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1.
Chem Biol Drug Des ; 91(2): 463-477, 2018 02.
Article in English | MEDLINE | ID: mdl-28905525

ABSTRACT

Due to the scarce biological profile, the pyrazolo[1,2-a]benzo[1,2,3,4]tetrazine-3-one scaffold (PBT) has been recently explored as promising core for potential anticancer candidates. Several suitably decorated derivatives (PBTs) exhibited antiproliferative activity in the low-micromolar range associated with apoptosis induction and cell cycle arrest on S phase. Herein, we selected the most active derivatives and submitted them to further biological explorations to deepen the mechanism of action. At first, a DNA targeting is approached by means of flow Linear Dichroism experiments so as to evaluate how small planar molecules might interact with DNA, including the interference with the catalytic cycle of topoisomerase II and the influence on the cleavable complex stabilization (poisoning effect). In support of the experimental data, in silico studies have been achieved to better understand the chemical space of the interactions. Interestingly some meaningful structural features, useful for further developments, were found. The 8,9-di-Cl substituted derivative revealed as the most effective in the intercalative process, as well as on the inhibition of catalytic activity of topoisomerase II. Predicted ADME studies confirm that PBTs are promising as potential drug candidates.


Subject(s)
Antineoplastic Agents/chemistry , Tetrazoles/chemistry , Animals , Antineoplastic Agents/metabolism , Antineoplastic Agents/pharmacology , Base Pairing , Binding Sites , DNA/chemistry , DNA/metabolism , DNA Cleavage/drug effects , DNA Topoisomerases, Type II/chemistry , DNA Topoisomerases, Type II/metabolism , Humans , Intercalating Agents/chemistry , Intercalating Agents/metabolism , Intercalating Agents/pharmacology , Molecular Docking Simulation , Protein Structure, Tertiary , Salmon/genetics , Tetrazoles/metabolism , Tetrazoles/pharmacology
2.
Chem Biol Drug Des ; 91(1): 39-49, 2018 01.
Article in English | MEDLINE | ID: mdl-28639390

ABSTRACT

A new series of 3-benzoylamino-5-(1H-imidazol-4-yl)methylaminobenzo[b]furans were synthesized and screened as antitumor agents. As a general trend, tested compounds showed concentration-dependent antiproliferative activity against HeLa and MCF-7 cancer cell lines, exhibiting GI50 values in the low micromolar range. In most cases, insertion of a methyl substituent on the imidazole moiety improved the antiproliferative activity. Therefore, methyl-imidazolyl-benzo[b]furans compounds were tested in cell cycle perturbation experiments, producing cell cycle arrest with proapoptotic effects. Their core similarity to known colchicine binding site binders led us to further study the structure features as antitubulin agents by in silico protocols.


Subject(s)
Antineoplastic Agents/chemical synthesis , Benzofurans/chemistry , Drug Design , Tubulin Modulators/chemical synthesis , Tubulin/metabolism , Antineoplastic Agents/pharmacology , Benzofurans/metabolism , Benzofurans/pharmacology , Binding Sites , Cell Cycle Checkpoints/drug effects , Cell Proliferation/drug effects , Colchicine/chemistry , Colchicine/metabolism , HeLa Cells , Humans , MCF-7 Cells , Molecular Docking Simulation , Protein Structure, Tertiary , Tubulin/chemistry , Tubulin Modulators/pharmacology
3.
Chem Commun (Camb) ; 53(54): 7521-7524, 2017 Jul 04.
Article in English | MEDLINE | ID: mdl-28631780

ABSTRACT

The sol-gel entrapment of nanostructured Bi2WO6 enhances the activity and the selectivity of the short-gap semiconductor in the sunlight-driven photo-oxidation of trans-ferulic and trans-cinnamic acid dissolved in water with air as the primary oxidant. Valuable products such as vanillin, benzaldehyde, benzoic acid and vanillic acid are obtained. This provides the proof of concept that photocatalysis could be a promising technology in tomorrow's solar biorefineries.


Subject(s)
Bismuth/chemistry , Photochemical Processes , Sunlight , Tungsten Compounds/chemistry , Tungsten/chemistry , Benzaldehydes/chemical synthesis , Benzaldehydes/chemistry , Benzoic Acid/chemical synthesis , Benzoic Acid/chemistry , Catalysis , Cinnamates/chemistry , Coumaric Acids/chemistry , Molecular Structure , Nanostructures/chemistry , Oxidation-Reduction , Vanillic Acid/chemical synthesis , Vanillic Acid/chemistry , Water/chemistry
4.
Chem Cent J ; 11: 22, 2017.
Article in English | MEDLINE | ID: mdl-28326128

ABSTRACT

Owing to new biotechnological production units mostly located in China, global supply of citric acid in the course of the last two decades rose from less than 0.5 to more than 2 million tonnes becoming the single largest chemical obtained via biomass fermentation and the most widely employed organic acid. Critically reviewing selected research achievements and production trends, we identify the reasons for which this polycarboxylic acid will become a key chemical in the emerging bioeconomy.Graphical abstractPalermo's Fabbrica Chimica Italiana Goldenberg today. In 1930 it was Europe's largest citric acid plant (photo courtesy of Aldo Ferrande).

5.
ACS Omega ; 2(11): 7991-7995, 2017 Nov 30.
Article in English | MEDLINE | ID: mdl-30023570

ABSTRACT

Analyzed by a quantitative method based on diffuse reflectance infrared Fourier transform spectroscopy, pectins extracted from different regions (outer skin, peel, and waste) of citrus fruits (red orange, lemon, and grapefruit) via microwave-assisted hydrodiffusion show significant variations. All polymers obtained are low-methoxyl pectins, with high contents in galacturonic acid regions. The degree of esterification (DE) of pectin extracted from different regions increases in the order waste < peel < outer skin for red orange, inverting for lemon. Thus, the pectins with the lowest DE are those extracted from red orange waste and lemon outer skin (∼25%). These findings open the route to nutraceutical- and pharmaceutical-grade pectins from citrus, in which the source fruit and its regions may be chosen, according to the desired DE.

6.
Chem Cent J ; 10: 63, 2016.
Article in English | MEDLINE | ID: mdl-27803730

ABSTRACT

BACKGROUND: Olive biophenols are emerging as a valued class of natural products finding practical application in the food, pharmaceutical, beverage, cosmetic and nutraceutical industries due to their powerful biological activity which includes antioxidant and antimicrobial properties. Olive mill waste water (OMWW), a by-product in olive oil manufacturing, is rich in biophenols such as hydroxytyrosol and tyrosol. The amount of biophenols depends on the cultivar, the geographical area of cultivation, and the seasonal conditions. The goal of this study was to develop a straightforward method to assess the economic value of OMWW via quantification of hydroxytyrosol and tyrosol. RESULTS: The amount of hydroxytyrosol and tyrosol phenolic compounds in the OMWW from four different cultivars grown in four different regions of Sicily was analyzed using liquid-liquid and solid-liquid analytical protocols developed ad hoc. Results showed significant differences amongst the different cultivars and their geographical origin. In all samples, the concentration of hydroxytyrosol was generally from 2 to 10 times higher than that of tyrosol. In general, the liquid-liquid extraction protocol gave higher amounts of extracted biophenols. The cultivar Cerasuola had the highest amount of both hydroxytyrosol and tyrosol. The cultivar Nocellara Etnea had the lowest content of both biophenols. CONCLUSIONS: A quick method to assess the economic value of olive mill waste water via quantification of hydroxytyrosol and tyrosol in olive phenolic enriched extracts is now available.

7.
Chem Cent J ; 10: 61, 2016.
Article in English | MEDLINE | ID: mdl-27790286

ABSTRACT

BACKGROUND: The introduction of an heterogeneously catalyzed gold-based alcohol oxidation process of broad applicability using a clean primary oxidant would be highly desirable. Gold is non toxic and carbonyl and carboxyl compounds are widely used to produce medicines, plastics, colorants, paints, detergents, fragrances, flavors, and other valued functional products. RESULTS: The sol-gel entrapment of gold nanoparticles in hybrid silica improves gold-based oxidation catalysis applied to the selective oxidation of alcohols with aqueous hydrogen peroxide as eco-friendly primary oxidant. Pronounced physical and chemical stabilization of the sol-gel entrapped Au nanoparticles is reflected in catalyst recyclability. CONCLUSIONS: Potential implications of these findings are significant, especially considering that the highly stable, mesoporous glassy catalyst is ideally suited for application in microreactors for carrying out the reaction under flow. Graphical abstractSelective oxidation of 2-phenylethanol over SiliaCat Au nanoparticle. Hydrogen peroxide is the clean oxidant.

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