Nikolaos Lougiakis

Athens, ESYE31, Greece

Last Updated: 09/26/2026

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Found 35 publications

Design and Synthesis of Novel Imidazo[4,5-c]pyridine Derivatives, Evaluation of Their Activity Against Hepatitis C Virus and In Silico Prediction of Their Binding Mode to NS4B Protein.

Design and Synthesis of Novel Imidazo[4,5-c]pyridine Derivatives, Evaluation of Their Activity Against Hepatitis C Virus and In Silico Prediction of Their Binding Mode to NS4B Protein.

Journal: ChemMedChem
Published: February 27, 2026

Author Correction: Generation of a selective senolytic platform using a micelle-encapsulated Sudan Black B conjugated analog.

Author Correction: Generation of a selective senolytic platform using a micelle-encapsulated Sudan Black B conjugated analog.

Journal: Nature aging
Published: January 31, 2025

Hit-to-Lead Optimization of Heterocyclic Carbonyloxycarboximidamides as Selective Antagonists at Human Adenosine A3 Receptor.

Hit-to-Lead Optimization of Heterocyclic Carbonyloxycarboximidamides as Selective Antagonists at Human Adenosine A3 Receptor.

Journal: Journal of medicinal chemistry
Published: July 29, 2024

Generation of a selective senolytic platform using a micelle-encapsulated Sudan Black B conjugated analog.

Generation of a selective senolytic platform using a micelle-encapsulated Sudan Black B conjugated analog.

Journal: Nature aging
Published: June 12, 2024

One-step rapid tracking and isolation of senescent cells in cellular systems, tissues, or animal models via GLF16.

One-step rapid tracking and isolation of senescent cells in cellular systems, tissues, or animal models via GLF16.

Journal: STAR protocols
Published: December 04, 2023

Hydrolytic Activity of Mitochondrial F1FO-ATP Synthase as a Target for Myocardial Ischemia-Reperfusion Injury: Discovery and In Vitro and In Vivo Evaluation of Novel Inhibitors.

Hydrolytic Activity of Mitochondrial F1FO-ATP Synthase as a Target for Myocardial Ischemia-Reperfusion Injury: Discovery and In Vitro and In Vivo Evaluation of Novel Inhibitors.

Journal: Journal of medicinal chemistry
Published: November 09, 2023

Novel H2S-Releasing Bifunctional Antihistamine Molecules with Improved Antipruritic and Reduced Sedative Actions.

Novel H2S-Releasing Bifunctional Antihistamine Molecules with Improved Antipruritic and Reduced Sedative Actions.

Journal: Journal of medicinal chemistry
Published: July 06, 2023

Synthesis, cytotoxic activity evaluation and mechanistic investigation of novel 3,7-diarylsubstituted 6-azaindoles.

Synthesis, cytotoxic activity evaluation and mechanistic investigation of novel 3,7-diarylsubstituted 6-azaindoles.

Journal: European journal of medicinal chemistry
Published: May 16, 2023

Discovery of New 1,4,6-Trisubstituted-1H-pyrazolo[3,4-b]pyridines with Anti-Tumor Efficacy in Mouse Model of Breast Cancer.

Discovery of New 1,4,6-Trisubstituted-1H-pyrazolo[3,4-b]pyridines with Anti-Tumor Efficacy in Mouse Model of Breast Cancer.

Journal: Pharmaceutics
Published: January 31, 2023

A fluorophore-conjugated reagent enabling rapid detection, isolation and live tracking of senescent cells.

A fluorophore-conjugated reagent enabling rapid detection, isolation and live tracking of senescent cells.

Journal: Molecular cell
Published: January 23, 2023

SIRT2i_Predictor: A Machine Learning-Based Tool to Facilitate the Discovery of Novel SIRT2 Inhibitors.

SIRT2i_Predictor: A Machine Learning-Based Tool to Facilitate the Discovery of Novel SIRT2 Inhibitors.

Journal: Pharmaceuticals (Basel, Switzerland)
Published: December 13, 2022

Dual A1/A3 Adenosine Receptor Antagonists: Binding Kinetics and Structure-Activity Relationship Studies Using Mutagenesis and Alchemical Binding Free Energy Calculations.

Dual A1/A3 Adenosine Receptor Antagonists: Binding Kinetics and Structure-Activity Relationship Studies Using Mutagenesis and Alchemical Binding Free Energy Calculations.

Journal: Journal of medicinal chemistry
Published: September 29, 2022
Showing 1-12 of 35

Last Updated: 09/26/2026