Affinity capillary electrophoresis and protein charge ladders are used together to measure the contributions of long-range electrostatic interactions to binding of substituted benzene sulfonamide inhibitors to derivatives of human carbonic anhydrase II. The results are analyzed by continuum electrostatic calculations, which afford a detailed analysis of interactions of individual members of a p...

The corrosion inhibition of carbon steel in 1.0 mol L HCl in the presence of an antibacterial sulfa drug Sulfathiazole, IUPAC name 4-amino-N-(1,3-thiazol-2-yl) benzene sulfonamide (TBSA) was investigated using mass loss and electrochemical measurements such as: potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). Surface chemistry was analyzed by X-ray photoelectron sp...

As a part of systematic investigation of biologically active compound, new azo dye ligand N-(4, 6-dimethylpyrimidin-2-yl)-4-((2-hydroxynaphthalen-1-yl) diazenyl) benzene sulfonamide has been synthesized by diazotization of 4-amino-N-(4, 6-dimethylpyrimidin-2-yl) benzenesulfonamide and coupled with coupling compound, naphthalen-2-ol. A new series of Ni (II), Cu (II), and Zn (II) complexes derive...

The selective inhibition of cancer-associated human carbonic anhydrase (CA) enzymes, specifically CA IX and XII, has been validated as a mechanistically novel approach toward personalized cancer management. Herein we report the design and synthesis of a panel of 24 novel glycoconjugate primary sulfonamides that bind to the extracellular catalytic domain of CA IX and XII. These compounds were sy...

In the title compound, C(24)H(24)Cl(4)N(2)O(4)S(2), the dihedral angles between the central benzene ring and the pendant rings are 58.09 (10) and 62.59 (10)°. The dihedral angle between the pendant rings is 81.64 (9)°. Both sulfonamide groups lie to the same side of the central ring but the C-S-N-C torsion angles [73.09 (16) and -117.35 (14)] and S-N-C-C torsion angles [-143.80 (14) and -111.45...

The asymmetric unit of the title compound, C(14)H(13)ClN(2)O(2)S·0.15H(2)O, a novel sulfonamide derivative, comprises two crystallographically independent mol-ecules (A and B) and a water mol-ecule of crystallization, which is partially occupied. One of the mol-ecules (B) is disordered over two positions (B and C) with refined site occupancies of 0.605 (10) and 0.395 (10). The dihedral angles b...

A series of novel isatine-sulphonamide derivatives have been synthesized by combining isatin derivatives with sulphonamides. The structure of the synthesized compounds were elucidated by spectral analysis (IR, NMR and Mass). Investigation of anti-HIV activity was done against HIV-1(IIIB) in MT-4 cells and HIV integrase inhibitory activity. 4-(1-acetyl-5-methyl-2-oxoindolin-3-ylideneamino)-N-(4,...