Rosanna Matucci

Author PubWeight™ 7.09‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Safety aspects of iodinated contrast media related to their physicochemical properties: a pharmacoepidemiology study in two Tuscany hospitals. Eur J Clin Pharmacol 2008 1.46
2 Calcium channel antagonists discovered by a multidisciplinary approach. J Med Chem 2006 0.85
3 Synthesis, affinity profile, and functional activity of muscarinic antagonists with a 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine structure. J Med Chem 2007 0.84
4 Pharmacological effects of 3-iodothyronamine (T1AM) in mice include facilitation of memory acquisition and retention and reduction of pain threshold. Br J Pharmacol 2013 0.83
5 1,4-dioxane, a suitable scaffold for the development of novel M₃ muscarinic receptor antagonists. J Med Chem 2012 0.81
6 The direct stimulation of Gi proteins by neuropeptide Y (NPY) in the rat left ventricle. Biochem Pharmacol 2002 0.80
7 Synthesis and biological evaluation of 2-mercapto-1,3-benzothiazole derivatives with potential antimicrobial activity. Arch Pharm (Weinheim) 2009 0.79
8 Synthesis and biological evaluation of chiral alpha-aminoanilides with central antinociceptive activity. J Med Chem 2007 0.78
9 Chiral aryloxyalkylamines: Selective 5-HT(1B/1D) activation and analgesic activity. ChemMedChem 2010 0.77
10 Design, synthesis and binding affinity of acetylcholine carbamoyl analogues. Bioorg Med Chem Lett 2013 0.76
11 Synthesis and cholinergic affinity of diastereomeric and enantiomeric isomers of 1-methyl-2-(2-methyl-1,3-dioxolan-4-yl)- pyrrolidine, 1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine and of Their iodomethylates. Bioorg Med Chem 2003 0.75
12 Highly chiral muscarinic ligands: the discovery of (2S,2'R,3'S,5'R)-1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine 3-sulfoxide methyl iodide, a potent, functionally selective, M2 partial agonist. J Med Chem 2006 0.75
13 Design, synthesis, and preliminary pharmacological evaluation of 4-aminopiperidine derivatives as N-type calcium channel blockers active on pain and neuropathic pain. J Med Chem 2004 0.75
14 Muscarinic subtype affinity and functional activity profile of 1-methyl-2-(2-methyl-1,3-dioxolan-4-yl)pyrrolidine and 1-methyl-2-(2-methyl-1,3-oxathiolan-5-yl)pyrrolidine derivatives. Biochem Pharmacol 2005 0.75
15 Muscarinic antagonists with multiple stereocenters: Synthesis, affinity profile and functional activity of isomeric 1-methyl-2-(2,2-alkylaryl-1,3-oxathiolan-5-yl)pyrrolidine sulfoxide derivatives. Bioorg Med Chem 2008 0.75
16 Does aspirin attenuate the beneficial effect of ACE inhibitors in elderly people with heart failure? Drugs Aging 2005 0.75
17 Muscarine-like compounds derived from a pyrolysis product of cellulose. Org Biomol Chem 2015 0.75
18 Molecular modulation of muscarinic antagonists. Synthesis and affinity profile of 2,2-diphenyl-2-ethylthio-acetic acid esters designed to probe the binding site cavity. Farmaco 2004 0.75
19 The conformational and property space of acetylcholine bound to muscarinic receptors: an entropy component accounts for the subtype selectivity of acetylcholine. Arch Biochem Biophys 2007 0.75
20 Synthesis and biological evaluation of a novel series of heterobivalent muscarinic ligands based on xanomeline and 1-[3-(4-butylpiperidin-1-yl)propyl]-1,2,3,4-tetrahydroquinolin-2-one (77-LH-28-1). J Med Chem 2014 0.75
21 Synthesis, affinity profile and functional activity of potent chiral muscarinic antagonists with a pyrrolidinylfuran structure. J Med Chem 2010 0.75
22 Synthesis and pharmacological characterization of chiral pyrrolidinylfuran derivatives: the discovery of new functionally selective muscarinic agonists. J Med Chem 2008 0.75
23 Properly substituted 1,4-dioxane nucleus favours the selective M3 muscarinic receptor activation. Bioorg Med Chem 2009 0.75
24 1,2,4-Benzothiadiazine-1,1-dioxide derivatives as ionotropic glutamate receptor ligands: synthesis and structure-activity relationships. Arch Pharm (Weinheim) 2014 0.75
25 Rapid novel divergent synthesis and muscarinic agonist profile of all four optical isomers of N,N,N-trimethyl(6-methyl-1,4-dioxan-2-yl)methanaminium iodide. Bioorg Med Chem Lett 2007 0.75