Synthesis of Ethynyl-Thiophene Derivatives, Antioxidant Properties and ADME Analysis

Konuş M., Algso M., Yılmaz C., Khorsheed B. A., Köroğlu A., Çetin D., ...Daha Fazla

ChemistrySelect, cilt.7, sa.12, 2022 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 7 Sayı: 12
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1002/slct.202200281
  • Dergi Adı: ChemistrySelect
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier
  • Anahtar Kelimeler: Ethynyl-thiophene, cross-coupling reaction, reducing power, antioxidant capacity, ADME, T, RADICALS
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

© 2022 Wiley-VCH GmbH.Herein, novel alkyne based organic compounds, 2-((2-(methylthio)phenyl)ethynyl)thiophene (MAT) and 2-ethynyl-3-(phenylethynyl)thiophene (DAT), were designed and synthesized via Pd-catalyst cross-coupling reactions. The isolated yields of MAT and DAT were obtained as 77 % and 96 %, respectively. After chemical characterization, radical scavenging activities and reduction power capacities of them were determined by DPPH, TEAC, phosphomolybdenum and reducing power methods. MAT showed higher radical scavenging activities than DAT, and comparable with the standard. Moreover, basic ADME properties were calculated in silico. Both of the newly synthesized derivatives were reported with the same moderate to good drug score of 0.42; and, having potential to pass through BBB and GI with no appointed toxic effects.