Atıf İçin Kopyala
Demirayak Ş., Yurttaş L., Karaburun A. Ç., Gündoğdu-Karaburun N., Kayağil İ.
LETTERS IN DRUG DESIGN & DISCOVERY, cilt.13, sa.6, ss.563-569, 2016 (SCI-Expanded)
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Yayın Türü:
Makale / Tam Makale
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Cilt numarası:
13
Sayı:
6
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Basım Tarihi:
2016
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Doi Numarası:
10.2174/1570180813999160429113316
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Dergi Adı:
LETTERS IN DRUG DESIGN & DISCOVERY
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus
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Sayfa Sayıları:
ss.563-569
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Anahtar Kelimeler:
Antitumor activity, aurone, benzofuranone, chalcone, cytotoxic activity, CANCER-CELL LINES, BIOLOGICAL EVALUATION, CHALCONE DERIVATIVES, ANTICANCER ACTIVITY, AURONES, INHIBITORS, AGENTS, DISCOVERY
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Anadolu Üniversitesi Adresli:
Evet
Özet
The synthesis of 2-arylidene 6-(2-aryl-2-oxoethoxy) benzofuran-3-one derivatives was reported and selected compounds were determined for their anticancer activity evaluation in National Cancer Institute NCI, USA according to the drug screening protocol of the institute against approximately 60 tumor cell lines derived from nine cancer diseases. Compound 3r, namely 2-(4-chlorobenzylidene)- 6-[2-(4-methoxyphenyl)-2-oxoethoxy] benzofuran-3-one exhibited the highest antitumor activity against non-small lung cancer cell lines.