Amgad Albohy

发表

Natural coumarins as potential anti-SARS-CoV-2 agents supported by docking analysis

G. Bringmann, U. Abdelmohsen, S. Bayoumi, 2021, RSC advances.

In vivo antiulcer activity, phytochemical exploration, and molecular modelling of the polyphenolic-rich fraction of Crepis sancta extract

P. Proksch, A. Disi, F. Youssef, 2019, Inflammopharmacology.

Anti‐Inflammatory, Antiallergic and COVID‐19 Main Protease (Mpro) Inhibitory Activities of Butenolides from a Marine‐Derived Fungus Aspergillus costaricaensis

Wenhan Lin, B. Konuklugil, Sherif S. Ebada, 2022, ChemistrySelect.

Anti-Inflammatory, Antiallergic, and COVID-19 Main Protease (Mpro) Inhibitory Activities of Butenolides from a Marine-Derived Fungus Aspergillus terreus

J. Horng, Wenhan Lin, T. Hwang, 2021, Molecules.

Substrate recognition of the membrane-associated sialidase NEU3 requires a hydrophobic aglycone.

D. Bundle, J. Klassen, C. Cairo, 2011, Biochemistry.

Inhibitor selectivity of a new class of oseltamivir analogs against viral neuraminidase over human neuraminidase enzymes.

B. M. Pinto, S. Mohan, C. Cairo, 2011, Bioorganic & medicinal chemistry.

SYNTHESIS AND DOCKING STUDIES OF NOVEL TETRAHYDROQUINAZOLINE DERIVATIVE AS PROMISING SCAFFOLD FOR ACETYLCHOLINE ESTERASE INHIBITION

Qais Abualassal, Sherif S. Ebada, Amgad Albohy, 2020 .

Bioactivity Potential of Marine Natural Products from Scleractinia-Associated Microbes and In Silico Anti-SARS-COV-2 Evaluation

G. Bringmann, U. Abdelmohsen, H. Ahmed, 2020, Marine drugs.

Biodiversity of N-acyl homoserine lactonase (aiiA) gene from Bacillus subtilis.

A. F. Basyony, Amgad Albohy, D. Almasri, 2022, Microbial pathogenesis.

Lonazolac analogues: molecular modeling, synthesis, and in vivo anti-inflammatory activity

K. Abouzid, J. Lehmann, D. A. Abou El Ella, 2009, Medicinal Chemistry Research.

2-Arylquinolines as novel anticancer agents with dual EGFR/FAK kinase inhibitory activity: synthesis, biological evaluation, and molecular modelling insights

Y. Pommier, K. Agama, Wagdy M. Eldehna, 2021, Journal of enzyme inhibition and medicinal chemistry.

Cytotoxic Potential of Green Synthesized Silver Nanoparticles of Lampranthus coccineus Extracts, Metabolic Profiling and Molecular Docking Study

M. Salem, E. Haggag, U. Abdelmohsen, 2020 .

Anti-inflammatory, antiallergic and COVID-19 protease inhibitory activities of phytochemicals from the Jordanian hawksbeard: identification, structure–activity relationships, molecular modeling and impact on its folk medicinal uses

P. Proksch, C. Janiak, Dina H El-Kashef, 2020, RSC advances.

Identifying the specific-targeted marine cerebrosides against SARS-CoV-2: an integrated computational approach

G. Bringmann, U. Abdelmohsen, A. Sayed, 2021, RSC advances.

Insight into substrate recognition and catalysis by the human neuraminidase 3 (NEU3) through molecular modeling and site-directed mutagenesis.

C. Cairo, R. Zheng, Amgad Albohy, 2010, Glycobiology.

Mapping substrate interactions of the human membrane-associated neuraminidase, NEU3, using STD NMR.

M. R. Richards, C. Cairo, Amgad Albohy, 2015, Glycobiology.

Identification of selective inhibitors for human neuraminidase isoenzymes using C4,C7-modified 2-deoxy-2,3-didehydro-N-acetylneuraminic acid (DANA) analogues.

A. Pshezhetsky, C. Cairo, Amgad Albohy, 2013, Journal of medicinal chemistry.

Dynamic Regulation of CD45 Lateral Mobility by the Spectrin-Ankyrin Cytoskeleton of T Cells*

Raibatak Das, Christopher W. Cairo, Daniel Coombs, 2010, The Journal of Biological Chemistry.

Structural Basis for Substrate Specificity of Mammalian Neuraminidases

A. Pshezhetsky, E. Korchagina, N. Bovin, 2014, PloS one.

Transforming iodoquinol into broad spectrum anti-tumor leads: Repurposing to modulate redox homeostasis.

F. Zouein, A. El-Yazbi, A. Hazzaa, 2021, Bioorganic chemistry.

Inhibition of human neuraminidase 3 (NEU3) by C9-triazole derivatives of 2,3-didehydro-N-acetyl-neuraminic acid.

C. Cairo, Mahendra Sandbhor, Amgad Albohy, 2010, Bioorganic & medicinal chemistry letters.

Isolation and Molecular Docking of Cytotoxic Secondary Metabolites from Two Red Sea Sponges of the Genus Diacarnus

P. Proksch, W. Ebrahim, Mona El-Neketi, 2021 .

Identification of Selective Nanomolar Inhibitors of the Human Neuraminidase, NEU4.

A. Pshezhetsky, C. Cairo, Amgad Albohy, 2013, ACS medicinal chemistry letters.

New Acaciin-Loaded Self-Assembled Nanofibers as MPro Inhibitors Against BCV as a Surrogate Model for SARS-CoV-2

E. Zahran, Soad A Mohamad, Amgad Albohy, 2021, International journal of nanomedicine.

Multitarget in silico studies of Ocimum menthiifolium, family Lamiaceae against SARS-CoV-2 supported by molecular dynamics simulation

M. M. Al-Sanea, M. Salem, T. Al-Warhi, 2020, Journal of biomolecular structure & dynamics.

Discovery of potent thieno[2,3-d]pyrimidine VEGFR-2 inhibitors: Design, synthesis and enzyme inhibitory evaluation supported by molecular dynamics simulations.

K. Abouzid, D. A. Abou El Ella, R. Serya, 2021, Bioorganic chemistry.

Importance of glutamine 189 flexibility in SARS-CoV-2 main protease: Lesson learned from in silico virtual screening of ChEMBL database and molecular dynamics

Mohamed A. Abdelrahman, Hany S. Ibrahim, Mohamed A. Said, 2021, European Journal of Pharmaceutical Sciences.

Synthesis, in vitro biological investigation, and molecular dynamics simulations of thiazolopyrimidine based compounds as corticotrophin releasing factor receptor-1 antagonists.

G. Liapakis, K. Abouzid, O. Chepurny, 2021, Bioorganic chemistry.

Metabolomic profiling of three Araucaria species, and their possible potential role against COVID-19

I. P. Bosko, M. M. Al-Sanea, A. Andrianov, 2021, Journal of biomolecular structure & dynamics.

Molecular Modeling Studies on Biochanin-A as a Potential Dual inhibitor for VEGFR-2 and Cyclin D1-CDK-4 Complex

S. Zada, M. Ramadan, M. Tolba, 2021 .

Sansevieria: An Evaluation Of Potential Cytotoxic Activity In Reference To Metabolomic And Molecular Docking Studies

M. Abdelatty, S. El-hawary, Amgad Albohy, 2021 .

Substrate recognition of the membrane-associated sialidase NEU3 requires a hydrophobic aglycone.

D. Bundle, C. Cairo, John S. Klassen, 2011, Biochemistry.