1 Ocak 2020 Dergi makalesi Açık Erişim

Kucukdumlu, Asligul; Tuncbilek, Meral; Guven, Ebru Bilget; Atalay, Rengul Cetin

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/5573</identifier>
  <creators>
    <creator>
      <creatorName>Kucukdumlu, Asligul</creatorName>
      <givenName>Asligul</givenName>
      <familyName>Kucukdumlu</familyName>
      <affiliation>Ankara Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Tuncbilek, Meral</creatorName>
      <givenName>Meral</givenName>
      <familyName>Tuncbilek</familyName>
      <affiliation>Ankara Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Guven, Ebru Bilget</creatorName>
      <givenName>Ebru Bilget</givenName>
      <familyName>Guven</familyName>
      <affiliation>Kadir Has Univ, Fac Engn &amp; Nat Sci, Dept Bioinformat &amp; Genet, TR-34083 Istanbul, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Atalay, Rengul Cetin</creatorName>
      <givenName>Rengul Cetin</givenName>
      <familyName>Atalay</familyName>
      <affiliation>Middle East Tech Univ, Grad Sch Informat, Dept Bioinformat, TR-06800 Ankara, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Design, Synthesis And In Vitro Cytotoxic Activity Of New 6,9-Disubstituted Purine Analogues</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2020</publicationYear>
  <dates>
    <date dateType="Issued">2020-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/5573</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.17344/acsi.2019.5196</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">A series of new 6,9-disubstituted purine analogs with 4-substituted piperazine at C-6 and 4-substituted benzyl at N-9 were designed and synthesized in four steps. All synthesized compounds (7-26) were screened initially for their in vitro anticancer activity on Huh7 liver, HCT116 colon and MCF7 breast carcinoma cell lines. Cytotoxic bioactivity studies revealed that all compounds screened, with compound 19 being the exception, were found to have promising cytotoxic activities at IC50 range of 0.05-21.8 mu M against cancer cells Huh7, HCT116 and MCF7. Among the prepared purine analogs, two of them (12 and 22) exhibited excellent cytotoxic activities, with IC50 0.08-0.13 mu M, on Huh7 cells comparable to camptothecin (CPT) and better than cladribine, fludarabine and 5-FU. Afterwards, the evaluation of cytotoxicity of the most potent purine analogs was screened against further hepatocellular cancer (HCC) cell lines. The 6-(4-(4-trifluoromethylphenyl)piperazine (12) and 6-(4-(3,4-dichlorophenyl)piperazine analogs (25) displayed a significant IC50 values (IC50 &amp;lt; 0.1-0.13 mu M) comparable to CPT and better cytotoxic bioactivity when compared with 5-FU, cladribine and fludarabine on HCC cells (Huh7 and HepG2).</description>
  </descriptions>
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