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机译:
Univ Naples 2, Dept Biochem Biophys & Gen Pathol, Vico L de Crecchio 7, I-80138 Naples, Italy;
TES Pharma Srl, Via P Togliatti 20, I-06073 Perugia, Italy;
Sapienza Univ Rome, Ist Pasteur Italia, Fdn Cenci Bolognetti, Dept Drug Chem & Technol, Ple A Moro 5, I-00185 Rome, ItalyUniv Bayreuth, Dept Biochem, D-95440 Bayreuth, Germany;
机译:Design of new potent and selective secretory phospholipase A(2) inhibitors. 6-Synthesis, structure-activity relationships and molecular modelling of 1-substituted-4-(4,5-dihydro-1,2,4-(4H)-oxadiazol-5-one-3-yl(methyl))-functionali zed aryl piperazin/one/dione derivatives.
机译:Novel analogues of Istaroxime, a potent inhibitor of Na(+),K(+)-ATPase: Synthesis, structure-activity relationship and 3D-quantitative structure-activity relationship of derivatives at position 6 on the androstane scaffold.
机译:Structure-activity relationship studies of 4-benzyl-1H-pyrazol-3-yl β-d-glucopyranoside derivatives as potent and selective sodium glucose co-transporter 1 (SGLT1) inhibitors with therapeutic activity on postprandial hyperglycemia