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Benedetta Maggio

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Recent Articles
11.
Raffa D, Maggio B, Plescia F, Cascioferro S, Raimondi M, Cancemi G, et al.
Bioorg Med Chem . 2015 Sep; 23(19):6305-16. PMID: 26344588
Several new 2-(2-phenoxyacetamido)benzamides 17a-v, 21 and 22 were synthesized by stirring in pyridine the acid chlorides 16a-e and the appropriate5-R-4-R₁-2-aminobenzamide 15a-e and initially evaluated in vitro for antiproliferative activity against...
12.
Cascioferro S, Raffa D, Maggio B, Raimondi M, Schillaci D, Daidone G
J Med Chem . 2015 Aug; 58(23):9108-23. PMID: 26280844
Here, we describe the most promising small synthetic organic compounds that act as potent Sortase A inhibitors and cater the potential to be developed as antivirulence drugs. Sortase A is...
13.
Maggio B, Raimondi M, Raffa D, Plescia F, Cascioferro S, Cancemi G, et al.
Eur J Med Chem . 2015 Apr; 96:98-104. PMID: 25874335
Based on the encouraging results found for 3,5-dimethyl-6-phenyl-8-(trifluoromethyl)-5,6-dihydropyrazolo[3,4-f][1,2,3,5]tetrazepin-4-(3H)-one 7 previously tested by us, as well as the consideration that heterocycle fused tetrazepinones bearing the 2-chloroethyl substituent show a better cytotoxic...
14.
Raffa D, Maggio B, Raimondi M, Cascioferro S, Plescia F, Cancemi G, et al.
Eur J Med Chem . 2015 Jan; 97:732-46. PMID: 25549911
In this review we report the recent advances in bioactive system containing pyrazole fused with a five membered heterocycle, covering the time span of the last decade. All of them...
15.
Maggio B, Raffa D, Raimondi M, Cusimano M, Plescia F, Cascioferro S, et al.
Eur J Med Chem . 2013 Dec; 72:1-9. PMID: 24333609
The reaction under reflux between 1-phenyl-3-R-5-methylaminopyrazoles and 2,5-hexanedione lead to 5,7:7,13-dimethanopyrazolo[3,4-b]pyrazolo[3',4':2,3]azepino[4,5-f]azocine derivatives 3b-g. These unusual molecules show the structural complexity of many biologically active natural products and are endowed with...
16.
Maggio B, Raffa D, Raimondi M, Daidone G
Molecules . 2013 Oct; 18(10):13096-110. PMID: 24152597
The compound 2-((1,3-dimethyl-1H-pyrazol-5-yl)(methyl)carbamoyl)benzene-diazonium hydrogen sulfate (10) was reacted with copper sulfate and sodium chloride, in the presence of ascorbic acid as reducing agent, to afford a mixture of the chlorinated...
17.
Meneghetti F, Maggio B
Acta Crystallogr Sect E Struct Rep Online . 2013 Oct; 69(Pt 10):o1583. PMID: 24098259
The central eight-membered ring of the title compound, C40H36N8O2, deviates from the ideal boat conformation because the bond between the exo-ethyl-ene group and the adjacent N atom is twisted by...
18.
Meneghetti F, Maggio B
Acta Crystallogr Sect E Struct Rep Online . 2013 Oct; 69(Pt 10):o1582. PMID: 24098258
In the title compound, C29H25N5O3, the dihedral angle between the benzene ring and the pendant quinazoline ring system (r.m.s. deviation = 0.036Å) is 87.60 (17)°. The equivalent angle between the...
19.
Raffa D, Maggio B, Raimondi M, Cusimano M, Amico G, Carollo A, et al.
Eur J Med Chem . 2013 Jun; 65:427-35. PMID: 23747810
Several new benzamides 4a-q were synthesized by stirring in pyridine the acid chlorides 3a-q with the appropriate anthranilamide derivatives 2a-g. Some of the synthesized compounds were evaluated for their in...
20.
Raimondi M, Maggio B, Raffa D, Plescia F, Cascioferro S, Cancemi G, et al.
Eur J Med Chem . 2012 Oct; 58:64-71. PMID: 23088933
Several new 4-diazopyrazole derivatives 6a-g and 9a-c were obtained by the reaction of 1-(R-substituted-phenyl)-3-(1,3-dimethyl-1H-pyrazol-5-yl)ureas 5a-g and N-(1,3-dimethyl-1H-pyrazol-5-yl)-2-(R-substituted-phenyl)acetamides 8a-c respectively with a sevenfold excess of nitrous acid in acetic acid solution....