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Discovery of N‐(phenylsulfonyl)thiazole‐2‐carboxamides as potent α‐glucosidase inhibitors.
- Published in:
- Drug Development Research, 2024, v. 85, n. 1, p. 1, doi. 10.1002/ddr.22128
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- Article
Quantitative structure-activity relationship (QSAR) directed the discovery of 3-(pyridin-2-yl)benzenesulfonamide derivatives as novel herbicidal agents.
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- Pest Management Science, 2018, v. 74, n. 1, p. 189, doi. 10.1002/ps.4693
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- Article
A new ligand system containing sulfanilamide and quinazolinone fragments: Synthesis, structure, and properties.
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- Russian Journal of General Chemistry, 2017, v. 87, n. 1, p. 66, doi. 10.1134/S1070363217010121
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- Article
Synthetic N-Alkyl/aralkyl-4-methyl-N-(naphthalen-1-yl)benzenesulfonamides as Potent Antibacterial Agents.
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- Pakistan Journal of Chemistry, 2015, v. 5, n. 1, p. 23, doi. 10.15228/2015.v05.i01.p04
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- Article
Synthesis and Screening of Some New N-Substituted Derivatives of N-(4-Methylpyridin-2-yl)benzenesulfonamides as Potential Antibacterial Agents.
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- Pakistan Journal of Chemistry, 2014, v. 4, n. 1, p. 6, doi. 10.15228/2014.v04.i01.p02
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- Article
Design and synthesis of novel sulfonamide substituted imidazobenzothiazole derivatives as radiosensitizers for anticancer therapy.
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- Nitte University Journal of Health Science, 2018, p. 33
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- Article
CAXII inhibitors: Potential sensitizers for immune checkpoint inhibitors in HCC treatment.
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- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.1052657
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- Article
Synthesis, molecular modeling, and biological evaluation of 4‐[5‐aryl‐3‐(thiophen‐2‐yl)‐4,5‐dihydro‐1<italic>H</italic>‐pyrazol‐1‐yl] benzenesulfonamides toward acetylcholinesterase, carbonic anhydrase I and II enzymes
- Published in:
- Chemical Biology & Drug Design, 2018, v. 91, n. 4, p. 854, doi. 10.1111/cbdd.13149
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- Article
Synthesis, QSAR studies, and metabolic stability of novel 2-alkylthio-4-chloro- N-(5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)benzenesulfonamide derivatives as potential anticancer and apoptosis-inducing agents.
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- Chemical Biology & Drug Design, 2017, v. 90, n. 3, p. 380, doi. 10.1111/cbdd.12955
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- Article
Synthesis and Biological Evaluation of a Series of 2-((1-substituted-1 H-1,2,3-triazol-4-yl)methylthio)-6-(naphthalen-1-ylmethyl)pyrimidin-4(3 H)-one As Potential HIV-1 Inhibitors.
- Published in:
- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 614, doi. 10.1111/cbdd.12524
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- Article
Synthesis, Molecular Docking, and Biological Evaluation of Some Novel Hydrazones and Pyrazole Derivatives as Anti-inflammatory Agents.
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- Chemical Biology & Drug Design, 2014, v. 84, n. 4, p. 473, doi. 10.1111/cbdd.12336
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- Article
Synthesis, Characterization, Antibacterial, a-Glucosidase Inhibition and Hemolytic Studies on Some New N-(2,3-Dimethylphenyl)benzenesulfonamide Derivatives.
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- Tropical Journal of Pharmaceutical Research, 2016, v. 115, n. 3, p. 591, doi. 10.4314/tjpr.v15i3.22
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- Article
Synthesis of Highly Substituted N-(Furan-3-ylmethylene)benzenesulfonamides by a Gold(I)-Catalyzed Oxidation/1,2-Alkynyl Migration/Cyclization Cascade.
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- Chemistry - A European Journal, 2014, v. 20, n. 45, p. 14868, doi. 10.1002/chem.201404229
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- Article
Synthesis of novel N‐aryl‐N‐(1H‐tetrazol‐5‐yl)benzenesulfonamides in water.
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- Applied Organometallic Chemistry, 2020, v. 34, n. 8, p. 1, doi. 10.1002/aoc.5706
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- Article
Green synthesis approach for novel benzenesulfonamide nanometer complexes with elaborated spectral, theoretical and biological treatments.
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- Applied Organometallic Chemistry, 2018, v. 32, n. 9, p. 1, doi. 10.1002/aoc.4460
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- Article
Polymer complexes. LXVIII. Spectroscopic studies of supramolecular copper(II) polymeric complexes of biologically active monomer derived from novel sulfa drug.
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- Applied Organometallic Chemistry, 2018, v. 32, n. 2, p. 1, doi. 10.1002/aoc.4059
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- Article
Progress in the development of human carbonic anhydrase inhibitors and their pharmacological applications: Where are we today?
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- Medicinal Research Reviews, 2020, v. 40, n. 6, p. 2485, doi. 10.1002/med.21713
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- Article
Continued Structural Exploration of Sulfocoumarin as Selective Inhibitor of Tumor-Associated Human Carbonic Anhydrases IX and XII.
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- Molecules, 2022, v. 27, n. 13, p. 4076, doi. 10.3390/molecules27134076
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- Article
Carbonic Anhydrase Inhibition with Sulfonamides Incorporating Pyrazole- and Pyridazinecarboxamide Moieties Provides Examples of Isoform-Selective Inhibitors.
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- Molecules, 2021, v. 26, n. 22, p. 7023, doi. 10.3390/molecules26227023
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- Article
Carbonic Anhydrase Inhibitors and Epilepsy: State of the Art and Future Perspectives.
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- Molecules, 2021, v. 26, n. 21, p. 6380, doi. 10.3390/molecules26216380
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- Article
The Glitazone Class of Drugs as Carbonic Anhydrase Inhibitors—A Spin-Off Discovery from Fragment Screening.
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- Molecules, 2021, v. 26, n. 10, p. 3010, doi. 10.3390/molecules26103010
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- Article
Bar Adsorptive Microextraction Coated with Carbon-Based Phase Mixtures for Performance-Enhancement to Monitor Selected Benzotriazoles, Benzothiazoles, and Benzenesulfonamides in Environmental Water Matrices.
- Published in:
- Molecules, 2020, v. 25, n. 9, p. 2133, doi. 10.3390/molecules25092133
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- Article
The Design and Synthesis of N-Xanthone Benzenesulfonamides as Novel Phosphoglycerate Mutase 1 (PGAM1) Inhibitors.
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- Molecules, 2018, v. 23, n. 6, p. 1396, doi. 10.3390/molecules23061396
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- Article
Novel Sulfamethoxazole Ureas and Oxalamide as Potential Antimycobacterial Agents.
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- Molecules, 2017, v. 22, n. 4, p. 535, doi. 10.3390/molecules22040535
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- Article
Synthesis and Pharmacological Evaluation of Novel Benzenesulfonamide Derivatives as Potential Anticonvulsant Agents.
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- Molecules, 2015, v. 20, n. 9, p. 17585, doi. 10.3390/molecules200917585
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- Article
4-Amino-substituted Benzenesulfonamides as Inhibitors of Human Carbonic Anhydrases.
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- Molecules, 2014, v. 19, n. 11, p. 17356, doi. 10.3390/molecules191117356
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- Article
Synthesis and Anti-Yeast Evaluation of Novel 2-Alkylthio-4-chloro-5-methyl-N-[imino-(1-oxo-(1H)-phthalazin-2-yl)methyl]benzenesulfonamide Derivatives.
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- Molecules, 2014, v. 19, n. 9, p. 13704, doi. 10.3390/molecules190913704
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- Article
Synthesis and Characterization of Celecoxib Derivatives as Possible Anti-Inflammatory, Analgesic, Antioxidant, Anticancer and Anti-HCV Agents.
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- Molecules, 2013, v. 18, n. 3, p. 3595, doi. 10.3390/molecules18033595
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- Article
Synthesis, Antibacterial and Antifungal Activity of Some New Pyrazoline and Pyrazole Derivatives.
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- Molecules, 2013, v. 18, n. 3, p. 2683, doi. 10.3390/molecules18032683
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- Article
4-(1H-Pyrazol-1-yl) Benzenesulfonamide Derivatives: Identifying New Active Antileishmanial Structures for Use against a Neglected Disease.
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- Molecules, 2012, v. 17, n. 11, p. 12961, doi. 10.3390/molecules171112961
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- Article
Newer, Older, and Alternative Agents for the Eradication of Helicobacter pylori Infection: A Narrative Review.
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- Antibiotics (2079-6382), 2023, v. 12, n. 6, p. 946, doi. 10.3390/antibiotics12060946
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- Article
Distinguishing tautomerism in the crystal structure of ( Z)- N-(5-ethyl-2,3-dihydro-1,3,4-thiadiazol-2-ylidene)-4-methylbenzenesulfonamide using DFT-D calculations and <sup>13</sup>C solid-state NMR.
- Published in:
- Acta Crystallographica Section C: Structural Chemistry, 2014, v. 70, n. 8, p. 784, doi. 10.1107/S2053229614015356
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- Article
Acid‐Catalyzed Rearrangements of 3‐Aryloxirane‐2‐Carboxamides: Novel DFT Mechanistic Insights.
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- ChemistryOpen, 2020, v. 9, n. 7, p. 743, doi. 10.1002/open.202000110
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- Article
Some N-(5-methyl-1,3,4-thiadiazol-2-yl)-4-[(3-substituted)ureido/thioureido]benzenesulfonamides as carbonic anhydrase I and II Inhibitors.
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- Marmara Pharmaceutical Journal, 2017, v. 21, n. 1, p. 89, doi. 10.12991/marupj.259885
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- Article
2‐Chloro‐5‐(1‐hydroxy‐3‐oxoisoindolin‐1‐yl)benzenesulfonamides as potential inhibitors of urease: Synthesis, in‐vitro and molecular modeling approach.
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- Journal of the Chinese Chemical Society, 2022, v. 69, n. 10, p. 1810, doi. 10.1002/jccs.202200295
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- Article
Reactions of a,ß-unsaturated N-benzenesulfonyl Imine - N-[(2 E)-3-phenyl-2-propen-1-ylidene]benzenesulfonamide with Methyllithium.
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- Journal of the Chinese Chemical Society, 2015, v. 62, n. 7, p. 573, doi. 10.1002/jccs.201500082
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- Article
Mechanism of covalent adsorption of benzenesulfonamide onto COOH- and COCl- functionalised carbon nanotubes.
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- Progress in Reaction Kinetics & Mechanism, 2016, v. 41, n. 1, p. 100, doi. 10.3184/146867816X14490560291507
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- Article
Cinnamaldehyde Attenuates the Progression of Rheumatoid Arthritis through Down-Regulation of PI3K/AKT Signaling Pathway.
- Published in:
- Inflammation, 2020, v. 43, n. 5, p. 1729, doi. 10.1007/s10753-020-01246-5
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- Article
Synthesis of Azasugar-Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 18, p. 2604, doi. 10.1002/ejoc.202100250
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- Article
Iron‐Catalyzed Electrophilic Amination of Sodium Sulfinates with Anthranils.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 9, p. 1466, doi. 10.1002/ejoc.202100010
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- Article
Synthesis of Tetrahydroquinoline-Embedded Bridged Benzothiaoxazepine-1,1-dioxides.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 45, p. 6671, doi. 10.1002/ejoc.201701152
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- Article
Repurposing of World-Approved Drugs for Potential Inhibition against Human Carbonic Anhydrase I: A Computational Study.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 16, p. 12619, doi. 10.3390/ijms241612619
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- Article
Benzenesulfonamides Incorporating Hydantoin Moieties Effectively Inhibit Eukaryoticand Human Carbonic Anhydrases.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 22, p. 14115, doi. 10.3390/ijms232214115
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- Article
MDM2-Based Proteolysis-Targeting Chimeras (PROTACs): An Innovative Drug Strategy for Cancer Treatment.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 19, p. 11068, doi. 10.3390/ijms231911068
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- Article
Suppression of Tumor Growth and Cell Migration by Indole-Based Benzenesulfonamides and Their Synergistic Effects in Combination with Doxorubicin.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 17, p. 9903, doi. 10.3390/ijms23179903
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- Article
Identification of Novel and Potent Indole-Based Benzenesulfonamides as Selective Human Carbonic Anhydrase II Inhibitors: Design, Synthesis, In Vitro, and In Silico Studies.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 5, p. 2540, doi. 10.3390/ijms23052540
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- Article
Efficacy of a Three Drug-Based Therapy for Neuroblastoma in Mice.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 13, p. 6753, doi. 10.3390/ijms22136753
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- Article
Carbonic Anhydrase Sensitivity to Pesticides: Perspectives for Biomarker Development.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 10, p. 3562, doi. 10.3390/ijms21103562
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- Article
Synthesis, Antitumor Evaluation, Molecular Modeling and Quantitative Structure–Activity Relationship (QSAR) of Novel 2-[(4-Amino-6-N-substituted-1,3,5-triazin-2-yl)methylthio]-4-chloro-5-methyl-N-(1H-benzo[d]imidazol-2(3H)-ylidene)Benzenesulfonamides
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- International Journal of Molecular Sciences, 2020, v. 21, n. 8, p. 2924, doi. 10.3390/ijms21082924
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- Article
Benzylaminoethyureido-Tailed Benzenesulfonamides: Design, Synthesis, Kinetic and X-ray Investigations on Human Carbonic Anhydrases.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 7, p. 2560, doi. 10.3390/ijms21072560
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- Article