1 Ocak 2011 Dergi makalesi Açık Erişim

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

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/21543</identifier>
  <creators>
    <creator>
      <creatorName>Kasimogullari, Rahmi</creatorName>
      <givenName>Rahmi</givenName>
      <familyName>Kasimogullari</familyName>
      <affiliation>Dumlupinar Univ, Fac Arts &amp; Sci, Dept Chem, Kutahya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Bulbul, Metin</creatorName>
      <givenName>Metin</givenName>
      <familyName>Bulbul</familyName>
      <affiliation>Dumlupinar Univ, Fac Arts &amp; Sci, Dept Chem, Kutahya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Mert, Samet</creatorName>
      <givenName>Samet</givenName>
      <familyName>Mert</familyName>
      <affiliation>Dumlupinar Univ, Fac Arts &amp; Sci, Dept Chem, Kutahya, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Guleryuz, Hulya</creatorName>
      <givenName>Hulya</givenName>
      <familyName>Guleryuz</familyName>
      <affiliation>Dumlupinar Univ, Fac Arts &amp; Sci, Dept Chem, Kutahya, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Synthesis Of 5-Amino-1,3,4-Thiadiazole-2-Sulphonamide Derivatives And Their Inhibition Effects On Human Carbonic Anhydrase Isozymes</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2011</publicationYear>
  <dates>
    <date dateType="Issued">2011-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/21543</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.3109/14756366.2010.491795</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">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 (</description>
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