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Pharmaceuticals (Basel, Switzerland)|April 23, 2022
Design, Synthesis, and Biological Evaluation of Novel Tomentosin Derivatives in NMDA-Induced ExcitotoxicityMohamed Zaki, Mohammed Loubidi, Tuğçe Bilgiç, et al.
Archiv Der Pharmazie|February 15, 2021
Design, synthesis, and evaluation of cytotoxic activities of arylnaphthalene lignans and aza-analogsEl-Mahdi Ourhzif, Arnaud Pâris, Isabelle Abrunhosa-Thomas, et al.
Current Organic Synthesis|February 25, 2020
Synthesis and Biological Evaluation of New Naphthoquinones DerivativesEl-Mahdi Ourhzif, Caroline Decombat, Isabelle Abrunhosa-Thomas, et al.
European Journal of Medicinal Chemistry|February 20, 2017
Synthesis of new heterocyclic compounds based on pyrazolopyridine scaffold and evaluation of their neuroprotective potential in MPP<sup>+</sup>-induced neurodegenerationJabrane Jouha, Mohammed Loubidi, Jamila Bouali, et al.
Molecules (Basel, Switzerland)|August 26, 2022
Antifungal and Cytotoxic Activity of Diterpenes and Bisnorsesquiterpenoides from the Latex of <i>Euphorbia resinifera</i> BergEl-Mahdi Ourhzif, Alessandra Ricelli, Venturina Stagni, et al.
Bioorganic Chemistry|July 23, 2021
Design, Hemiysnthesis, crystal structure and anticancer activity of 1, 2, 3-triazoles derivatives of totarolYassine Laamari, Ali Oubella, Abdoullah Bimoussa, et al.
European Journal of Medicinal Chemistry|January 12, 2018
Efficient synthesis and first regioselective C-6 direct arylation of imidazo[2,1-c][1,2,4]triazine scaffold and their evaluation in H<sub>2</sub>O<sub>2</sub>-induced oxidative stressMohammed Loubidi, Jabrane Jouha, Zahira Tber, et al.
Scientific Reports|June 23, 2026
Design and synthesis of 2,5-di(pyridin-4-yl)-1,3,4-oxadiazole: structural elucidation, DFT insights, and preliminary in silico biological evaluationChaimaa Hatim, Abdessamad Benabbou, Said Jebbari, et al.
European Journal of Medicinal Chemistry|January 17, 2021
Evaluation of the cellular protection by novel spiropyrazole compounds in dopaminergic cell deathJamila Zaiter, Achraf Hibot, Abderrafia Hafid, et al.
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