Gianluca Santoni - Publications

Affiliations: 
Univ Grenoble Alpes 
Area:
Acetylcholinesterase, Crystallography, Molecular simulations

10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Lalut J, Santoni G, Karila D, Lecoutey C, Davis A, Nachon F, Silman I, Sussman J, Weik M, Maurice T, Dallemagne P, Rochais C. Novel multitarget-directed ligands targeting acetylcholinesterase and σ receptors as lead compounds for treatment of Alzheimer's disease: Synthesis, evaluation, and structural characterization of their complexes with acetylcholinesterase. European Journal of Medicinal Chemistry. 162: 234-248. PMID 30447434 DOI: 10.1016/J.Ejmech.2018.10.064  0.604
2018 Santoni G, de Sousa J, De la Mora E, Dias J, Jean L, Sussman JL, Silman I, Renard PY, Brown RCD, Weik M, Baati R, Nachon F. Structure-based optimization of non-quaternary reactivators of acetylcholinesterase inhibited by organophosphorus nerve agents. Journal of Medicinal Chemistry. PMID 30125110 DOI: 10.1021/Acs.Jmedchem.8B00592  0.671
2018 Dolles D, Hoffmann M, Gunesch S, Marinelli O, Möller J, Santoni G, Chatonnet A, Lohse MJ, Wittmann HJ, Strasser A, Nabissi M, Maurice T, Decker M. Structure-Activity Relationships and Computational Investigations into the Development of Potent and Balanced Dual-Acting Butyrylcholinesterase Inhibitors and Human Cannabinoid Receptor 2 Ligands with Pro-Cognitive in Vivo Profiles. Journal of Medicinal Chemistry. PMID 29400965 DOI: 10.1021/Acs.Jmedchem.7B01760  0.324
2017 Brazzolotto X, Igert A, Guillon V, Santoni G, Nachon F. Bacterial Expression of Human Butyrylcholinesterase as a Tool for Nerve Agent Bioscavengers Development. Molecules (Basel, Switzerland). 22. PMID 29077024 DOI: 10.3390/molecules22111828  0.341
2014 Kliachyna M, Santoni G, Nussbaum V, Renou J, Sanson B, Colletier JP, Arboléas M, Loiodice M, Weik M, Jean L, Renard PY, Nachon F, Baati R. Design, synthesis and biological evaluation of novel tetrahydroacridine pyridine- Aldoxime and -Amidoxime hybrids as efficient uncharged reactivators of nerve agent-Inhibited human acetylcholinesterase European Journal of Medicinal Chemistry. 78: 455-467. PMID 24704618 DOI: 10.1016/J.Ejmech.2014.03.044  0.498
2014 Oueis E, Santoni G, Ronco C, Syzgantseva O, Tognetti V, Joubert L, Romieu A, Weik M, Jean L, Sabot C, Nachon F, Renard PY. Reaction site-driven regioselective synthesis of AChE inhibitors Organic and Biomolecular Chemistry. 12: 156-161. PMID 24216754 DOI: 10.1039/C3Ob42109K  0.632
2013 Carletti E, Colletier JP, Schopfer LM, Santoni G, Masson P, Lockridge O, Nachon F, Weik M. Inhibition pathways of the potent organophosphate CBDP with cholinesterases revealed by X-ray crystallographic snapshots and mass spectrometry. Chemical Research in Toxicology. 26: 280-9. PMID 23339663 DOI: 10.1021/Tx3004505  0.645
2008 Quaglia W, Piergentili A, Del Bello F, Farande Y, Giannella M, Pigini M, Rafaiani G, Carrieri A, Amantini C, Lucciarini R, Santoni G, Poggesi E, Leonardi A. Structure-activity relationships in 1,4-benzodioxan-related compounds. 9. 1 From 1,4-benzodioxane to 1,4-dioxane ring as a promising template of novel α1D-adrenoreceptor antagonists, 5-HT1A full agonists, and cytotoxic agents Journal of Medicinal Chemistry. 51: 6359-6370. PMID 18817363 DOI: 10.1021/jm800461k  0.33
2008 Antonini I, Santoni G, Lucciarini R, Amantini C, Dal Ben D, Volpini R, Cristalli G. Synthesis and antitumor evaluation of bis aza-anthracene-9,10-diones and bis aza-anthrapyrazole-6-ones Journal of Medicinal Chemistry. 51: 997-1006. PMID 18232651 DOI: 10.1021/jm7013937  0.32
2006 Antonini I, Santoni G, Lucciarini R, Amantini C, Sparapani S, Magnano A. Synthesis and biological evaluation of new asymmetrical bisintercalators as potential antitumor drugs Journal of Medicinal Chemistry. 49: 7198-7207. PMID 17125272 DOI: 10.1021/jm0606793  0.328
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