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[13] L. Puccetti, G. Fasolis, D. Vullo, Z. H. Chohan, A. Scoz-zafavab and C. T. Supuranb, “Carbonic Anhydrase Inhibitors. Inhibition of Cytosolic/Tumor-Associated Carbonic Anhy-drase Isozymes I, II, IX, and XII with Schiff Bases Incorpo-rating Chromone and Aromatic Sulfonamide Moieties, and Their Zinc Complexes,” Bioorganic & Medical Chemistry Letter, Vol. 15, 2005, pp.
3096-3101.doi:10.1016/j.bmcl.2005.04.055
has been cited by the following article:
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TITLE:
Synthesis, Structure Analysis and Antibacterial Activity of New Potent Sulfonamide Derivatives
AUTHORS:
Abdulhakeem Alsughayer, Abdel-Zaher A. Elassar, Seham Mustafa, Fakhreia Al Sagheer
KEYWORDS:
Sulfonamide, Sulfa drug, Gram positive, Gram negative bacteria
JOURNAL NAME:
Journal of Biomaterials and Nanobiotechnology,
Vol.2 No.2,
February
15,
2011
ABSTRACT: Modification of sulfonamid drug using different principles of chemical reactions was investigated. These reactions involve the condensation of an amino group with triethyl orthoformate and dimethylformamide dimethyl acetal. Ability of sulfa to condense with active keto compounds, like ethyl pyruvate and piprazine carboxyaldehye was studied. Alkyation of sulfa with different chloro derivatives was also reported. The structure of the isolated compound was elucidated and confirmed using elemental analysis and spectral data. The bioactivity of the ob-tained compounds was investigated against different gram positive and gram negative bacteria. The study reveals that most of the modified drugs show high to moderate antibacterial activity.