Exploring the therapeutic potential of chalcones in oncology: A comprehensive review

CS Yadav, I Azad, AR Khan, N Ahmad… - Current Bioactive …, 2024 - ingentaconnect.com
Chalcone is a bioactive flavonoid found in various plants, such as Angelica archangelica,
Pueraria lobata, and Glycyrrhiza glabra. It has been studied extensively in the field of …

Quassinoids from Eurycoma longifolia as Potential Dihydrofolate Reductase Inhibitors: A Computational Study

NM Yunos, MG Al-Thiabat… - Current …, 2024 - benthamdirect.com
Background: Quassinoids are degraded triterpene compounds that can be obtained from
various species of the Simaroubaceae plant family, including Eurycoma longifolia …

Potential Serotonin 5-HT2A Receptor Agonist of Psychoactive Components of Silene undulata Aiton: LC-MS/MS, ADMET, and Molecular Docking Studies

MB Alhawarri, S Olimat - Current Pharmaceutical Biotechnology, 2025 - benthamdirect.com
Background Silene undulata is historically used for inducing vivid and prophetic lucid
dreams, but limited information exists on its phytochemical composition and potential …

Exploring the Anticancer Potential of Furanpydone A: A Computational Study on its Inhibition of MTHFD2 Across Diverse Cancer Cell Lines

MB Alhawarri - Cell Biochemistry and Biophysics, 2024 - Springer
Cancer poses a significant global health challenge due to its high mortality rate and complex
treatment strategies. Methylenetetrahydrofolate dehydrogenase 2 (MTHFD2), which is …

[HTML][HTML] Computational Insight of Oleracone L, Portulacatone B, and Portulacatal from Portulaca oleracea L. as Potential Anticholinesterase Inhibitors for Alzheimer's

SO Alshammari - Processes, 2024 - mdpi.com
Alzheimer's disease, characterized by a decline in cognitive functions, is frequently
associated with decreased levels of acetylcholine due to the overactivity of …

Synthesis, characterization and bioactivity of new pyridine-2(H)-one, nicotinonitrile, and furo[2,3-b]pyridine derivatives

MM Ibrahim, MN Azmi, MB Alhawarri, NNSNM Kamal… - Molecular Diversity, 2024 - Springer
Pyridone heterocycles, such as furo [2, 3-b] pyridines, have emerged as prominent scaffolds
in medicinal chemistry due to their versatile pharmacological properties, including significant …

Investigating the potential of mono-chalcone compounds in targeting breast cancer receptors through network pharmacology, molecular docking, molecular dynamics …

NZ Ismail, M Khairuddean, MM Alidmat, S Abubakar… - 3 Biotech, 2024 - Springer
The study aims to investigate various aspects of synthesized mono-chalcone compounds 5
and 8 concerning breast cancer, including network pharmacology, molecular docking …

[PDF][PDF] Synthesis, Characterization and Glyoxalase inhibitory activity of 4, 6-Diheteroarylpyrimidine-2-amine derivatives: In vitro and in silico studies

MM Alidmat, MB Alhawarri, M Al-Refai… - Egyptian Journal of …, 2024 - ejchem.journals.ekb.eg
Abstract New series of 4, 6-diheteroarylpyrimidine-2ـamines (4a-e) and (5a-c) were
prepared by cyclization of particular chalcones (2) or (3) with guanidine nitrate in the …

Targeting necroptosis in MCF-7 breast cancer cells: In Silico insights into 8,12-dimethoxysanguinarine from Eomecon Chionantha through molecular docking …

MB Alhawarri, MG Al-Thiabat, A Dubey, A Tufail… - PloS one, 2025 - journals.plos.org
Breast cancer remains a significant challenge in oncology, highlighting the need for
alternative therapeutic strategies that target necroptosis to overcome resistance to …

Identification and Absorption–Distribution–Metabolism–Excretion–Toxicity Prediction of Potential MTHFD2 Enzyme Inhibitors from Urtica dioica Ethanolic Leaf Extract

SO Alshammari - Processes, 2024 - mdpi.com
This study aimed to explore the potential of Urtica dioica (U. dioica) ethanolic leaf extract for
cancer treatment by identifying its components, evaluating its effects on cancer cell lines …