Works by Ali, Taha F. S.
Results: 21
Cyclodextrin Enhances Corneal Tolerability and Reduces Ocular Toxicity Caused by Diclofenac.
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- Oxidative Medicine & Cellular Longevity, 2018, p. 1, doi. 10.1155/2018/5260976
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- Article
Antiproliferative potential of moluccella laevis L. aerial parts family lamiaceae (labiatae), supported by phytochemical investigation and molecular docking study.
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- Natural Product Research, 2022, v. 36, n. 5, p. 1391, doi. 10.1080/14786419.2021.1876046
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- Article
Antidepressant potential of Mesembryanthemum cordifolium roots assisted by metabolomic analysis and virtual screening.
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- Natural Product Research, 2021, v. 35, n. 23, p. 5493, doi. 10.1080/14786419.2020.1788019
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- Article
Indole-based FLT3 inhibitors and related scaffolds as potential therapeutic agents for acute myeloid leukemia.
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- BMC Chemistry, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s13065-023-00981-8
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- Article
Design and synthesis of new dihydropyrimidine/sulphonamide hybrids as promising anti-inflammatory agents via dual mPGES-1/5-LOX inhibition.
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- Frontiers in Chemistry, 2024, p. 1, doi. 10.3389/fchem.2024.1387923
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- Article
Applying Different Techniques to Improve the Bioavailability of Candesartan Cilexetil Antihypertensive Drug.
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- Drug Design, Development & Therapy, 2020, v. 14, p. 1851, doi. 10.2147/dddt.s248511
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- Article
A Dithiol Compound Binds to the Zinc Finger Protein TRAF6 and Suppresses Its Ubiquitination.
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- ChemMedChem, 2017, v. 12, n. 23, p. 1935, doi. 10.1002/cmdc.201700399
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- Article
Front Cover: A Dithiol Compound Binds to the Zinc Finger Protein TRAF6 and Suppresses Its Ubiquitination (ChemMedChem 23/2017).
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- ChemMedChem, 2017, v. 12, n. 23, p. 1906, doi. 10.1002/cmdc.201700735
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- Article
Novel Inhibitor for Downstream Targeting of Transforming Growth Factor-β Signaling to Suppress Epithelial to Mesenchymal Transition and Cell Migration.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 9, p. 5047, doi. 10.3390/ijms23095047
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- Article
New antiproliferative 3-substituted oxindoles inhibiting EGFR/VEGFR-2 and tubulin polymerization.
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- Molecular Diversity, 2024, v. 28, n. 2, p. 563, doi. 10.1007/s11030-023-10603-z
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- Article
Combination of an Oxindole Derivative with (−)-β-Elemene Alters Cell Death Pathways in FLT3/ITD + Acute Myeloid Leukemia Cells.
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- Molecules, 2023, v. 28, n. 13, p. 5253, doi. 10.3390/molecules28135253
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- Article
In Vitro and In Silico Evaluation of Anticancer Activity of New Indole-Based 1,3,4-Oxadiazoles as EGFR and COX-2 Inhibitors.
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- Molecules, 2020, v. 25, n. 21, p. 5190, doi. 10.3390/molecules25215190
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- Article
Antiproliferative S-Trityl-l-Cysteine -Derived Compounds as SIRT2 Inhibitors: Repurposing and Solubility Enhancement.
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- Molecules, 2019, v. 24, n. 18, p. 3295, doi. 10.3390/molecules24183295
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- Article
Design, Synthesis, and Biological Evaluation of Novel 1,3,4-Thiadiazole Derivatives as Potential Antitumor Agents against Chronic Myelogenous Leukemia: Striking Effect of Nitrothiazole Moiety.
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- Molecules, 2018, v. 23, n. 1, p. 59, doi. 10.3390/molecules23010059
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- Article
Discovery and Anticancer Screening of Novel Oxindole-Based Derivative Bearing Pyridyl Group as Potent and Selective Dual FLT3/CDK2 Kinase Inhibitor.
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- Pharmaceuticals (14248247), 2024, v. 17, n. 5, p. 659, doi. 10.3390/ph17050659
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- Article
Discovery of Azaindolin-2-One as a Dual Inhibitor of GSK3β and Tau Aggregation with Potential Neuroprotective Activity.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 4, p. N.PAG, doi. 10.3390/ph15040426
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- Article
New Multi-Targeted Antiproliferative Agents: Design and Synthesis of IC261-Based Oxindoles as Potential Tubulin, CK1 and EGFR Inhibitors.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 11, p. 1114, doi. 10.3390/ph14111114
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- Article
Discovery of oxindole‐based FLT3 inhibitors as a promising therapeutic lead for acute myeloid leukemia carrying the oncogenic ITD mutation.
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- Archiv der Pharmazie, 2023, v. 356, n. 2, p. 1, doi. 10.1002/ardp.202200407
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- Article
An antifibrotic compound that ameliorates hyperglycaemia and fat accumulation in cell and HFD mouse models.
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- Diabetologia, 2024, v. 67, n. 11, p. 2568, doi. 10.1007/s00125-024-06260-y
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- Article
In silico drug discovery of SIRT2 inhibitors from natural source as anticancer agents.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-28226-7
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- Article
In silico drug discovery of SIRT2 inhibitors from natural source as anticancer agents.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-28226-7
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- Article