/Anti-infective Activity

2009

heterocyclic scaffoldanti-infective activity13-dipolar cycloaddition reactionanti-tumor activitySettore CHIM/08 - Chimica Farmaceutica
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New imidazo[1,2-c]pyrrolo[3,2-e]pyrimidinone derivatives as potential DNA-binders

2008

imidazo[12-c]pyrrolo[32-e]pyrimides DNA-bindersSettore CHIM/08 - Chimica Farmaceutica
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An Updated Review on the Synthesis and Antibacterial Activity of Molecular Hybrids and Conjugates Bearing Imidazole Moiety

2020

The rapid growth of serious infections caused by antibiotic resistant bacteria, especially the nosocomial ESKAPE pathogens, has been acknowledged by Governments and scientists and is one of the world’s major health problems. Various strategies have been and are currently investigated and developed to reduce and/or delay the bacterial resistance. One of these strategies regards the design and development of antimicrobial hybrids and conjugates. This unprecedented critical review, in which our continuing interest in the synthesis and evaluation of the bioactivity of imidazole derivatives is testified, aims to summarise and comment on the results obtained from the end of the 1900s until Februa…

imidazoles molecular hybrids molecular conjugates antibacterials antibiotic resistance synthesis bioactivity antibioticsantibiotic resistancesynthesismedicine.drug_classAntibioticsPharmaceutical ScienceReviewMicrobial Sensitivity Tests010402 general chemistry01 natural sciencesantibioticsAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundAntibiotic resistancelcsh:Organic chemistryDrug DiscoveryDrug Resistance BacterialmedicineImidazoleMoietyPhysical and Theoretical Chemistryantibacterialsmolecular conjugatesBacteria010405 organic chemistrymolecular hybridsOrganic ChemistryImidazolesSettore CHIM/06 - Chimica OrganicaBacterial InfectionsAntimicrobialCombinatorial chemistrySettore CHIM/08 - Chimica Farmaceutica0104 chemical sciencesAnti-Bacterial AgentschemistryChemistry (miscellaneous)bioactivityMolecular MedicineAntibacterial activityLinkerConjugateMolecules
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DA-Phen, a new dopamine aminoacid conjugate: in vivo testing and molecular modeling as dopaminergic modulator

2014

in vivo testingDopaminergic modulatormolecular modelingSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSettore BIO/14 - FarmacologiaSettore CHIM/08 - Chimica Farmaceuticaaminoacid conjiugate
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DERIVATI TIENO[3,2-d]-1,2,3-TRIAZIN-4(3H)ONI ANELLATI:UNA NUOVA CLASSE DI INIBITORI DI AURORA CHINASI A

2012

inibitoriAurora chinasi ASettore CHIM/08 - Chimica Farmaceuticatienotriazinoni
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