Hazim Aljewari
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Author
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Hazim Aljewari's research investigates the synthesis and biological evaluation of natural products and their analogs, focusing on compounds like Ipomoeassin F. His work includes exploring the pharmacophore of these molecules through molecular editing and docking studies, aiming to understand their antitumor potential. Aljewari also studies the purification of enzymes, such as L-asparaginase from *Escherichia coli*, for potential therapeutic applications against cancer cell lines. His research extends to materials science, including the development of covalent organic frameworks for biomolecule separation and the removal of toxins like microcystin-LR from water using enzymatic linearization and ultrafiltration. He has collaborated with researchers at the University of Arkansas at Fayetteville, including Robert Beitle, Faisal Alqhtani, Lei Guo, and Jerry A. Thornhill.
Metrics
- h-index: 6
- Publications: 12
- Citations: 159
Selected Publications
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A Metal-Organic Framework Decorated Filter For Fractionation and Isolation of Proteins Using Uio-66-Nh2 (2025)
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Improved Catalytic Reaction of Biotemplated Palladium Nanoparticles through Immobilized Metal Affinity Purification (2023)
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Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F (2022)
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Microcystin-LR Removal from Water via Enzymatic Linearization and Ultrafiltration (2022)
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Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor (2022)
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Cationic Covalent Organic Framework as an Ion Exchange Material for Efficient Adsorptive Separation of Biomolecules (2021)
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Study of Pneumococcal Surface Protein, PspA, Incorporated in Poly(Vinyl Alcohol) Hydrogel Membranes (2020)
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Recombinant peptide fusion construction for protein‐templated catalytic palladium nanoparticles (2020)
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Revealing the Pharmacophore of Ipomoeassin F through Molecular Editing (2016)
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Total Synthesis and Biological Evaluation of Ipomoeassin F and Its Unnatural 11R-Epimer (2015)
Collaboration Network
Top Collaborators
- Total Synthesis and Biological Evaluation of Ipomoeassin F and Its Unnatural 11R-Epimer
- Revealing the Pharmacophore of Ipomoeassin F through Molecular Editing
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Total Synthesis and Biological Evaluation of Ipomoeassin F and Its Unnatural 11R-Epimer
- Revealing the Pharmacophore of Ipomoeassin F through Molecular Editing
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Total Synthesis and Biological Evaluation of Ipomoeassin F and Its Unnatural 11R-Epimer
- Revealing the Pharmacophore of Ipomoeassin F through Molecular Editing
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Cationic Covalent Organic Framework as an Ion Exchange Material for Efficient Adsorptive Separation of Biomolecules
- Recombinant peptide fusion construction for protein‐templated catalytic palladium nanoparticles
- Improved Catalytic Reaction of Biotemplated Palladium Nanoparticles through Immobilized Metal Affinity Purification
- A Metal-Organic Framework Decorated Filter For Fractionation and Isolation of Proteins Using Uio-66-Nh2
- Cationic Covalent Organic Framework as an Ion Exchange Material for Efficient Adsorptive Separation of Biomolecules
- Recombinant peptide fusion construction for protein‐templated catalytic palladium nanoparticles
- Improved Catalytic Reaction of Biotemplated Palladium Nanoparticles through Immobilized Metal Affinity Purification
- A Metal-Organic Framework Decorated Filter For Fractionation and Isolation of Proteins Using Uio-66-Nh2
- Microcystin-LR Removal from Water via Enzymatic Linearization and Ultrafiltration
- Study of Pneumococcal Surface Protein, PspA, Incorporated in Poly(Vinyl Alcohol) Hydrogel Membranes
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
- Synthesis, Biological Evaluation and Docking Studies of Ring-Opened Analogues of Ipomoeassin F
- Biology-directed and in silico-aided design liberates a potent, simplified and ipomoeassin-F-derived Sec61 inhibitor
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