Publications by authors named "Matteo A Tallarida"

Article Synopsis
  • - The study focuses on creating hybrid molecules as a strategy for drug discovery, emphasizing the significance of 1,2,3-triazole as a key component in medicinal chemistry.
  • - Researchers designed and synthesized new 1,2,3-triazole hybrids incorporating isatine and phenolic elements, utilizing a click chemistry approach for efficient synthesis.
  • - A molecular docking study identified four therapeutic targets for these hybrids, with the most promising results related to 5-lipoxygenase, which plays a role in inflammation.
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  • - Naringenin (NRG) is shown to counteract mitochondrial dysfunction, which is important in preventing cardiovascular diseases, by selectively inhibiting the FF-ATPase enzyme involved in ATP hydrolysis.
  • - NRG interacts with FF-ATPase in a way that blocks energy transmission, particularly when calcium (Ca) ions are present, illustrating its preference for the enzyme activated by Ca over magnesium (Mg).
  • - The study indicates that NRG helps protect against cell injury in cerebral endothelial cells, restoring cell viability and function after salt-induced damage, while also improving mitochondrial activity.
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  • A method for creating polysubstituted spirocyclopropyl oxindoles using rare-earth metal salts, specifically Sc(OTf), has been developed.
  • This technique involves a multicomponent reaction that showcases high diastereoselectivity, achieving ratios of up to 94:6 for the different isomers.
  • Computational studies suggest that the unique properties of the metal, such as its ability to coordinate and its preference for oxygen, are crucial in producing the predominant isomer in the reaction.
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In this paper, we evaluated the potential of two synthesized bio-based polyurethane foams, PU1 and PU2, for the removal of diesel and gasoline from water mixtures. We started the investigation with the experiment in batch. The total sorption capacity S (g/g) for the diesel/water system was slightly higher with respect to gasoline/water, with a value of 62 g/g for PU1 and 65 g/g for PU2.

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An efficient, eco-compatible, and very cheap method for the construction of fully substituted pyrazoles (Pzs) via eliminative nitrilimine-alkene 1,3-dipolar cycloaddition (ENAC) reaction was developed in excellent yield and high regioselectivity. Enaminones and nitrilimines generated in situ were selected as dipolarophiles and dipoles, respectively. A deep screening of the employed base, solvent, and temperature was carried out to optimize reaction conditions.

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1,2,3-triazoles are versatile building blocks with growing interest in medicinal chemistry. For this reason, organic chemistry focuses on the development of new synthetic pathways to obtain 1,2,3-triazole derivatives, especially with pyridine moieties. In this work, a novel series of 1,5-disubstituted-1,2,3-triazoles functionalized with pyrimidine nucleobases were prepared via 1,3-dipolar cycloaddition reaction in a regioselective manner for the first time.

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Aminyl radicals are nitrogen-centered radicals of interest in synthetic strategies involving C-N bond formation due to their high reactivity. These intermediate radicals are generated by the reaction of an organic azide with tributyltin hydride (BuSnH) in the presence of substoichiometric amounts of azobisisobutyronitrile (AIBN). In this work, we report the regioselective rearrangement of azanorbornanic ([2.

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The compromised viability and function of cardiovascular cells are rescued by small molecules of triazole derivatives (Tzs), identified as 3a and 3b, by preventing mitochondrial dysfunction. The oxidative phosphorylation improves the respiratory control rate in the presence of Tzs independently of the substrates that energize the mitochondria. The FF-ATPase, the main candidate in mitochondrial permeability transition pore (mPTP) formation, is the biological target of Tzs and hydrophilic F domain of the enzyme is depicted as the binding region of Tzs.

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In the present work, we proved the efficacy of cellulose citrate to remove methylene blue (MB) from artificially contaminated water. MB is a widely used dye, but because of its chemical aromatic structure, it is significantly stable with quite slow biodegradation, causing consequent serious health problems for people and significant environmental pollution. Cellulose citrate, the bio-adsorbent proposed and studied by us to remediate water polluted by MB, is produced by a green, cheap and fast procedure that makes use of two abundant natural products, cellulose and citric acid.

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A novel series of bio-based polyurethane composite foams was prepared, employing a cellulose-derived polyol for chain extension and cellulose-citrate as a thickener additive. The utilized polyol was obtained from the reduction reaction of cellulose-derived bio-oil through the use of sodium borohydride and iodine. Primarily, we produced both rigid and flexible polyurethane foams through chain extension of the prepolymers.

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In this study we evaluated the oil adsorption capacity of an aliphatic polyurethane foam (PU ) and two of its composites, produced through surface coating using microparticles of silica (PU-Si ) and activated carbon (PU-ac ). The oil adsorption capacity in diesel was improved up to 36% using the composite with silica and up to 50% using the composite with activated carbon with respect to the initial PU . Excellent performances were retained in gasoline and motor oil.

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The mitochondrial permeability transition pore (mPTP), a high-conductance channel triggered by a sudden Ca concentration increase, is composed of the F F -ATPase. Since mPTP opening leads to mitochondrial dysfunction, which is a feature of many diseases, a great pharmacological challenge is to find mPTP modulators. In our study, the effects of two 1,5-disubstituted 1,2,3-triazole derivatives, five-membered heterocycles with three nitrogen atoms in the ring and capable of forming secondary interactions with proteins, were investigated.

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Nucleobase-containing isoxazolidines spiro-bonded to an indane core have been synthesized in very good yields by regio- and diastereoselective 1,3-dipolar cycloaddition starting from indanyl nitrones and -vinylnucleobases by using environmentally benign microwave technology. The contemporary presence of various structural groups that are individually active scaffolds of different typology of drugs, has directed us to speculate that these compounds may act as inhibitors of MDM2-p53 interaction. Therefore, both computational calculations and antiproliferative screening against A549 human lung adenocarcinoma cells and human SH-SY5Y neuroblastoma cells were carried out to support this hypothesis.

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A series of ketonitrones derived from isatin and indanone (INs) were synthesized and evaluated for their antiproliferative activities against several human cancer cell lines. Then, the antioxidant properties of these substrates were measured by the DPPH test to report their biological activity in terms of their action. In particular, one substrate has showed very high biological and scavenging activity, probably due to the strong correlation between its spin trapping activity and structure.

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