Your browser doesn't support javascript.
loading
Disubstituted 4-Chloro-3-nitrophenylthiourea Derivatives: Antimicrobial and Cytotoxic Studies.
Bielenica, Anna; Sanna, Giuseppina; Madeddu, Silvia; Giliberti, Gabriele; Stefanska, Joanna; Koziol, Anna E; Savchenko, Oleksandra; Strzyga-Lach, Paulina; Chrzanowska, Alicja; Kubiak-Tomaszewska, Grazyna; Struga, Marta.
  • Bielenica A; Department of Biochemistry, Medical University, 02-097 Warszawa, Poland. abielenica@wum.edu.pl.
  • Sanna G; Department of Biomedical Sciences, Section of Microbiology and Virology, University of Cagliary, Cittadella Universitaria, 09042 Monserrato, Italy. g.sanna@unica.it.
  • Madeddu S; Department of Biomedical Sciences, Section of Microbiology and Virology, University of Cagliary, Cittadella Universitaria, 09042 Monserrato, Italy. silvia.madeddu@unica.it.
  • Giliberti G; Department of Biomedical Sciences, Section of Microbiology and Virology, University of Cagliary, Cittadella Universitaria, 09042 Monserrato, Italy. ggiliberti@unica.it.
  • Stefanska J; Department of Pharmaceutical Microbiology, Medical University, 02-007 Warszawa, Poland. jstefanska@wum.edu.pl.
  • Koziol AE; Faculty of Chemistry, Maria Curie-Sklodowska University, 20-031 Lublin, Poland. anna.koziol@poczta.umcs.lublin.pl.
  • Savchenko O; Ecotech Complex, Maria Curie-Sklodowska University, 20-031 Lublin, Poland. oleksandra.savchenko@poczta.umcs.lublin.pl.
  • Strzyga-Lach P; Department of Biochemistry, Medical University, 02-097 Warszawa, Poland. paulina.strzyga@gmail.com.
  • Chrzanowska A; Department of Biochemistry, Medical University, 02-097 Warszawa, Poland. chrzanow.a@gmail.com.
  • Kubiak-Tomaszewska G; Department of Biochemistry and Pharmacogenomics, Faculty of Pharmacy, Medical University of Warsaw, 02-097 Warszawa, Poland. grazynakubiak@poczta.onet.pl.
  • Struga M; Department of Biochemistry, Medical University, 02-097 Warszawa, Poland. mstruga@wum.edu.pl.
Molecules ; 23(10)2018 Sep 21.
Article en En | MEDLINE | ID: mdl-30248936
ABSTRACT
4-Chloro-3-nitrophenylthioureas 1⁻30 were synthesized and tested for their antimicrobial and cytotoxic activities. Compounds exhibited high to moderate antistaphylococcal activity against both standard and clinical strains (MIC values 2⁻64 µg/mL). Among them derivatives with electron-donating alkyl substituents at the phenyl ring were the most promising. Moreover, compounds 1⁻6 and 8⁻19 were cytotoxic against MT-4 cells and various other cell lines derived from human hematological tumors (CC50 ≤ 10 µM). The influence of derivatives 11, 13 and 25 on viability, mortality and the growth rate of immortalized human keratinocytes (HaCaT) was observed.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feniltiourea / Queratinocitos / Antibacterianos Límite: Humans Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feniltiourea / Queratinocitos / Antibacterianos Límite: Humans Idioma: En Año: 2018 Tipo del documento: Article