Design and Synthesis of Novel Polycycles Based on the 3H-pyrrolo/6,7- dihydropyrido[1,2-a]indole scaffold as Templates for Pharmaceutical Development (Articolo in rivista)

Type
Label
  • Design and Synthesis of Novel Polycycles Based on the 3H-pyrrolo/6,7- dihydropyrido[1,2-a]indole scaffold as Templates for Pharmaceutical Development (Articolo in rivista) (literal)
Anno
  • 2011-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/jhet.710 (literal)
Alternative label
  • M. Derudas, N. Pala, V. Sanna, R. Dallocchio, A. Dessì, A. M. Roggio, M. Sechi (2011)
    Design and Synthesis of Novel Polycycles Based on the 3H-pyrrolo/6,7- dihydropyrido[1,2-a]indole scaffold as Templates for Pharmaceutical Development
    in Journal of heterocyclic chemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • M. Derudas, N. Pala, V. Sanna, R. Dallocchio, A. Dessì, A. M. Roggio, M. Sechi (literal)
Pagina inizio
  • 1161 (literal)
Pagina fine
  • 1168 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 48 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 8 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Cardiff University, Università di Sassari, Porto Conte Ricerche, CNR (literal)
Titolo
  • Design and Synthesis of Novel Polycycles Based on the 3H-pyrrolo/6,7- dihydropyrido[1,2-a]indole scaffold as Templates for Pharmaceutical Development (literal)
Abstract
  • In the course of our work aimed at developing novel heterocycles of pharmaceutical interest, we designed and synthesized several polycyclic templates as potential substrates to be used in drug design. We obtained a set of condensed ring systems as versatile structural platforms to generate potential DNA-interactive agents and/or reversible inhibitors of enzymes such as topoisomerases, poly(ADPribose) polymerase-1 (PARP-1), telomerase, and, in particular, cyclin dependent kinases. Herein, we report the design, synthesis, structural investigation, and preliminary DNA-binding affinity of these heteroaromatic systems. (literal)
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