Match tier
Likely match
Presence
Current · Arkansas
Last published
2026
Sources
OpenAlex · ORCID
Refreshed
2026-08-16
H
Hazim Aljewari
This is a likely match — the affiliation was inferred from OpenAlex, ORCID, and web sources but has not been fully confirmed. Treat with appropriate caution.
Researcher
Faculty Researcher
6 h-index
12 pubs
159 cited
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Hazim Aljewari's research focuses on the intersection of materials science and biological applications, particularly in areas related to separation technologies and drug discovery. His work includes the development of novel materials like cationic covalent organic frameworks and metal-organic frameworks for biomolecule separation, as well as the investigation of microcystin-LR removal from water using enzymatic linearization and ultrafiltration. Aljewari also engages in the synthesis and evaluation of potential therapeutic agents, including ring-opened analogues of ipomoeassin F and simplified ipomoeassin-F-derived Sec61 inhibitors, employing biological evaluation and computational docking studies. He has published 12 papers, with his work attracting 159 citations and an h-index of 6. Aljewari collaborates 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 11<i>R</i>-Epimer (2015)
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
3 shared publications
In database
- 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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