α-Amino acid derivatives as proton pump inhibitors and potent anti-ulcer agents

α-Amino acid derivatives as proton pump inhibitors and potent anti-ulcer agents Discovery, synthesis, and biological evaluation of novel pyrrole derivatives as highly selective potassium-competitive acid blockers Nicotinamide Derivatives as a New Class of Gastric H⁺/K⁺-ATPase Inhibitors. 1. Synthesis and Structure−Activity Relationships of N-Substituted 2-(Benzhydryl- and benzylsulfinyl)nicotinamides Synthesis and antiulcer activity of N-substituted N'-[3-[3-(piperidinomethyl)phenoxy]propyl]ureas: histamine H2-receptor antagonists with potent mucosal protective activity Reversible Inhibitors of the Gastric (H+/K+)-ATPase. 5. Substituted 2,4-Diaminoquinazolines and Thienopyrimidines Substituted methoxybenzyl-sulfonyl- 1H -benzo[d]imidazoles evaluated as effective H + /K + -ATPase inhibitors and anti-ulcer therapeutics Anti-Helicobacter pyloriAgents. 1. 2-(Alkylguanidino)-4-furylthiazoles and Related Compounds Discovery of a Novel Pyrrole Derivative 1-[5-(2-Fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl]-N-methylmethanamine Fumarate (TAK-438) as a Potassium-Competitive Acid Blocker (P-CAB) Studies on antiulcer drugs. 7. 2-Guanidino-4-pyridylthiazoles as histamine H2-receptor antagonists with potent gastroprotective effects against nonsteroidal antiinflammatory drug-induced injury Arylamino containing hydroxamic acids as potent urease inhibitors for the treatment of Helicobacter pylori infection