Emidio Camaioni
Affiliations: | 1997-1999 | University of Perugia, Perugia, Umbria, Italy |
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Ferri M, Alunno M, Greco FA, et al. (2020) Fragment based drug design and diversity-oriented synthesis of carboxylic acid isosteres. Bioorganic & Medicinal Chemistry. 28: 115731 |
Mammoli A, Coletti A, Ballarotto M, et al. (2020) New Insights from Crystallographic Data: Diversity of Structural Motifs and Molecular Recognition Properties between Groups of IDO1 Structures. Chemmedchem |
Cerra B, Macchiarulo A, Carotti A, et al. (2020) Enantioselective HPLC Analysis to Assist the Chemical Exploration of Chiral Imidazolines. Molecules (Basel, Switzerland). 25 |
Buonvicino D, Mazzola F, Zamporlini F, et al. (2018) Identification of the Nicotinamide Salvage Pathway as a New Toxification Route for Antimetabolites. Cell Chemical Biology |
Coletti A, Greco FA, Dolciami D, et al. (2017) Advances in indoleamine 2,3-dioxygenase 1 medicinal chemistry. Medchemcomm. 8: 1378-1392 |
Carotti A, Ianni F, Camaioni E, et al. (2017) N-Decyl-S-trityl-(R)-cysteine, a new chiral selector for "green" ligand-exchange chromatography applications. Journal of Pharmaceutical and Biomedical Analysis |
Liscio P, Carotti A, Asciutti S, et al. (2014) Scaffold hopping approach on the route to selective tankyrase inhibitors. European Journal of Medicinal Chemistry. 87: 611-23 |
Marchand JR, Carotti A, Passeri D, et al. (2014) Investigating the allosteric reverse signalling of PARP inhibitors with microsecond molecular dynamic simulations and fluorescence anisotropy. Biochimica Et Biophysica Acta. 1844: 1765-72 |
Liscio P, Carotti A, Asciutti S, et al. (2014) Design, synthesis, crystallographic studies, and preliminary biological appraisal of new substituted triazolo[4,3-b]pyridazin-8-amine derivatives as tankyrase inhibitors. Journal of Medicinal Chemistry. 57: 2807-12 |
Antonyan A, De A, Vitali LA, et al. (2014) Evaluation of (arene)Ru(II) complexes of curcumin as inhibitors of dipeptidyl peptidase IV. Biochimie. 99: 146-52 |