F. Palluotto

发表

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.

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.

Indenocinnoline derivatives as G-quadruplex binders, topoisomerase IIα inhibitors and antiproliferative agents.

B. Gatto, Grigoris Zoidis, M. Catto, 2017, Bioorganic & medicinal chemistry.

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

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

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.

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

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

Quinolino[3,4-b]quinoxalines and pyridazino[4,3-c]quinoline derivatives: Synthesis, inhibition of topoisomerase IIα, G-quadruplex binding and cytotoxic properties.

B. Gatto, Grigoris Zoidis, M. Catto, 2016, European journal of medicinal chemistry.