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Investigation of α‐glucosidase and α‐amylase inhibitory effects of phenoxy chalcones and molecular modeling studies.
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- Journal of Molecular Recognition, 2023, v. 36, n. 11, p. 1, doi. 10.1002/jmr.3061
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Chalcones bearing nitrogen‐containing heterocyclics as multi‐targeted inhibitors: Design, synthesis, biological evaluation and molecular docking studies.
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- Journal of Molecular Recognition, 2023, v. 36, n. 7, p. 1, doi. 10.1002/jmr.3020
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Design, in Silico Studies and Biological Evaluation of New Chiral Thiourea and 1,3‐Thiazolidine‐4,5‐dione Derivatives.
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- Chemistry & Biodiversity, 2023, v. 20, n. 8, p. 1, doi. 10.1002/cbdv.202300626
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Synthesis and structure-activity relationship study: Anticancer chalcones derived from 4'-morpholinoacetophenone.
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- Marmara Pharmaceutical Journal, 2017, v. 21, n. 4, p. 949, doi. 10.12991/mpj.2017.18
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Synthesis of benzoyl hydrazones having 4-hydroxy-3,5-dimethoxy phenyl ring, their biological activities, and molecular modeling studies on enzyme inhibition activities.
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- Turkish Journal of Chemistry, 2022, v. 46, n. 1, p. 236, doi. 10.3906/kim-2107-7
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Synthesis and biological evaluation of novel chalcones bearing morpholine moiety as antiproliferative agents.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 2, p. 482, doi. 10.3906/kim-1705-28
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Studies on Hydrazide–Hydrazones Derivatives As Acetylcholinesterase Inhibitors.
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- Journal of Marmara University Institute of Health Sciences, 2015, v. 5, n. 1, p. 10, doi. 10.5455/musbed.20141117035707
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Novel fluorine‐containing chiral hydrazide‐hydrazones: Design, synthesis, structural elucidation, antioxidant and anticholinesterase activity, and in silico studies.
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- Chirality, 2019, v. 31, n. 8, p. 603, doi. 10.1002/chir.23102
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Synthesis of novel chiral metal complexes derived from chiral thiosemicarbazide ligands as potential antioxidant agents.
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- Chirality, 2019, v. 31, n. 6, p. 434, doi. 10.1002/chir.23069
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Synthesis of Novel Chiral Sulfonamide-Bearing 1,2,4-Triazole-3-thione Analogs Derived from D- and L-Phenylalanine Esters as Potential Anti-Influenza Agents.
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- Chirality, 2016, v. 28, n. 6, p. 495, doi. 10.1002/chir.22607
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Synthesis,.
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- Chirality, 2015, v. 27, n. 2, p. 177, doi. 10.1002/chir.22408
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In silico modeling of α-glucosidase, aldose reductase, and PPAR-γ with benzoyl/sulfonyl hydrazone derivatives using molecular docking, ADMET, and molecular dynamics simulations.
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- Journal of Research in Pharmacy, 2023, v. 27, n. 4, p. 1567, doi. 10.29228/jrp.442
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Synthesis, characterization, antituberculosis activity and computational studies on novel Schiff bases of 1,3,4-thiadiazole derivatives.
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- Journal of Research in Pharmacy, 2020, v. 24, n. 6, p. 793, doi. 10.35333/jrp.2020.232
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Design and Synthesis of Novel Thioureas Derived from 4-(4-Fluorophenoxy)aniline as Anticancer Agents.
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- Journal of the Chinese Chemical Society, 2017, v. 64, n. 3, p. 321, doi. 10.1002/jccs.201600193
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Synthesis, Antioxidant and Some Enzyme Inhibition Activities of New Sulfonyl Hydrazones and their Molecular Docking Simulations.
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- Pharmaceutical Chemistry Journal, 2022, v. 56, n. 4, p. 559, doi. 10.1007/s11094-022-02674-3
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