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Synthesis, biological activities, and molecular docking studies of triazolo[4,3‐b]triazine derivatives as a novel class of α‐glucosidase and α‐amylase inhibitors.
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- Archiv der Pharmazie, 2024, v. 357, n. 7, p. 1, doi. 10.1002/ardp.202300628
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- Article
Novel quinazolines bearing 1,3,4-thiadiazole-aryl urea derivative as anticancer agents: design, synthesis, molecular docking, DFT and bioactivity evaluations.
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- BMC Chemistry, 2024, v. 18, p. 1, doi. 10.1186/s13065-024-01119-0
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- Article
Tannic acid-mediated synthesis of flower-like mesoporous MnO<sub>2</sub> nanostructures as T<sub>1</sub>–T<sub>2</sub> dual-modal MRI contrast agents and dual-enzyme mimetic agents.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41598-0
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Tannic acid-mediated synthesis of flower-like mesoporous MnO<sub>2</sub> nanostructures as T<sub>1</sub>–T<sub>2</sub> dual-modal MRI contrast agents and dual-enzyme mimetic agents.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41598-0
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Imidazo[1,2-c]quinazolines as a novel and potent scaffold of α-glucosidase inhibitors: design, synthesis, biological evaluations, and in silico studies.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-42549-5
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- Article
Tannic acid-mediated synthesis of flower-like mesoporous MnO<sub>2</sub> nanostructures as T<sub>1</sub>–T<sub>2</sub> dual-modal MRI contrast agents and dual-enzyme mimetic agents.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41598-0
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- Article
Synthesis, α-Glucosidase inhibitory activity and docking studies of Novel Ethyl 1,2,3-triazol-4-ylmethylthio-5,6-diphenylpyridazine-4-carboxylate derivatives.
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- BMC Chemistry, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s13065-023-00973-8
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Synthesis, α-Glucosidase inhibitory activity and docking studies of Novel Ethyl 1,2,3-triazol-4-ylmethylthio-5,6-diphenylpyridazine-4-carboxylate derivatives.
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- BMC Chemistry, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s13065-023-00973-8
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CuONPs/MWCNTs/carbon paste modified electrode for determination of tramadol: theoretical and experimental investigation.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-34569-y
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Thienopyrimidine‐based agents bearing diphenylurea: Design, synthesis, and evaluation of antiproliferative and antiangiogenic activity.
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- Archiv der Pharmazie, 2023, v. 356, n. 3, p. 1, doi. 10.1002/ardp.202200349
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Ultrasound‐promoted 1,3‐dipolar cycloaddition of azomethine yields for synthesis of dispiropyrrolidineoxindole derivatives in hexyltriphenylphosphonium bromide as an ionic liquid, and the evaluation of their anti‐cancer activity.
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- Journal of Heterocyclic Chemistry, 2023, v. 60, n. 3, p. 416, doi. 10.1002/jhet.4595
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Bioengineered synthesis of phytochemical-adorned green silver oxide (Ag<sub>2</sub>O) nanoparticles via Mentha pulegium and Ficus carica extracts with high antioxidant, antibacterial, and antifungal activities.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-26021-4
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Green and four-component cyclocondensation synthesis and in silico docking of new polyfunctionalized pyrrole derivatives as the potential anticholinesterase agents.
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- Molecular Diversity, 2022, v. 26, n. 6, p. 3021, doi. 10.1007/s11030-021-10362-9
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Green and one-pot synthesis of novel amidoalkyl naphthols using triethanolammonium acetate [(OHCH<sub>2</sub>CH<sub>2</sub>)<sub>3</sub>NH][OAc]) ionic liquid and their anti-H.pylori activity.
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- Research on Chemical Intermediates, 2022, v. 48, n. 10, p. 4049, doi. 10.1007/s11164-022-04803-9
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Antidiabetic and neuroprotective effects of a novel repaglinide analog.
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- Journal of Biochemical & Molecular Toxicology, 2022, v. 36, n. 9, p. 1, doi. 10.1002/jbt.23125
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2-(Nitroaryl)-5-Substituted-1,3,4-Thiadiazole Derivatives with Antiprotozoal Activities: In Vitro and In Vivo Study.
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- Molecules, 2022, v. 27, n. 17, p. 5559, doi. 10.3390/molecules27175559
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Design, synthesis and evaluation of novel tetrahydropyridothienopyrimidin-ureas as cytotoxic and anti-angiogenic agents.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-13515-4
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Synthesis of new 2-(5-(5-nitrofuran-2-yl)-1,3,4-thiadiazol-2-ylimino)thiazolidin-4-one derivatives as anti-MRSA and anti-H. pylori agents.
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- BMC Chemistry, 2022, v. 16, n. 1, p. 1, doi. 10.1186/s13065-022-00829-7
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Synthesis of novel 2‐acetamide‐5‐phenylthio‐1,3,4‐thiadiazole‐containing phenyl urea derivatives as potential VEGFR‐2 inhibitors.
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- Archiv der Pharmazie, 2022, v. 355, n. 3, p. 1, doi. 10.1002/ardp.202100397
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- Article
New Antimicrobial Nitro Heteroaryl-1,3,4-Thiadiazole Derivatives Containing Piperazinyl Benzonitrile Moiety: Synthesis and in silico Study.
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- Journal of Computational Biophysics & Chemistry, 2022, v. 21, n. 2, p. 249, doi. 10.1142/S2737416521410052
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- Article
Design, synthesis, molecular docking, and in vitro α-glucosidase inhibitory activities of novel 3-amino-2,4-diarylbenzo[4,5]imidazo[1,2-a]pyrimidines against yeast and rat α-glucosidase.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91473-z
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- Article
A QSAR Study for the Prediction of Inhibitory Activity of Coumarin Derivatives for the Treatment of Alzheimer's Disease.
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- Arabian Journal for Science & Engineering (Springer Science & Business Media B.V. ), 2021, v. 46, n. 6, p. 5523, doi. 10.1007/s13369-020-05064-7
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Chromone–lipoic acid conjugate: Neuroprotective agent having acceptable butyrylcholinesterase inhibition, antioxidant and copper-chelation activities.
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- DARU: Journal of Pharmaceutical Sciences, 2021, v. 29, p. 23, doi. 10.1007/s40199-020-00378-1
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Synthesis and radioligand‐binding assay of 2,5‐disubstituted thiadiazoles and evaluation of their anticonvulsant activities.
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- Archiv der Pharmazie, 2020, v. 353, n. 12, p. 1, doi. 10.1002/ardp.202000066
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- Article
Design and synthesis of benzodiazepine-1,2,3-triazole hybrid derivatives as selective butyrylcholinesterase inhibitors.
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- Molecular Diversity, 2020, v. 24, n. 4, p. 997, doi. 10.1007/s11030-019-10008-x
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Design, synthesis, molecular docking study, and antibacterial evaluation of some new fluoroquinolone analogues bearing a quinazolinone moiety.
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- DARU: Journal of Pharmaceutical Sciences, 2020, v. 28, p. 661, doi. 10.1007/s40199-020-00373-6
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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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Bucladesine Attenuates Spatial Learning and Hippocampal Mitochondrial Impairments Induced by 3, 4-Methylenedioxymethamphetamine (MDMA).
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- Neurotoxicity Research, 2020, v. 38, n. 1, p. 38, doi. 10.1007/s12640-020-00183-3
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Evaluation of hepatic CYP2D1 activity and hepatic clearance in type I and type II diabetic rat models, before and after treatment with insulin and metformin.
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- DARU: Journal of Pharmaceutical Sciences, 2020, v. 28, p. 479, doi. 10.1007/s40199-020-00350-z
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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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A comparison between Suzuki cross‐coupling reaction and direct arylation in the synthesis of new antibacterial imidazo‐pyrazines/pyridazines.
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- Journal of Heterocyclic Chemistry, 2020, v. 57, n. 4, p. 1770, doi. 10.1002/jhet.3902
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- Article
An efficient and targeted synthetic approach towards new highly substituted 6-amino-pyrazolo[1,5-a]pyrimidines with α-glucosidase inhibitory activity.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-59079-z
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- Article
Proton Pump Inhibitor-Treated H. pylori Adjust Cell Envelope Fatty Acid and Cholesterol Content to Survive.
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- Archives of Iranian Medicine (AIM), 2020, v. 23, n. 1, p. 7
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- Article
Synthesis and Activity Evaluation of New Benzofuran-1,3,4-Oxadiazole Hybrids Against Wood-Degrading Fungi.
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- BioResources, 2020, v. 15, n. 1, p. 1085, doi. 10.15376/biores.15.1.1085-1097
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- Article
Green Decarboxylative Aminoalkylation of Coumarin‐3‐Carboxylic Acids.
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- ChemistrySelect, 2019, v. 4, n. 46, p. 13695, doi. 10.1002/slct.201902872
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- Article
Novel 5-(nitrothiophene-2-yl)-1,3,4-Thiadiazole Derivatives: Synthesis and Antileishmanial Activity against promastigote stage of Leishmania major.
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- Iranian Journal of Pharmaceutical Research, 2019, v. 18, n. 4, p. 1816, doi. 10.22037/ijpr.2019.14547.12476
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In Vitro Interaction of Geldanamycin with Triazoles and Echinocandins Against Common and Emerging Candida Species.
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- Mycopathologia, 2019, v. 184, n. 5, p. 607, doi. 10.1007/s11046-019-00370-7
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- Article
N-(5-(Trifluoromethyl)-1,3,4-Thiadiazol-2-Yl)Benzamide and Benzothioamide Derivatives Induce Apoptosis Via Caspase-Dependent Pathway.
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- Pharmaceutical Chemistry Journal, 2019, v. 53, n. 6, p. 521, doi. 10.1007/s11094-019-02031-x
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Design, synthesis, biological evaluation, and molecular dynamics of novel cholinesterase inhibitors as anti‐Alzheimer's agents.
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- Archiv der Pharmazie, 2019, v. 352, n. 7, p. N.PAG, doi. 10.1002/ardp.201800352
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- Article
Hexyltriphenylphosphonium Bromide as an Absolutely Chemoselective Ionic Liquid Catalyst in the Three‐Component Reaction of Aryl Aldehydes, Acetophenones and Malononitrile.
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- ChemistrySelect, 2019, v. 4, n. 20, p. 6190, doi. 10.1002/slct.201901076
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- Article
3‐Aryl Coumarin Derivatives Bearing Aminoalkoxy Moiety as Multi‐Target‐Directed Ligands against Alzheimer's Disease.
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- Chemistry & Biodiversity, 2019, v. 16, n. 5, p. N.PAG, doi. 10.1002/cbdv.201800436
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- Article
Graphene Oxide Incorporated Strontium Nanoparticles as a Highly Efficient and Green Acid Catalyst for One-Pot Synthesis of Tetramethyl-9-aryl-hexahydroxanthenes and 13-Aryl-5H-dibenzo[b,i]xanthene-5,7,12,14(13H)-tetraones Under Solvent-Free Conditions.
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- Catalysis Letters, 2019, v. 149, n. 4, p. 1075, doi. 10.1007/s10562-019-02675-0
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- Article
Trastuzumab‐monomethyl auristatin E conjugate exhibits potent cytotoxic activity in vitro against HER2‐positive human breast cancer.
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- Journal of Cellular Physiology, 2019, v. 234, n. 3, p. 2693, doi. 10.1002/jcp.27085
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A novel and reusable magnetic nanocatalyst developed based on graphene oxide incorporated strontium nanoparticles for the facial synthesis of β‐enamino ketones under solvent‐free conditions.
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- Applied Organometallic Chemistry, 2019, v. 33, n. 1, p. N.PAG, doi. 10.1002/aoc.4644
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Simultaneous targeting of HSP90 and lanosterol 14a-demethylase could reverse azole resistance in some Candida species.
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- Current Medical Mycology, 2018, v. 4, p. 36, doi. 10.18502/cmm.4.S1.2018.179
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A one-pot, three-component, solvent-free synthesis of novel 6H-chromeno[3',4':5,6]pyrido[2,3-d]pyrimidine-triones under microwave irradiation.
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- Journal of Chemical Research, 2018, v. 42, n. 12, p. 604, doi. 10.3184/174751918X15414289771620
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N-substituted piperazinyl sarafloxacin derivatives: synthesis and in vitro antibacterial evaluation.
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- DARU: Journal of Pharmaceutical Sciences, 2018, v. 26, p. 1, doi. 10.1007/s40199-018-0226-0
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- Article
New 7-piperazinylquinolones containing (benzo[d]imidazol-2-yl)methyl moiety as potent antibacterial agents.
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- Molecular Diversity, 2018, v. 22, n. 4, p. 815, doi. 10.1007/s11030-018-9834-3
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- Article
Copper-catalyzed synthesis of 2,3-disubstituted quinazolin-4(3H)-ones from benzyl-substituted anthranilamides.
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- Heterocyclic Communications, 2018, v. 24, n. 5, p. 267, doi. 10.1515/hc-2018-0051
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- Article
Synthesis, evaluation, and molecular docking studies of aryl urea‐triazole‐based derivatives as anti‐urease agents.
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- Archiv der Pharmazie, 2018, v. 351, n. 7, p. 1, doi. 10.1002/ardp.201800005
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- Article