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Profil bibliographique

Hamada S. Abulkhair

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

81Publications signalées
2674Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Synthesis and biological activitySynthesis and Biological EvaluationClick Chemistry and ApplicationsCancer therapeutics and mechanismsSynthesis and Characterization of Heterocyclic Compounds

Les publications récentes

Accès ouvert 2026 article OpenAlex

Pyridone-based EZH2 inhibitor anticancer candidates: synthetic approaches, comparative analysis, and future perspectives

Hamada S. Abulkhair

Enhancer of Zeste Homolog 2 (EZH2) is a major epigenetic regulator whose dysregulation drives oncogenesis through aberrant trimethylation of H3K27 and silencing tumor-suppressor genes. Pyridone-based small molecules have emerged as the dominant chemotype for targeting the SET domain of EZH2, enabling potent, …

0 citations Figshare
Accès ouvert 2026 article OpenAlex

Pyridone-based EZH2 inhibitor anticancer candidates: synthetic approaches, comparative analysis, and future perspectives

Hamada S. Abulkhair

Enhancer of Zeste Homolog 2 (EZH2) is a major epigenetic regulator whose dysregulation drives oncogenesis through aberrant trimethylation of H3K27 and silencing tumor-suppressor genes. Pyridone-based small molecules have emerged as the dominant chemotype for targeting the SET domain of EZH2, enabling potent, …

0 citations Figshare
Accès ouvert 2026 article OpenAlex

Pyridone-based EZH2 inhibitor anticancer candidates: synthetic approaches, comparative analysis, and future perspectives

Hamada S. Abulkhair

Enhancer of Zeste Homolog 2 (EZH2) is a major epigenetic regulator whose dysregulation drives oncogenesis through aberrant trimethylation of H3K27 and silencing tumor-suppressor genes. Pyridone-based small molecules have emerged as the dominant chemotype for targeting the SET domain of EZH2, enabling potent, …

id, Égypte (code pays fourni par la source)

0 citations Future Medicinal Chemistry
2026 article OpenAlex

Therapeutic Horizons in Targeting EZH2 With Dual and Non‐PROTAC Inhibitor Molecules: Recent Achievements, Comparative Analysis, and Future Perspectives

Hamada S. Abulkhair

The aberrant overexpression of Enhancer of Zeste Homolog 2 (EZH2) endorses uncontrolled cell proliferation and metastasis across multiple malignancies. These make EZH2 an attractive biological target for the development of potential anticancer molecules. Following the approval of Tazemetostat, the last 5 years …

Égypte (code pays fourni par la source)

0 citations Archiv der Pharmazie
Accès ouvert 2026 article OpenAlex

Therapeutic horizons in the development of PROTAC-based EZH2 inhibitors: recent achievements, comparative analysis, and future perspectives

Hamada S. Abulkhair

= 34 nM in EOL-1 cells) with concentration- and time-dependent activity, establishing a benchmark for efficient EZH2 elimination. Compounds P3 (72) and P4 (73) (VHL-based) and U3i (44) (CRBN-based) also demonstrated potent dual biochemical and cellular profiles. Recent findings emphasize structure-activity trends, …

Égypte (code pays fourni par la source)

2 citations RSC Advances
Accès ouvert 2026 article OpenAlex

Rational design and synthesis of Co( ii ), Ni( ii ) and Cu( ii ) complexes bearing 1,2,4-triazole scaffold for biological applications

Azza A. Hassoon, Hamada S. Abulkhair, Ranim H. Ashour, Mariam M. Abdelsamea et autres

The synthesis of 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole (AHMT) metal complexes, followed by comprehensive physico-chemical characterization, evaluation of their biological applications and molecular docking studies.

Égypte (code pays fourni par la source)

0 citations RSC Advances
Accès ouvert 2025 article OpenAlex

α-Glucosidase-targeting 1,2,4-triazole antidiabetic candidates: comparative analysis and future perspectives

Hamada S. Abulkhair

Diabetes mellitus develops because of the disturbance in carbohydrate metabolism. The therapeutic goal for antidiabetic medications is to manage blood glucose level and to prevent hyperglycemia-associated complications. α-Glucosidase inhibitors represent one of the widely used oral hypoglycemics. This review highlights the potential …

Égypte, id (code pays fourni par la source)

6 citations Future Medicinal Chemistry

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