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Bioorganic & Medicinal Chemistry|November 26, 2008
Design and synthesis of novel dihydroquinoline-3-carboxylic acids as HIV-1 integrase inhibitorsMario Sechi, Giuseppe Rizzi, Alessia Bacchi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|September 9, 2014
Peptidomimetics as protein arginine deiminase 4 (PAD4) inhibitorsAndrea Trabocchi, Nicolino Pala, Ilga Krimmelbein, et al.
RSC Medicinal Chemistry|March 4, 2026
Harnessing oligonucleotide architecture for potent multivalent inhibition of human carbonic anhydrasesEslam M Abbass, Federico Ladu, Justine Mansot, et al.
Scientific Reports|October 26, 2018
Fisetin targets YB-1/RSK axis independent of its effect on ERK signaling: insights from in vitro and in vivo melanoma modelsMario Sechi, Rahul K Lall, Saheed O Afolabi, et al.
Molecular Pharmaceutics|February 18, 2011
HIV-1 IN strand transfer chelating inhibitors: a focus on metal bindingAlessia Bacchi, Mauro Carcelli, Carlotta Compari, et al.
European Journal of Medicinal Chemistry|July 5, 2014
Antiretroviral activity of metal-chelating HIV-1 integrase inhibitorsMauro Carcelli, Dominga Rogolino, Mario Sechi, et al.
Journal of Medicinal Chemistry|February 11, 2011
Targeted biocompatible nanoparticles for the delivery of (-)-epigallocatechin 3-gallate to prostate cancer cellsVanna Sanna, Gianfranco Pintus, Anna Maria Roggio, et al.
Scientific Reports|February 2, 2017
Targeted nanoparticles encapsulating (-)-epigallocatechin-3-gallate for prostate cancer prevention and therapyVanna Sanna, Chandra K Singh, Rahime Jashari, et al.
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