Search Results - "Vigorita, Maria Gabriella"
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In vitro antiproliferative activity against human colon cancer cell lines of representative 4-thiazolidinones. Part I
Published in Bioorganic & medicinal chemistry letters (01-09-2005)“…The characterization of two cyclooxygenase isoforms (COX), the rate-limiting enzyme for the synthesis of prostaglandins (PGs) from arachidonic acid, has…”
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Evaluation of in vitro aldose redutase inhibitory activity of 5-arylidene-2,4-thiazolidinediones
Published in Bioorganic & medicinal chemistry letters (15-07-2007)“…A number of 5-arylidene-2,4-thiazolidinediones containing a hydroxy or a carboxymethoxy group in their 5-benzylidene moiety have been synthesised and evaluated…”
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In vitro advanced antimycobacterial screening of isoniazid-related hydrazones, hydrazides and cyanoboranes: Part 14
Published in Bioorganic & medicinal chemistry letters (16-05-2005)“…The in vitro antimycobacterial activities of some isoniazid derivatives are reported. As a part of an ongoing search for new isoniazid-related…”
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5-Arylidene-2,4-thiazolidinediones as inhibitors of protein tyrosine phosphatases
Published in Bioorganic & medicinal chemistry (01-08-2007)“…4-(5-Arylidene-2,4-dioxothiazolidin-3-yl)methylbenzoic acids ( 2) were synthesized and evaluated in vitro as inhibitors of PTP1B and LMW-PTP, two protein…”
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Synthesis and in vitro evaluation of 5-arylidene-3-hydroxyalkyl-2-phenylimino-4-thiazolidinones with antidegenerative activity on human chondrocyte cultures
Published in Bioorganic & medicinal chemistry (15-12-2007)“…5-Arylidene-3-hydroxyalkyl-2-phenylimino-4-thiazolidinones ( 7, 8) were synthesized and evaluated for their antidegenerative activity on human chondrocyte…”
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In vitro aldose reductase inhibitory activity of 5-benzyl-2,4-thiazolidinediones
Published in Bioorganic & medicinal chemistry (15-01-2006)“…Several 5-benzyl-2,4-thiazolidinediones ( 5– 7) were synthesised and tested as in vitro aldose reductase (ALR2) inhibitors. Most of them, particularly…”
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In Vitro Antimycobacterial Activities of 2′-Monosubstituted Isonicotinohydrazides and Their Cyanoborane Adducts
Published in Antimicrobial Agents and Chemotherapy (01-02-2002)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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Modeling and biological evaluation of 3,3′-(1,2-ethanediyl)bis[2-(4-methoxyphenyl)-thiazolidin-4-one], a new synthetic cyclooxygenase-2 inhibitor
Published in European journal of pharmacology (12-07-2002)“…Within the series of chiral 3,3′-(1,2-ethanediyl)bis[2-arylthiazolidin-4-ones], the 3,4-dimethoxyphenyl substituted derivative was found in the primary…”
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Facile Biocatalytic Access to 9-Fluorenylmethyl Polyglycosides: Evaluation of Antiviral Activity on Immunocompetent Cells
Published in ChemMedChem (15-09-2008)“…The biological activities of a series of mono‐ and oligosaccharides (β‐xylosides and α‐glucosides) of 9‐fluorenylmethanol were investigated together with…”
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9-Fluorenon-4-carboxamides: synthesis, conformational analysis, anti-HSV-2, and immunomodulatory evaluation. Note II
Published in ARKIVOC (28-04-2004)Get full text
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5-Arylidene-2-imino-4-thiazolidinones: Design and synthesis of novel anti-inflammatory agents
Published in Bioorganic & medicinal chemistry (01-07-2005)“…[Display omitted] The synthesis and pharmacological activity of 5-arylidene-2-imino-4-thiazolidinones ( 3a– 8a) are described. All derivatives exhibited…”
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Structure–activity relationships and molecular modelling of 5-arylidene-2,4-thiazolidinediones active as aldose reductase inhibitors
Published in Bioorganic & medicinal chemistry (15-04-2005)“…[Display omitted] The structure–activity relationships (SARs) of 5-arylidene-2,4-thiazolidinediones active as aldose reductase inhibitors (ARIs) were extended…”
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Rational Design, Synthesis, Biophysical and Antiproliferative Evaluation of Fluorenone Derivatives with DNA G-Quadruplex Binding Properties
Published in ChemMedChem (06-04-2010)“…Molecular modeling studies carried out with experimental DNA models with the sequence d[AG3(T2AG3)3] suggest that the introduction of a net positive charge…”
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In vitro advanced antimycobacterial screening of cobalt(II) and copper(II) complexes of fluorinated isonicotinoylhydrazones
Published in Bioorganic & medicinal chemistry letters (06-12-2004)“…The in vitro antimycobacterial activities of metalcomplexes 1, 2 are reported. The in vitro antimycobacterial activity of cobalt(II) and copper(II) complexes…”
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2/4-Substituted-9-fluorenones and their O-glucosides as potential immunomodulators and anti-herpes simplex virus-2 agents. Part 5
Published in European journal of medicinal chemistry (01-12-2008)“…In pursuing a research on the antiviral and immunomodulatory activity of tilorone congeners, two new series of compounds were prepared and pharmacologically…”
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Tetraplex DNA specific ligands based on the fluorenone-carboxamide scaffold
Published in Bioorganic & medicinal chemistry letters (01-05-2007)“…A series of fluorenone-carboxamide compounds was analyzed with regard to DNA binding properties by UV spectroscopy and competition dialysis methods. The…”
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Biocatalysed synthesis of β- O-glucosides from 9-fluorenon-2-carbohydroxyesters. Part 3: IFN-inducing and anti-HSV-2 properties
Published in Bioorganic & medicinal chemistry (16-05-2005)“…[Display omitted] In pursuing research on the antiviral, interferon (IFN)-inducing tilorone congeners, a new series of fluoren-carboxyhydroxyesters has been…”
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Configurational assignments of the diastereomers of 3,3′-(1,2-ethanediyl)bis[2-(3-fluorophenyl)-5-methyl-4-thiazolidinone] derivative with four stereogenic centers
Published in Journal of heterocyclic chemistry (01-03-2001)“…Diastereomers of antiinflammatory/analgesic and antihistaminic 3,3′[(1,2‐ethanediyl)bis(2‐aryl‐4‐thiazo‐lidinone)] derivatives possessing two stereogenic…”
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2'-[1-(4-Fluorophenyl)ethyl]isonicotino-κN-hydrazide-Cyanoborane
Published in Acta crystallographica. Section C, Crystal structure communications (15-07-1998)Get full text
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