Structure-activity relationship of acridine derivatives to amyloid aggregation of lysozyme (Articolo in rivista)

Type
Label
  • Structure-activity relationship of acridine derivatives to amyloid aggregation of lysozyme (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.bbagen.2011.01.007 (literal)
Alternative label
  • Andrea Antosova (1), Beatrice Chelli (2), Eva Bystrenova (2), Katarina Siposova (1), Francesco Valle (2), Jan Imrich (3), Maria Vilkova (3), Pavol Kristian (3), Fabio Biscarini (2), Zuzana Gazova (1) (2010)
    Structure-activity relationship of acridine derivatives to amyloid aggregation of lysozyme
    in Biochimica et biophysica acta. G, General subjects (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Andrea Antosova (1), Beatrice Chelli (2), Eva Bystrenova (2), Katarina Siposova (1), Francesco Valle (2), Jan Imrich (3), Maria Vilkova (3), Pavol Kristian (3), Fabio Biscarini (2), Zuzana Gazova (1) (literal)
Pagina inizio
  • 465 (literal)
Pagina fine
  • 474 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://dx.doi.org/10.1016/j.bbagen.2011.01.007 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 1810 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 10 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 4 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • (1) Department of Biophysics, Institute of Experimental Physics, Slovak Academy of Sciences, Kosice, Slovakia (2) Istituto per lo Studio dei Materiali Nanostrutturati, ISMN CNR, Bologna, Italy (3) Institute of Chemical Sciences, P. J. Safarik University, Kosice, Slovakia (literal)
Titolo
  • Structure-activity relationship of acridine derivatives to amyloid aggregation of lysozyme (literal)
Abstract
  • We have studied the effect of acridine derivatives on the amyloid aggregation of lysozyme to investigate the acridine structure-activity relationship. The activity of the effective planar acridines was characterized by the half-maximum depolymerization concentration DC50 and half-maximal inhibition concentration IC50. For the most effective acridine derivatives we examined their interaction with DNA and their effect on cell viability in order to investigate their eventual influence on cells. We thus identified planar acridine derivatives with intensive anti-amyloid activity (IC50 and DC50 values in micromolar range), low cytotoxicity and weak ability to interfere with the processes in the cell. (literal)
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