Synhesis and genotoxic activities of five 2-aryl-substituted-benzothiazole derivatives

Zeytinoglu H., Meryc A., Tuylu B., Ergene E.

REVISTA DE CHIMIE, cilt.57, sa.12, ss.1247-1252, 2006 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 57 Sayı: 12
  • Basım Tarihi: 2006
  • Dergi Adı: REVISTA DE CHIMIE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1247-1252
  • Eskişehir Osmangazi Üniversitesi Adresli: Hayır

Özet

Five 2-aryl-substituted-benzothiazoles were synthesized from o-amino-thiophenol and their structural assignments were made by H-1-NMR. Mutagenicily of derivatives was tested by Salmonella microsome assay using TA98 and TA100.2-m-tolil-benzothiazole and 2-p-tolil-benzothiazole whose phenyl rings possess methyl group showed significant mutagenic activity in T100, whereas they were cytotoxic for TA98. 2-pyridin-2-yl-benzothiazole was weakly mutagenic. Tested compounds may show different genotoxicity regarding to electronic properly of alkyl substituent which is attached to phenyl ring at the second position of benzothiazole.