1. Investigation of the effects of the proton transfer salts of 2-aminopyridine derivatives with 5-sulfosalicylic acid and their Cu(II) complexes on cancer-related carbonic anhydrases: CA IX and CA XII
- Author
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Ekrem Tunca, Cengiz Yenikaya, Halil İlkimen, Metin Bülbül, Rukiye Saygılı Canlıdinç, Tunca, Ekrem, Bülbül, Metin, İlkimen, Halil, Saygılı Canlıdinç, Rukiye, and Yenikaya, Cengiz
- Subjects
Proton ,General Chemical Engineering ,02 engineering and technology ,010402 general chemistry ,01 natural sciences ,Biochemistry ,Isozyme ,Medicinal chemistry ,Industrial and Manufacturing Engineering ,Carbonic Anhydrase ,chemistry.chemical_compound ,Materials Chemistry ,Ic50 values ,2-Aminopyridine ,Cancer ,Sulfosalicylic acid ,General Chemistry ,Proton Transfer Salt ,021001 nanoscience & nanotechnology ,In vitro ,0104 chemical sciences ,chemistry ,5-Sulfosalicylic Acid ,Metal Complex ,0210 nano-technology - Abstract
Six novel proton transfer compounds (15-20) obtained from 5-sulfosalicylic acid (1) and 2-aminopyridine derivatives [2-amino-3-benzyloxypyridine (2), 2-amino-3-hydroxylpyridine (3), 2-amino-3-methylpyridine (4), 2-amino-3-nitropyridine (5), 2-amino-3-nitro-4-methylpyridine (6) and 2-amino-3-nitro-6-methylpyridine (7)] and their Cu(II) complexes (21-26) along with the Cu(II) complexes of 2-7 (9-14) have been prepared and characterized by spectroscopic techniques. The in vitro inhibition effects of all compounds on CA IX and CA XII isozymes as well as on hCA I and hCA II were investigated and the results were compared. The inhibition studies showed that the synthesized compounds are more selective to CA XII isozyme. The hydratase IC50 values of the compounds were determined as in the range of 15.61 +/- 2.32 mu M-99.02 +/- 4.99 mu M for hCA I, 22.36 +/- 0.75 mu M-77.03 +/- 4.03 mu M for hCA II, 23.90 +/- 1.67 mu M-138.63 +/- 5.45 mu M for CA IX, and 9.50 +/- 1.16 mu M-693.15 +/- 8.96 mu M for CA XII. The inhibition data have been analyzed using one-way analysis of variance for multiple comparisons (p < 0.0001).
- Published
- 2020