Synthesis and Anticancer Activity of Some 1H-inden-1-one Substituted (Heteroaryl)Acetamide Derivatives

Karaburun A. Ç., Gündoğdu-Karaburun N., Yurttaş L., Kayağil İ., Demirayak Ş.

LETTERS IN DRUG DESIGN & DISCOVERY, cilt.16, sa.2, ss.111-118, 2019 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 16 Sayı: 2
  • Basım Tarihi: 2019
  • Doi Numarası: 10.2174/1570180815666180606081042
  • Dergi Adı: LETTERS IN DRUG DESIGN & DISCOVERY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.111-118
  • Anahtar Kelimeler: Anticancer activity, aurone analogue, benzothiazoleacetamide, 2,3-dihydro-1H-inden-1-one, thiazoleacetamide, leukaemia, BIOLOGICAL EVALUATION, DRUG DISCOVERY, POTENT, INHIBITORS, CHROMAN-4-ONE, FLAVONES, CHROMONE, DESIGN
  • Anadolu Üniversitesi Adresli: Evet

Özet

Background: The synthesis of 2-[3/4-((6-substituted-1-oxo-2,3-dihydro-1H-inden-2ylidene) methyl)phenoxy]-N-(heteroaryl)acetamide derivatives and the investigation of their anticancer activity were studied.