Marinella Roberti

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Bagnolini G, Milano D, Manerba M, et al. (2020) Synthetic lethality in pancreatic cancer: discovery of a new RAD51-BRCA2 small molecule disruptor that inhibits homologous recombination and synergizes with olaparib. Journal of Medicinal Chemistry
Linciano P, Cullia G, Borsari C, et al. (2020) Identification of a 2,4-diaminopyrimidine scaffold targeting Trypanosoma brucei pteridine reductase 1 from the LIBRA compound library screening campaign. European Journal of Medicinal Chemistry. 189: 112047
Roberti M, Schipani F, Bagnolini G, et al. (2019) Rad51/BRCA2 disruptors inhibit homologous recombination and synergize with olaparib in pancreatic cancer cells. European Journal of Medicinal Chemistry. 165: 80-92
Uliassi E, Peña-Altamira LE, Morales AV, et al. (2018) A focused library of psychotropic analogs with neuroprotective and neuroregenerative potential. Acs Chemical Neuroscience
Porru E, Franco P, Calabria D, et al. (2018) Combined analytical approaches to define biodistribution and biological activity of semi-synthetic berberrubine, the active metabolite of natural berberine. Analytical and Bioanalytical Chemistry
Bruno F, Castelli G, Vitale F, et al. (2017) Effects of trans-stilbene and terphenyl compounds on different strains of Leishmania and on cytokines production from infected macrophages. Experimental Parasitology
Falchi F, Giacomini E, Masini T, et al. (2017) Synthetic lethality triggered by combining Olaparib with BRCA2-Rad51 disruptors. Acs Chemical Biology
Manerba M, Di Ianni L, Govoni M, et al. (2017) LDH inhibition impacts on heat shock response and induces senescence of hepatocellular carcinoma cells. European Journal of Pharmaceutical Sciences : Official Journal of the European Federation For Pharmaceutical Sciences. 105: 91-98
Jeřábek J, Uliassi E, Guidotti L, et al. (2016) Tacrine-resveratrol fused hybrids as multi-target-directed ligands against Alzheimer's disease. European Journal of Medicinal Chemistry. 127: 250-262
Rupiani S, Guidotti L, Manerba M, et al. (2016) Synthesis of natural urolithin M6, a galloflavin mimetic, as a potential inhibitor of lactate dehydrogenase A. Organic & Biomolecular Chemistry