4 results on '"Maria Jose España De Marco"'
Search Results
2. Contributors
- Author
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Ashok Agarwal, Gulzhanat Aimagambetova, Ibrahim Alkatout, M. Al Naqbi, Luis Alonso Pacheco, Nicola Arrighi, Domenico Baldini, Giorgio Maria Baldini, Helena Ban Frangež, Federica Barbagallo, Caio Parente Barbosa, Erlisa Bardhi, Amy Barrie, Murat Basar, Gizem Bektas, Chiara Benedetto, Bianca Bianco, Luca Boeri, Giovanni Buzzaccarini, Aldo E. Calogero, Alison Campbell, Rossella Cannarella, Domenico Carone, Andrea Roberto Carosso, Jose Carugno, Donatella Caserta, Sandrine Chamayou, Michael Chapman, Stephanie Cheung, Denise Maria Christofolini, Laura Cimino, Isabella Cobuzzi, Michele Compagnone, Rosita A. Condorelli, Anna Consoli, Andrea Coscia, Mauro Cozzolino, Andrea Crafa, Angela Cuccarollo, Konstantinos Dafopoulos, Rhianna Davies, Rossana Di Paola, Panagiotis Drakopoulos, Maria Jose España De Marco, Bernadette Evangelisti, Ala'a Farkouh, Federico Ferrari, Filippo Alberto Ferrari, Necati Findikli, Carlo Foresta, Damaris Freytag, Andrea Garolla, Simone Garzon, Ghina Ghazeeri, Veronika Günther, Timur Gurgan, Alayman Hussein, Pieraldo Inaudi, Nina Jančar, Channa N. Jayasena, Juan Manuel Jiménez Tuñón, Derek Keating, Olena M. Kocur, Vilmante Kodyte, Dalal Kojok, William Kutteh, Antonio Simone Laganà, Stella Lancuba, Sandro La Vignera, Ahmad Majzoub, Roberto Marci, Aine McNally, Noemi Lucia Mercaldo, Mariana Miguens, Suks Minhas, Helene Mitchell, Laura M. Mongioì, Laura Nieto Pascual, Wendy Norton, Franco Odicino, Engin Oral, Pinar Ozcan, Gianpiero D. Palermo, Stefano Palomba, Michail Papapanou, Sergio Papier, Livia Pellegrini, Stamatios Petousis, Edoardo Pozzi, Nikolaos Prapas, Martina Ratti, Alberto Revelli, Zev Rosenwaks, Alessandro Ruffa, Claudia Saganuma, Hassan N. Sallam, Nooman H. Sallam, Andrea Salonia, Fernando Sánchez Martín, Pascual Sánchez Martín, Enrico Sartori, Benedetta Scarselli, Omar Sefrioui, Charalampos Siristatidis, Rachel Smith, Ilaria Soave, Michele Tanada, Basil C. Tarlatzis, Milan Terzic, Marta Tesone, Marcos Sean Thomson, Bulut Varli, Amerigo Vitagliano, Antoine Watrelot, Philip Xie, and Ivan Henrique Yoshida
- Published
- 2023
- Full Text
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3. Design and Optimization of Quinazoline Derivatives: New Non-nucleoside Inhibitors of Bovine Viral Diarrhea Virus
- Author
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Rocío A. Rosas, Leandro Battini, Gabriela Araceli Fernandez, Eliana F. Castro, Daniela M. Fidalgo, Lucia Cavallaro, Ana M. Bruno, Natalia S. Adler, Maria Jose España de Marco, Matias Fabiani, and Mariela Bollini
- Subjects
viruses ,BVDV inhibitors ,Context (language use) ,medicine.disease_cause ,01 natural sciences ,pharmacokinetics in vitro properties ,Virus ,lcsh:Chemistry ,purl.org/becyt/ford/1 [https] ,03 medical and health sciences ,chemistry.chemical_compound ,Flaviviridae ,PHARMACOKINETICS IN VITRO PROPERTIES ,RNA polymerase ,medicine ,purl.org/becyt/ford/1.4 [https] ,RDRP PROTEIN ,RdRp protein ,purl.org/becyt/ford/1.6 [https] ,BVDV INHIBITORS ,Original Research ,030304 developmental biology ,quinazoline derivatives ,0303 health sciences ,Mutation ,biology ,010405 organic chemistry ,Pestivirus ,QUINAZOLINE DERIVATIVES ,General Chemistry ,biology.organism_classification ,Virology ,molecular dynamics ,In vitro ,0104 chemical sciences ,Chemistry ,lcsh:QD1-999 ,chemistry ,MOLECULAR DYNAMICS ,Nucleoside - Abstract
Bovine viral diarrhea virus (BVDV) belongs to the Pestivirus genus (Flaviviridae). In spite of the availability of vaccines, the virus is still causing substantial financial losses to the livestock industry. In this context, the use of antiviral agents could be an alternative strategy to control and reduce viral infections. The viral RNA-dependent RNA polymerase (RdRp) is essential for the replication of the viral genome and constitutes an attractive target for the identification of antiviral compounds. In a previous work, we have identified potential molecules that dock into an allosteric binding pocket of BVDV RdRp via a structure-based virtual screening approach. One of them, N-(2-morpholinoethyl)-2-phenylquinazolin-4-amine [1, 50% effective concentration (EC50) = 9.7 ± 0.5 μM], was selected to perform different chemical modifications. Among 24 derivatives synthesized, eight of them showed considerable antiviral activity. Molecular modeling of the most active compounds showed that they bind to a pocket located in the fingers and thumb domains in BVDV RdRp, which is different from that identified for other non-nucleoside inhibitors (NNIs) such as thiosemicarbazone (TSC). We selected compound 2-[4-(2-phenylquinazolin-4-yl)piperazin-1-yl]ethanol (1.9; EC50 = 1.7 ± 0.4 μM) for further analysis. Compound 1.9 was found to inhibit the in vitro replication of TSC-resistant BVDV variants, which carry the N264D mutation in the RdRp. In addition, 1.9 presented adequate solubility in different media and a high-stability profile in murine and bovine plasma. Fil: Fernandez, Gabriela A.. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: Castro, Eliana Florencia. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Microbiología, Inmunología y Biotecnología. Cátedra de Virología; Argentina. Instituto Nacional de Tecnologia Agropecuaria. Centro de Investigacion En Ciencias Veterinarias y Agronomicas. Instituto de Virologia E Innovaciones Tecnologicas. - Consejo Nacional de Investigaciones Cientificas y Tecnicas. Oficina de Coordinacion Administrativa Pque. Centenario. Instituto de Virologia E Innovaciones Tecnologicas.; Argentina Fil: Rosas, Rocio Ayelen. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Microbiología, Inmunología y Biotecnología. Cátedra de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Fidalgo, Daniela Marina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: Adler, Natalia Sol. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: Battini, Leandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: España de Marco, Maria Jose. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Microbiología, Inmunología y Biotecnología. Cátedra de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Fabiani, Matias. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Microbiología, Inmunología y Biotecnología. Cátedra de Virología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Bruno, Ana María. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Orgánica. Química Orgánica II; Argentina Fil: Bollini, Mariela. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: Cavallaro, Lucia Vicenta. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Microbiología, Inmunología y Biotecnología. Cátedra de Virología; Argentina
- Published
- 2020
4. Identification of potent bovine viral diarrhea virus inhibitors by a structure-based virtual screening approach
- Author
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Maria Jose España de Marco, Matias Fabiani, Juan José Casal, Gabriela Araceli Fernandez, Leandro Battini, Mariela Bollini, Ana M. Bruno, Eliana F. Castro, and Lucia Cavallaro
- Subjects
viruses ,In silico ,Clinical Biochemistry ,Drug Evaluation, Preclinical ,Pharmaceutical Science ,Microbial Sensitivity Tests ,Molecular Dynamics Simulation ,01 natural sciences ,Biochemistry ,Antiviral Agents ,Virus ,chemistry.chemical_compound ,Structure-Activity Relationship ,RNA polymerase ,Drug Discovery ,Animals ,Molecular Biology ,Virtual screening ,Diarrhea Viruses, Bovine Viral ,biology ,Dose-Response Relationship, Drug ,Molecular Structure ,010405 organic chemistry ,Chemistry ,Organic Chemistry ,Pestivirus ,RNA ,biology.organism_classification ,Virology ,Small molecule ,In vitro ,0104 chemical sciences ,010404 medicinal & biomolecular chemistry ,Molecular Medicine ,Cattle - Abstract
Bovine viral diarrhea virus (BVDV) is a pestivirus whose infection in cattle is globally distributed. The use of antivirals could complement vaccination as a tool of control and reduce economic losses. The RNA-dependent RNA polymerase (RdRp) of the virus is essential for its genome replication and constitutes an attractive target for the identification of antivirals. With the aim of obtaining selective BVDV inhibitors, the crystal structure of BVDV RdRp was used to perform a virtual screening. Approximately 15,000 small molecules from commercial and in-house databases were evaluated and several structurally different compounds were tested in vitro for antiviral activity. Interestingly, of twelve evaluated compounds, five were active and displayed EC50 values in the sub and low-micromolar range. Time of drug addition experiment and measured intracellular BVDV RNA showed that compound 7 act during RNA synthesis. Molecular Dynamics and MM/PBSA calculation were done to characterize the interaction of the most active compounds with RdRp, which will allow future ligand optimization. These studies highlight the use of in silico screening to identify a new class of BVDV inhibitors.
- Published
- 2018
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