Search results for "Farmaceutica"

showing 10 items of 582 documents

Nuovi inibitori di Aurora chinasi A come target biologico coinvolto nei processi carcinogenici

2011

Identificando Aurora chinasi A come target elettivo per l’inibizione dell’espansione tumorale è stato sfruttato l’approccio computazionale per effettuare un virtual screening su una libreria “in house” di strutture molecolari. L’analisi dei dati computazionali ha permesso di identificare nei derivati della serie pirido[3’,2’:4,5]furo[3,2-d]-1,2,3-triazin-4(3H)one di tipo 3 nuovi composti a potenziale attività inibitoria sul sito ATP-asico di Aurora chinasi A. La sintesi del sistema triciclico-eteroaromatico 3 prevede la diazotazione della 3-amino-furopiridina 1 e conseguente reazione di copulazione con una serie di ammine primarie opportunamente scelte, permettendo l’isolamento delle 3-tria…

Aurora chinasi A antitumorale pirido[3’2’:45]furo[32-d]-123-triazin-4(3H)one triazeniSettore CHIM/08 - Chimica Farmaceutica
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Evaluación etnobotanica de la Yareta (Azorella compacta) en Arequipa (Perú) y sus posibles aplicaciones

2013

Abstract – Ethnobotanical study of the Yareta Arequipa plant (Azorella compacta Phil) and its possible applications. – The aim of this work is the ethnobotanical characterisation of the Yareta Arequipa plant (Azorella compacta Phil), to report indications about the uses of the Yareata plant by “Salinas y Aguada Blanca” National Reserve (RNSAB) populations and to find its possible applications. The survey has been lead on nine communities of the Arequipa Region (Peru), it concerned the actual degree of conservation of the plants, the botanical description and classification, the ecological characterization, the use and the distribution in ethnomedicine and ethnopharmacology and all the uses …

Azorella compacta Phil ethnobotany biodiversity plant preservationSettore BIO/15 - Biologia FarmaceuticaSettore AGR/02 - Agronomia E Coltivazioni Erbacee
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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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Docking of indolo- and pyrrolo-pyrimidines to DNA. New DNA-interactive polycycles from amino-indoles/pyrroles and BMMA

2004

New indolo- and pyrrolo-pyrimidines of type 1-4 were studied for their ability to form stable complexes with DNA fragments. The calculated free energies of binding were found in the range -8.39 ÷ -16.72 Kcal/mol. The docking studies revealed a common binding mode with the chromophore intercalated between GC base pairs whereas the side chain lies along the minor groove.

Base pairStereochemistryOrganic ChemistryChromophoreSettore CHIM/08 - Chimica Farmaceuticalcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrychemistryDocking (molecular)Docking DNA interaction indolopyrimidine pyrrolopyrimidine aminoindoles aminopyrroles BMMASide chainFree energiesDNAMinor groove
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Pharmacophore modeling e screening in silico di nuovi inibitori della proteina antiapoptotica Bcl-xl

2008

Bcl-xlpharmacophore modelingin silico screeningapoptosiSettore CHIM/08 - Chimica Farmaceutica
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Synthesis, antiproliferative activity, and mechanism of action of new benzamido derivatives

2011

The cinnamoyl anthranilamides represent a class of biological active substances of great importance in medicinal chemistry. Moreover, despite their wide range of biological activities, a review of the literature revealed that no anticancer activity is described for this kind of substances. Starting from the 2-cinnamamido-5-iodobenzamide, resulted able to inhibit the leukemic cell line K-562 proliferation with a percent of inhibition of 74% at 10M concentration, we undertake the following structural modifications on cinnamamidobenzamide skeleton: the introduction of various substituents both on the benzamido and the cinnamamido moieties, the substitution of olefinic bond with the ethane, et…

Benzamido derivatives antiproliferative activity cell cycleSettore CHIM/08 - Chimica Farmaceutica
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Immuno-oncological treatment of Non-Small-Cell Lung Cancer (NSCLC) in advanced stage with Nivolumab

2023

Immuno-oncology marked a therapeutic revolution in the treatment of cancer. Thanks to the new strategy that aims to awaken the immune system to fight cancer cells, there has been a change in the clinical course in the treatment of advanced Non-Small Cell Lung Cancer (NSCLC). Our study aimed to evaluate the therapeutic efficacy of nivolumab monotherapy in the treatment of patients with advanced stage IIIB/IV non-small cell lung cancer beyond the second line. The results showed a progression-free survival of 7.35 months and an improvement in the quality of life of patients compared to other treatments. In addition, no type 3 and type 4 adverse reactions were detected in patients treated with …

Biochemistry (medical)Settore BIO/14 - FarmacologiacancerPlant ScienceSettore MED/49 - Scienze Tecniche Dietetiche Applicateimmuno-oncologyNivolumab.Settore CHIM/08 - Chimica FarmaceuticaGeneral Biochemistry Genetics and Molecular Biologylung
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The Essential Oil of Thymbra capitata and its Application as A Biocide on Stone and Derived Surfaces

2019

Many chemicals used nowadays for the preservation of cultural heritage pose a risk to both human health and the environment. Thus, it is desirable to find new and eco-friendly biocides that can replace the synthetic ones. In this regard, plant essential oils represent effective alternatives to synthetic substances for the preservation of historical monuments. Thymbra capitata (syn. Thymus capitatus) is a medicinal and aromatic plant growing in the Mediterranean area and endowed with important pharmacological properties related to its essential oil. Among them, the antimicrobial ones make the T. capitata essential oil an ideal candidate for industrial applications

BiocideStone surface<i>Thymbra capitata</i>02 engineering and technologyPlant Science01 natural sciencesThymbra capitataessential oillaw.inventionchemistry.chemical_compoundHuman healthfoodstone surfaceslawnatural biocideThymbra capitataCarvacrolSettore BIO/15 - Biologia FarmaceuticaEcology Evolution Behavior and SystematicsEssential oilSettore CHIM/02 - Chimica FisicaEcology010405 organic chemistryChemistrybiological inhibitionBotanySettore CHIM/06 - Chimica Organicacultural heritage021001 nanoscience & nanotechnologyPulp and paper industryfood.food0104 chemical sciencesbiodeteriogensPickering emulsionQK1-989CapitataBiodeteriogenMediterranean areaThymus capitatus0210 nano-technologyPlants
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Chemical composition of essential oil from Italian populations of Artemisia alba Turra (Asteraceae).

2012

The use of essential oils as chemotaxonomic markers could be useful for the classification of Artemisia species and to caracterize biodiversity in the different populations. An analysis of the chemical composition of four essential oils from Italian populations of Artemisia alba Turra (collected in Sicily, Marche and Abruzzo) was investigated. In this paper an in depth study of the significant differences observed in the composition of these oils is reported.

BiodiversityPharmaceutical ScienceGas Chromatography-Mass SpectrometryArticleessential oilAnalytical Chemistrylaw.inventionArtemisia albalawDrug DiscoveryBotanyOils VolatilePlant OilsSettore BIO/15 - Biologia FarmaceuticaPhysical and Theoretical ChemistryChemical compositionArtemisia alba; essential oil; biodiversity; α-bisabolone oxide A; davanone DEssential oilα-bisabolone oxide AbiologyEcologyOrganic Chemistryfood and beveragesdavanone DSettore CHIM/06 - Chimica OrganicaBiodiversityAsteraceaebiology.organism_classificationArtemisiaItalyChemistry (miscellaneous)MonoterpenesMolecular MedicineArtemisia<em>Artemisia alba</em>; essential oil; biodiversity; α-bisabolone oxide A; davanone DMolecules (Basel, Switzerland)
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Chemical Composition of the Essential Oils of Three Species of the Apiaceae Family Growing Wild in Sicily: Bonannia graeca, Eryngium maritimum and Op…

2013

n the present study the chemical composition of the essential oils from aerial parts of Bonannia graeca (L.) Halácsy and Opopanax chironium (L.) Kock, and from aerial parts and roots of Eryngium maritimum L. was evaluated by GC and GC-MS. α-Pinene (15.2%) and β-pinene were recognized as the main constituents of B. graeca, whereas the aerial parts of O. chironium contained mainly the diterpene cembrene and the coumarin angelicin. In both aerial parts and roots of E. maritimum germacrene D (10.4% and 15.9%, respectively) and 2,4,5-trimethylbenzaldehyde (8.3% and 6.7%) were the most abundant components

Bonannia graecaCembreneα-pineneEryngium maritimumSettore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia FarmaceuticaGermacrene DOpopanax chironiumEssential oilApiaceae
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