Leandros Skaltsounis

Prof. Dr. Leandros Skaltsounis

Department of Pharmacognosy and Natural Product Chemistry, Faculty of Pharmacy, National and Kapodistrian University of Athens, Panepistimioupoli, Zografou, GR-15771, Athens, Greece

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

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

Representative Publications

View All Publications
26 September 2013 in Planta Medica
Verified
Journal Article
Closed access
PDF file
PKPeriklis Kanakis
Periklis Kanakis
ATAikaterini Termentzi
Aikaterini Termentzi
TMThomas Michel
Thomas Michel
Evangelos GikasEvangelos Gikas
Evangelos Gikas
MHMaria Halabalaki
Maria Halabalaki
LSLeandros Skaltsounis
Leandros Skaltsounis
The aim of the current study was the qualitative exploration and quantitative monitoring of key olive secondary metabolites in different production steps (drupes, paste, first and final oil) throughout a virgin olive oil production line. The Greek variety Koroneiki was selected as one of the most representative olives, which is rich in biological active compounds. For the first time, an HPLC-Orbitrap platform was employed for both qualitative and quantitative purposes. Fifty-two components belonging to phenyl alcohols, secoiridoids, flavonoids, triterpenes, and lactones were identified based on HRMS and HRMS/MS data. Nine biologically and chemically significant metabolites were quantitatively determined throughout the four production steps. Drupes and paste were found to be rich in several components, which are not present in the final oil. The current study discloses the chemical nature of different olive materials in a successive and integrated way and reveals new sources of high added value constituents of olives.

3 September 2013 in Natural Product Reports
Verified
Journal Article
Closed access
PDF file
AAAikaterini Argyropoulou
Aikaterini Argyropoulou
NANektarios Aligiannis
Nektarios Aligiannis
Ioannis TrougakosIoannis Trougakos
Ioannis Trougakos
LSLeandros Skaltsounis
Leandros Skaltsounis
Covering: up to the end of June 2013 Ageing is a complex molecular process driven by diverse molecular pathways and biochemical events that are promoted by both environmental and genetic factors. Specifically, ageing is defined as a time-dependent decline of functional capacity and stress resistance, associated with increased chance of morbidity and mortality. These effects relate to age-related gradual accumulation of stressors that result in increasingly damaged biomolecules which eventually compromise cellular homeostasis. Nevertheless, the findings that genetic or diet interventions can increase lifespan in evolutionarily diverse organisms indicate that mortality can be postponed. Natural compounds represent an extraordinary inventory of high diversity structural scaffolds that can offer promising candidate chemical entities in the major healthcare challenge of increasing healthspan and/or delaying ageing. Herein, those natural compounds (either pure forms or extracts) that have been found to delay cellular senescence or in vivo ageing will be critically reviewed and summarized according to affected cellular signalling pathways. Moreover, the chemical structures of the identified natural compounds along with the profile of extracts related to their bioactive components will be presented and discussed. Finally, novel potential molecular targets for screening natural compounds for anti-ageing activity, as well as the idea that anti-ageing interventions represent a systemic approach that is also effective against age-related diseases will be discussed.

25 September 2008 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
KVKonstantina Vougogiannopoulou
Konstantina Vougogiannopoulou
YFYoan Ferandin
Yoan Ferandin
KBKarima Bettayeb
Karima Bettayeb
VMVassilios Myrianthopoulos
Vassilios Myrianthopoulos
LOLozach Olivier
Lozach Olivier
LMLAURENT MEIJER
LAURENT MEIJER

23 March 2017 in Molecules
Verified
Journal Article
Open access
PDF file
ECEliza Chaita
Eliza Chaita
GLGeorge Lambrinidis
George Lambrinidis
MCMaria-Christina Cheimonidi
Maria-Christina Cheimonidi
AAAdamantia Agalou
Adamantia Agalou
Dimitris BeisDimitris Beis
Dimitris Beis
NANektarios Aligiannis
Nektarios Aligiannis
In therapeutic interventions associated with melanin hyperpigmentation, tyrosinase is regarded as a target enzyme as it catalyzes the rate-limiting steps in mammalian melanogenesis. Since many known agents have been proven to be toxic, there has been increasing impetus to identify alternative tyrosinase inhibitors, especially from natural sources. In this study, we investigated 900 extracts from Greek plants for potential tyrosinase inhibitive properties. Among the five most potent extracts, the methanol extract of Morus alba wood (MAM) demonstrated a significant reduction in intracellular tyrosinase and melanin content in B16F10 melanoma cells. Bioassay-guided isolation led to the acquisition of twelve compounds: oxyresveratrol (1), kuwanon C (2), mulberroside A (3), resorcinol (4), dihydrooxyresveratol (5), trans-dihydromorin (6), 2,4,3′-trihydroxydihydrostilbene (7), kuwanon H (8), 2,4-dihydroxybenzaldehyde (9), morusin (10), moracin M (11) and kuwanon G (12). Among these, 2,4,3′-trihydroxydihydrostilbene (7) is isolated for the first time from Morus alba and constitutes a novel potent tyrosinase inhibitor (IC50 0.8 ± 0.15). We report here for the first time dihydrooxyresveratrol (5) as a potent natural tyrosinase inhibitor (IC50 0.3 ± 0.05). Computational docking analysis indicated the binding modes of six tyrosinase inhibitors with the aminoacids of the active centre of tyrosinase. Finally, we found both MAM extract and compounds 1, 6 and 7 to significantly suppress in vivo melanogenesis during zebrafish embryogenesis.

6 November 2012 in ACS Medicinal Chemistry Letters
Verified
Journal Article
Open access
VMVassilios Myrianthopoulos
Vassilios Myrianthopoulos
MKMarina Kritsanida
Marina Kritsanida
NGNicolas Gaboriaud-Kolar
Nicolas Gaboriaud-Kolar
Prokopios MagiatisProkopios Magiatis
Prokopios Magiatis
YFYoan Ferandin
Yoan Ferandin
LSLeandros Skaltsounis
Leandros Skaltsounis
DYRK kinases are involved in alternative pre-mRNA splicing as well as in neuropathological states such as Alzheimer's disease and Down syndrome. In this study, we present the design, synthesis, and biological evaluation of indirubins as DYRK inhibitors with enhanced selectivity. Modifications of the bis-indole included polar or acidic functionalities at positions 5′ and 6′ and a bromine or a trifluoromethyl group at position 7, affording analogues that possess high activity and pronounced specificity. Compound 6i carrying a 5′-carboxylate moiety demonstrated the best inhibitory profile. A novel inverse binding mode, which forms the basis for the improved selectivity, was suggested by molecular modeling and confirmed by determining the crystal structure of DYRK2 in complex with 6i. Structure–activity relationships were further established, including a thermodynamic analysis of binding site water molecules, offering a structural explanation for the selective DYRK inhibition.

1 March 2023 in Plants
Verified
Journal Article
Open access
PDF file
EKEleftherios Kalpoutzakis
Eleftherios Kalpoutzakis
Theodoros ChatzimitakosTheodoros Chatzimitakos
Theodoros Chatzimitakos
Vassilis AthanasiadisVassilis Athanasiadis
Vassilis Athanasiadis
SMSofia Mitakou
Sofia Mitakou
NANektarios Aligiannis
Nektarios Aligiannis
Stavros I. LalasStavros I. Lalas
Stavros I. Lalas
Oxidative damages are responsible for many adverse health effects and food deterioration. The use of antioxidant substances is well renowned, and as such, much emphasis is placed on their use. Since synthetic antioxidants exhibit potential adverse effects, plant-derived antioxidants are a preferable solution. Despite the myriads of plants that exist and the fact that numerous studies have been carried out so far, there are many species that have not been examined so far. Many plants under research exist in Greece. Trying to fill this research gap, the total phenolics content and antioxidant activity of seventy methanolic extracts from parts of Greek plants were evaluated. The total phenolics content was measured by the Folin–Ciocalteau assay. Their antioxidant capacity was calculated by the 2,2-Diphenyl-1-picrylhydrazyl (DPPH) scavenging test, the Rancimat method based on conductometric measurements, and the thermoanalytical method DSC (Differential Scanning Calorimetry). The tested samples were obtained from several parts of fifty-seven Greek plant species belonging to twenty-three different families. Both a remarkably high phenolic content (with gallic acid equivalents varying between 311.6 and 735.5 mg/g of extract) and radical scavenging activity (IC50 values ranged from 7.2 to 39.0 μg/mL) were found in the extract of the aerial parts of Cistus species (C. creticus subsp. creticus, C. creticus subsp. eriocephalus, C. monspeliensis, C. parviflorus and C. salviifolius), Cytinus taxa (C. hypocistis subsp. hypocistis, C. hypocistis subsp. orientalis and C. ruber), and Sarcopoterium spinosum. Furthermore, the sample of Cytinus ruber showed the highest protection factor (PF = 1.276) regarding the Rancimat method, which was similar to that of butylated hydroxytoluene (BHT) (PF = 1.320). The results indicated that these plants are rich in antioxidant compounds, potentiating their use either as food additives to enhance the antioxidant properties of food products, or protect them from oxidation, or as sources for the preparation of food supplements with antioxidant properties.