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Panagiotis Marakos
Researcher at National and Kapodistrian University of Athens
Publications - 100
Citations - 1340
Panagiotis Marakos is an academic researcher from National and Kapodistrian University of Athens. The author has contributed to research in topics: Acridone & Tautomer. The author has an hindex of 18, co-authored 96 publications receiving 1175 citations. Previous affiliations of Panagiotis Marakos include Masaryk University & University of Michigan.
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Synthesis and antiviral activity evaluation of some new 6-substituted 3-(1-adamantyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles.
Marina Kritsanida,Anastasia Mouroutsou,Panagiotis Marakos,Nicole Pouli,S. Papakonstantinou‐Garoufalias,Christophe Pannecouque,Myriam Witvrouw,Erik De Clercq +7 more
TL;DR: A number of novel 3,6-disubstituted 1,2,4-triazolo[3, 4-b][1,3,4]thiadiazole derivatives, containing the adamantyl moiety, were synthesized and examined in various viral test systems.
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Robust, universal biomarker assay to detect senescent cells in biological specimens
Konstantinos Evangelou,Nikolaos Lougiakis,Sophia V. Rizou,Athanassios Kotsinas,Dimitris Kletsas,Daniel Muñoz-Espín,Nikolaos G. Kastrinakis,Nicole Pouli,Panagiotis Marakos,Paul A. Townsend,Manuel Serrano,Jiri Bartek,Vassilis G. Gorgoulis,Vassilis G. Gorgoulis,Vassilis G. Gorgoulis +14 more
TL;DR: A lipophilic, biotin‐linked Sudan Black B (SBB) analogue suitable for sensitive and specific, antibody‐enhanced detection of lipofuscin‐containing senescent cells in any biological material is designed and synthesized.
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Synthesis antimicrobial and antifungal activity of some new 3 substituted derivatives of 4-(2,4-dichlorophenyl)-5-adamantyl-1H-1,2,4-triazole.
TL;DR: The synthesis of a series of substituted hydrazones and thiazolidinones and some of them exhibited moderate activity against Candida albicans were tested for antimicrobial and antifungal activity.
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Design, synthesis and antiproliferative activity of some new azapyranoxanthenone aminoderivatives.
TL;DR: Some novel aminosubstituted azapyranoxanthenones, bearing structural similarity to the acridone alkaloid acronycine, have been designed and synthesized and exhibited interesting cytotoxic activity against the human solid tumor cell line.
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Fused xanthone derivatives as antiproliferative agents.
Nicole Pouli,Panagiotis Marakos +1 more
TL;DR: The furanoxanthone psorospermin is a highly promising isolated xanthone derivative exhibiting significant cytotoxicity through a novel mechanism of action, being an irreversible topoisomerase II poison and it was selected for further development as an antineoplastic agent.