1 Ocak 2019 Dergi makalesi Açık Erişim

Arslan, Tayfun; Cakir, Nezaket; Keles, Turgut; Yiklioglu, Zekeriya B.; Senturk, Murat

Dublin Core

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  <dc:creator>Arslan, Tayfun</dc:creator>
  <dc:creator>Cakir, Nezaket</dc:creator>
  <dc:creator>Keles, Turgut</dc:creator>
  <dc:creator>Yiklioglu, Zekeriya B.</dc:creator>
  <dc:creator>Senturk, Murat</dc:creator>
  <dc:date>2019-01-01</dc:date>
  <dc:description>In this study, 1,2,3-triazole substituted metal-free and metallo phthalocyanines (4, 5, 6) and their water soluble derivatives (4a, 5a, 6a) were designed, synthesized for the first time and tested in vitro on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes. Most phthalocyanines exhibited good inhibitory activities on these enzymes. Among the six phthalocyanines and starting compounds, 4a showed the most interesting profile as a submicromolar selective inhibitor of AChE (IC50 = 0.040 mu M) and 5a showed the most effective inhibitor of BChE (IC50 = 0.1198 mu M).</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/70639</dc:identifier>
  <dc:identifier>oai:zenodo.org:70639</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>BIOORGANIC CHEMISTRY 90</dc:source>
  <dc:title>Triazole substituted metal-free, metallo-phthalocyanines and their water soluble derivatives as potential cholinesterases inhibitors: Design, synthesis and in vitro inhibition study</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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