Personal profile
Research interests
The Elgendy Lab specializes in drug discovery and medicinal chemistry, engaging in a comprehensive range of activities associated with various aspects of drug development. Their primary objective is to advance the field of medicinal chemistry by designing and synthesizing novel therapeutic agents.
Elgendy lab has predominantly focused on (a) the design and synthesis of modulators of nuclear hormone receptors (e.g., REV-ERB, ERR, LXR, FXR, and TLX) to validate these targets for the treatment of challenging diseases such as muscle injuries, Alzheimer’s disease, atherosclerosis, cancer, Fatty liver diseases, and pain.
The recent drug discovery efforts by Elgendy lab have been concentrated on three primary areas. Firstly, they are developing Central Nervous System (CNS)-active 5-HT3 receptor antagonists to treat neuropathic pain. Secondly, they are designing and developing new inhibitors of the mitochondrial protein complex to treat type 2 diabetes, metabolic dysfunction-associated steatotic liver disease (MASLD), and neurodegenerative diseases. Lastly, they are working on discovering inhibitors of Cholesterol 25-hydroxylase (CH25H) to treat Alzheimer's disease.
Dr. Elgendy incorporates computational methods such as quantitative structure activity relationships, pharmacophore modeling, and virtual screening in his drug discovery pipeline to accelerate the process of drug discovery and optimization.
Available to Mentor:
- PhD Students
- Post-Baccalaureate Students
- Postdocs
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Collaborations and top research areas from the last five years
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A Gut-Restricted Liver X Receptor Agonist Ameliorates Liver Injury in Experimental Short Bowel Syndrome
Kim, A., Alligood, D. M., Maram, L., Phelps, H. M., Cameron, M., DeRousse, J. T., Han, J., Dunning, T. J., Mintz, R. L., Park, A., Lee, D. D., Davis, D. L., Huckstep, C. G., Field, R. L., Hegazy, L., Zinselmeyer, B. H., Brestoff, J. R., Martin, C. A., Warner, B. W. & Elgendy, B. & 1 others, , May 2026, In: Gastroenterology. 170, 5, p. 1017-1032 16 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Link opens in a new tab Scopus citations -
Chemical optimization of the exercise mimetic SLU-PP-332 enables insight into estrogen-related receptor signaling
Okda, H. E., Zhao, P., Hayes, M., Duvall, C., Quillin, E., Fang, H., Mohammed, B. M., Hegazy, L., Burris, T. P. & Elgendy, B., Apr 2026, In: International Journal of Biological Macromolecules. 355, 151450.Research output: Contribution to journal › Article › peer-review
Open Access -
Discovery of BE2012, a First-in-Class REV-ERBα/β Antagonist with Favorable Selectivity and Pharmacokinetics, and In Vivo Efficacy in Inducing Key Myogenic Factors for Muscle Repair upon Acute Muscle Injury
Maram, L., Valfort, A. C., Homaidur Rahman, M., Okda, H. E., Elagawany, M., Politte, H., Appourchaux, K., Bedia-Diaz, G., Côté, I., Hegazy, L., Burris, T. P. & Elgendy, B., Jan 8 2026, In: Journal of Medicinal Chemistry. 69, 1, p. 439-465 27 p.Research output: Contribution to journal › Article › peer-review
1 Link opens in a new tab Scopus citations -
Edaravone: Advances on cytoprotective effects, pharmacological properties, and mechanisms of action
Dakroub, F., Awada, B., Abdelhady, S., Shaito, A. A., Eid, A. H., Walker, J., Mondello, S., Bondi, C. O., Moro, F., Elgendy, B., Wang, K. K., Zanier, E. R., Mechref, Y. & Kobeissy, F., Jan 2026, In: Pharmacological Reviews. 78, 1, 100101.Research output: Contribution to journal › Review article › peer-review
5 Link opens in a new tab Scopus citations -
Erratum to “Edaravone: Advances on cytoprotective effects, pharmacological properties, and mechanisms of action”(Pharmacological Reviews, (2026), 78, 1, (100101), (S0031699725075106), 10.1016/j.pharmr.2025.100101)
Dakroub, F., Awada, B., Abdelhady, S., Shaito, A. A., Eid, A. H., Walker, J., Mondello, S., Bondi, C. O., Moro, F., Elgendy, B., Wang, K. K., Zanier, E. R., Mechref, Y. & Kobeissy, F., Mar 2026, In: Pharmacological Reviews. 78, 2, 100114.Research output: Contribution to journal › Comment/debate
Open Access