Davide Bonanni

ScholarGPS® ID: 71437010229565

Affiliation

University of Modena and Reggio Emilia, Modena and Reggio Emilia, Italy

Affiliation History

Field

Physical Sciences and Mathematics

Discipline

Chemistry

Top Specialties

Medicinal Chemistry | Scaffolding

Metrics Summary

Publication Count

Predicted Citations

429

Predicted h-index

Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

Publications
Books
Patents
NIH/NSF

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Discovery of potent pyrrolo-pyrimidine and purine HDAC inhibitors for the treatment of advanced prostate cancer (journal article) Moi, Davide \| Bonanni, Davide \| Belluti, Silvia \| Linciano, Pasquale \| Citarella, Andrea \| Franchini, Silvia \| Sorbi, Claudia \| Imbriano, Carol \| Pinzi, Luca \| Rastelli, Giulio European Journal of Medicinal Chemistry, volume 260 (2023). 10.1016/j.ejmech.2023.115730 Cited by (4) \| Cite \| Source
Development of machine learning classifiers to predict compound activity on prostate cancer cell lines (journal article) Bonanni, Davide \| Pinzi, Luca \| Rastelli, Giulio Journal of Cheminformatics, volume 14, issue 1 (2022). 10.1186/s13321-022-00647-y Cited by (2) \| Cite \| Source
Synthesis of potent and selective HDAC6 inhibitors led to unexpected opening of a quinazoline ring (journal article) Moi, Davide \| Citarella, Andrea \| Bonanni, Davide \| Pinzi, Luca \| Passarella, Daniele \| Silvani, Alessandra \| Giannini, Clelia \| Rastelli, Giulio RSC Advances, volume 12, issue 18, pages 11548-11556 (2022). 10.1039/D2RA01753A Cited by (9) \| Cite \| Source
Dual Targeting Strategies on Histone Deacetylase 6 (HDAC6) and Heat Shock Protein 90 (Hsp90) (journal article) Bonanni, Davide \| Citarella, Andrea \| Moi, Davide \| Pinzi, Luca \| Bergamini, Elisa \| Rastelli, Giulio Current Medicinal Chemistry, volume 29, issue 9, pages 1474-1502 (2022). 10.2174/0929867328666210902145102 Cited by (12) \| Cite \| Source
Hydroxamic Acid Derivatives: From Synthetic Strategies to Medicinal Chemistry Applications (journal article) Citarella, Andrea \| Moi, Davide \| Pinzi, Luca \| Bonanni, Davide \| Rastelli, Giulio ACS Omega, volume 6, issue 34, pages 21843-21849 (2021). 10.1021/acsomega.1c03628 Cited by (43) \| Cite \| Source
Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2-Hydroxypyrazolo[1,5- a ]pyridine Scaffold: SAR of the Biphenyl Moiety (journal article) Sainas, Stefano \| Giorgis, Marta \| Circosta, Paola \| Gaidano, Valentina \| Bonanni, Davide \| Pippione, Agnese C. \| Bagnati, Renzo \| Passoni, Alice \| Qiu, Yaqi \| Cojocaru, Carina Florina \| ... \| Lolli, Marco L. Journal of Medicinal Chemistry, volume 64, issue 9, pages 5404-5428 (2021). 10.1021/acs.jmedchem.0c01549 Cited by (22) \| Cite \| Source
Computational Method for Structure-Based Analysis of SAR Transfer (journal article) Bonanni, Davide \| Lolli, Marco L. \| Bajorath, Jürgen Journal of Medicinal Chemistry, volume 63, issue 3, pages 1388-1396 (2020). 10.1021/acs.jmedchem.9b01931 Cited by (4) \| Cite \| Source
Exploration of [2 + 2 + 2] cyclotrimerisation methodology to prepare tetrahydroisoquinoline-based compounds with potential aldo–keto reductase 1C3 target affinity (journal article) Santos, Ana R. N. \| Sheldrake, Helen M. \| Ibrahim, Ali I. M. \| Danta, Chhanda Charan \| Bonanni, Davide \| Daga, Martina \| Oliaro-Bosso, Simonetta \| Boschi, Donatella \| Lolli, Marco L. \| Pors, Klaus MedChemComm, volume 10, issue 8, pages 1476-1480 (2019). 10.1039/C9MD00201D Cited by (3) \| Cite \| Source
Bioisosteres of Indomethacin as Inhibitors of Aldo-Keto Reductase 1C3 (journal article) Lolli, Marco L. \| Carnovale, Irene M. \| Pippione, Agnese C. \| Wahlgren, Weixiao Y. \| Bonanni, Davide \| Marini, Elisabetta \| Zonari, Daniele \| Gallicchio, Margherita \| Boscaro, Valentina \| Goyal, Parveen \| ... \| Boschi, Donatella ACS Medicinal Chemistry Letters, volume 10, issue 4, pages 437-443 (2019). 10.1021/acsmedchemlett.8b00484 Cited by (33) \| Cite \| Source
Targeting Myeloid Differentiation Using Potent 2-Hydroxypyrazolo[1,5- a ]pyridine Scaffold-Based Human Dihydroorotate Dehydrogenase Inhibitors (journal article) Sainas, Stefano \| Pippione, Agnese C. \| Lupino, Elisa \| Giorgis, Marta \| Circosta, Paola \| Gaidano, Valentina \| Goyal, Parveen \| Bonanni, Davide \| Rolando, Barbara \| Cignetti, Alessandro \| ... \| Lolli, Marco L. Journal of Medicinal Chemistry, volume 61, issue 14, pages 6034-6055 (2018). 10.1021/acs.jmedchem.8b00373 Cited by (57) \| Cite \| Source
Targeting Myeloid Differentiation Using Potent 2-Hydroxypyrazolo[1,5-a]pyridine Scaffold-Based Human Dihydroorotate Dehydrogenase Inhibitors (journal article) Sainas, Stefano \| Pippione, Agnese Chiara \| Lupino, Elisa \| Giorgis, Marta \| Circosta, Paola \| Gaidano, Valentina \| Goyal, Parveen \| bonanni, davide \| Rolando, Barbara \| Cignetti, Alessandro \| ... \| Lolli, Marco L. Journal of Medicinal Chemistry, volume 61, issue 14, pages 6034-6055 (2018). 10.2210/pdb6fmd/pdb Cited by (3) \| Cite \| Source
Discovery and development of novel salicylate synthase (MbtI) furanic inhibitors as antitubercular agents (journal article) Chiarelli, Laurent R. \| Mori, Matteo \| Barlocco, Daniela \| Beretta, Giangiacomo \| Gelain, Arianna \| Pini, Elena \| Porcino, Marianna \| Mori, Giorgia \| Stelitano, Giovanni \| Costantino, Luca \| ... \| Meneghetti, Fiorella European Journal of Medicinal Chemistry, volume 155 (2018). 10.1016/j.ejmech.2018.06.033 Cited by (53) \| Cite \| Source
Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid. (journal article) Pippione, Agnese Chiara \| Carnovale, Irene Maria \| Bonanni, Davide \| Sini, Marcella \| Goyal, Parveen \| Marini, Elisabetta \| Pors, Klaus \| Adinolfi, Salvatore \| Zonari, Daniele \| Festuccia, Claudio \| ... \| Lolli, Marco L. European Journal of Medicinal Chemistry, volume 150 (2018). 10.2210/pdb6f2u/pdb Cited by (3) \| Cite \| Source \| Open Access
Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid (journal article) Pippione, Agnese Chiara \| Carnovale, Irene Maria \| Bonanni, Davide \| Sini, Marcella \| Goyal, Parveen \| Marini, Elisabetta \| Pors, Klaus \| Adinolfi, Salvatore \| Zonari, Daniele \| Festuccia, Claudio \| ... \| Lolli, Marco Lucio European Journal of Medicinal Chemistry, volume 150 (2018). 10.1016/j.ejmech.2018.03.040 Cited by (41) \| Cite \| Source \| Open Access
Hydroxytriazole derivatives as potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors discovered by bioisosteric scaffold hopping approach (journal article) Pippione, Agnese C. \| Giraudo, Alessandro \| Bonanni, Davide \| Carnovale, Irene M. \| Marini, Elisabetta \| Cena, Clara \| Costale, Annalisa \| Zonari, Daniele \| Pors, Klaus \| Sadiq, Maria \| ... \| Lolli, Marco L. European Journal of Medicinal Chemistry, volume 139 (2017). 10.1016/j.ejmech.2017.08.046 Cited by (35) \| Cite \| Source \| Open Access
Mutations responsible for Mycobacterium tuberculosis isoniazid resistance in Italy. (journal article) Rindi, L \| Bianchi, L \| Tortoli, E \| Lari, N \| Bonanni, D \| Garzelli, C The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease, volume 9, issue 1 (2005). Cited by (8) \| Cite