Alberto Cerri
University of Urbino(IT)Sigma Tau (Italy)(IT)
Publications by Year
Research Areas
Steroid Chemistry and Biochemistry, Inflammatory mediators and NSAID effects, Ion Transport and Channel Regulation, Synthetic Organic Chemistry Methods, Hormonal Regulation and Hypertension
Most-Cited Works
- → Synthesis and pharmacological activity of a series of dihydro-1H-pyrrolo[1,2-a]imidazole-2,5(3H,6H)-diones, a novel class of potent cognition enhancers(1993)68 cited
- → 17β-(3-Furyl)-5β-androstane-3β,14β,17α-triol (PST 2238). A Very Potent Antihypertensive Agent with a Novel Mechanism of Action(1997)50 cited
- → A general, [1+4] approach to the synthesis of 3(5)-substituted pyrazoles from aldehydes(1998)43 cited
- → Structure-Based Design and Synthesis of Novel Potent Na+,K+-ATPase Inhibitors Derived from a 5α,14α-Androstane Scaffold as Positive Inotropic Compounds(2003)39 cited
- → 17α-O-(Aminoalkyl)oxime Derivatives of 3β,14β-Dihydroxy-5β-androstane and 3β-Hydroxy-14-oxoseco-D-5β-androstane as Inhibitors of Na+,K+-ATPase at the Digitalis Receptor(2001)31 cited
- → 17β-O-Aminoalkyloximes of 5β-Androstane-3β,14β-diol with Digitalis-like Activity: Synthesis, Cardiotonic Activity, Structure−Activity Relationships, and Molecular Modeling of the Na+,K+-ATPase Receptor(2000)30 cited
- → A New Approach to the Design of Novel Inhibitors of Na+,K+-ATPase: 17α-Substituted Seco-D 5β-Androstane as Cassaine Analogues(1998)29 cited
- → Development of a practical and sustainable strategy for the synthesis of ST1535 by an iron-catalyzed Kumada cross-coupling reaction(2014)24 cited
- → Novel Analogues of Istaroxime, a Potent Inhibitor of Na+,K+-ATPase: Synthesis and Structure−Activity Relationship(2008)23 cited
- → Synthesis, Cardiotonic Activity, and Structure−Activity Relationships of 17β-Guanylhydrazone Derivatives of 5β-Androstane-3β,14β-diol Acting on the Na+,K+-ATPase Receptor(1997)22 cited