V. D. Piaz

发表

Synthesis and Evaluation of Some Pyrazolo[3,4-d]pyridazinones and Analogues as PDE 5 Inhibitors Potentially Useful as Peripheral Vasodilator Agents

V. D. Piaz, M. C. Castellana, C. Vergelli, 2002, Journal of enzyme inhibition and medicinal chemistry.

Synthesis of pyrrolo[2,3-d]pyridazinones as potent, subtype selective PDE4 inhibitors

V. D. Piaz, C. Vergelli, M. Giovannoni, 2007, Journal of enzyme inhibition and medicinal chemistry.

4,5-Functionalized 6-Phenyl-3(2H)-pyridazinones: Synthesis and Evaluation of Antinociceptive Activity.

V. D. Piaz, M. Giovannoni, D. Barlocco, 1996 .

4,5-Functionalized 6-phenyl-3(2H)-pyridazinones: synthesis and evaluation of antinociceptive activity

V. D. Piaz, M. Giovannoni, D. Barlocco, 1996 .

Synthesis and evaluation of some 4,5-disubstituted 6-phenyl-3(2H)-pyridazinones as hypotensive agents

V. D. Piaz, M. Giovannoni, R. Laguna, 1994 .

A new two-step procedure for functionalized-3(2H)-pyridazinones through homolytic substitution of 3-chloropyridazines

V. D. Piaz, M. Giovannoni, G. Ciciani, 1993 .

Diels-alder reactions on 5-acetyl-2-methyl-4-nitro-6-phenylpyridazin-3(2H)-one: A new facet of the pyridazine system

V. D. Piaz, M. Giovannoni, D. Giomi, 1993 .

Reductive cleavage of isoxazolo[3,4-d]pyridazinones : a synthetic approach to various 4,5-functionalized 3(2H)-pyridazinones

V. D. Piaz, M. Giovannoni, G. Ciciani, 1991 .

New synthetic approach to pyrazolo[3,4-d]pyridazin-7(6H)-one ring system

V. D. Piaz, M. Giovannoni, G. Ciciani, 1989 .

Isoxazolo[3,4-d]pyridazin-7(6H)-ones. Synthesis of 3-unsubstituted derivatives a reinvestigation

V. D. Piaz, M. Giovannoni, G. Ciciani, 1991 .

4-Amino-3(2H)-pyridazinones bearing arylpiperazinylalkyl groups and related compounds: synthesis and antinociceptive activity.

M. Scheideler, V. D. Piaz, C. Vergelli, 2003, Farmaco.

Antiinflammatory and antiplatelet activity of new 5-acyl-6-aryl-pyridazine derivatives

V. D. Piaz, L. Raimondi, G. Ciciani, 1988 .

Isoxazolo(3,4-d)pyridazin-7(6H)-ones: Synthesis of 3-Unsubstituted Derivatives: A Reinvestigation.

V. D. Piaz, M. Giovannoni, G. Ciciani, 1992 .

Pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazin-7(8H)-one: a new heterocyclic ring system from isoxazolopyridazinones

V. D. Piaz, S. Chimichi, G. Ciciani, 1986 .

New functionalized pyrazoles from isoxazolopyridazinones

V. D. Piaz, S. Chimichi, G. Ciciani, 1985 .

1,2,3,4-Tetrahydro-1,2-diazepine derivatives from isoxazolo[3,4-d]pyridazin-7(6H)-ones

V. D. Piaz, S. Chimichi, G. Ciciani, 1984 .

Condensation of some 3‐methylisoxazolo[3,4‐d]pyridazin‐7(6H)ones with aromatic aldehydes

S. Pinzauti, V. D. Piaz, P. Lacrimini, 1976 .

4‐Amino‐3(2H)‐pyridazinones Bearing Arylpiperazinylalkyl Groups and Related Compounds: Synthesis and Antinociceptive Activity.

M. Scheideler, V. D. Piaz, C. Vergelli, 2004 .

4-Nitro-1,2-oxazoles from Hydroximic Acid Chlorides

S. Pinzauti, V. D. Piaz, P. Lacrimini, 1975 .

Mono- and Di-substituted 5,6-Diphenyl-3-alkylaminopyridazines Active as ACAT Inhibitors

A. Gelain, B. Kwon, L. Toma, 2002 .

5,6-Diphenylpyridazine derivatives as acyl-CoA:cholesterol acyltransferase inhibitors.

L. Toma, Y. K. Kim, V. D. Piaz, 2001, Journal of medicinal chemistry.

Heterocyclic-fused 3(2H)-pyridazinones as potent and selective PDE IV inhibitors: Further structure-activity relationships and molecular modelling studies

V. D. Piaz, M. Giovannoni, V. Segarra, 1998 .

The use of 3,5‐dimethyl‐4‐nitroisoxazole for the preparation of α,β‐unsaturated aromatic acids

V. D. Piaz, D. Donati, P. Sarti-fantoni, 1980 .

Design, synthesis and evaluation of N-benzoylindazole derivatives and analogues as inhibitors of human neutrophil elastase.

A. Khlebnikov, V. D. Piaz, C. Vergelli, 2011, Bioorganic & medicinal chemistry.

α2‐Agonists as analgesic agents

C. Ghelardini, V. D. Piaz, C. Vergelli, 2009, Medicinal research reviews.

Mono‐ and Di‐Substituted 5,6‐Diphenyl‐3‐alkylaminopyridazines Active as ACAT Inhibitors.

A. Gelain, B. Kwon, L. Toma, 2002 .

5,6-dinitrophenyl and 5-aminophenyl-6-nitrophenyl analogues of the acat inhibitor 5,6-diphenyl-3-alkylaminopyridazines

G. Celentano, B. Kwon, L. Toma, 2000 .

New Synthesis of Differently Fused Pyridazinoquinolines

V. D. Piaz, C. Vergelli, M. Giovannoni, 1999 .

Selective ACAT inhibitors as promising antihyperlipidemic, antiathero-sclerotic and anti-Alzheimer drugs.

V. D. Piaz, C. Vergelli, M. Giovannoni, 2003, Mini reviews in medicinal chemistry.

New Pyrazolo[1′,5′:1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as Potent and Selective PDE5 Inhibitors.

V. D. Piaz, C. Vergelli, M. Giovannoni, 2005 .