Search Results - "Porretta, GC"

Research on antibacterial and antifungal agents. XI. Synthesis and antimicrobial activity of N-heteroaryl benzylamines and their Schiff bases by Fioravanti, R, Biava, M, Porretta, GC, Landolfi, C, Simonetti, N, Villa, A, Conte, E, Porta-Puglia, A

“…The synthesis and antimicrobial activity of new N-heteroaryl benzylamines and their Schiff bases are reported. Antifungal data were compared with those…”
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Antimycobacterial compounds. New pyrrole derivatives of BM212 by Biava, Mariangela, Porretta, Giulio Cesare, Deidda, Delia, Pompei, Raffaello, Tafi, Andrea, Manetti, Fabrizio

“…We have identified BM212 as a lead compound among a series of pyrrole derivatives with good in vitro activity against mycobacteria and candidae. First studies…”
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Importance of the thiomorpholine introduction in new pyrrole derivatives as antimycobacterial agents analogues of BM 212 by Biava, Mariangela, Cesare Porretta, Giulio, Deidda, Delia, Pompei, Raffaello, Tafi, Andrea, Manetti, Fabrizio

“…During the course of our investigations in the field of azole antimicrobial agents, we have identified BM 212, a pyrrole derivative with good in vitro activity…”
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1,5-Diarylpyrrole-3-acetic Acids and Esters as Novel Classes of Potent and Highly Selective Cyclooxygenase-2 Inhibitors by Biava, Mariangela, Porretta, Giulio Cesare, Cappelli, Andrea, Vomero, Salvatore, Manetti, Fabrizio, Botta, Maurizio, Sautebin, Lidia, Rossi, Antonietta, Makovec, Francesco, Anzini, Maurizio

“…A small set of substituted 1,5-diarylpyrrole-3-acetic and -glyoxylic acid derivatives have been synthesized, and their cyclooxygenase (COX-1 and COX-2)…”
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Antimycobacterial compounds. Optimization of the BM 212 structure, the lead compound for a new pyrrole derivative class by Biava, Mariangela, Porretta, Giulio Cesare, Poce, Giovanna, Deidda, Delia, Pompei, Raffaello, Tafi, Andrea, Manetti, Fabrizio

“…Previously we have identified BM 212, a pyrrole derivative with good in vitro activity against mycobacteria and a four-feature pharmacophore model derived from…”
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Bactericidal Activities of the Pyrrole Derivative BM212 against Multidrug-Resistant and Intramacrophagic Mycobacterium tuberculosis Strains by DEIDDA, D, LAMPIS, G, FIORAVANTI, R, BIAVA, M, PORRETTA, G. C, ZANETTI, S, POMPEI, R

“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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New pyrrole derivatives as antimycobacterial agents analogs of BM212 by Biava, Mariangela, Fioravanti, Rossella, Porretta, Giulio Cesare, Deidda, Delia, Maullu, Carlo, Pompei, Raffaello

“…During the course of our investigations in the field of azole antimicrobial agents, we have identified BM212 a pyrrole derivative with good in vitro activity…”
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β-Aminomethylation of N-aryl- and N-azaheteroaryl-substituted methyl 2,5-dimethylpyrrole-3-carboxylates. Kinetic effect of the N-pyrrole substituent by Biava, Mariangela, Porretta, Giulio Cesare, Giorgi, Giorgio, Sleiter, Giancarlo

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Building a pharmacophore model for a novel class of antitubercular compounds by Manetti, F, Corelli, F, Biava, M, Fioravanti, R, Porretta, G.C, Botta, M

“…Starting from a set of 32 antitubercular compounds, for the first time a three-dimensional pharmacophore model has been derived through a computational…”
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Chromatographic resolution and pharmacological investigation of some imidazole derivatives by Quaglia, M.G., Bossù, E., Porretta, G.C., Biava, M., Fioravanti, R., Romanelli, L., Leonardi, A.

“…Some N-phenylethylimidazoles have a chiral carbon atom in their structure. These compounds were obtained by non-stereoselective synthesis and their…”
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Antimycobacterial activity of new ortho-, meta- and para-toluidine derivatives by Biava, Mariangela, Fioravanti, Rossella, Porretta, Giulio Cesare, Sleiter, Giancarlo, Deidda, Delia, Lampis, Giorgio, Pompei, Raffaello

“…Novel toluidine derivatives are described. Some of them showed an interesting in vitro activity against Mycobacterium tuberculosis, M. smegmatis, M. marinum,…”
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The Antifungal Agent 1-[2-(4-Chlorobenzylamino)benzyl]-1H-imidazole by Ettorre, A., Biava, M., Fioravanti, R., Porretta, G. C.

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Synthesis and microbiological evaluations of (N-heteroaryl) arylmethanamines and their Schiff bases by Fioravanti, R, Biava, M, Donnarumma, S, Porretta, G C, Simonetti, N, Villa, A, Porta-Puglia, A, Deidda, D, Maulla, C, Pompei, R

“…The synthesis as well as the antimicrobial and antiviral activities of new (N-heteroaryl)arylmethanamines and their Schiff bases are reported. None of the…”
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Study of the Mannich reaction: beta-amino-methylation of N-aryl and N-azaheteroaryl-substituted 2,5-dimethylpyrroles, compounds with potential biological activity by Biava, M, Fioravanti, R, Porretta, G C, Frachey, G, Mencarelli, P, Sleiter, G, Perazzi, M E, Simonetti, N, Villa, A

“…Owing to the increasing need of drugs for the treatment of a variety of fungal and bacterial opportunistic infections, a study has been started with the aim of…”
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Antifungal agents. 7. Dichlorophenylpyrrylimidazolylmethane derivatives: synthesis and antifungal activities by Massa, S, Mai, A, Ragno, R, Porretta, G C, Retico, A, Simonetti, G, Artico, M

“…The synthesis and antifungal activities of some dichlorophenyl-1H-pyrrol-2-yl-1H-imidazol-1-ylmethane derivatives substituted at pyrrole nitrogen are reported…”
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Antimicrobial activity of a new derivative: N-(4-chlorobenzyl)-2-(1H-imidazol-1-ylmethyl)benzenamine by Panico, S, Villa, A, Simonetti, N, Porretta, G C, Scalzo, M

“…The activity of a new antifungal agent, an imidazolylmethylaniline derivative (XX H), synthesized by the authors, has been studied in vitro and in vivo…”
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The synthesis of 4H-pyrrolo[2,1-c] [1,4] benzoxazine by Artico, Marino, Porretta, Giulio Cesare, De Martino, Giovanni

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Research on compounds with antiblastic activity. 43. Synthesis of 9H-pyrrolo-(1,2-a)-indole derivatives by Artico, M, Giuliano, R, Porretta, G C, Scalzo, M

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