Aida A. Azzouny-El

Dokki, GZ 12622, Egypt

Last Updated: 09/26/2026

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Found 16 publications

Design, synthesis, biological evaluation and computational studies of novel phthalimides as dual COX-2/5-LOX inhibitors.

Design, synthesis, biological evaluation and computational studies of novel phthalimides as dual COX-2/5-LOX inhibitors.

Journal: Molecular diversity

Published: November 13, 2025

Design and synthesis of new 1,3,4-oxadiazole-1,2,3,4-tetrahydroisoquinoline hybrids as selective COX-2 inhibitors.

Design and synthesis of new 1,3,4-oxadiazole-1,2,3,4-tetrahydroisoquinoline hybrids as selective COX-2 inhibitors.

Journal: Bioorganic chemistry

Published: July 12, 2025

Design, synthesis and anti-inflammatory assessment of certain substituted 1,2,4-triazoles bearing tetrahydroisoquinoline scaffold as COX 1/2-inhibitors.

Design, synthesis and anti-inflammatory assessment of certain substituted 1,2,4-triazoles bearing tetrahydroisoquinoline scaffold as COX 1/2-inhibitors.

Journal: Bioorganic chemistry

Published: May 08, 2024

Design and synthesis of new quinazolinone derivatives: investigation of antimicrobial and biofilm inhibition effects.

Design and synthesis of new quinazolinone derivatives: investigation of antimicrobial and biofilm inhibition effects.

Journal: Molecular diversity

Published: September 30, 2023

Synthetic non-toxic anti-biofilm agents as a strategy in combating bacterial resistance.

Synthetic non-toxic anti-biofilm agents as a strategy in combating bacterial resistance.

Journal: European journal of medicinal chemistry

Published: August 11, 2023

Experimental design optimization of simultaneous enantiomeric separation of atenolol and chlorthalidone binary mixture by high-performance liquid chromatography using polysaccharide-based stationary phases.

Experimental design optimization of simultaneous enantiomeric separation of atenolol and chlorthalidone binary mixture by high-performance liquid chromatography using polysaccharide-based stationary phases.

Journal: Chirality

Published: December 09, 2020

Design and synthesis of novel parabanic acid derivatives as anticonvulsants.

Design and synthesis of novel parabanic acid derivatives as anticonvulsants.

Journal: Bioorganic chemistry

Published: August 02, 2019

Design, synthesis and anticancer evaluation of novel 1,3-benzodioxoles and 1,4-benzodioxines.

Design, synthesis and anticancer evaluation of novel 1,3-benzodioxoles and 1,4-benzodioxines.

Journal: European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences

Published: June 15, 2019

Synthesis, molecular modeling studies, and anticonvulsant evaluation of novel 1-((2-hydroxyethyl)(aryl)amino)-N-substituted cycloalkanecarboxamides and their acetate esters.

Synthesis, molecular modeling studies, and anticonvulsant evaluation of novel 1-((2-hydroxyethyl)(aryl)amino)-N-substituted cycloalkanecarboxamides and their acetate esters.

Journal: Archiv der Pharmazie

Published: September 08, 2018

Structure-retention relationship for enantioseparation of selected fluoroquinolones.

Structure-retention relationship for enantioseparation of selected fluoroquinolones.

Journal: Chirality

Published: February 18, 2018

Enantioseparation of Substituted 1, 3-Diazaspiro [4.5]Decan-4-Ones: HPLC Comparative Study on Different Polysaccharide Type Chiral Stationary Phases.

Enantioseparation of Substituted 1, 3-Diazaspiro [4.5]Decan-4-Ones: HPLC Comparative Study on Different Polysaccharide Type Chiral Stationary Phases.

Journal: Journal of chromatographic science

Published: February 27, 2017

Anticonvulsant profiles of certain new 6-aryl-9-substituted-6,9-diazaspiro-[4.5]decane-8,10-diones and 1-aryl-4-substituted-1,4-diazaspiro[5.5]undecane-3,5-diones.

Anticonvulsant profiles of certain new 6-aryl-9-substituted-6,9-diazaspiro-[4.5]decane-8,10-diones and 1-aryl-4-substituted-1,4-diazaspiro[5.5]undecane-3,5-diones.

Journal: International journal of molecular sciences

Published: August 19, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026