A. Antonello

Prazosin-related compounds. Effect of transforming the piperazinylquinazoline moiety into an aminomethyltetrahydroacridine system on the affinity for alpha1-adrenoreceptors.

A. Cavalli, A. Minarini, M. Rosini, 2003, Journal of medicinal chemistry.

Polymethylene tetraamine backbone as template for the development of biologically active polyamines

V. Tumiatti, A. Minarini, M. Rosini, 2003, Medicinal research reviews.

Design, synthesis and biological evaluation of ambenonium derivatives as AChE inhibitors.

A. Cavalli, V. Andrisano, M. Bartolini, 2003, Farmaco.

Design, synthesis, and biological evaluation of prazosin-related derivatives as multipotent compounds.

V. Tumiatti, M. Rosini, C. Melchiorre, 2005, Journal of medicinal chemistry.

A route to the thapsigargins from (S)-carvone providing a substrate-controlled total synthesis of trilobolide, nortrilobolide, and thapsivillosin F.

S. Ley, S. Oliver, Martin D. Smith, 2003, Angewandte Chemie.

Total synthesis of five thapsigargins: guaianolide natural products exhibiting sub-nanomolar SERCA inhibition.

S. P. Andrews, S. Ley, S. Oliver, 2007, Chemistry.

Synthesis of the thapsigargins.

S. Christensen, S. Ley, A. Woolford, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Multitarget-directed drug design strategy: a novel molecule designed to block epidermal growth factor receptor (EGFR) and to exert proapoptotic effects.

A. Cavalli, M. Rosini, M. Bolognesi, 2006, Journal of medicinal chemistry.