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Design and synthesis of new N-thioacylated ciprofloxacin derivatives as urease inhibitors with potential antibacterial activity.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-17993-4
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- Article
Design and synthesis of novel nitrothiazolacetamide conjugated to different thioquinazolinone derivatives as anti-urease agents.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05736-4
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- Article
Study Of General Health Among Tehran University Of Medical Sciences Hospital’s Administrators.
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- Payavard Salamat, 2014, v. 8, n. 1, p. 13
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- Article
Rational Design, Synthesis, in Vitro, and in Silico Studies of Chlorophenylquinazolin‐4(3H)‐One Containing Different Aryl Acetohydrazides as Tyrosinase Inhibitors.
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- Chemistry & Biodiversity, 2022, v. 19, n. 7, p. 1, doi. 10.1002/cbdv.202100964
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- Article
New thioxothiazolidinyl-acetamides derivatives as potent urease inhibitors: design, synthesis, in vitro inhibition, and molecular dynamic simulation.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-022-27234-3
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- Article
Discovery of direct inhibitor of KRAS oncogenic protein by natural products: a combination of pharmacophore search, molecular docking, and molecular dynamic studies.
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- Research in Pharmaceutical Sciences, 2020, v. 15, n. 3, p. 226, doi. 10.4103/1735-5362.288425
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- Article
Synthesis, molecular docking, and antiepileptic activity of novel phthalimide derivatives bearing amino acid conjugated anilines.
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- Research in Pharmaceutical Sciences, 2019, v. 14, n. 6, p. 534, doi. 10.4103/1735-5362.272562
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Synthesis, Biological Evaluation and Molecular Docking of Deferasirox and Substituted 1,2,4‐Triazole Derivatives as Novel Potent Urease Inhibitors: Proposing Repositioning Candidate.
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- Chemistry & Biodiversity, 2020, v. 17, n. 5, p. 1, doi. 10.1002/cbdv.201900710
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- Article
Design, Synthesis, Molecular Docking, and Cholinesterase Inhibitory Potential of Phthalimide‐Dithiocarbamate Hybrids as New Agents for Treatment of Alzheimer's Disease.
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- Chemistry & Biodiversity, 2019, v. 16, n. 11, p. N.PAG, doi. 10.1002/cbdv.201900370
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- Article
Design, synthesis, biological evaluation, and docking study of new acridine‐9‐carboxamide linked to 1,2,3‐triazole derivatives as antidiabetic agents targeting α‐glucosidase.
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- Journal of Heterocyclic Chemistry, 2020, v. 57, n. 12, p. 4348, doi. 10.1002/jhet.4142
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- Article
Design, synthesis and antibacterial activity evaluation of novel 2‐(4‐((1‐aryl‐1H‐1,2,3‐triazol‐4‐yl)methoxy)phenyl)2‐(2‐oxoazetidin‐1‐yl)acetamide derivatives.
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- Journal of Heterocyclic Chemistry, 2020, v. 57, n. 12, p. 4254, doi. 10.1002/jhet.4131
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- Article
Efficient one‐pot synthesis of novel 6′,9′‐dihydro‐2H,7′H‐spiro[pyrimidine‐5,8′‐[1,3]dioxolo[4,5‐f]quinoline]‐2,4,6(1H,3H)‐trione derivatives under mild and "green" reaction conditions
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- Journal of Heterocyclic Chemistry, 2020, v. 57, n. 8, p. 3161, doi. 10.1002/jhet.4023
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Screening of 20 Commonly Used Iranian Traditional Medicinal Plants Against Urease.
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- Iranian Journal of Pharmaceutical Research, 2014, v. 13, p. 195
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- Article
Design and synthesis of 2,4‐dioxochroman‐pyridinium‐phenylacetamide derivatives as new anti‐Alzheimer agents: in vitro and in silico studies.
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- Journal of the Chinese Chemical Society, 2020, v. 67, n. 10, p. 1910, doi. 10.1002/jccs.202000013
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- Article
Benzoylquinazolinone derivatives as new potential antidiabetic agents: α‐Glucosidase inhibition, kinetic, and docking studies.
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- Journal of the Chinese Chemical Society, 2020, v. 67, n. 5, p. 856, doi. 10.1002/jccs.201900268
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- Article
New 4‐phenylpiperazine‐carbodithioate‐N‐phenylacetamide hybrids: Synthesis, in vitro and in silico evaluations against cholinesterase and α‐glucosidase enzymes.
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- Archiv der Pharmazie, 2022, v. 355, n. 5, p. 1, doi. 10.1002/ardp.202100313
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- Article
Design, synthesis, and α‐glucosidase‐inhibitory activity of phenoxy‐biscoumarin–N‐phenylacetamide hybrids.
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- Archiv der Pharmazie, 2021, v. 354, n. 12, p. 1, doi. 10.1002/ardp.202100179
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Synthesis, characterization, molecular docking, and biological activities of coumarin–1,2,3‐triazole‐acetamide hybrid derivatives.
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- Archiv der Pharmazie, 2020, v. 353, n. 10, p. 1, doi. 10.1002/ardp.202000109
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- Article
New 1,2,3‐triazole–(thio)barbituric acid hybrids as urease inhibitors: Design, synthesis, in vitro urease inhibition, docking study, and molecular dynamic simulation.
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- Archiv der Pharmazie, 2020, v. 353, n. 9, p. 1, doi. 10.1002/ardp.202000023
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How to establish infrastructures to achieve more efficient regenerative medicine?
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- Cell & Tissue Banking, 2023, v. 24, n. 1, p. 1, doi. 10.1007/s10561-022-10028-2
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Cell-based approaches towards treating age-related macular degeneration.
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- Cell & Tissue Banking, 2020, v. 21, n. 3, p. 339, doi. 10.1007/s10561-020-09826-3
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Synthesis and biological evaluation of a new series of benzofuran‐1,3,4‐oxadiazole containing 1,2,3‐triazole‐acetamides as potential α‐glucosidase inhibitors.
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- Journal of Biochemical & Molecular Toxicology, 2021, v. 35, n. 4, p. 1, doi. 10.1002/jbt.22688
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Recent Advances in Alkyne Hydroamination as a Powerful Tool for the Construction of C−N Bonds.
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- Asian Journal of Organic Chemistry, 2020, v. 9, n. 7, p. 969, doi. 10.1002/ajoc.202000092
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Synthesis, α‐glucosidase Inhibition, in silico Pharmacokinetic, and Docking Studies Of Thieno[2,3‐b]Quinoline‐Acetamide Derivatives as New Anti‐Diabetic Agents.
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- ChemistrySelect, 2022, v. 7, n. 44, p. 1, doi. 10.1002/slct.202104482
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Diabetes and Heart Failure: Multi-Omics Approaches.
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- Frontiers in Physiology, 2021, v. 12, p. 1, doi. 10.3389/fphys.2021.705424
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Recent strategies in the synthesis of thiophene derivatives: highlights from the 2012–2020 literature.
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- Molecular Diversity, 2021, v. 25, n. 4, p. 2571, doi. 10.1007/s11030-020-10128-9
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Design and synthesis of 4,5-diphenyl-imidazol-1,2,3-triazole hybrids as new anti-diabetic agents: in vitro α-glucosidase inhibition, kinetic and docking studies.
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- Molecular Diversity, 2021, v. 25, n. 2, p. 877, doi. 10.1007/s11030-020-10072-8
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Synthesis and molecular docking studies of new aryl imeglimin derivatives as a potent antidiabetic agent in a diabetic zebrafish model.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-60206-3
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- Article