Effect of coordination to antimony(III) on the antifungal activity of 2-acetylpyridine- and 2-benzoylpyridine-derived hydrazones

Antimony(III) [Sb(L)Cl2] complexes were obtained with 2-acetylpyridine-phenylhydrazone (H2AcPh), 2-acetylpyridine-para-chloro-phenylhydrazone (H2AcpClPh), 2-acetylpyridine-para-nitro-phenylhydrazone (H2AcpNO2Ph) and 2-acetylpyridine-para-hydroxy-phenylhydrazone (H2AcpOHPh) along with the 2-benzoylpyridine-phenylhydrazone analogs H2BzPh, H2BzpClPh, H2BzpNO2Ph, H2BzpOHPh (HL). [Sb(2BzpClPh)Cl2], complex (6), (IC50 = 4.91 ± 1.20 μmol L−1) was as active as nystatin (IC50 = 4.44 ± 0.76 μmol L−1) and twofold more active than H2BzpClPh (IC50 = 10.05 ± 0.67 μmol L−1) against Candida dubliniensis. While H2BzpClPh proved to be inactive against Candida glabrata, 6 (IC50 = 10.11 ± 0.64 μmol L−1) was more active than miconazole nitrate (IC50 = 19.50 ± 4.53 μmol L−1). Similarly, H2BzpNO2Ph revealed to be inactive against Candida lusitaniae whereas complex [Sb(2BzpNO2Ph)Cl2] (7) (IC50 = 8.54 ± 2.21 μmol L−1) proved to be as active as nystatin (IC50 = 5.31 ± 0.84 μmol L−1).

[Sb(2BzpClPh)Cl2], complex (6), was as active as nystatin and twofold more active than the free hydrazone H2BzpClPh against Candida dubliniensis. While H2BzpClPh proved to be inactive against Candida glabrata, complex (6) was more active than miconazole nitrate.Figure optionsDownload as PowerPoint slide