Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Enza Di Modugno"'
Autor:
Stefania Contini, Emiliangelo Ratti, Aldo Feriani, Frank E. Blaney, David G. Trist, Karen L Roberts, Fabio Maria Sabbatini, Romano Di Fabio, Damiano Ghirlanda, Daniele Donati, Angela Worby, Stefano Provera, Mario Mattioli, Yves St-Denis, Roberto Arban, Elettra Fazzolari, Emiliano Castiglioni, Francesca Pavone, Simone Spada, Enza Di Modugno, Carla Marchioro, Giovanni Bernasconi, Arnaldo Nalin, Anna Mingardi, Anna Maria Capelli, Daniele Andreotti, Simone Braggio, Gabriella Gentile
Publikováno v:
Journal of Medicinal Chemistry. 51:7370-7379
To identify new CRF(1) receptor antagonists, an attempt to modify the bis-heterocycle moiety present in the top region of the dihydropyrrole[2,3]pyridine template was made following new pharmacophoric hypothesis on the CRF(1) receptor antagonists bin
Publikováno v:
Burger's Medicinal Chemistry and Drug Discovery
This chapter reviews the history of β-lactams from the discovery of penicillin in 1928 to the more recently studied and the current trends in the field. The most relevant aspects related to the mechanism of action of β-lactams are covered, and the
Autor:
Alessandro Casnati, Giorgio Tarzia, Enza Di Modugno, Francesco Sansone, Andrea Pochini, Massimo Fabbi, Rocco Unguro, Nicola Pelizzi
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 6:2699-2704
Biologically active Vancomycin antibiotic mimics have been synthesized by linking two opposite aromatic nuclei of a calix[4]arene derivative in the cone conformation with a polifunctional bridge containing D-or L-alanine units and diethylentriamine s
Publikováno v:
Rapid Communications in Mass Spectrometry. 9:883-887
Complexation in aqueous solutions between vancomycin, ristocetin A, teicoplanin and two bacterial cell-wall analogues, Ac2-L-Lys-D-Ala-D-Ala (tripeptide) and Ac-D-Ala-D-Ala (dipeptide) has been examined by positive-ion electrospray mass spectrometry
Autor:
Emily Lin, Zhiyong Luo, Dimitri E. Grigoriadis, Marion Lanier, Xiaohu Zhang, Romano Di Fabio, Yves St. Denis, John E. Tellew, Enza Di Modugno, John Saunders, Deborah H. Slee, John P. Williams, Sam R. J. Hoare, Manisha Moorjani
Publikováno v:
Bioorganicmedicinal chemistry letters. 20(24)
Antagonists of the corticotropin-releasing factor (CRF) neuropeptide may prove effective in treating stress and anxiety related disorders. In an effort to identify antagonists with improved physico-chemical properties a new series of CRF1 antagonists
Autor:
Aldo Balsamo, Armando Rossello, Enza Di Modugno, Marco Macchia, Silvia Barontini, Federico Calvani, Daniela Gentili, Antonio Felici
Publikováno v:
ChemInform. 30
The synthesis and the antimicrobial properties of a new series of cephalosporinic β-lactam antibiotics is described. The data reported in the present paper show the potential of this type of substituted cephalosporins as new anti Gram-positive antib
Autor:
Elisabetta Orlandini, Elisa Nuti, Marco Macchia, Aldo Balsamo, Armando Rossello, Simona Rapposelli, Enza Di Modugno
Publikováno v:
ChemInform. 36
Selected 7beta-(benzo[a]dihydrocarbazolyloxyacetyl)-substituted cephalosporins (1a-e) were synthesised and tested for their antimicrobial activity against Gram-positive and Gram-negative clinical pathogens. All compounds synthesised (1a-e) showed an
Autor:
Aldo Balsamo, Elisabetta Orlandini, Enza Di Modugno, Elisa Nuti, Simona Rapposelli, Marco Macchia, Armando Rossello
Selected 7beta-(benzo[a]dihydrocarbazolyloxyacetyl)-substituted cephalosporins (1a-e) were synthesised and tested for their antimicrobial activity against Gram-positive and Gram-negative clinical pathogens. All compounds synthesised (1a-e) showed an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::715d8825306011d3054a725aede61882
http://hdl.handle.net/11568/204921
http://hdl.handle.net/11568/204921
Autor:
Aldo Balsamo, Federico Calvani, Silvia Barontini, Armando Rossello, Marco Macchia, Enza Di Modugno, Antonio Felici, Daniela Gentili
Publikováno v:
Bioorganicmedicinal chemistry letters. 9(7)
The synthesis and the antimicrobial properties of a new series of cephalosporinic beta-lactam antibiotics is described. The data reported in the present paper show the potential of this type of substituted cephalosporins as new anti Gram-positive ant