Design and Development of New Benzopyrazole Derivatives as Selective Inhibitors of Helicobacter pylori IMPDH

Abstract Helicobacter pylori ( H. pylori ) is a Gram‐negative bacterial pathogen responsible for gastritis, peptic ulcers, and gastric cancer. Current treatment regimens involve triple or quadruple antibiotic therapies; however, the rise in antibiotic resistance necessitates the development of alternative therapeutic strategies. This study explores the potential of targeting H. pylori inosine‐5‐monophosphate dehydrogenase ( Hp IMPDH), a crucial enzyme in purine nucleotide biosynthesis essential for bacterial proliferation. A novel series of benzopyrazole derivatives was designed and synthesized as potential Hp IMPDH inhibitors. Biochemical assays revealed that the synthesized compounds exhibited potent inhibitory activity, with SN‐8.1 and SN‐8.2 displaying IC 50 values of 0.122 and 0.187 µM, respectively. These compounds showed minimal inhibition of human IMPDH2, suggesting selectivity toward the bacterial enzyme. Molecular docking studies further confirmed strong binding affinities at the Hp IMPDH active site. Cytotoxicity assays indicated that the compounds were nontoxic at the tested concentrations. These findings demonstrate that benzopyrazole‐based Hp IMPDH inhibitors offer a promising strategy for the development of new anti‐ H. pylori agents.