Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents (Articolo in rivista)

Type
Label
  • Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents (Articolo in rivista) (literal)
Anno
  • 2000-01-01T00:00:00+01:00 (literal)
Alternative label
  • Campiani, G ; Fabbrini, M; Morelli, E ; Nacci, V ; Greco, G ; Novellino, E ; Maga, G ; Spadari, S ; Bergamini, A; Faggioli, E ; Uccella, I ; Bolacchi, F ; Marini, S; Coletta, M; Fracasso, C; Caccia, S (2000)
    Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents
    in Antiviral chemistry & chemotherapy (Online)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Campiani, G ; Fabbrini, M; Morelli, E ; Nacci, V ; Greco, G ; Novellino, E ; Maga, G ; Spadari, S ; Bergamini, A; Faggioli, E ; Uccella, I ; Bolacchi, F ; Marini, S; Coletta, M; Fracasso, C; Caccia, S (literal)
Pagina inizio
  • 141 (literal)
Pagina fine
  • 145 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 11 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Univ Salerno, Fac Farm, Dipartimento Sci Farmaceut, I-84084 Salerno, Italy Univ Siena, Dipartimento Farmaco Chim Tecnol, I-53100 Siena, Italy Univ Naples Federico II, Dipartimento Chim Farmaceut & Tossicol, I-80131 Naples, Italy CNR, Ist Genet Biochim & Evoluzionist, I-27100 Pavia, Italy Univ Roma Tor Vergata, Dipartimento Sanita Pubbl & Biol Cellulare, I-00133 Rome, Italy Univ Roma Tor Vergata, Dipartimento Med Sperimentale & Sci Biochim, I-00133 Rome, Italy Ist Ric Farmacol Mario Negri, I-20157 Milan, Italy (literal)
Titolo
  • Non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis and biological evaluation of novel quinoxalinylethylpyridylthioureas as potent antiviral agents (literal)
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