Abdullah A. Elgazar
Kafr Ash Shaykh, SHR, Egypt
Last Updated: 09/26/2026
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Found 30 publications
Egyptian fennel honey as a potential sustainable and economical alternative to manuka honey: a multi-parameter comparative study.
Journal: RSC advances
Published: April 03, 2026
Unveiling the wound-healing potential of Pisum sativum aerial biomass through integrated bioassay-guided, LC-MS/MS, and network pharmacology approaches.
Journal: BMC complementary medicine and therapies
Published: November 15, 2025
Thiazolidinedione-based dual inhibitors of α-amylase and aldose reductase: Design, in vitro evaluation, and in vivo hypoglycemic activity.
Journal: Bioorganic & medicinal chemistry
Published: October 18, 2025
Design, synthesis, and biological evaluation of quinazoline-benzohydrazide and quinazoline-benzothiazole hybrids uncovering a dual EGFR/VEGFR-2 inhibitor with pronounced cytotoxic activity against triple-negative breast Cancer.
Journal: Bioorganic & medicinal chemistry
Published: September 15, 2025
Editorial: Multi-target drug discovery and design for complex health disorders.
Journal: Frontiers in pharmacology
Published: May 22, 2025
Khellin Mitigates Cisplatin-Induced Renal Injury by Targeting Oxidative Stress, Inflammation, and Apoptosis: Integration of Network Pharmacology, Molecular Docking, and Preclinical Validation.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: April 11, 2025
Click Chemistry-Aided Synthesis of Triazole-Tethered Benzothiazoles as Novel Multifunctional Agents Against Alzheimer's Disease.
Journal: Archiv der Pharmazie
Published: January 28, 2025
"Triazole-linked thiazolidinedione-Benzothiazole hybrids: Design and biological evaluation as AChE inhibitors".
Journal: Bioorganic chemistry
Published: December 27, 2024
New phenylpiperazine-thiazolidine-2,4-dione hybrids targeting MAO inhibition: Synthesis, biological evaluation, kinetic study and in silico insights.
Journal: Bioorganic & medicinal chemistry
Published: December 16, 2024
Design, Synthesis, Pharmacological Evaluation of Quinazolin-4(3H)-Ones Bearing Urea Functionality as Potential VEGFR-2 Inhibitors.
Journal: Drug design, development and therapy
Published: September 18, 2024
Design, synthesis, and in vitro and in vivo biological evaluation of triazolopyrimidine hybrids as multitarget directed anticancer agents.
Journal: RSC advances
Published: September 17, 2024
S-Alkylated quinazolin-4(3H)-ones as dual EGFR/VEGFR-2 kinases inhibitors: design, synthesis, anticancer evaluation and docking study.
Journal: RSC advances
Published: July 03, 2024
Last Updated: 09/26/2026