http://www.cnr.it/ontology/cnr/individuo/prodotto/ID285510
Carbonic anhydrase inhibitors. Phenols incorporating 2-or 3-pyridyl-ethenylcarbonyl and tertiary amine moieties strongly inhibit Saccharomyces cerevisiae beta-carbonic anhydrase (Articolo in rivista)
- Type
- Label
- Carbonic anhydrase inhibitors. Phenols incorporating 2-or 3-pyridyl-ethenylcarbonyl and tertiary amine moieties strongly inhibit Saccharomyces cerevisiae beta-carbonic anhydrase (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.3109/14756366.2013.806497 (literal)
- Alternative label
Bilginer, Sinan; Unluer, Elif; Gul, Halise Inci; Mete, Ebru; Isik, Semra; Vullo, Daniela; Ozensoy-Guler, Ozen; Beyaztas, Serap; Capasso, Clemente; Supuran, Claudiu T. (2014)
Carbonic anhydrase inhibitors. Phenols incorporating 2-or 3-pyridyl-ethenylcarbonyl and tertiary amine moieties strongly inhibit Saccharomyces cerevisiae beta-carbonic anhydrase
in Journal of enzyme inhibition and medicinal chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Bilginer, Sinan; Unluer, Elif; Gul, Halise Inci; Mete, Ebru; Isik, Semra; Vullo, Daniela; Ozensoy-Guler, Ozen; Beyaztas, Serap; Capasso, Clemente; Supuran, Claudiu T. (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Ataturk University; Ataturk University; University of Florence; Yildirim Beyazit Univ; Consiglio Nazionale delle Ricerche (CNR); University of Florence (literal)
- Titolo
- Carbonic anhydrase inhibitors. Phenols incorporating 2-or 3-pyridyl-ethenylcarbonyl and tertiary amine moieties strongly inhibit Saccharomyces cerevisiae beta-carbonic anhydrase (literal)
- Abstract
- A series of phenols incorporating tertiary amine and trans-pyridylethenyl-carbonyl moieties were assayed as inhibitors of the beta-carbonic anhydrase (CA, EC 4.2.1.1) from Saccharomyces cerevisiae, ScCA. One of these compounds was a low nanomolar ScCA inhibitor, whereas the remaining ones inhibited the enzyme with K(I)s in the range of 23.5-95.4 nM. The off-target human (h) isoforms hCA I and hCA II were much less inhibited by these phenols, with K(I)s in the range of 0.78-23.5 mu M (hCA I) and 10.8-52.4 mu M (hCA II). The model organism S. cerevisiae and this particular enzyme may be useful for detecting antifungals with a novel mechanism of action compared to the classical azole drugs to which significant drug resistance emerged. (literal)
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