Works about BENZENESULFONAMIDES
Results: 254
Cover Feature: Structure‐Activity Relationship of Fluorinated Benzenesulfonamides as Inhibitors of Amyloid‐β Aggregation (Chem. Eur. J. 58/2024).
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- Chemistry - A European Journal, 2024, v. 30, n. 58, p. 1, doi. 10.1002/chem.202485804
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In vitro and in silico interactions of antiulcer, glucocorticoids and urological drugs on human carbonic anhydrase I and II isozymes.
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- Biopharmaceutics & Drug Disposition, 2022, v. 43, n. 2, p. 47, doi. 10.1002/bdd.2309
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Synthesis and Antibacterial and Immunobiological Activity of Ethyl-1-(4-Aminosulfonylphenyl)-5-Aryl-3-Hydroxy-2-Oxo-3-Pyrroline-4-Carboxylates.
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- Pharmaceutical Chemistry Journal, 2016, v. 49, n. 10, p. 677, doi. 10.1007/s11094-016-1351-z
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Synthesis and characterization of polysulfanilamide and its copolymers: bioactivity and drug release.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 7, p. 418, doi. 10.1007/s11094-012-0813-1
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Synthesis and antiviral activity of sterically hindered o-aminophenol derivatives.
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- Pharmaceutical Chemistry Journal, 2012, v. 46, n. 7, p. 414, doi. 10.1007/s11094-012-0812-2
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Molecular and crystal structure of a novel Schiff base: 4-methyl-N-[2-[(2-methyl-4-oxo-quinazoline-3-yl)iminomethyl]phenyl]benzenesulfonamide.
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- Journal of Structural Chemistry, 2017, v. 58, n. 2, p. 366, doi. 10.1134/S0022476617020214
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Synthesis of β-Glycosyl Amides from N -Glycosyl Dinitrobenzenesulfonamides.
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- Journal of Carbohydrate Chemistry, 2012, v. 31, n. 4-6, p. 353, doi. 10.1080/07328303.2012.663431
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Synthesis and pharmacological effects of novel benzenesulfonamides carrying benzamide moiety as carbonic anhydrase and acetylcholinesterase inhibitors.
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- Turkish Journal of Chemistry, 2020, v. 44, n. 6, p. 1601, doi. 10.3906/kim-2007-37
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Synthesis, spectral characterisation, electrochemical, and fluorescence studies of biologically active novel Schiff base complexes derived from E-4-(2-hydroxy-3- methoxybenzlideneamino)-N-(pyrimidin-2-yl)benzenesulfonamide.
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- Turkish Journal of Chemistry, 2014, v. 38, n. 4, p. 521, doi. 10.3906/kim-1301-83
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Crystal structure correlations with the intrinsic thermodynamics of human carbonic anhydrase inhibitor binding.
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- PeerJ, 2018, p. 1, doi. 10.7717/peerj.4412
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Identification of new 4-(6-oxopyridazin-1-yl)benzenesulfonamides as multi-target anti-inflammatory agents targeting carbonic anhydrase, COX-2 and 5-LOX enzymes: synthesis, biological evaluations and modelling insights.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2201407
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Antihistamines, phenothiazine-based antipsychotics, and tricyclic antidepressants potently activate pharmacologically relevant human carbonic anhydrase isoforms II and VII.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2188147
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Potent carbonic anhydrase I, II, IX and XII inhibition activity of novel primary benzenesulfonamides incorporating bis-ureido moieties.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2185762
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Diversely N-substituted benzenesulfonamides dissimilarly bind to human carbonic anhydrases: crystallographic investigations of N-nitrosulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2178430
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Dependence on linkers' flexibility designed for benzenesulfonamides targeting discovery of novel hCA IX inhibitors as potent anticancer agents.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 2765, doi. 10.1080/14756366.2022.2130285
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Benzenesulfonamides with different rigidity-conferring linkers as carbonic anhydrase inhibitors: an insight into the antiproliferative effect on glioblastoma, pancreatic, and breast cancer cells.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1857, doi. 10.1080/14756366.2022.2091557
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4-Anilinoquinazoline-based benzenesulfonamides as nanomolar inhibitors of carbonic anhydrase isoforms I, II, IX, and XII: design, synthesis, in-vitro, and in-silico biological studies.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 994, doi. 10.1080/14756366.2022.2055553
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4-(3-Alkyl/benzyl-guanidino)benzenesulfonamides as selective carbonic anhydrase VII inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2022, v. 37, n. 1, p. 1568, doi. 10.1080/14756366.2022.2080816
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Investigation of pesticides on honey bee carbonic anhydrase inhibition.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 1923, doi. 10.1080/14756366.2020.1835885
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Synthesis and biological evaluation of novel 3-(quinolin-4-ylamino)benzenesulfonamides as carbonic anhydrase isoforms I and II inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1457, doi. 10.1080/14756366.2019.1652282
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Appraisal of anti-protozoan activity of nitroaromatic benzenesulfonamides inhibiting carbonic anhydrases from Trypanosoma cruzi and Leishmania donovani.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2019, v. 34, n. 1, p. 1164, doi. 10.1080/14756366.2019.1626375
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Carbonic anhydrase inhibition with a series of novel benzenesulfonamide-triazole conjugates.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 1565, doi. 10.1080/14756366.2018.1513927
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Synthesis, carbonic anhydrase I and II inhibition studies of the 1,3,5-trisubstituted-pyrazolines.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 189, doi. 10.1080/14756366.2016.1244533
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Designing, synthesis and bioactivities of 4-[3-(4-hydroxyphenyl)-5-aryl-4,5-dihydro-pyrazol-1-yl]benzenesulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 169, doi. 10.1080/14756366.2016.1243536
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3D QSAR studies, pharmacophore modeling, and virtual screening of diarylpyrazole–benzenesulfonamide derivatives as a template to obtain new inhibitors, using human carbonic anhydrase II as a model protein.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2017, v. 32, n. 1, p. 688, doi. 10.1080/14756366.2016.1241781
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Selective inhibition of human carbonic anhydrase IX in Xenopus oocytes and MDA-MB-231 breast cancer cells.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 38, doi. 10.1080/14756366.2016.1217854
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Study of reactivity of cyanoacetohydrazonoethyl- N -ethyl- N -methyl benzenesulfonamide: preparation of novel anticancer and antimicrobial active heterocyclic benzenesulfonamide derivatives and their molecular docking against dihydrofolate reductase.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 7, doi. 10.1080/14756366.2016.1217851
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Synthesis and bioactivity studies on new 4-(3-(4-Substitutedphenyl)-3a,4-dihydro-3 H -indeno[1,2-c]pyrazol-2-yl) benzenesulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 6, p. 1619, doi. 10.3109/14756366.2016.1160077
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Design, synthesis and biological evaluation of N -(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 174, doi. 10.1080/14756366.2016.1197221
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Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, p. 1, doi. 10.1080/14756366.2016.1181627
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Synthesis of 4-(2-substituted hydrazinyl)benzenesulfonamides and their carbonic anhydrase inhibitory effects.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 4, p. 568, doi. 10.3109/14756366.2015.1047359
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Synthesis and inhibition potency of novel ureido benzenesulfonamides incorporating GABA as tumor-associated carbonic anhydrase IX and XII inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2016, v. 31, n. 2, p. 205, doi. 10.3109/14756366.2015.1014477
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Fluorinated pyrrolidines and piperidines incorporating tertiary benzenesulfonamide moieties are selective carbonic anhydrase II inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 5, p. 737, doi. 10.3109/14756366.2014.963072
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Exploring QSARs of some benzenesulfonamides incorporating cyanoacrylamide moieties as a carbonic anhydrase inhibitors (specifically against tumor-associated isoforms IX and XII).
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 4, p. 519, doi. 10.3109/14756366.2014.948435
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Inhibition of human carbonic anhydrase isozymes I, II, IX and XII with a new series of sulfonamides incorporating aroylhydrazone-, [1,2,4]triazolo[3,4-b][1,3,4]thiadiazinyl- or 2-(cyanophenylmethylene)-1,3,4-thiadiazol-3(2H)-yl moieties.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2015, v. 30, n. 1, p. 52, doi. 10.3109/14756366.2013.877897
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Synthesis, molecular modeling and NAD(P)H:quinone oxidoreductase 1 inducer activity of novel cyanoenone and enone benzenesulfonamides.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 6, p. 840, doi. 10.3109/14756366.2013.858146
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Dual evaluation of some novel 2-amino-substituted coumarinylthiazoles as anti-inflammatory-antimicrobial agents and their docking studies with COX-1/COX-2 active sites.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 4, p. 476, doi. 10.3109/14756366.2013.805755
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Synthesis and blood glucose lowering activity of some novel benzenesulfonylthiourea derivatives substituted with 4-aryl-1-oxophthalazin-2(1H)yl-ones.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 3, p. 362, doi. 10.3109/14756366.2013.782300
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Benzenesulfonamides with benzimidazole moieties as inhibitors of carbonic anhydrases I, II, VII, XII and XIII.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 1, p. 124, doi. 10.3109/14756366.2012.757223
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Synthesis and anti-inflammatory activity of celecoxib like compounds.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 5, p. 1105, doi. 10.3109/14756366.2012.710847
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Synthesis and in vitro antitumor and antimicrobial activity of some 2,3-diaryl-7-methyl-4,5,6,7-tetrahydroindazole and 3,3a,4,5,6,7-hexahydroindazole derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 3, p. 495, doi. 10.3109/14756366.2011.653354
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Synthesis and antibacterial activity of novel 4-chloro-2-mercaptobenzenesulfonamide derivatives.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2013, v. 28, n. 1, p. 41, doi. 10.3109/14756366.2011.625024
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Carbonic Anhydrases inhibitory effects of new benzenesulfonamides synthesized by using superacid chemistry.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2012, v. 27, n. 6, p. 886, doi. 10.3109/14756366.2011.638921
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Sulfapyridine-like benzenesulfonamide derivatives as inhibitors of carbonic anhydrase isoenzymes I, II and VI.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2012, v. 27, n. 6, p. 818, doi. 10.3109/14756366.2011.617745
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Evaluation of DNase I inhibitory activity on synthetic halogenated chalcone derivatives.
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- Macedonian Pharmaceutical Bulletin / Makedonsko Farmacevtski Bilten, 2023, v. 69, p. 267, doi. 10.33320/maced.pharm.bull.2023.69.03.130
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Carbonic anhydrases enhance activity of endogenous Na‐H exchangers and not the electrogenic Na/HCO<sub>3</sub> cotransporter NBCe1‐A, expressed in Xenopus oocytes.
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- Journal of Physiology, 2020, v. 598, n. 24, p. 5821, doi. 10.1113/JP280143
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Carbonic anhydrase is not a relevant nitrite reductase or nitrous anhydrase in the lung.
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- Journal of Physiology, 2019, v. 597, n. 4, p. 1045, doi. 10.1113/JP275894
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A Novel Fully-Human Potency-Matched Dual Cytokine-Antibody Fusion Protein Targets Carbonic Anhydrase IX in Renal Cell Carcinomas.
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- Frontiers in Oncology, 2019, p. 1, doi. 10.3389/fonc.2019.01228
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Carbonic anhydrase inhibition by antiviral drugs in vitro and in silico.
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- Journal of Molecular Recognition, 2023, v. 36, n. 12, p. 1, doi. 10.1002/jmr.3063
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Investigation of the effects of some pesticides on carbonic anhydrase isoenzymes.
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- Journal of Molecular Recognition, 2023, v. 36, n. 9, p. 1, doi. 10.1002/jmr.3048
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