An integrated approach (synthetic, structural and biological) to the study of aroylhydrazone salts (CROSBI ID 254242)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Vrdoljak, Višnja ; Prugovečki, Biserka ; Primožič, Ines ; Hrenar, Tomica ; Cvijanović, Danijela ; Parlov Vuković, Jelena ; Odžak, Renata ; Skočibušić, Mirjana ; Prugovečki, Stjepan ; Lovrić, Jasna ; Matković-Čalogović, Dubravka ; Cindrić, Marina
engleski
An integrated approach (synthetic, structural and biological) to the study of aroylhydrazone salts
The reaction of two methoxy substituted salinazid-based hydrazones, 4-methoxysalicylaldehyde isonicotinoyl hydrazone (L1) and 3-methoxysalicylaldehyde isonicotinoyl hydrazone (L2) with HCl, HBr, HNO3 and H2SO4 in methanol yielded salts of different stoichiometries (1:1 or 2:1) and/or polymorphic forms. In such a way (HL1)+X− and (HL2)+X−salts where X = Cl, Br, NO3, HSO4, as well as [H(L1)2]+Br− and (HL1)2+SO4 2− were obtained. Solid state properties and propensity for transformation between different forms in solution were also investigated. Crystal structures were solved by the single-crystal X-ray diffraction method and by the powder diffraction method. Details of anion binding with the isoniazid functionality are discussed. The aroylhydrazone salts were evaluated for cytotoxic activity in vitro. All compounds exhibited weak cytotoxicity against THP-1 and no cytotoxicity against HepG2 cells. In a preliminary antimicrobial screening assay, these compounds were not only active against antibiotic susceptible Gram-positive, but also exhibited antibacterial effects on a wide range of multidrug-resistant Gram-positive as well as multidrug resistant Gram-negative bacterial pathogens.
Aroylhyderazone salts ; Polymorphic forms ; Cytotoxic activity ; Antibacterial effects
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Podaci o izdanju
42 (14)
2018.
11697-11707
objavljeno
1144-0546
1369-9261
10.1039/c8nj01457d
Povezanost rada
Kemija