Paola Ruggeri
Overview
Explore the profile of Paola Ruggeri including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
24
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0
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Recent Articles
1.
Ippoliti I, Da Cas R, Marano G, Annunziata A, Salvi E, Ruggeri P, et al.
Recenti Prog Med
. 2024 Nov;
115(11):566-567.
PMID: 39550666
Objectives: To assess the safety profile of dietary supplements with a focus on those purchased online or reported via the internet. Results: Among the 2,367 reports of Adverse Reactions (ARs)...
2.
Da Cas R, Ippoliti I, Ruggeri P, Annunziata A, Civitelli G, Vischetti E, et al.
Recenti Prog Med
. 2023 Aug;
114(9):532-533.
PMID: 37530007
No abstract available.
3.
Bolchi C, Valoti E, Gotti C, Fasoli F, Ruggeri P, Fumagalli L, et al.
J Med Chem
. 2015 Jul;
58(16):6665-77.
PMID: 26225816
Some unichiral analogues of 2R,2'S-2-(1'-methyl-2'-pyrrolidinyl)-7-hydroxy-1,4-benzodioxane, a potent and selective α4β2-nAChR partial agonist, were designed by opening dioxane and replacing hydroxyl carbon with nitrogen. The resulting 3-pyridyl and m-hydroxyphenyl ethers have...
4.
Chiodini G, Pallavicini M, Zanotto C, Bissa M, Radaelli A, Straniero V, et al.
Eur J Med Chem
. 2014 Dec;
89:252-65.
PMID: 25462242
A SAR study was performed on 3-substituted 2,6-difluorobenzamides, known inhibitors of the essential bacterial cell division protein FtsZ, through a series of modifications first of 2,6-difluoro-3-nonyloxybenzamide and then of its...
5.
Bolchi C, Valoti E, Straniero V, Ruggeri P, Pallavicini M
J Org Chem
. 2014 Jun;
79(14):6732-7.
PMID: 24945589
2-Substituted 1,4-benzodioxanes, such as 2-cyano-, 2-methoxycarbonyl-, 2-aminocarbonyl-, and 2-formyl-1,4-benzodioxane, are key synthons that for the most part are never described as enantiomers or are inadequately characterized for enantiomeric purity. They...
6.
Straniero V, Pallavicini M, Chiodini G, Ruggeri P, Fumagalli L, Bolchi C, et al.
Bioorg Med Chem Lett
. 2014 May;
24(13):2924-7.
PMID: 24821376
Mimetics of the C-terminal CAAX tetrapeptide of Ras protein were designed as farnesyltransferase (FTase) inhibitors (FTIs) by replacing AA with o-aryl or o-heteroaryl substituted p-hydroxy- or p-aminobenzoic acid, while maintaining...