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DOI 10.3109/14756366.2013.782299

Медицинская библиотека · Journal of enzyme inhibition and medicinal chemistry · 2013

Synthesis and characterization of a proton transfer salt between 2,6-pyridinedicarboxylic acid and 2-aminobenzothiazole, and its complexes and their inhibition studies on carbonic anhydrase isoenzymes.

İlkimen Halil, Yenikaya Cengiz, Sarı Musa, Bülbül Metin, Tunca Ekrem, Dal Hakan

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

A novel proton transfer compound (HABT)(+)(Hdipic)(-) (1) obtained from ABT and H2dipic and its metal complexes (2-5) have been prepared and characterized by spectroscopic techniques. Single crystal X-ray diffraction method has also been applied to 2 and 5. While complex 2 has a distorted octahedral conformation, 5 exhibits a distorted square pyramidal structure. The structures of 3 and 4 might be proposed as octahedral according to experimental data. All compounds were also evaluated for their in vitro inhibition effects on hCA I and II for their hydratase and esterase activities. Although there is no inhibition for hydratase activities, all compounds have inhibited the esterase activities of hCA I and II. The comparison of the inhibition studies of 1-5 to parent compounds indicates that 1-5 have superior inhibitory effects. The inhibition effects of 2-5 are also compared to inhibitory properties of the metal complexes of ABT and H2dipic, revealing an improved transfection profile.

Для цитирования: İlkimen Halil, Yenikaya Cengiz, Sarı Musa, Bülbül Metin, Tunca Ekrem, Dal Hakan. Synthesis and characterization of a proton transfer salt between 2,6-pyridinedicarboxylic acid and 2-aminobenzothiazole, and its complexes and their inhibition studies on carbonic anhydrase isoenzymes.. Journal of enzyme inhibition and medicinal chemistry. 2013. DOI: 10.3109/14756366.2013.782299.

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