Intracellular Binding of Novel Fluorinated Compounds to Carbonic Anhydrase Isoforms Explored by In-Cell <sup>19</sup>F NMR. [PDF]
Costantino A +8 more
europepmc +1 more source
An ureido-substituted benzenesulfonamide carbonic anhydrase inhibitor exerts a potent antitumor effect in vitro and in vivo. [PDF]
Gazzaroli G +12 more
europepmc +1 more source
Design, synthesis, biological evaluation and in silico studies of 2-anilino- 4-(benzimidazol- 1-yl)pyrimidine scaffold as antitumor agents. [PDF]
Al-Rasheed LS +6 more
europepmc +1 more source
Development of Novel Sulfonamide-Based Pyrazole-Clubbed Pyrazoline Derivatives: Synthesis, Biological Evaluation, and Molecular Docking Study. [PDF]
Zala M +5 more
europepmc +1 more source
Novel Derivatives of 3-Amino-4-hydroxy-benzenesulfonamide: Synthesis, Binding to Carbonic Anhydrases, and Activity in Cancer Cell 2D and 3D Cultures. [PDF]
Vainauskas V +12 more
europepmc +1 more source
Theoretical Basis for Refractive Index Changes Resulting from Solution Phase Molecular Interaction. [PDF]
Kammer MN, Kussrow AK, Bornhop DJ.
europepmc +1 more source
ortho-Acylation attempt of benzenesulfonamide afforded the corresponding hemiaminal as major product. The in situ reduction of the reaction mixture, reported herein, directly provided 2-hydroxyalkyl benzenesulfonamide, an important pharmacophoric element for designing drug-like scaffolds. Its application is demonstrated through designing a novel series
P Praveen Kumar, J Moses Babu, K Vyas
exaly +4 more sources

