1 Ocak 2011 Dergi makalesi Açık Erişim

Kasimogullari, Rahmi; Bulbul, Metin; Mert, Samet; Guleryuz, Hulya

Dublin Core

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  <dc:creator>Kasimogullari, Rahmi</dc:creator>
  <dc:creator>Bulbul, Metin</dc:creator>
  <dc:creator>Mert, Samet</dc:creator>
  <dc:creator>Guleryuz, Hulya</dc:creator>
  <dc:date>2011-01-01</dc:date>
  <dc:description>In this study, some novel inhibitors were synthesised from the further stage reactions of 4-benzoyl-1-(4-nitrophenyl)-5-phenyl-1H-pyrazole-3-carbonyl chloride with 5-amino-1,3,4-thiadiazole-2-sulphonamide 1 (inhibitor 1). They were characterised by elemental and spectral (</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/21543</dc:identifier>
  <dc:identifier>oai:zenodo.org:21543</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY 26(2) 231-237</dc:source>
  <dc:title>Synthesis of 5-amino-1,3,4-thiadiazole-2-sulphonamide derivatives and their inhibition effects on human carbonic anhydrase isozymes</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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