Luigi Scipione

Prof. Luigi Scipione

Sapienza University of Rome, Rome, Lazio, Italy
orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 July 2021 in Molecules
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Journal Article
Open access
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Valentina Noemi MadiaValentina Noemi Madia
Valentina Noemi Madia
Daniela De VitaDaniela De Vita
Daniela De Vita
DIDavide Ialongo
Davide Ialongo
VTValeria Tudino
Valeria Tudino
ALAlessandro De Leo
Alessandro De Leo
Antonella MessoreAntonella Messore
Antonella Messore
Growing attention to environmental protection leads food industries to adopt a model of “circular economy” applying safe and sustainable technologies to recover, recycle and valorize by-products. Therefore, by-products become raw material for other industries. Tomato processing industry produces significant amounts of by-products, consisting of skins and seeds. Tomato skin is very rich in lycopene, and from its seeds, high nutritional oil can be extracted. Alternative use of the two fractions not only could cut disposal costs but also allow one to extract bioactive compounds and an oil with a high nutritional value. This review focused on the recent advance in extraction of lycopene, whose beneficial effects on health are widely recognized.

28 January 2015 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
GCGiuliana Cuzzucoli Crucitti
Giuliana Cuzzucoli Crucitti
MMMathieu Métifiot
Mathieu Métifiot
LPLuca Pescatori
Luca Pescatori
AMAntonella Messore
Antonella Messore
Valentina Noemi MadiaValentina Noemi Madia
Valentina Noemi Madia
RSRoberto Di Santo
Roberto Di Santo

1 March 2014 in Bioorganic & Medicinal Chemistry Letters
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Journal Article
Closed access
Daniela De VitaDaniela De Vita
Daniela De Vita
LFLaura Friggeri
Laura Friggeri
FDFelicia Diodata D'Auria
Felicia Diodata D'Auria
Fabiana PandolfiFabiana Pandolfi
Fabiana Pandolfi
FPFrancesco Piccoli
Francesco Piccoli
STSilvano Tortorella
Silvano Tortorella

1 January 2017 in Journal of Enzyme Inhibition and Medicinal Chemistry
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Journal Article
Open access
Francesco SaccolitiFrancesco Saccoliti
Francesco Saccoliti
GAGabriella Angiulli
Gabriella Angiulli
GPGiovanni Pupo
Giovanni Pupo
LPLuca Pescatori
Luca Pescatori
Valentina Noemi MadiaValentina Noemi Madia
Valentina Noemi Madia
AIAndrea Ilari
Andrea Ilari
The study presented here aimed at identifying a new class of compounds acting against Leishmania parasites, the causative agent of Leishmaniasis. For this purpose, the thioether derivatives of our in-house library have been evaluated in whole-cell screening assays in order to determine their in vitro activity against Leishmania protozoan. Among them, promising results have been achieved with compound RDS 777 (6-(sec-butoxy)-2-((3-chlorophenyl)thio)pyrimidin-4-amine) (IC50 = 29.43 µM), which is able to impair the mechanism of the parasite defence against the reactive oxygen species by inhibiting the trypanothione reductase (TR) with high efficiency (Ki 0.25 ± 0.18 µM). The X-ray structure of L. infantum TR in complex with RDS 777 disclosed the mechanism of action of this compound that binds to the catalytic site and engages in hydrogen bonds the residues more involved in the catalysis, namely Glu466', Cys57 and Cys52, thereby inhibiting the trypanothione binding and avoiding its reduction.

14 January 2021 in Expert Opinion on Therapeutic Patents
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Journal Article
Closed access
Martina BortolamiMartina Bortolami
Martina Bortolami
DRDaniele Rocco
Daniele Rocco
AMAntonella Messore
Antonella Messore
RSRoberto Di Santo
Roberto Di Santo
Roberta CostiRoberta Costi
Roberta Costi
Fabiana PandolfiFabiana Pandolfi
Fabiana Pandolfi
Introduction – AD, the most common form of dementia, has a multifactorial etiology, and the current therapy (AChEIs and memantine) is unable to interrupt its progress and fatal outcome. This is reflected in the research programs that are oriented toward the development of new therapeutics able to operate on multiple targets involved in the disease progression. Areas covered – The patents from 2016 to present regarding the use of AChEIs in AD, concerns the development of new AChEIs, multitarget or multifunctional ligands, or the associations of currently used AChEIs with other compounds acting on different targets involved in the AD. Expert opinion – The development of new multitarget AChEIs promises to identify compounds with great therapeutic potential but requires more time and effort in order to obtain drugs with the optimal pharmacodynamic profile. Otherwise, the research on new combinations of existing drugs, with known pharmacodynamic and ADME profile, could shorten the time and reduce the costs to develop a new therapeutic treatment for AD. From the analyzed data, it seems more likely that a response to the urgent need to develop effective treatments for AD therapy could come more quickly from studies on drug combinations than from the development of new AChEIs.

14 October 2013 in Journal of Medicinal Chemistry
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Journal Article
Closed access
Roberta CostiRoberta Costi
Roberta Costi
MMMathieu Métifiot
Mathieu Métifiot
Francesca EspositoFrancesca Esposito
Francesca Esposito
GCGiuliana Cuzzucoli Crucitti
Giuliana Cuzzucoli Crucitti
LPLuca Pescatori
Luca Pescatori
RSRoberto Di Santo
Roberto Di Santo