This paper describes a method based on magnetic levitation (MagLev) that is capable of indirectly measuring the binding of unlabeled ligands to unlabeled protein. We demonstrate this method by measuring the affinity of unlabeled bovine carbonic anhydrase (BCA) for a variety of ligands (most of which are benzene sulfonamide derivatives). This method utilizes porous gel beads that are functionali...

It is important for the prevention and treatment of colibacillosis to monitor drug resistance in Escherichia coli. To choose effective drugs to prevent and control avian colibacillosis in North China, we investigated the resistance of 164 E. coli isolates (from Beijing, Tianjin, Inner Mongolia, Shanxi, and Hebei regions of China) to commonly used clinical sulfonamide antibiotics using a drug su...

N,N-dichloropolystyrene sulfonamide as a decontaminant was synthesized in 5 steps from styrene monomer. Styrene was first polymerized. Then, sulfonation reaction was performed by H2SO4 (c) followed by chlorination with POCl3 obtain chlorosulfonated polystyrene. Amidification reaction was then applied to get sulfonamide resin. Sulfonamide resin was treat...

Two general classes of compounds interfere with the synthesis of the hormone thyroxine in the thyroid gland. These are the thiocarbamides and what will be referred to here as the “aromatic” antithyroid compounds. The present state of knowledge on the mechanism and locus of action of these substances has been reviewed recently (l-3). There appears to be general agreement that the thiocarbamides ...

While normal kidneys are relatively sensitive to ionizing radiation (IR), renal cell carcinoma (RCC) is considered radioresistant. Carbonic anhydrase IX (CA9), an enzyme that maintains intracellular pH by carbon dioxide dissolution, is upregulated in the majority of RCC, but not in normal kidneys. Since regulation of intracellular pH may enhance radiation effects, we hypothesized that inhibitio...

A flexible and short synthesis of sulfonamide-bridged di-, tri-, tetra-, and octasaccharide glycomimetics was accomplished by reaction of glycosyl thioacetates with amino sugar substrates. The chemistry to incorporate the sulfonamide linker in place of a native O-glycosidic bond was broadly scoped, allowing access to head-to-head (1↔1) and head-to-tail (1→2), (1→3), (1→4), and (1→6) sulfonamide...

A feature of sulfonamide therapy for bacterial infections is that species of bacteria differ in their resistance to the antibacterial action of the compounds. It is also recognized that strains of microorganisms within the same species display variations in susceptibility. A disconcerting and confusing factor associated with chemotherapy, which appears to be assuming increasing clinical signifi...

3 0 9 (celecoxib and valdecoxib) could possibly cross react with sulfonamides. The sulfonamide-type reactions (erythema multiforme, Stevens Johnson syndrome, toxic epidermal necrolysis (TEN) and maculopapular rash) were found to be twice as common with celecoxib as with rofecoxib. The pathogenesis of these reactions is likely to be the same as for sulfonamide induced reactions – T cell mediated...