Sergio De Munari - Concepedia

Author

Sergio De Munari

Sigma Tau (Italy)

Also Known As

S. DE MUNARI, S. De Munari, Sergio De Munari

Publications

631

Citations

H-Index

Concepts

All Affiliations

Sigma Tau (Italy)CTI BioPharma (United Kingdom)Ospedale San Carlo

About

Sergio De Munari is an author at Sigma Tau (Italy) specializing in pharmacology, natural sciences, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	7	7	297
2	Biochemistry	7	7	316
3	Medicine	5	5	118
4	Engineering	3	3	186
5	Biomolecular Engineering	2	2	44

Sergio De Munari

Publications

621

Citations

H-Index

Page 1

	Year	Citations
Discovery of a Potent, Selective, and Orally Active Proteasome Inhibitor for the Treatment of Cancer Bruce D. Dorsey, Mohamed Iqbal, Sankar Chatterjee, Journal of Medicinal Chemistry	2008	146
Hypervalent Iodine Oxidants: Structure and Kinetics of the Reactive Intermediates in the Oxidation of Alcohols and 1,2-Diols by <i>o</i>-Iodoxybenzoic Acid (IBX) and Dess−Martin Periodinane. A Comparative <sup>1</sup>H-NMR Study Sergio De Munari, M. FRIGERIO, Marco Santagostino The Journal of Organic Chemistry Chemical EngineeringChemical KineticsBenzyl AlcoholEngineeringBiochemistry	1996	142
Pharmacological Profile of the Novel Inotropic Agent (E,Z)-3-((2-Aminoethoxy)imino)androstane-6,17-dione Hydrochloride (PST2744) R. Micheletti, Giovan Giuseppe Mattera, Marcella Rocchetti, Journal of Pharmacology and Experimental Therapeutics	2002	64
Structure-Based Design and Synthesis of Novel Potent Na<sup>+</sup>,K<sup>+</sup>-ATPase Inhibitors Derived from a 5α,14α-Androstane Scaffold as Positive Inotropic Compounds Sergio De Munari, Alberto Cerri, Mauro Gobbini, Journal of Medicinal Chemistry Positive Inotropic CompoundsBioorganic ChemistryChemical BiologyDigitalis-like ActivityPharmaceutical Chemistry	2003	39
Asymetric dihydroxylations via chiral oxazolidines Lino Colombo, Cesare Gennari, Giovanni Poli, Tetrahedron Letters Chiral OxazolidinesOrganic ChemistryStereoselective SynthesisPharmacologyAsymmetric Catalysis	1985	39
Stereospecificity in the transformation of α-aminoacids into fluoroacids F. Faustini, Sergio De Munari, Achille Panzeri, Tetrahedron Letters Stereoselective SynthesisFluorous SynthesisBiochemistry	1981	36
Stability of Boronic Esters to Hydrolysis: A Comparative Study Raffaella Bernardini, Ambrogio Oliva, Alessandro Paganelli, Chemistry Letters EngineeringOrganic ChemistryAbstract Boronic EstersChemistryPharmaceutical Chemistry	2009	34
17α-<i>O</i>-(Aminoalkyl)oxime Derivatives of 3β,14β-Dihydroxy-5β-androstane and 3β-Hydroxy-14-oxoseco-D-5β-androstane as Inhibitors of Na<sup>+</sup>,K<sup>+</sup>-ATPase at the Digitalis Receptor Mauro Gobbini, Paolo Barassi, Alberto Cerri, Journal of Medicinal Chemistry Molecular PharmacologyMedicinal ChemistryBioorganic ChemistryBiochemistryDigitalis Na	2001	31
A New Approach to the Design of Novel Inhibitors of Na<sup>+</sup>,K<sup>+</sup>-ATPase: 17α-Substituted Seco-D 5β-Androstane as Cassaine Analogues Sergio De Munari, Paolo Barassi, Alberto Cerri, Journal of Medicinal Chemistry	1998	29
Synthesis and Inotropic Activity of 1-(<i>O</i>-Aminoalkyloximes) of Perhydroindene Derivatives as Simplified Digitalis-like Compounds Acting on the Na<sup>+</sup>,K<sup>+</sup>-ATPase Alberto Cerri, Nicoletta Almirante, Paolo Barassi, Journal of Medicinal Chemistry Drug TargetBioorganic ChemistryAldo-keto ReductaseCorresponding Digitalis 17Beta-aminoalkyloximesChemistry	2001	21

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