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Sahar M. Abou‐Seri

Observed names: Abou-Seri, Sahar M, Abou-Seri, Sahar M., Sahar Abou-Serid, Sahar M Abou-Seri, Sahar M Abou-seri, Sahar M. Abou-Seri, Sahar M. Abou-seri, Sahar M. Abouseri, Sahar Mahmoud Abou-Seri, Sahar Mahmoud Abou‐Seri
Institution: Cairo University
OpenAlex ID: A5073430332
Celecoxib analogs bearing benzofuran moiety as cyclooxygenase-2 inhibitors: Design, synthesis and evaluation as potential anti-inflammatory agents
2014 · Ghaneya Sayed Hassan, Sahar Mahmoud Abou-Seri, et al. · European Journal of Medicinal Chemistry · 159
1-Piperazinylphthalazines as potential VEGFR-2 inhibitors and anticancer agents: Synthesis and in vitro biological evaluation
2015 · Sahar M. Abou-Seri, Wagdy M. Eldehna, et al. · European Journal of Medicinal Chemistry · 145
Synthesis and biological evaluation of novel coumarin–pyrazoline hybrids endowed with phenylsulfonyl moiety as antitumor agents
2012 · Kamilia M. Amin, Amal A.M. Eissa, et al. · European Journal of Medicinal Chemistry · 136
Isatin-pyrazole benzenesulfonamide hybrids potently inhibit tumor-associated carbonic anhydrase isoforms IX and XII
2015 · Hany S. Ibrahim, Sahar M. Abou-Seri, et al. · European Journal of Medicinal Chemistry · 120
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Synthesis and antitumor activity of pyrido [2,3-d]pyrimidine and pyrido[2,3-d] [1,2,4]triazolo[4,3-a]pyrimidine derivatives that induce apoptosis through G1 cell-cycle arrest
2014 · Mohamed Fares, Sahar Mahmoud Abou-Seri, et al. · European Journal of Medicinal Chemistry · 119
Novel indole-thiazolidinone conjugates: Design, synthesis and whole-cell phenotypic evaluation as a novel class of antimicrobial agents
2018 · Mahmoud F. Abo-Ashour, Wagdy M. Eldehna, et al. · European Journal of Medicinal Chemistry · 116
3-Hydrazinoisatin-based benzenesulfonamides as novel carbonic anhydrase inhibitors endowed with anticancer activity: Synthesis, in vitro biological evaluation and in silico insights
2019 · Mahmoud F. Abo-Ashour, Wagdy M. Eldehna, et al. · European Journal of Medicinal Chemistry · 111
Synthesis of 3-substituted-2-oxoindole analogues and their evaluation as kinase inhibitors, anticancer and antiangiogenic agents
2006 · Ashraf H. Abadi, Sahar M. Abou-Seri, et al. · European Journal of Medicinal Chemistry · 109
Increasing the binding affinity of VEGFR-2 inhibitors by extending their hydrophobic interaction with the active site: Design, synthesis and biological evaluation of 1-substituted-4-(4-methoxybenzyl)phthalazine derivatives
2016 · Wagdy M. Eldehna, Sahar M. Abou-Seri, et al. · European Journal of Medicinal Chemistry · 104
Amido/ureidosubstituted benzenesulfonamides-isatin conjugates as low nanomolar/subnanomolar inhibitors of the tumor-associated carbonic anhydrase isoform XII
2016 · Wagdy M. Eldehna, Mohamed Fares, et al. · European Journal of Medicinal Chemistry · 90
Synthesis and in vitro cytotoxic activity of novel pyrazolo[3,4-d]pyrimidines and related pyrazole hydrazones toward breast adenocarcinoma MCF-7 cell line
2011 · Ghaneya Sayed Hassan, Hanan Hassan Kadry, et al. · Bioorganic & Medicinal Chemistry · 83
Synthesis and biological evaluation of novel 2,4′-bis substituted diphenylamines as anticancer agents and potential epidermal growth factor receptor tyrosine kinase inhibitors
2010 · Sahar Mahmoud Abou-Seri · European Journal of Medicinal Chemistry · 79
Novel hydrazido benzenesulfonamides-isatin conjugates: Synthesis, carbonic anhydrase inhibitory activity and molecular modeling studies
2018 · Mahmoud F. Abo-Ashour, Wagdy M. Eldehna, et al. · European Journal of Medicinal Chemistry · 73
Novel synthesized SLC-0111 thiazole and thiadiazole analogues: Determination of their carbonic anhydrase inhibitory activity and molecular modeling studies
2019 · Mahmoud F. Abo-Ashour, Wagdy M. Eldehna, et al. · Bioorganic Chemistry · 70
Novel 3-substituted coumarins as selective human carbonic anhydrase IX and XII inhibitors: Synthesis, biological and molecular dynamics analysis
2020 · Mohamed A. Abdelrahman, Hany S. Ibrahim, et al. · European Journal of Medicinal Chemistry · 69
Sulfonamide-based ring-fused analogues for CAN508 as novel carbonic anhydrase inhibitors endowed with antitumor activity: Design, synthesis, and in vitro biological evaluation
2020 · Mohamed A. Said, Wagdy M. Eldehna, et al. · European Journal of Medicinal Chemistry · 69
Design, synthesis and anticancer activity of new monastrol analogues bearing 1,3,4-oxadiazole moiety
2017 · Fatma A.F. Ragab, Sahar M. Abou-Seri, et al. · European Journal of Medicinal Chemistry · 68
Synthesis, biological and molecular dynamics investigations with a series of triazolopyrimidine/triazole-based benzenesulfonamides as novel carbonic anhydrase inhibitors
2019 · Mohamed A. Said, Wagdy M. Eldehna, et al. · European Journal of Medicinal Chemistry · 67
Design, synthesis, in vitro and in vivo evaluation of novel pyrrolizine-based compounds with potential activity as cholinesterase inhibitors and anti-Alzheimer's agents
2019 · Nehad Abou-Elmagd El-Sayed, Awatef El-Said Farag, et al. · Bioorganic Chemistry · 67
Bis-isatin hydrazones with novel linkers: Synthesis and biological evaluation as cytotoxic agents
2015 · Hany S. Ibrahim, Sahar M. Abou-seri, et al. · European Journal of Medicinal Chemistry · 67
Newly synthesized series of oxoindole–oxadiazole conjugates as potential anti-SARS-CoV-2 agents: in silico and in vitro studies
2022 · Rana M. El-Masry, Ahmed A. Al-Karmalawy, et al. · New Journal of Chemistry · 66
Design, synthesis and vasorelaxant evaluation of novel coumarin–pyrimidine hybrids
2011 · Kamilia M. Amin, Fadi M. Awadalla, et al. · Bioorganic & Medicinal Chemistry · 65
Comparative Study of the Synthetic Approaches and Biological Activities of the Bioisosteres of 1,3,4-Oxadiazoles and 1,3,4-Thiadiazoles over the Past Decade
2022 · Rana M. El-Masry, Hanan H. Kadry, et al. · Molecules · 63
Indoline ureas as potential anti-hepatocellular carcinoma agents targeting VEGFR-2: Synthesis, in vitro biological evaluation and molecular docking
2015 · Wagdy M. Eldehna, Mohamed Fares, et al. · European Journal of Medicinal Chemistry · 63
Design and synthesis of pyrimidine-5-carbonitrile hybrids as COX-2 inhibitors: Anti-inflammatory activity, ulcerogenic liability, histopathological and docking studies
2020 · Abdallah M. Alfayomy, Salah A. Abdel-Aziz, et al. · Bioorganic Chemistry · 62
Works count: 93
Citation count: 3,401
H-index: 34
I10-index: 64
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