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Relevant bibliographies by topics / –Aminobenzenesulfonamide

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Academic literature on the topic '–Aminobenzenesulfonamide'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "–Aminobenzenesulfonamide"

1

Benmebarek, Sabrina, Mhamed Boudraa, Sofiane Bouacida, Hocine Merazig та George Dénès. "Bis(4-aminobenzenesulfonamide-κN4)dichloridozinc". Acta Crystallographica Section E Structure Reports Online 70, № 1 (2013): m28—m29. http://dx.doi.org/10.1107/s160053681303417x.

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Kaneda, Kyosuke. "Synthesis of Cyclic Compounds Containing Aminobenzenesulfonamide." YAKUGAKU ZASSHI 140, no. 9 (2020): 1087–94. http://dx.doi.org/10.1248/yakushi.20-00139.

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3

Kravchenya, N. A. "Selective N-acylation of 4-aminobenzenesulfonamide." Pharmaceutical Chemistry Journal 23, no. 4 (1989): 332–34. http://dx.doi.org/10.1007/bf00758426.

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4

Güzel-Akdemir, Özlen, Atilla Akdemir, Nilgün Karalı, and Claudiu T. Supuran. "Discovery of novel isatin-based sulfonamides with potent and selective inhibition of the tumor-associated carbonic anhydrase isoforms IX and XII." Organic & Biomolecular Chemistry 13, no. 23 (2015): 6493–99. http://dx.doi.org/10.1039/c5ob00688k.

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A series of 2/3/4-[(2-oxo-1,2-dihydro-3H-indol-3-ylidene)amino]benzenesulfonamides, obtained from substituted isatins and 2-, 3- or 4-aminobenzenesulfonamide, showed low nanomolar inhibitory activity against the tumor associated carbonic anhydrases IX and XII.

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5

H. Naser, Noor, Monther F. Mahdi, Tagreed N-A Omar, and Amar A. Fadhil. "Synthesis and Preliminary Pharmacological Evaluation of New Analogues of Diclofenac as Potential Anti-inflammatory Agents." Iraqi Journal of Pharmaceutical Sciences ( P-ISSN: 1683 - 3597 , E-ISSN : 2521 - 3512) 20, no. 1 (2017): 25–32. http://dx.doi.org/10.31351/vol20iss1pp25-32.

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A group of amine derivatives [4-aminobenzenesulfonamide derivatives, 2-aminopyridine and 2-aminothiazole] incorporated to Î±-carbon of diclofenac a well known non-steroidal anti-inflammatory drug (NSAID) to increase bulkiness were designed and synthesized for evaluation as a potential anti-inflammatory agents with expected COX-2 selectivity. In vivo acute anti-inflammatory activity of the selected final compounds (9, 12 and 13) was evaluated in rats using egg-white induced edema model of inflammation in a dose equivalent to (3 mg/Kg) of diclofenac sodium. All tested compounds produced a signif

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6

F. Mahdi, Monther. "Synthesis and Preliminary Pharmacological Evaluation of Aminobenzensulfonamides Derivatives of Mefenamic Acid as a Potential Anti-inflammatory Agents." Iraqi Journal of Pharmaceutical Sciences ( P-ISSN: 1683 - 3597 , E-ISSN : 2521 - 3512) 17, no. 1 (2017): 7–15. http://dx.doi.org/10.31351/vol17iss1pp7-15.

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A group of amino derivatives [4-aminobenzenesulfonamide,4-amino-NÂ¹ methylbenzenesulfonamide, or NÂ¹-(4-aminophenylsulfonyl)acetamide] bound to carboxyl group of mefenamic acid a well known nonsteroidal anti-inflammatory drugs (NSAIDs) were designed and synthesized for evaluation as a potential anti-inflammatory agent. In vivo acute anti-inflammatory activity of the final compounds (9, 10 and 11) was evaluated in rat using egg-white induced edema model of inflammation in a dose equivalent to (7.5mg/Kg) of mefenamic acid. All tested compounds produced a significant reduction in paw edema with r

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7

Gein, V. L., O. V. Nazarets, A. V. Romanova, et al. "Synthesis and biological activity of 4-aryl-2-hydroxy-4-oxo-<i>N</i>-(2-sulfamoylphenyl)but-2-enamides." Журнал общей химии 93, no. 5 (2023): 664–69. http://dx.doi.org/10.31857/s0044460x23050025.

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The reaction of methyl esters of 4-aryl-2-hydroxy-4-oxobut-2-enoic (aroylpyruvic) acids with 2-aminobenzenesulfonamide in glacial acetic acid in the presence of anhydrous sodium acetate, 4-aryl-2-hydroxy-4-oxo N -(2-sulfamoylphenyl)but-2-enamides were obtained. The analgesic and antimicrobial activity of the obtained compounds was studied.

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8

S. Salem, Bader, Monther F. Mahdi, and Mohammed H. Mohammed. "Synthesis and Preliminary Pharmacological Study of Sulfonamide Conjugates with Ibuprofen and Indomethacin as New Anti-Inflammatory Agents." Iraqi Journal of Pharmaceutical Sciences ( P-ISSN: 1683 - 3597 , E-ISSN : 2521 - 3512) 18, no. 2 (2017): 39–45. http://dx.doi.org/10.31351/vol18iss2pp39-45.

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4-aminobenzenesulfonamide conjugates of ibuprofen (compound 10) and indomethacin (compound 11) have been designed and synthesized by the reaction of sulfanilamide (compound 7) with 2-(4-isobutylphenyl) propanoic acid (ibuprofen) and 2-(1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl)acetic acid (indomethacin) for the evaluation as potential anti-inflammatory agents with expected selectivity against COX-2 enzyme. In vivo acute anti-inflammatory activity of the synthesized final compounds (10 and 11) was evaluated in rats using egg-white induced edema model of inflammation in a dose equival

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9

Nasser, Noor H., Nethal H. Hammud, Samer A. Hasan, Abbas Hamid Abdalsadh, and Ahmed kareem Hussein. "Design and Synthesis of new Naproxen Analogues as Potential Anti-inflammatory Agents." Al Mustansiriyah Journal of Pharmaceutical Sciences 17, no. 1 (2018): 9. http://dx.doi.org/10.32947/ajps.v17i1.61.

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4-aminobenzenesulfonamide derivatives were linked to α-carbon of naproxen a non-selective non-steroidal anti-inflammatory drug (NSAID) to increase its size, so; increase its selectivity toward COX-2 enzyme, rather than COX-1 enzyme, that lead to reduce gastrointestinal side effects of this drug.The chemical structures of the synthesized compounds and their intermediates were confirmed and characterized using elemental microanalysis (CHN), FTIR, and other physicochemical properties like melting points, Rf values.

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10

González, Myriam, María Ovejero-Sánchez, Alba Vicente-Blázquez, et al. "Microtubule Destabilizing Sulfonamides as an Alternative to Taxane-Based Chemotherapy." International Journal of Molecular Sciences 22, no. 4 (2021): 1907. http://dx.doi.org/10.3390/ijms22041907.

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Pan-Gyn cancers entail 1 in 5 cancer cases worldwide, breast cancer being the most commonly diagnosed and responsible for most cancer deaths in women. The high incidence and mortality of these malignancies, together with the handicaps of taxanes—first-line treatments—turn the development of alternative therapeutics into an urgency. Taxanes exhibit low water solubility that require formulations that involve side effects. These drugs are often associated with dose-limiting toxicities and with the appearance of multi-drug resistance (MDR). Here, we propose targeting tubulin with compounds directe

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Books on the topic "–Aminobenzenesulfonamide"

1

N, Paruta Anthony, Piekos Ryszard, and International Union of Pure and Applied Chemistry., eds. 4-Aminobenzenesulfonamides. Pergamon Press, 1988.

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2

N, Paruta Anthony, and Piekos Ryszard, eds. 4-aminobenzenesulfonamides. Pergamon, 1989.

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3

N, Paruta Anthony, Piekos Ryszard, and International Union of Pure and Applied Chemistry., eds. 4-Aminobenzenesulfonamides. Pergamon Press, 1988.

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4

4-aminobenzenesulfonamides. Pergamon, 1988.

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5

4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/c2009-0-01253-7.

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6

Paruta, Anthony N. 4-Aminobenzenesulfonamides. Pergamon Pr, 1988.

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7

Paruta, Anthony N. 4-Aminobenzenesulfonamides. Pergamon Pr, 1988.

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8

Paruta, Anthony N. 4-Aminobenzenesulfonamides. Pergamon Pr, 1988.

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Paruta, Anthony N. 4-Aminobenzenesulfonamides. Pergamon Pr, 1988.

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10

Paruta, A. N., and R. Piekos. 4-Aminobenzenesulfonamides: 6-Membered Heterocyclic Substituents and Miscellaneous Systems. Elsevier Science & Technology Books, 2013.

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Book chapters on the topic "–Aminobenzenesulfonamide"

1

Scholar, Eric M., and William B. Pratt. "The Antimetabolites: The Sulfonamides and Trimethoprim (Trimethoprim-Sulfamethoxazole)." In The Antimicrobial Drugs. Oxford University PressNew York, NY, 2000. http://dx.doi.org/10.1093/oso/9780195125283.003.0007.

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Abstract The sufonamides were the first effective chemotherapeutic agents to be used systematically for the treatment of bacterial infections. Sulfonamide-containing compounds were synthesized early in this century by German chemists for use as dyes. Their therapeutic potential was not exploited until 1935, when Domagk demonstrated that one of these dyes, prontosil, was effective in treating mice infected with streptococci. Later it was found that prontosil is metabolized in the tissues to para aminobenzenesulfonamide ( sulfanilamide), the chemotherapeutically active part of the molecule. Subs

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2

"SOLUBILITY DATA SERIES." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50001-5.

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"Front Matter." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50002-7.

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"Copyright." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50003-9.

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Kertes, A. S. "FOREWORD." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50004-0.

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"PREFACE." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50005-2.

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7

Cohen-Adad, R., S. Lindenbaum, J. W. Lorimer, A. N. Paruta, R. Piekos, and M. Salomon. "INTRODUCTION TO THE SERIES ON SOLUBILITY OF SOLIDS IN LIQUIDS: SUBSERIES ON PHARMACEUTICALS." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50006-4.

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8

"STRUCTURES." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50007-6.

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9

"aminosulfonylbenzene compounds." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50008-8.

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10

"pyridinylbenzene compounds." In 4–Aminobenzenesulfonamides. Elsevier, 1989. http://dx.doi.org/10.1016/b978-0-08-034710-3.50009-x.

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