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Structure-based design and synthesis of novel potent Na+,K+ -ATPase inhibitors derived from a 5alpha,14alpha-androstane scaffold as positive inotropic compounds.

Prassis Istituto Di Ricerche Sigma-Tau

A new approach to the design of novel inhibitors of Na+,K+-ATPase: 17alpha-substituted seco-D 5beta-androstane as cassaine analogues.

Prassis Istituto Di Ricerche Sigma-Tau

Antiulcer agents. 4-substituted 2-guanidinothiazoles: reversible, competitive, and selective inhibitors of gastric H+,K(+)-ATPase.

Pfizer

 

Alteration of Na⁺ permeability in human erythrocytes as studied by ²³Na-NMR and inhibition of the kidney Na⁺,K⁺-ATPase activities with saponins: Interaction of Gleditsia saponins with human erythrocyte membranes

TBA