Search results for "Farmaceutica"

showing 10 items of 582 documents

Ni(II) and Zn(II) Schiff Base complexes: B-DNA vs G4-DNA binding

2015

Settore CHIM/03 - Chimica Generale E InorganicaSettore BIO/10 - BiochimicaSettore CHIM/08 - Chimica FarmaceuticaNi(II) Schiff bases Zn(II) Schiff bases complexes with B-DNA complexes with G4-DNA
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The influence of substitution in the quinoxaline nucleus on 1,3-dipolar cycloaddition reactions

2013

The reaction mechanism of 1,3-dipolar cycloadditions of both symmetric and unsymmetric benzo-condensed diazines with a nitrilimine dipole, to give two different mono- and bis-cycloadducts, in tetrahydrofuran (THF) solution, was studied by DFT calculatio ns. The results obtained show that each 1,3-dipolar cycloaddition reaction always proceeds by a two steps mechanism, in which the first intermediate shows only one covalent bond between the beta carbon of the nitrilimine and the aromatic nitrogen of the diazine molecule. The structure and energy content of the two transition states of the two cycloaddition steps, in the case of the unsymmetric benzo-condensed diazine, nicely explains why the…

Settore CHIM/03 - Chimica Generale E InorganicaSettore CHIM/08 - Chimica FarmaceuticaDFT calculations 13-Dipolar cycloaddition reactions Quinoxalines Reaction mechanism
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Design of copper(II) complexes as potential anticancer prodrugs

The fibroblast growth factor receptors (FGFR) are tyrosine kinases that are present in many types of endothelial and tumor cells and play an important role in cell growth, survival, and migration as well as in maintaining tumor angiogenesis (1). FGFR genetic alterations are frequently observed in cancer, suggesting that FGFR inhibition may be a promising therapy in patients harboring these lesions (2). In particular, molecules with structural properties similar to Ponatinib, a known inhibitor of FGFR, that shows a selective interaction for the ATP binding site of the isoform 4 of these receptors (FGFR4), are being considered. Molecular modeling studies have been conducted to design novel po…

Settore CHIM/03 - Chimica Generale E Inorganicacopper(II) complexesFGFR4PonatinibSettore CHIM/08 - Chimica Farmaceutica
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The Interaction of Small Molecules with Biomolecules

2014

The binding of small molecules with biological targets is associated to interesting chemical and biological properties of the resulting supramolecular systems. We have recently reported on the synthesis and characterization of cationic first row transition metal complexes and the study of their DNA binding properties, in aqueous solutions at neutral pH, essentially investigated by viscosimetry and spectroscopic techniques such as circular dichroism, absorption and fluorescence in the UV-visible wavelength range. Of course, such procedure cannot furnish atomic level details of the molecule-DNA interaction. Computational Chemistry may provide support for the interpretation of experimental dat…

Settore CHIM/03 - Chimica Generale E Inorganicatransition metal complexes DNA binding properties Molecular Dynamics G-quadruplexSettore CHIM/08 - Chimica Farmaceutica
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Bioactive Azoles with Three Heteroatoms

2010

This issue is dedicated to scientists belonging to either or both the fields of heterocyclic and medicinal chemistry. Nowadays, pharmaceutical industries are more and more dedicating their research towards different use or applications of the same molecule rather than towards the development of new drugs. In the latter decades, in fact, the time which is necessary since a given molecule is synthesized to when it is approved as a drug has significantly increased. Therefore, the development of time-saving methodologies such as combinatorial chemistry and computationally driven drug design has attracted the interest of several organic and medicinal chemists. Many of the molecules tested in-vit…

Settore CHIM/06 - Chimica OrganicaBioactive Compounds Azoles HeterocyclesSettore CHIM/08 - Chimica Farmaceutica
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Essential oil composition and antibacterial activity of Anthemis mixta L. and Anthemis tomentosa L. (Asteraceae)

2012

In the present study the chemical composition of the essential oils from aerial parts and roots of Anthemis mixta L. and A. tomentosa L. was evaluated by GC and GC-MS, and their antibacterial activity tested against ten bacterial species. Hexadecanoic acid (15.2%) was recognized as the main constituent of A. mixta, together with τ-cadinol (6.7%), while in both aerial parts and roots of A. tomentosa nonacosane (21.9% and 20.7%), heptacosane (8.1% and 6.0%), hexadecanoic acid (8.1% and 27.1%) and hexahydrofarnesylacetone (6.8% and 5.5%) prevailed. The oils from aerial parts of both species showed a good activity against Gram-positive bacteria. These results suggest that the plants could be po…

Settore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia FarmaceuticaEssential oil antibacterial activity Anthemis mixta L. Anthemis tomentosa L. Asteraceae
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Sintesi e valutazione biologica di 1,2,4-ossadiazoli analoghi del Linezolid

2011

Settore CHIM/06 - Chimica Organicaoxadiazoles Linezolid anti-microbials oxazolidinonesSettore CHIM/08 - Chimica Farmaceutica
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Synthesis and biological evaluation of new 1,2,4-oxadiazole derivatives of Topsentin

Settore CHIM/08 - Chimica Farmaceutica124-oxadiazoles Topsentin Topsentin derivatives 124-oxadiazole topsentin derivatives
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ANALOGHI DELL'ALCALOIDE MARINO NORTOPSENTINA: SINTESI ED ATTIVITA' ANTITUMORALE

2009

Settore CHIM/08 - Chimica FarmaceuticaANALOGHI DELL'ALCALOIDE MARINO NORTOPSENTINA
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NEW 5-DIMETHYL-3-HETEROARYL-1H-4-ONN-AZOXYCYANIDES: SYNTHESIS AND ANTIMICOTICAL ACTIVITY.

2014

In the field of infectious diseases, in the last years an increasingly high importance is ascribed to mycosis as causes of illness and mortality in particularly susceptible patients: leukemia, organ transplant, AIDS and immunosuppressed patients, creating clinical and epidemiological problems. Although several drugs are available, antifungal spectrum is still limited especially for invasive infections, which often have fatal results. We previously reported the 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 rin…

Settore CHIM/08 - Chimica FarmaceuticaAZOXYCYANIDES ANTIMICOTICAL AGENTS
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