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Biological properties and conformational studies of amphiphilic Pd(II) and Ni(II) complexes bearing functionalized aroylaminocarbo-N-thioylpyrrolinate units.
Poyraz, Samet; Belveren, Samet; Aydinoglu, Sabriye; Ulger, Mahmut; de Cózar, Abel; de Gracia Retamosa, Maria; Sansano, Jose M; Döndas, H Ali.
Afiliación
  • Poyraz S; Department of Chemistry, Faculty of Pharmacy, Mersin University, Yenisehir, 33169 Mersin, Turkey.
  • Belveren S; Department of Chemistry, Faculty of Pharmacy, Mersin University, Yenisehir, 33169 Mersin, Turkey.
  • Aydinoglu S; Department of Basic Pharmaceutical Sciences, Faculty of Pharmacy, Çukurova University, Balcali 01330, Adana, Turkey.
  • Ulger M; Department of Pharmaceutical Microbiology, Faculty of Pharmacy, Mersin University, Yenisehir, 33169 Mersin, Turkey.
  • de Cózar A; Departamento de Química Orgánica I, Facultad de Química. Universidad del País Vasco/Euskal Herriko Unibertsitatea UPV/EHU, Centro de Innovación en Química Avanzada (ORFEO-CINQA) and Donostia International Physics Center (DIPC), P. K. 1072, E-20018 San Sebastián, Spain.
  • de Gracia Retamosa M; IKERBASQUE, Basque Foundation of Science, Plaza Euskadi 5, 48009, Bilbao, Spain.
  • Sansano JM; University of Alicante, Department of Organic Chemistry, Centro de Innovación en Química Avanzada (ORFEO-CINQA) and Instituto de Síntesis Orgánica (ISO), PO Box 99, 03080 Alicante, Spain.
  • Döndas HA; University of Alicante, Department of Organic Chemistry, Centro de Innovación en Química Avanzada (ORFEO-CINQA) and Instituto de Síntesis Orgánica (ISO), PO Box 99, 03080 Alicante, Spain.
Beilstein J Org Chem ; 17: 2812-2821, 2021.
Article en En | MEDLINE | ID: mdl-34925620
A series of novel palladium(II) and nickel(II) complexes of multifunctionalized aroylaminocarbo-N-thioylpyrrolinates were synthesized and characterized by analytical and spectroscopic techniques. The biological properties of the freshly prepared compounds were screened against S. aureus, B. subtilis, A. hydrophila, E. coli, and A. baumannii bacteria and antituberculosis activity against M. tuberculosis H37Rv strains. Also, the antifungal activity was studied against C. albicans, C. tropicalis, and C. glabrata standard strains. A deep conformational survey was monitored using DFT calculations with the aim to explain the importance of the final conformation in the biological experimental results.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Beilstein J Org Chem Año: 2021 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Beilstein J Org Chem Año: 2021 Tipo del documento: Article País de afiliación: Turquía