F. Campagna

发表

Synthesis and biophysical evaluation of arylhydrazono-1H-2-indolinones as β-amyloid aggregation inhibitors.

G. Palazzo, A. De Stradis, M. Catto, 2011, European journal of medicinal chemistry.

β‐D‐Glucosyl Conjugates of Highly Potent Inhibitors of Blood Coagulation Factor Xa Bearing 2‐Chorothiophene as a P1 Motif

M. Romano, C. Altomare, M. Lograno, 2012, ChemMedChem.

Design, synthesis and biological evaluation of indane-2-arylhydrazinylmethylene-1,3-diones and indol-2-aryldiazenylmethylene-3-ones as beta-amyloid aggregation inhibitors.

A. De Stradis, M. Catto, A. Carotti, 2010, European journal of medicinal chemistry.

A convenient synthesis of nitriles from primary amides under mild conditions

Giovanni Casini, A. Carotti, F. Campagna, 1977 .

Targeting monoamine oxidases with multipotent ligands: an emerging strategy in the search of new drugs against neurodegenerative diseases.

F. Leonetti, O. Nicolotti, M. Catto, 2011, Current medicinal chemistry.

Design, synthesis and biological evaluation of benzo[e][1,2,4]triazin-7(1H)-one and [1,2,4]-triazino[5,6,1-jk]carbazol-6-one derivatives as dual inhibitors of beta-amyloid aggregation and acetyl/butyryl cholinesterase.

P. Koutentis, A. De Stradis, M. Catto, 2012, European journal of medicinal chemistry.

Mannich base approach to 5‐methoxyisatin 3‐(4‐isopropylphenyl)hydrazone: A water‐soluble prodrug for a multitarget inhibition of cholinesterases, beta‐amyloid fibrillization and oligomer‐induced cytotoxicity

O. Nicolotti, M. Catto, L. Pisani, 2017, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Synthesis and biological evaluation of pyridazino[4,3-b]indoles and indeno[1,2-c]pyridazines as new ligands of central and peripheral benzodiazepine receptors.

M. P. Mascia, E. Maciocco, A. Carotti, 2003, Farmaco.

Benzodiazepine Receptor Affinities, Behavioral, and Anticonvulsant Activity of 2-Aryl-2,5-dihydropyridazino[4,3-b]indol- 3(3H)-ones in Mice

R. Mckernan, P. Giusti, A. Carotti, 2000, Pharmacology Biochemistry and Behavior.

An Easy, High-Yield Conversion of Aldoximes to Nitriles

R. Ballini, A. Carotti, F. Campagna, 1979 .

Synthesis, central and peripheral benzodiazepine receptor affinity of pyrazole and pyrazole-containing polycyclic derivatives.

E. Maciocco, A. Carotti, F. Campagna, 2004, Farmaco.

Insights into Structure-Activity Relationships of 3-Arylhydrazonoindolin-2-One Derivatives for Their Multitarget Activity on β-Amyloid Aggregation and Neurotoxicity

M. de Candia, F. De Santis, M. Catto, 2018, Molecules.

Synthesis and monoamine oxidase inhibitory activity of new pyridazine-, pyrimidine- and 1,2,4-triazine-containing tricyclic derivatives.

B. Testa, F. Leonetti, M. Catto, 2007, Journal of medicinal chemistry.

SYNTHESIS OF NEW HETEROCYCLIC RING SYSTEMS: INDENO[2,1-B]-BENZO[G]INDOLIZINE AND INDENO[1',2':5,4]PYRROLO[2,1-A]PHTHALAZINE

Angelo Carotti, Giovanni Casini, Giovanni Casini, 1990 .

Chemical and Catalytic Reductive Isomerization of [1,3]Oxazino[2,3-a]isoquinolines to [1,3]Oxazino[3,2-b]isoquinolines

Giovanni Casini, A. Carotti, F. Campagna, 1988 .

Synthesis and antibacterial activity of pyridazino[4,3-b]indole-4-carboxylic acids carrying different substituents at N-2.

A. Rosato, A. Carotti, F. Campagna, 2002, Farmaco.

Synthesis and structure-affinity relationships at the central benzodiazepine receptor of pyridazino[4,3-b]indoles and indeno[1,2-c]pyridazines.

G. Genchi, A. Carotti, F. Campagna, 1999, Bioorganic & medicinal chemistry.

Structure-activity relationships of 2-aryl-2,5-dihydropyridazino [4,3-b]indol-3(3H)-ones at the benzodiazepine receptor.

G. Genchi, G. De Sarro, A. Carotti, 1996, Bioorganic & medicinal chemistry.

2-Aryl-2,5-dihydropyridazino[4,3-b]indol-3(3H)-ones: novel rigid planar benzodiazepine receptor ligands.

G. Genchi, G. De Sarro, A. Carotti, 1993, Bioorganic & medicinal chemistry.

Inhibition of carbonic anhydrase by substituted benzenesulfonamides. A reinvestigation by QSAR and molecular graphics analysis

R. Langridge, T. Klein, A. Carotti, 1989 .

Cyclic amidine analogues of taurine and homotaurine: synthesis and effects on rat skeletal muscle.

A. De Luca, S. Pierno, A. Carotti, 1994, Farmaco.

Effects of taurine analogues on chloride channel conductance of rat skeletal muscle fibers: a structure-activity relationship investigation

S. Pierno, D. Conte Camerino, A. Carotti, 1994, Naunyn-Schmiedeberg’s Archives of Pharmacology.

Design, synthesis, and biological evaluation of glycine-based molecular tongs as inhibitors of Abeta1-40 aggregation in vitro.

E. Sotelo, P. Acquafredda, M. Catto, 2008, Bioorganic & medicinal chemistry.

1,3-Dialkyl-8-(hetero)aryl-9-OH-9-deazaxanthines as potent A2B adenosine receptor antagonists: design, synthesis, structure-affinity and structure-selectivity relationships.

M. Loza, J. Brea, F. Leonetti, 2008, Bioorganic & medicinal chemistry.

Investigation on the influence of (Z)-3-(2-(3-chlorophenyl)hydrazono)-5,6-dihydroxyindolin-2-one (PT2) on β-amyloid(1-40) aggregation and toxicity.

G. Palazzo, F. Arnesano, A. De Stradis, 2014, Archives of biochemistry and biophysics.

Hydroxylation of 5H-3-Oxo-2,3,6,7,8,9-hexahydroimidazo[1,2-a]azepine derivatives by molecular oxygen

Giovanni Casini, A. Carotti, F. Campagna, 1990 .

Synthesis of 12-mono- and di-substituted 8-aza-11-oxasteroids

A. Carotti, C. Altomare, F. Campagna, 1986, Steroids.

Heterocyclic steroids. II. Synthesis of some spiro derivatives of 7,8‐diaza‐11‐oxasteroids

A. Carotti, C. Altomare, F. Campagna, 1983 .

An Efficient Route to Biologically Active 5H-Indeno(1,2-c)pyridazin-5- ones.

A. Carotti, C. Altomare, F. Campagna, 1993 .