Search Results - "Nasser S.M. Ismail"
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Molecular modeling based approach, synthesis and in vitro assay to new indole inhibitors of hepatitis C NS3/4A serine protease
Published in Bioorganic & medicinal chemistry (01-01-2011)“…In an attempt to identify potential HCV NS3 protease inhibitors lead compounds, a series of novel indoles (10a–g) was designed. Molecular modeling study,…”
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Design, synthesis and biological study of novel pyrido[2,3-d]pyrimidine as anti-proliferative CDK2 inhibitors
Published in European journal of medicinal chemistry (01-12-2011)“…The design and synthesis of a small library of 4-aminopyrido[2,3-d]pyrimidine derivatives is reported. The potential activity of these compounds as CDK2/Cyclin…”
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Design and Synthesis of New CDK2 Inhibitors Containing Thiazolone and Thiazolthione Scafold with Apoptotic Activity
Published in Chemical & pharmaceutical bulletin (01-01-2021)“…Cyclin dependent kinase 2 (CDK2) inhibition is a well-established strategy for treating cancer. Different series of novel thiazolone (1, 7–9) together with…”
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Therapeutic Potential of Vanillin and its Main Metabolites to Regulate the Inflammatory Response and Oxidative Stress
Published in Mini reviews in medicinal chemistry (01-01-2019)“…Many phenolic compounds found in foods and medicinal plants have shown interesting therapeutic potential and have attracted the attention of the pharmaceutical…”
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Synthesis and biological activity of new 18β-glycyrrhetinic acid derivatives
Published in Arabian journal of chemistry (01-05-2016)“…In an attempt to find out new, potent and safe anti-inflammatory molecules and as a contribution in the chemistry of triterpenes, a series of…”
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Regioselective synthesis and molecular modeling study of vasorelaxant active 7,9-dioxa-1,2-diaza-spiro[4.5]dec-2-ene-6,10-diones
Published in European journal of medicinal chemistry (01-09-2010)“…Nitrilimines (PhC −:N +:NR′) generated in situ from hydrazonoyl chlorides 2a,b reacted regioselectively with 5-arylidene-2,2-dimethyl[1,3]dioxane-4,6-diones…”
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Analogs design, synthesis and biological evaluation of peptidomimetics with potential anti-HCV activity
Published in Bioorganic & medicinal chemistry (15-05-2013)“…Peptidomimetics bearing a C-terminal carboxylate or vinyl sulfonate functionality as HCV NS3 protease inhibitors. Two series of peptidomimetics were designed,…”
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Recent advances in 4-aminoquinazoline based scaffold derivatives targeting EGFR kinases as anticancer agents
Published in Future Journal of Pharmaceutical Sciences (01-06-2016)“…Quinazoline derivatives are fused heterocyclic ring systems which have been explored for their inhibitory activity towards various protein kinase enzymes and…”
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A molecular docking study repurposes FDA approved iron oxide nanoparticles to treat and control COVID-19 infection
Published in European journal of pharmaceutical sciences (01-10-2020)“…COVID-19, is a disease resulting from the SARS-CoV-2 global pandemic. Due to the current global emergency and the length of time required to develop specific…”
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Medicinal attributes of pyrazolo[1,5-a]pyrimidine based scaffold derivatives targeting kinases as anticancer agents
Published in Future Journal of Pharmaceutical Sciences (01-12-2016)“…Pyrazolo pyrimidines are fused heterocyclic ring systems which known as bioisosteres of adenine, that are necessary for every aspect of cell life…”
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Pyrazolo[3,4-d]pyrimidine based scaffold derivatives targeting kinases as anticancer agents
Published in Future Journal of Pharmaceutical Sciences (01-06-2016)“…Pyrazolopyrimidines are fused heterocyclic ring systems which structurally can consider as bioisosteres of adenine, which is fundamental for every aspect of…”
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Alkaloids: Therapeutic Potential against Human Coronaviruses
Published in Molecules (Basel, Switzerland) (24-11-2020)“…Alkaloids are a class of natural products known to have wide pharmacological activity and have great potential for the development of new drugs to treat a wide…”
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Discovery of pyrazolo[3,4-]pyrimidine and pyrazolo[4,3-][1,2,4]triazolo[1,5-]pyrimidine derivatives as novel CDK2 inhibitors: synthesis, biological and molecular modeling investigations
Published in RSC advances (17-05-2022)“…CDK2 inhibition is an appealing target for cancer treatment that targets tumor cells in a selective manner. A new set of small molecules featuring the…”
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Synthesis and QSAR study of novel cytotoxic spiro[3 H-indole-3,2′(1′ H)-pyrrolo[3,4- c]pyrrole]-2,3′,5′(1 H,2′ aH,4′ H)-triones
Published in European journal of medicinal chemistry (2012)“…1,3-Dipolar cycloaddition reaction of 1-aryl-1 H-pyrrole-2,5-diones 1a-e with non-stabilized azomethine ylides, generated in situ via decarboxylative…”
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Design, synthesis and QSAR studies of dispiroindole derivatives as new antiproliferative agents
Published in European journal of medicinal chemistry (01-10-2013)“…A variety of 4′-aryl-3-(arylmethylidene)-1″-[(cyclic-amino)methylene]-1′-methyl-dispiro[cyclohexane-1,3′-pyrrolidine-2′,3″-[3H]indole]-2,2″(1″H)-diones 4a–u…”
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Development of pyrolo[2,3-c]pyrazole, pyrolo[2,3-d]pyrimidine and their bioisosteres as novel CDK2 inhibitors with potent in vitro apoptotic anti-proliferative activity: Synthesis, biological evaluation and molecular dynamics investigations
Published in Bioorganic chemistry (01-10-2023)“…[Display omitted] •A novel series of pyrolo[2,3-c]pyrazole, pyrolo[2,3-c]isoaxazole and pyrolo[2,3-d]pyrimidine, pyrolo[3,2-c]pyridine & indole scaffolds were…”
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Design, synthesis and biological evaluation of certain CDK2 inhibitors based on pyrazole and pyrazolo[1,5-a] pyrimidine scaffold with apoptotic activity
Published in Bioorganic chemistry (01-05-2019)“…[Display omitted] •19 Compounds were screened against CDK2/cyclin A2 enzyme.•Target compounds were assessed in vitro against MCF-7, HepG2, A549 and Caco-2…”
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Design, synthesis and molecular modeling study of certain VEGFR-2 inhibitors based on thienopyrimidne scaffold as cancer targeting agents
Published in Bioorganic chemistry (01-03-2019)“…[Display omitted] •25 compounds were screened against VEGFR-2 kinase enzyme.•Selected compounds were assessed in vitro against full NCI 60 cell lines.•10a…”
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Novel series of 6-(2-substitutedacetamido)-4-anilinoquinazolines as EGFR-ERK signal transduction inhibitors in MCF-7 breast cancer cells
Published in European journal of medicinal chemistry (15-07-2018)“…Epidermal growth factor receptor (EGFR) signaling pathway has been previously investigated for its significant role in the progression of different types of…”
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Design and Synthesis of New Quinoxaline Derivatives as Anticancer Agents and Apoptotic Inducers
Published in Molecules (Basel, Switzerland) (25-03-2019)“…The quinoxaline scaffold is a promising platform for the discovery of active chemotherapeutic agents. Three series of quinoxaline derivatives were synthesized…”
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