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Synthesis, characterization and antiglaucoma activity of some novel pyrazole derivatives of 5-amino-1,3,4-thiadiazole-2-sulfonamide

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dc.creator Kasimogullari, Rahmi
dc.creator Bulbul, Metin
dc.creator Arslan, B. Seckin
dc.creator Gokce, Başak
dc.date 2010-10-31T22:00:00Z
dc.date.accessioned 2020-10-06T10:49:50Z
dc.date.available 2020-10-06T10:49:50Z
dc.identifier 99d4b335-6322-456b-80eb-61386dd228d2
dc.identifier 10.1016/j.ejmech.2010.07.041
dc.identifier https://avesis.sdu.edu.tr/publication/details/99d4b335-6322-456b-80eb-61386dd228d2/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/67229
dc.description Pyrazole carboxylic acid derivatives of 5-amino-1,3,4-thiadiazole-2-sulfonamide (inhibitor 1) were synthesized from ethyl 3-(chlorocarbonyl)-1-(3-nitrophenyl)-5-phenyl-1H-pyrazole-4-carboxylate compound. The inhibitory effects of inhibitor 1, acetazolamide (AAZ) and of 11 newly synthesized amides (5a-b, 6, 7a-g, and 8) on hydratase and esterase activities of carbonic anhydrase isoenzymes (hCA-I and hCA-II) have been studied in vitro. The comparison of newly synthesized amides to inhibitor 1 and to AAZ indicated that the new derivatives inhibit CA isoenzymes and they are more potent inhibitors than the parent inhibitor 1 and AAZ. (C) 2010 Elsevier Masson SAS. All rights reserved.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Synthesis, characterization and antiglaucoma activity of some novel pyrazole derivatives of 5-amino-1,3,4-thiadiazole-2-sulfonamide
dc.type info:eu-repo/semantics/article


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