28 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
27172398	20	An Unusual Natural Product Primary Sulfonamide: Synthesis, Carbonic Anhydrase Inhibition, and Protein X-ray Structures of Psammaplin C.	Griffith University
26805033	426	Kinetically Selective Inhibitors of Human Carbonic Anhydrase Isozymes I, II, VII, IX, XII, and XIII.	Uppsala University
26347950	32	Phosphate Chemical Probes Designed for Location Specific Inhibition of Intracellular Carbonic Anhydrases.	Griffith University
25468040	77	Inhibition studies of new ureido-substituted sulfonamides incorporating a GABA moiety against human carbonic anhydrase isoforms I-XIV.	TBA
25358084	143	Discovery and characterization of novel selective inhibitors of carbonic anhydrase IX.	Vilnius University
25245672	5	Substituted thieno[2,3-b]thiophenes and related congeners: Synthesis,ß-glucuronidase inhibition activity, crystal structure, and POM analyses.	King Saud University
23394791	177	4-Substituted-2,3,5,6-tetrafluorobenzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, XII, and XIII.	Vilnius University Institute Of Biotechnology
23010455	108	Synthesis of C-cinnamoyl glycosides and their inhibitory activity against mammalian carbonic anhydrases.	Universidad Nacional De La Plata
22892213	168	Natural product coumarins that inhibit human carbonic anhydrases.	Griffith University
23067387	105	Tricyclic sulfonamides incorporating benzothiopyrano[4,3-c]pyrazole and pyridothiopyrano[4,3-c]pyrazole effectively inhibita- andß-carbonic anhydrase: X-ray crystallography and solution investigations on 15 isoforms.	Universit£
22487176	109	Flavones and structurally related 4-chromenones inhibit carbonic anhydrases by a different mechanism of action compared to coumarins.	Universit£
22440859	176	Design of [(2-pyrimidinylthio)acetyl]benzenesulfonamides as inhibitors of human carbonic anhydrases.	Vilnius University
20674354	79	Carbonic anhydrase inhibitors. Antioxidant polyphenols effectively inhibit mammalian isoforms I-XV.	Universit£
20605094	91	Carbonic anhydrase inhibitors. The X-ray crystal structure of human isoform II in adduct with an adamantyl analogue of acetazolamide resides in a less utilized binding pocket than most hydrophobic inhibitors.	University Of Florida
20028100	78	The coumarin-binding site in carbonic anhydrase accommodates structurally diverse inhibitors: the antiepileptic lacosamide as an example and lead molecule for novel classes of carbonic anhydrase inhibitors.	Universit£
22365761	144	New chemotypes acting as isozyme-selective carbonic anhydrase inhibitors with low affinity for the offtarget cytosolic isoform II.	Universit£
21821413	65	Synthesis of rhodamine B-benzenesulfonamide conjugates and their inhibitory activity against humana- and bacterial/fungalß-carbonic anhydrases.	Ecole Nationale Sup£Rieure De Chimie De Montpellier
21515057	153	Sulfonamides incorporating 1,3,5-triazine moieties selectively and potently inhibit carbonic anhydrase transmembrane isoforms IX, XII and XIV over cytosolic isoforms I and II: Solution and X-ray crystallographic studies.	Universit£
21620713	25	Conformational variability of different sulfonamide inhibitors with thienyl-acetamido moieties attributes to differential binding in the active site of cytosolic human carbonic anhydrase isoforms.	University Of Florida
20926301	77	Indapamide-like benzenesulfonamides as inhibitors of carbonic anhydrases I, II, VII, and XIII.	Institute Of Biotechnology
20889345	94	4-[N-(substituted 4-pyrimidinyl)amino]benzenesulfonamides as inhibitors of carbonic anhydrase isozymes I, II, VII, and XIII.	Vilnius University
21679053	22	Acetaldehyde-derived modifications on cytosolic human carbonic anhydrases.	University Of Tampere And Tampere University Hospital
26773755	20	Synthesis and tyrosinase inhibition activity of trans-stilbene derivatives.	Indian Institute Of Integrative Medicine