Giuseppe Campiani
Affiliations: | University of Siena, Italy, Siena, Toscana, Italy |
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Publications
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| Papa A, Pasquini S, Galvani F, et al. (2022) Development of potent and selective FAAH inhibitors with improved drug-like properties as potential tools to treat neuroinflammatory conditions. European Journal of Medicinal Chemistry. 246: 114952 |
| Guidi A, Prasanth Saraswati A, Relitti N, et al. (2020) (+)-(R)- and (-)-(S)-Perhexiline maleate: Enantioselective synthesis and functional studies on Schistosoma mansoni larval and adult stages. Bioorganic Chemistry. 102: 104067 |
| Frydenvang K, Pickering DS, Kshirsagar GU, et al. (2020) The ionotropic glutamate receptor GluA2 in complex with bicyclic pyrimidinedione-based compounds: when small compound modifications have distinct effects on binding interactions. Acs Chemical Neuroscience |
| Sirous H, Campiani G, Brogi S, et al. (2020) Computer-Driven Development of an in Silico Tool for Finding Selective Histone Deacetylase 1 Inhibitors. Molecules (Basel, Switzerland). 25 |
| Relitti N, Saraswati AP, Federico S, et al. (2020) Telomerase-based Cancer Therapeutics: A Review on their Clinical Trials. Current Topics in Medicinal Chemistry. 20: 433-457 |
| Battah B, Chemi G, Butini S, et al. (2019) A Repurposing Approach for Uncovering the Anti-Tubercular Activity of FDA-Approved Drugs with Potential Multi-Targeting Profiles. Molecules (Basel, Switzerland). 24 |
| Saccoccia F, Brindisi M, Gimmelli R, et al. (2019) Screening and phenotypical characterization of Schistosoma mansoni histone deacetylase 8 (SmHDAC8) inhibitors as multi-stage antischistosomal agents. Acs Infectious Diseases |
| Grillo A, Chemi G, Brogi S, et al. (2019) Development of novel multipotent compounds modulating endocannabinoid and dopaminergic systems. European Journal of Medicinal Chemistry. 183: 111674 |
| Sirous H, Chemi G, Campiani G, et al. (2019) An integrated in silico screening strategy for identifying promising disruptors of p53-MDM2 interaction. Computational Biology and Chemistry. 83: 107105 |
| Sirous H, Chemi G, Gemma S, et al. (2019) Identification of Novel 3-Hydroxy-pyran-4-One Derivatives as Potent HIV-1 Integrase Inhibitors Using Structure-Based Combinatorial Library Design Approach. Frontiers in Chemistry. 7: 574 |