Francesca Fruttarolo

Synthesis and Biological Evaluation of 2- and 3-Aminobenzo[<i>b</i>]thiophene Derivatives as Antimitotic Agents and Inhibitors of Tubulin Polymerization

Romeo Romagnoli, Pier Giovanni Baraldi, María Dora Carriòn et al. · Journal of Medicinal Chemistry · 2007 · 141 citations

Pharmaceutical Science, Bioorganic Chemistry, Colchicine Site +17

Design, Synthesis, and Biological Evaluation of New 8-Heterocyclic Xanthine Derivatives as Highly Potent and Selective Human A_2BAdenosine Receptor Antagonists

Pier Giovanni Baraldi, Mojgan Aghazadeh Tabrizi, Delia Preti et al. · Journal of Medicinal Chemistry · 2004 · 97 citations · Full text

Combinatorial Chemistry, Medicinal Chemistry, Adenosine Receptors +15

Synthesis and biological effects of a new series of 2-amino-3-benzoylthiophenes as allosteric enhancers of A1-adenosine receptor

Pier Giovanni Baraldi, Abdel Naser Zaid, Ilaria Lampronti et al. · Bioorganic & Medicinal Chemistry Letters · 2000 · 77 citations

Molecular Pharmacology, Biological Effects, Biochemistry +7

Design, Synthesis, and Biological Evaluation of C⁹- and C²-Substituted Pyrazolo[4,3-<i>e</i>]-1,2,4-triazolo[1,5-<i>c</i>]pyrimidines as New A_2Aand A₃Adenosine Receptors Antagonists

Pier Giovanni Baraldi, Francesca Fruttarolo, Mojgan Aghazadeh Tabrizi et al. · Journal of Medicinal Chemistry · 2003 · 74 citations · Full text

N6-[(Hetero)aryl/(cyclo)alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5′-N-ethylcarboxamido-adenosines: The first example of adenosine-related structures with potent agonist activity at the human A2B adenosine receptor

Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi et al. · Bioorganic & Medicinal Chemistry · 2007 · 64 citations · Full text

Molecular Pharmacology, Potent Agonist Activity, Biochemistry +9