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Phaeodactylum tricornutum as a model organism for testing the membrane penetrability of sulphonamide carbonic anhydrase inhibitors.
Rogato, Alessandra; Del Prete, Sonia; Nocentini, Alessio; Carginale, Vincenzo; Supuran, Claudiu T; Capasso, Clemente.
Afiliação
  • Rogato A; a Institute of Bioscience and BioResources, CNR , Naples , Italy.
  • Del Prete S; b Department of Integrative Marine Ecology , Stazione Zoologica Anton Dohrn , Naples , Italy.
  • Nocentini A; a Institute of Bioscience and BioResources, CNR , Naples , Italy.
  • Carginale V; c Neurofarba Department, University of Florence, Polo Scientifico , Sesto Fiorentino , Florence , Italy.
  • Supuran CT; a Institute of Bioscience and BioResources, CNR , Naples , Italy.
  • Capasso C; c Neurofarba Department, University of Florence, Polo Scientifico , Sesto Fiorentino , Florence , Italy.
J Enzyme Inhib Med Chem ; 34(1): 510-518, 2019 Dec.
Article em En | MEDLINE | ID: mdl-30688123
ABSTRACT
Carbonic anhydrases (CAs) are ubiquitous metalloenzymes, which started to be investigated in detail in pathogenic, as well as non-pathogenic species since their pivotal role is to accelerate the physiological CO2 hydration/dehydration reaction significantly. Here, we propose the marine unicellular diatom Phaeodactylum tricornutum as a model organism for testing the membrane penetrability of CA inhibitors (CAIs). Seven inhibitors belonging to the sulphonamide type and possessing a diverse scaffold have been explored for their in vitro inhibition of the whole diatom CAs and the in vivo inhibitory effect on the growth of P. tricornutum. Interesting, inhibition of growth was observed, in vivo, demonstrating that this diatom is a good model for testing the cell wall penetrability of this class of pharmacological agents. Considering that many pathogens are difficult and dangerous to grow in the laboratory, the growth inhibition of P. tricornutum with different such CAIs may be subsequently used to design inhibition studies of CAs from pathogenic organisms.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Sulfonamidas / Inibidores da Anidrase Carbônica / Anidrases Carbônicas / Diatomáceas Idioma: En Revista: J Enzyme Inhib Med Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Sulfonamidas / Inibidores da Anidrase Carbônica / Anidrases Carbônicas / Diatomáceas Idioma: En Revista: J Enzyme Inhib Med Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Itália