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Synthesis and Antimicrobial Activity of 6-Thioxo-6,7-dihydro-2H-[1,2,4]triazino[2,3-c]-quinazolin-2-one Derivatives.
Nosulenko, Inna S; Voskoboynik, Olexii Yu; Berest, Galina G; Safronyuk, Sergiy L; Kovalenko, Sergiy I; Kamyshnyi, Oleksandr M; Polishchuk, Nataliya M; Sinyak, Raisa S; Katsev, Andrey V.
Afiliación
  • Nosulenko IS; Department of Organic and Bioorganic Chemistry, Zaporizhzhia State Medical University, Mayakovsky ave., 26, 69035, Zaporizhzhia, Ukraine.
  • Voskoboynik OY; Department of Organic and Bioorganic Chemistry, Zaporizhzhia State Medical University, Mayakovsky ave., 26, 69035, Zaporizhzhia, Ukraine.
  • Berest GG; Department of Pharmacognosy, Pharmaceutical chemistry and Technologies, Department of post-graduate education, Zaporizhzhia State Medical University, Mayakovsky ave., 26, 69035, Zaporizhzhia, Ukraine.
  • Safronyuk SL; Department of Pharmacy, Crimean State Medical University, 95006, Simferopol, Ukraine.
  • Kovalenko SI; Department of Organic and Bioorganic Chemistry, Zaporizhzhia State Medical University, Mayakovsky ave., 26, 69035, Zaporizhzhia, Ukraine.
  • Kamyshnyi OM; Department of Microbiology, Virology and Immunology, Zaporizhzhia State Medical University, Mayakovsky ave., 26, 69035, Zaporizhzhia, Ukraine.
  • Polishchuk NM; Department of Microbiology, Virology and Immunology, Zaporizhzhia State Medical University, Mayakovsky ave., 26, 69035, Zaporizhzhia, Ukraine.
  • Sinyak RS; Department of Organic and Bioorganic Chemistry, Zaporizhzhia State Medical University, Mayakovsky ave., 26, 69035, Zaporizhzhia, Ukraine.
  • Katsev AV; Department of General Chemistry, Crimean State Medical University, 95006, Simferopol, Ukraine.
Sci Pharm ; 82(3): 483-500, 2014.
Article en En | MEDLINE | ID: mdl-25853063
Potassium 8-R(1)-9-R(2)-10-R(3)-3-R-2-oxo-2H-[1,2,4]triazino[2,3-c]quinazoline-6-thiolates 2.1-2.26 were synthesized via cyclocondensation of 6-R-3-(3-R(1)-4-R(2)-5-R(3)-aminophenyl)-1,2,4-triazin-5-ones 1.1-1.26 with carbon disulfide, potassium hydroxide, and ethanol or with potassium O-ethyl dithiocarbonate in 2-propanol. The corresponding thiones 3.1-3.26 were obtained by treatment of 2.1-2.26 with hydrochloric acid. It was found that the nature of the substituents in positions 3, 4, and 5 of the corresponding 6-R-3-(3-R(1)-4-R(2)-5-R(3)-aminophenyl)-1,2,4-triazin-5-ones were affected on the terms of the reaction. The structures of compounds were proven by a complex of physicochemical methods ((1)H, (13)C NMR, LC-MS, and EI-MS). The results of the antibacterial and antifungal activity assay allowed the determination of the high sensitivity of Staphylococcus aureus ATCC 25923 (MIC 6.25-100 µg/mL, MBC 12.5-200 µg/mL) to the synthesized compounds.
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Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Sci Pharm Año: 2014 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: Sci Pharm Año: 2014 Tipo del documento: Article