Dergi makalesi Açık Erişim

Novel indole-based melatonin analogues: Evaluation of antioxidant activity and protective effect against amyloid beta-induced damage

Gurer-Orhan, Hande; Karaaslan, Cigdem; Ozcan, Senem; Firuzi, Omidreza; Tavakkoli, Marjan; Saso, Luciano; Suzen, Sibel


MARC21 XML

<?xml version='1.0' encoding='UTF-8'?>
<record xmlns="http://www.loc.gov/MARC21/slim">
  <leader>00000nam##2200000uu#4500</leader>
  <datafield tag="909" ind1="C" ind2="O">
    <subfield code="p">user-tubitak-destekli-proje-yayinlari</subfield>
    <subfield code="o">oai:zenodo.org:56107</subfield>
  </datafield>
  <datafield tag="520" ind1=" " ind2=" ">
    <subfield code="a">Oxidative stress has been recognized as a contributing factor in ageing and various diseases including cancer and neuropathological disorders. Indole derivatives such as the neurohormone melatonin (MLT) constitute an important class of therapeutic agent in medicinal chemistry. MLT can scavenge different reactive oxygen species and can also stimulate the synthesis of antioxidant enzymes. As a part of our ongoing studies, a series of new indole-based hydrazide/hydrazone derivatives were synthesized as MLT analogues. Their antioxidant activity was investigated in human erythrocytes by evaluating their reducing effect against oxidation of a redox-sensitive fluorescent probe. Possible inherent cytotoxicity of the compounds was investigated in CHO-K1 cells by lactate dehydrogenase leakage test. Protection of neuronal PC12 cells against amyloid beta-induced damage was examined by MTT assay and their ability in reduction of ROS generation induced by amyloid beta was tested. MLT analogues having an o-halogenated aromatic moiety exhibited effective antioxidant properties without having any membrane-damaging effect. Moreover, derivatives having o-halogenated and dihalogenated aromatic side chain significantly protected neuronal cells at concentrations of 10 and 100 mu M. In conclusion, MLT derivatives represent promising scaffolds for discovery of effective antioxidant and neuroprotective agents. (C) 2016 Elsevier Ltd. All rights reserved.</subfield>
  </datafield>
  <datafield tag="980" ind1=" " ind2=" ">
    <subfield code="a">publication</subfield>
    <subfield code="b">article</subfield>
  </datafield>
  <datafield tag="540" ind1=" " ind2=" ">
    <subfield code="a">Creative Commons Attribution</subfield>
    <subfield code="u">http://www.opendefinition.org/licenses/cc-by</subfield>
  </datafield>
  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Gurer-Orhan, Hande</subfield>
    <subfield code="u">Ege Univ, Fac Pharm, Dept Pharmaceut Toxicol, TR-35100 Izmir, Turkey</subfield>
  </datafield>
  <datafield tag="856" ind1="4" ind2=" ">
    <subfield code="z">md5:656bd83b35469f3e5fa6c5ebbe203f83</subfield>
    <subfield code="s">284</subfield>
    <subfield code="u">https://aperta.ulakbim.gov.trrecord/56107/files/bib-db131a7b-aa00-4afe-b1d9-16e629e18ed6.txt</subfield>
  </datafield>
  <controlfield tag="005">20210315235952.0</controlfield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2016-01-01</subfield>
  </datafield>
  <datafield tag="024" ind1=" " ind2=" ">
    <subfield code="a">10.1016/j.bmc.2016.02.039</subfield>
    <subfield code="2">doi</subfield>
  </datafield>
  <datafield tag="542" ind1=" " ind2=" ">
    <subfield code="l">open</subfield>
  </datafield>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Novel indole-based melatonin analogues: Evaluation of antioxidant activity and protective effect against amyloid beta-induced damage</subfield>
  </datafield>
  <datafield tag="909" ind1="C" ind2="4">
    <subfield code="v">24</subfield>
    <subfield code="p">BIOORGANIC &amp; MEDICINAL CHEMISTRY</subfield>
    <subfield code="c">1658-1664</subfield>
    <subfield code="n">8</subfield>
  </datafield>
  <datafield tag="650" ind1="1" ind2="7">
    <subfield code="a">cc-by</subfield>
    <subfield code="2">opendefinition.org</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Karaaslan, Cigdem</subfield>
    <subfield code="u">Ankara Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Ozcan, Senem</subfield>
    <subfield code="u">Ege Univ, Fac Pharm, Dept Pharmaceut Toxicol, TR-35100 Izmir, Turkey</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Firuzi, Omidreza</subfield>
    <subfield code="u">Shiraz Univ Med Sci, Med &amp; Nat Prod Chem Res Ctr, Shiraz, Iran</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Tavakkoli, Marjan</subfield>
    <subfield code="u">Shiraz Univ Med Sci, Med &amp; Nat Prod Chem Res Ctr, Shiraz, Iran</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Saso, Luciano</subfield>
    <subfield code="u">Univ Roma La Sapienza, Dept Physiol &amp; Pharmacol Vittorio Erspamer, Ple Aldo Moro 5, I-00185 Rome, Italy</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Suzen, Sibel</subfield>
    <subfield code="u">Ankara Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey</subfield>
  </datafield>
  <controlfield tag="001">56107</controlfield>
  <datafield tag="980" ind1=" " ind2=" ">
    <subfield code="a">user-tubitak-destekli-proje-yayinlari</subfield>
  </datafield>
</record>
53
9
görüntülenme
indirilme
Görüntülenme 53
İndirme 9
Veri hacmi 2.6 kB
Tekil görüntülenme 51
Tekil indirme 9

Alıntı yap