H
Hazim Aljewari Data-verified
Affiliation confirmed via AI analysis of OpenAlex, ORCID, and web sources.
Researcher
faculty
6 h-index
12 pubs
159 cited
Research Areas
Biography and Research Information
OverviewAI-generated summary
Hazim Aljewari's research investigates the application of advanced materials for separation and purification processes, particularly in biological contexts. His work has explored the use of Cationic Covalent Organic Frameworks for biomolecule separation and Metal-Organic Frameworks decorated filters for protein fractionation and isolation. Aljewari has also studied methods for removing contaminants from water, including microcystin-LR removal through enzymatic linearization and ultrafiltration. Additionally, his research includes the synthesis and biological evaluation of potential therapeutic agents, such as ring-opened analogues of Ipomoeassin F, and the development of simplified, biologically directed inhibitors. His publications also touch upon enhancing catalytic reactions using immobilized metal affinity purification and exploring the biological effects of specific molecular structures. Aljewari's scholarship metrics include an h-index of 6, with 12 total publications and 158 total citations.
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)
Collaboration Network
Top Collaborators
Imann Mosleh
Pfizer (United States) (US)
3 shared publications
- Cationic Covalent Organic Framework as an Ion Exchange Material for Efficient Adsorptive Separation of Biomolecules
- 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
Robert Beitle
Oldham Council (GB)
3 shared publications
- Cationic Covalent Organic Framework as an Ion Exchange Material for Efficient Adsorptive Separation of Biomolecules
- 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
Sarah O’Keefe
University of Manchester (GB)
2 shared publications
- 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
Pratiti Bhadra
Saarland University (DE)
2 shared publications
- 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
Kwabena B. Duah
Ball State University (US)
2 shared publications
- 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
Guanghui Zong
University of Maryland, College Park (US)
2 shared publications
- 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
Levise Tenay
Saarland University (DE)
2 shared publications
- 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
Lauren Andrews
Ball State University (US)
2 shared publications
- 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
Hayden Schneider
Ball State University (US)
2 shared publications
- 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
Ashley G. Anderson
Saarland University (DE)
2 shared publications
- 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
Zhijian Hu
Feinstein Institute for Medical Research (US)
2 shared publications
- 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
Belinda S. Hall
University of Surrey (GB)
2 shared publications
- 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
Rachel E. Simmonds
University of Surrey (GB)
2 shared publications
- 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
Volkhard Helms
Saarland University (DE)
2 shared publications
- 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
Stephen High
University of Manchester (GB)
2 shared publications
- 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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