Identification of Human Leukotriene A4 Hydrolase Inhibitors Using Structure-Based Pharmacophore Modeling and Molecular Docking by Audat, Suaad A, Al-Shar'i, Nizar A, Al-Oudat, Buthina A, Bryant-Friedrich, Amanda, Bedi, Mel F, Zayed, Aref L, Al-Balas, Qosay A

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Novel Chrysin-De-Allyl PAC-1 Hybrid Analogues as Anticancer Compounds: Design, Synthesis, and Biological Evaluation by Al-Oudat, Buthina A, Ramapuram, Hariteja, Malla, Saloni, Audat, Suaad A, Hussein, Noor, Len, Jenna M, Kumari, Shikha, Bedi, Mel F, Ashby, Jr, Charles R, Tiwari, Amit K

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Synthesis of C3′ Modified Nucleosides for Selective Generation of the C3′-Deoxy-3′-thymidinyl Radical: A Proposed Intermediate in LEE Induced DNA Damage by Audat, Suaad A. S, Trzasko Love, CherylAnn, Al-Oudat, Buthina A. S, Bryant-Friedrich, Amanda C

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Design, synthesis and biological evaluation of novel glyoxalase I inhibitors possessing diazenylbenzenesulfonamide moiety as potential anticancer agents by Al-Oudat, Buthina A., Jaradat, Hana'a M., Al‑Balas, Qosay A., Al-Shar'i, Nizar A., Bryant-Friedrich, Amanda, Bedi, Mel F.

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Structural optimization and biological evaluation of quinoline/naphthalene-based glyoxalase-I inhibitors as anti-cancer candidates by Al-Oudat, Buthina A., Abu Al fool, Bushra S., Audat, Suaad A., Al-Shar’i, Nizar A., Al-Balas, Qosay A., Zayed, Aref, Bryant-Friedrich, Amanda

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Lead optimization and biological evaluation of diazenylbenzenesulfonamides inhibitors against glyoxalase-I enzyme as potential anticancer agents by Al-Oudat, Buthina A., Al-Shar'i, Nizar A., Al‑Balas, Qosay A., Audat, Suaad A., Alqudah, Mohammad A.Y., Hamzah, Ali H., Hallak, Ramez W., Bedi, Mel, Bryant-Friedrich, Amanda

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Generation of the first structure-based pharmacophore model containing a selective "zinc binding group" feature to identify potential glyoxalase-1 inhibitors by Al-Balas, Qosay, Hassan, Mohammad, Al-Oudat, Buthina, Alzoubi, Hassan, Mhaidat, Nizar, Almaaytah, Ammar

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Design, synthesis, and biological evaluation of SMYD3 inhibitors possessing N-thiazole benzenesulfonamide moiety as potential anti-cancer agents by Audat, Suaad Abdallah, Al-Shar'i, Nizar A., Al-Oudat, Buthina Abdallah, Alnabulsi, Soraya

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Design, synthesis, and biologic evaluation of novel chrysin derivatives as cytotoxic agents and caspase-3/7 activators by Al-Oudat, Buthina Abdallah, Alqudah, Mohammad Ali, Audat, Suaad Abdallah, Al-Balas, Qosay Ali, El-Elimat, Tamam, Hassan, Mohammad Abdelhafeez, Frhat, Islam Nawaf, Azaizeh, Marwah Mohammad

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Design, Synthesis and Biological Evaluation of 1,4-Benzenesulfonamide Derivatives as Glyoxalase I Inhibitors by Audat, Suaad Abdallah, Al-Balas, Qosay Ali, Al-Oudat, Buthina Abdallah, Athamneh, Mo'ad Jamil, Bryant-Friedrich, Amanda

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3′-Modified oligodeoxyribonucleotides for the study of 2-deoxyribose damage in DNA by Al-Oudat, Buthina, Salyer, Alex, Trabbic, Kevin, Bryant-Friedrich, Amanda

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Generation of the First Structure-Based Pharmacophore Model Containing a Selective #8220;Zinc Binding Group #8221; Feature to Identify Potential Glyoxalase-1 Inhibitors by Qosay Al-Balas, Mohammad Hassan, Buthina Al-Oudat, Hassan Alzoubi, Nizar Mhaidat, Ammar Almaaytah

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