159 articles for thisTarget

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PMID	Data	Article Title	Organization
28256371	83	Synthesis of bulky-tailed sulfonamides incorporating pyrido[2,3-d][1,2,4]triazolo[4,3-a]pyrimidin-1(5H)-yl) moieties and evaluation of their carbonic anhydrases I, II, IV and IX inhibitory effects.	University of Wollongong
28161252	64	Synthesis and biological evaluation of cyclic imides incorporating benzenesulfonamide moieties as carbonic anhydrase I, II, IV and IX inhibitors.	King Saud University
28237553	76	Human carbonic anhydrase inhibitory profile of mono- and bis-sulfonamides synthesized via a direct sulfochlorination of 3- and 4-(hetero)arylisoxazol-5-amine scaffolds.	Saint Petersburg State University
28109946	84	Novel indolin-2-one-based sulfonamides as carbonic anhydrase inhibitors: Synthesis, in vitro biological evaluation against carbonic anhydrases isoforms I, II, IV and VII and molecular docking studies.	Kafrelsheikh University
28075587	102	Design and Synthesis of Novel Nonsteroidal Anti-Inflammatory Drugs and Carbonic Anhydrase Inhibitors Hybrids (NSAIDs-CAIs) for the Treatment of Rheumatoid Arthritis.	University of Florence
12565948	120	Modelling of carbonic anhydrase inhibitory activity of sulfonamides using molecular negentropy.	A.P.S. University
28111158	100	Synthesis of isoxazole-containing sulfonamides with potent carbonic anhydrase II and VII inhibitory properties.	Abant Izzet Baysal University
27919611	60	Discovery of 4-sulfamoyl-phenyl-ß-lactams as a new class of potent carbonic anhydrase isoforms I, II, IV and VII inhibitors: The first example of subnanomolar CA IV inhibitors.	National Institute of Pharmaceutical Education and Research (NIPER)
27876475	68	Microwave assisted synthesis of novel tetrazole/sulfonamide derivatives based on octahydroacridine, xanthene and chromene skeletons as inhibitors of the carbonic anhydrases isoforms I, II, IV and VII.	Dumlupinar University
27144971	60	PEGylated Bis-Sulfonamide Carbonic Anhydrase Inhibitors Can Efficiently Control the Growth of Several Carbonic Anhydrase IX-Expressing Carcinomas.	Temple University
27172398	20	An Unusual Natural Product Primary Sulfonamide: Synthesis, Carbonic Anhydrase Inhibition, and Protein X-ray Structures of Psammaplin C.	Griffith University
27298005	92	Microwave assisted synthesis of novel acridine-acetazolamide conjugates and investigation of their inhibition effects on human carbonic anhydrase isoforms hCA I, II, IV and VII.	Dumlupinar University
26498394	105	Inhibition of mammalian carbonic anhydrase isoforms I-XIV with a series of phenolic acid esters.	Universit£
26498393	116	New natural product carbonic anhydrase inhibitors incorporating phenol moieties.	Aristotle University of Thessaloniki
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
24689792	54	Cyclic secondary sulfonamides: unusually good inhibitors of cancer-related carbonic anhydrase enzymes.	Griffith University
23010455	108	Synthesis of C-cinnamoyl glycosides and their inhibitory activity against mammalian carbonic anhydrases.	Universidad Nacional De La Plata
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£
22687439	51	Synthesis and carbonic anhydrase inhibitory properties of novel bromophenols and their derivatives including natural products: vidalol B.	Atat£Rk University
22487176	109	Flavones and structurally related 4-chromenones inhibit carbonic anhydrases by a different mechanism of action compared to coumarins.	Universit£
21211980	47	Characterization and anions inhibition studies of ana-carbonic anhydrase from the teleost fish Dicentrarchus labrax.	Ondokuz Mayis 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
20472429	80	Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron-containing aromatic sulfamide with mammalian isoforms I-XV.	Istituto Di Biostrutture E Bioimmagini-Cnr
20363633	67	Thioether benzenesulfonamide inhibitors of carbonic anhydrases II and IV: structure-based drug design, synthesis, and biological evaluation.	Pfizer
20185318	132	Carbonic anhydrase inhibitors. Inhibition of mammalian isoforms I-XIV with a series of natural product polyphenols and phenolic acids.	Universit£
19911821	273	Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins.	Universita Degli Studi Di Firenze
19854054	18	Nitric oxide-donating carbonic anhydrase inhibitors for the treatment of open-angle glaucoma.	Nicox Research Institute
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£
19269822	75	Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I, II, III, VII and XIII with less investigated inorganic anions.	Universit£
19186056	60	A thiabendazole sulfonamide shows potent inhibitory activity against mammalian and nematode alpha-carbonic anhydrases.	Universit£
18990571	65	Carbonic anhydrase inhibitors: 2-substituted-1,3,4-thiadiazole-5-sulfamides act as powerful and selective inhibitors of the mitochondrial isozymes VA and VB over the cytosolic and membrane-associated carbonic anhydrases I, II and IV.	Ecole Nationale Sup£Rieure De Chimie De Montpellier
18359629	84	Carbonic anhydrase inhibitors: the X-ray crystal structure of ethoxzolamide complexed to human isoform II reveals the importance of thr200 and gln92 for obtaining tight-binding inhibitors.	Istituto Di Biostrutture E Bioimmagini-Cnr
17475500	130	Carbonic anhydrases as targets for medicinal chemistry.	Universit£
17376683	63	Carbonic anhydrase inhibitors. Inhibition of isoforms I, II, IV, VA, VII, IX, and XIV with sulfonamides incorporating fructopyranose-thioureido tails.	Ecole Nationale Sup£Rieure De Chimie De Montpellier
17314045	11	Phosph(on)ate as a zinc-binding group in metalloenzyme inhibitors: X-ray crystal structure of the antiviral drug foscarnet complexed to human carbonic anhydrase I.	Universit£
16290146	30	Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II"selective" inhibitor celecoxib.	Istituto Di Biostrutture E Bioimmagini-Cnr
15686931	84	Carbonic anhydrase inhibitors. Inhibition of the membrane-bound human and bovine isozymes IV with sulfonamides.	Universit£
15664814	55	Carbonic anhydrase inhibitors. Inhibition of isozymes I, II, IV, V, and IX with anions isosteric and isoelectronic with sulfate, nitrate, and carbonate.	Universit£
15501038	68	Carbonic anhydrase inhibitors: inhibition of the membrane-bound human isozyme IV with anions.	Universit£
15357993	82	Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the methanoarchaeon Methanobacterium thermoautotrophicum (Cab) with anions.	Universit£
15139757	105	Carbonic anhydrase inhibitors: synthesis and topical intraocular pressure lowering effects of fluorine-containing inhibitors devoid of enhanced reactivity.	Universit£
11906288	713	Carbonic anhydrase inhibitors. A general approach for the preparation of water-soluble sulfonamides incorporating polyamino-polycarboxylate tails and of their metal complexes possessing long-lasting, topical intraocular pressure-lowering properties.	Universit£
11784136	100	Carbonic anhydrase inhibitors: anticonvulsant sulfonamides incorporating valproyl and other lipophilic moieties.	University of Namur
11123998	141	Carbonic anhydrase inhibitors: water-soluble 4-sulfamoylphenylthioureas as topical intraocular pressure-lowering agents with long-lasting effects.	Universit£
11087579	465	Carbonic anhydrase inhibitors: perfluoroalkyl/aryl-substituted derivatives of aromatic/heterocyclic sulfonamides as topical intraocular pressure-lowering agents with prolonged duration of action.	Universit£
10479300	383	Carbonic anhydrase inhibitors: synthesis of water-soluble, aminoacyl/dipeptidyl sulfonamides possessing long-lasting intraocular pressure-lowering properties via the topical route.	Universit£
10411484	176	Carbonic anhydrase inhibitors. Synthesis of water-soluble, topically effective, intraocular pressure-lowering aromatic/heterocyclic sulfonamides containing cationic or anionic moieties: is the tail more important than the ring?	Universit£
15012984	192	Carbonic anhydrase inhibitors: the first selective, membrane-impermeant inhibitors targeting the tumor-associated isozyme IX.	Slovak Academy of Sciences
14698154	26	Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with the antipsychotic drug sulpiride.	Bruker-Axs
14684331	24	Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX.	Universit£
12643899	127	Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozyme IX with aromatic and heterocyclic sulfonamides.	Universit£
12617904	46	Carbonic anhydrase inhibitors: SAR and X-ray crystallographic study for the interaction of sugar sulfamates/sulfamides with isozymes I, II and IV.	Universit£
14611846	101	Carbonic anhydrase inhibitors: topically acting antiglaucoma sulfonamides incorporating esters and amides of 3- and 4-carboxybenzolamide.	Universit£
12039560	377	Carbonic anhydrase inhibitors. Preparation of potent sulfonamides inhibitors incorporating bile acid tails.	Universit£
11229775	204	Carbonic anhydrase inhibitors: synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma properties.	Universit£
11425561	197	Carbonic anhydrase inhibitors: 4-sulfamoyl-benzenecarboxamides and 4-chloro-3-sulfamoyl-benzenecarboxamides with strong topical antiglaucoma properties.	Universit£
10762051	66	Carbonic anhydrase inhibitors: topical sulfonamide antiglaucoma agents incorporating secondary amine moieties.	Universit£
10843231	129	Carbonic anhydrase inhibitors: synthesis of N-morpholylthiocarbonylsulfenylamino aromatic/heterocyclic sulfonamides and their interaction with isozymes I, II and IV.	Universit£
22365761	144	New chemotypes acting as isozyme-selective carbonic anhydrase inhibitors with low affinity for the offtarget cytosolic isoform II.	Universit£
22245047	135	Structure-activity relationships for the interaction of 5,10-dihydroindeno[1,2-b]indole derivatives with human and bovine carbonic anhydrase isoforms I, II, III, IV and VI.	Ondokuz Mayis University
22230050	82	Synthesis and carbonic anhydrase inhibitory properties of novel cyclohexanonyl bromophenol derivatives.	Artvin£Oruh University
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£
21549597	71	Synthesis and crystallographic analysis of new sulfonamides incorporating NO-donating moieties with potent antiglaucoma action.	U.O. Oculistica Az. Usl 3
21377369	60	Purification and inhibition studies with anions and sulfonamides of ana-carbonic anhydrase from the Antarctic seal Leptonychotes weddellii.	Universit£
20590092	273	Polyamines inhibit carbonic anhydrases by anchoring to the zinc-coordinated water molecule.	Universita Degli Studi Di Firenze
19527930	53	The protein tyrosine kinase inhibitors imatinib and nilotinib strongly inhibit several mammalian alpha-carbonic anhydrase isoforms.	University of Tampere and Tampere University Hospital
19121582	15	Carbonic anhydrase inhibitors: inhibition studies of a coral secretory isoform with inorganic anions.	Centre Scientifique De Monaco
16759856	9	N-hydroxyurea--a versatile zinc binding function in the design of metalloenzyme inhibitors.	Università
15780631	55	Carbonic anhydrase inhibitors. Inhibition of isozymes I, II, IV, V and IX with complex fluorides, chlorides and cyanides.	Università
15745821	21	Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with organic phosphates and phosphonates.	University of Montpellier
15664815	45	Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with carboxylates.	Università
15501037	27	Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with phosphates, carbamoyl phosphate, and the phosphonate antiviral drug foscarnet.	Università
15081040	4	Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with a topically acting antiglaucoma sulfonamide.	Bruker-Axs
12873509	4	Carbonic anhydrase inhibitors: X-ray crystallographic structure of the adduct of human isozyme II with a bis-sulfonamide-two heads are better than one?	Università
32519851	164	Sulfonamide Inhibitors of Human Carbonic Anhydrases Designed through a Three-Tails Approach: Improving Ligand/Isoform Matching and Selectivity of Action.	University of Firenze
32435377	30	Glycomimetic Based Approach toward Selective Carbonic Anhydrase Inhibitors.	Universit£
30996772	55	-Nitrosulfonamides as Carbonic Anhydrase Inhibitors: A Promising Chemotype for Targeting Chagas Disease and Leishmaniasis.	University of Florence
10649985	390	Carbonic anhydrase inhibitors: synthesis of membrane-impermeant low molecular weight sulfonamides possessing in vivo selectivity for the membrane-bound versus cytosolic isozymes.	Università
32364386	184	Phenyl(thio)phosphon(amid)ate Benzenesulfonamides as Potent and Selective Inhibitors of Human Carbonic Anhydrases II and VII Counteract Allodynia in a Mouse Model of Oxaliplatin-Induced Neuropathy.	University of Florence
32031797	96	Discovery of Potent Dual-Tailed Benzenesulfonamide Inhibitors of Human Carbonic Anhydrases Implicated in Glaucoma and in Vivo Profiling of Their Intraocular Pressure-Lowering Action.	University of Wollongong
31255926	46	Sulfamates in drug design and discovery: Pre-clinical and clinical investigations.	University of Sharjah
31794211	138	"A Sweet Combination": Developing Saccharin and Acesulfame K Structures for Selectively Targeting the Tumor-Associated Carbonic Anhydrases IX and XII.	University of Florence
31515057	20	Highly hydrophilic 1,3-oxazol-5-yl benzenesulfonamide inhibitors of carbonic anhydrase II for reduction of glaucoma-related intraocular pressure.	Saint Petersburg State University
31476557	164	From random to rational: A discovery approach to selective subnanomolar inhibitors of human carbonic anhydrase IV based on the Castagnoli-Cushman multicomponent reaction.	Saint Petersburg State University
31401537	45	Synthesis of novel tellurides bearing benzensulfonamide moiety as carbonic anhydrase inhibitors with antitumor activity.	University of Florence
31287314	52	Synthesis and Evaluation of Carbonic Anhydrase Inhibitors with Carbon Monoxide Releasing Properties for the Management of Rheumatoid Arthritis.	Universit£
31136893	176	Benzensulfonamides bearing spyrohydantoin moieties act as potent inhibitors of human carbonic anhydrases II and VII and show neuropathic pain attenuating effects.	University of Florence
31740053	1887	Halogenated and di-substituted benzenesulfonamides as selective inhibitors of carbonic anhydrase isoforms.	Vilnius University
31539777	92	Continued exploration and tail approach synthesis of benzenesulfonamides containing triazole and dual triazole moieties as carbonic anhydrase I, II, IV and IX inhibitors.	Kurukshetra University
30553625	761	Pyrrolidinone-bearing methylated and halogenated benzenesulfonamides as inhibitors of carbonic anhydrases.	Kaunas University of Technology
31413806	65	Bis-benzoxaboroles: Design, Synthesis, and Biological Evaluation as Carbonic Anhydrase Inhibitors.	Universit£
26678172	70	Inhibition of carbonic anhydrase isoforms I, II, IV, VII and XII with carboxylates and sulfonamides incorporating phthalimide/phthalic anhydride scaffolds.	King Saud University
24300919	55	Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studies.	Universit£
24103430	78	Inhibition of human carbonic anhydrase isoforms I-XIV with sulfonamides incorporating fluorine and 1,3,5-triazine moieties.	Universit£
30496988	25	Pharmaceutical and medicinal significance of sulfur (S	Wuhan University of Technology
16458003	158	QSAR study on topically acting sulfonamides incorporating GABA moieties: a molecular connectivity approach.	A.P.S. University
11831900	8	Structural aspects of isozyme selectivity in the binding of inhibitors to carbonic anhydrases II and IV.	University of Pennsylvania
30193219	114	Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity.	Department of University of Florence
30344913	24	Famotidine, an Antiulcer Agent, Strongly Inhibits	University of Florence
29685656	8	Synthesis, structure and bioactivity of primary sulfamate-containing natural products.	Griffith University
29571155	124	Synthesis of novel 4-functionalized 1,5-diaryl-1,2,3-triazoles containing benzenesulfonamide moiety as carbonic anhydrase I, II, IV and IX inhibitors.	Kurukshetra University
28947945	72	Discovery of New Selenoureido Analogues of 4-(4-Fluorophenylureido)benzenesulfonamide as Carbonic Anhydrase Inhibitors.	University of Florence
28802125	92	Novel 4/3-((4-oxo-5-(2-oxoindolin-3-ylidene)thiazolidin-2-ylidene)amino) benzenesulfonamides: Synthesis, carbonic anhydrase inhibitory activity, anticancer activity and molecular modelling studies.	Kafrelsheikh University
29746127	195	Discovery of Novel Nonsteroidal Anti-Inflammatory Drugs and Carbonic Anhydrase Inhibitors Hybrids (NSAIDs-CAIs) for the Management of Rheumatoid Arthritis.	Ege University Bornova
29305297	480	Benzimidazole design, synthesis, and docking to build selective carbonic anhydrase VA inhibitors.	Vilnius University
30006175	644	Design of two-tail compounds with rotationally fixed benzenesulfonamide ring as inhibitors of carbonic anhydrases.	Vilnius University
29909339	84	Design and synthesis of novel benzenesulfonamide containing 1,2,3-triazoles as potent human carbonic anhydrase isoforms I, II, IV and IX inhibitors.	Kurukshetra University
29684705	72	Dual-tail arylsulfone-based benzenesulfonamides differently match the hydrophobic and hydrophilic halves of human carbonic anhydrases active sites: Selective inhibitors for the tumor-associated hCA IX isoform.	Egyptian Russian University
29635168	140	2-Benzylpiperazine: A new scaffold for potent human carbonic anhydrase inhibitors. Synthesis, enzyme inhibition, enantioselectivity, computational and crystallographic studies and in vivo activity for a new class of intraocular pressure lowering agents.	University of Florence
29912561	40	4-Substituted Benzenesulfonamides Incorporating Bi/Tricyclic Moieties Act as Potent and Isoform-Selective Carbonic Anhydrase II/IX Inhibitors.	Universit£
29259736	70	Synthesis of Novel Selenides Bearing Benzenesulfonamide Moieties as Carbonic Anhydrase I, II, IV, VII, and IX Inhibitors.	University of Florence
29259754	76	Discovery of New Sulfonamide Carbonic Anhydrase IX Inhibitors Incorporating Nitrogenous Bases.	University of Florence
29057059	82	Lucky Switcheroo: Dramatic Potency and Selectivity Improvement of Imidazoline Inhibitors of Human Carbonic Anhydrase VII.	Saint Petersburg State University
28277280	43	Bortezomib inhibits mammalian carbonic anhydrases.	Universit£
28302505	120	Evaluation of selenide, diselenide and selenoheterocycle derivatives as carbonic anhydrase I, II, IV, VII and IX inhibitors.	Universit£
23914927	24	Inhibition of mammalian carbonic anhydrases I-XIV with grayanotoxin III: solution and in silico studies.	University of Calgary
22299585	46	Analysis of saponins and phenolic compounds as inhibitors of a-carbonic anhydrase isoenzymes.	Ege University
22299576	44	Metronidazole-coumarin conjugates and 3-cyano-7-hydroxy-coumarin act as isoform-selective carbonic anhydrase inhibitors.	Ecole Nationale Superieure De Chimie De Montpellier
22299577	12	Three new aromatic sulfonamide inhibitors of carbonic anhydrases I, II, IV and XII.	Universit?? Di Firenze
22168126	43	Carbonic anhydrase inhibitors: in vitro inhibition of a isoforms (hCA I, hCA II, bCA III, hCA IV) by flavonoids.	Ondokuz Mayis University
22145694	64	Simple methanesulfonates are hydrolyzed by the sulfatase carbonic anhydrase activity.	Agri Ibrahim Cecen University
22050606	36	a-Carbonic anhydrases are sulfatases with cyclic diol monosulfate esters.	Dumlupinar University
15499999	35	Benzolamide is not a membrane-impermeant carbonic anhydrase inhibitor.	UniversitÀ Degli Studi Di Firenze
11916140	21	Carbonic anhydrase activity modulators: synthesis of inhibitors and activators incorporating 2-substituted-thiazol-4-yl-methyl scaffolds.	UniversitÀ
19703035	60	Which carbonic anhydrases are targeted by the antiepileptic sulfonamides and sulfamates?	Istituto Di Biostrutture E Bioimmagini-Cnr
19731956	72	Carbonic anhydrase inhibitors. Comparison of aliphatic sulfamate/bis-sulfamate adducts with isozymes II and IX as a platform for designing tight-binding, more isoform-selective inhibitors.	Cnr
19119014	12	Carbonic anhydrase inhibitors. Comparison of chlorthalidone, indapamide, trichloromethiazide, and furosemide X-ray crystal structures in adducts with isozyme II, when several water molecules make the difference.	Universita Degli Studi Di Firenze
19128966	80	Carbonic anhydrase inhibitors: the membrane-associated isoform XV is highly inhibited by inorganic anions.	Universita Degli Studi Di Firenze
18579385	132	Carbonic anhydrase inhibitors: inhibition of mammalian isoforms I-XIV with a series of substituted phenols including paracetamol and salicylic acid.	Universita Degli Studi Di Firenze
18819811	195	Carbonic anhydrase inhibitors: synthesis and inhibition studies against mammalian isoforms I-XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides.	Istanbul University
18374572	100	Carbonic anhydrase inhibitors. Interaction of indapamide and related diuretics with 12 mammalian isozymes and X-ray crystallographic studies for the indapamide-isozyme II adduct.	Universita Degli Studi Di Firenze
18640037	48	Carbonic anhydrase inhibitors. Interaction of the antitumor sulfamate EMD 486019 with twelve mammalian carbonic anhydrase isoforms: Kinetic and X-ray crystallographic studies.	Universita Degli Studi Di Firenze
14971907	180	Carbonic anhydrase inhibitors. Inhibition of mitochondrial isozyme V with aromatic and heterocyclic sulfonamides.	Universita Degli Studi Di Firenze
15084132	88	Carbonic anhydrase inhibitors. Design of selective, membrane-impermeant inhibitors targeting the human tumor-associated isozyme IX.	Canadian Institutes of Health Research
14736236	20	Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognition.	University of Marburg
17125255	77	Carbonic anhydrase inhibitors: clash with Ala65 as a means for designing inhibitors with low affinity for the ubiquitous isozyme II, exemplified by the crystal structure of the topiramate sulfamide analogue.	Universite Montpellier Ii
12747790	171	Carbonic anhydrase inhibitors. Inhibition of tumor-associated isozyme IX by halogenosulfanilamide and halogenophenylaminobenzolamide derivatives.	University of Agricultural Sciences and Veterinary Medicine
10882008	93	2H-Thieno[3,2-e]- and [2,3-e]-1,2-thiazine-6-sulfonamide 1,1-dioxides as ocular hypotensive agents: synthesis, carbonic anhydrase inhibition and evaluation in the rabbit.	Alcon Research
11020282	512	Carbonic anhydrase and matrix metalloproteinase inhibitors: sulfonylated amino acid hydroxamates with MMP inhibitory properties act as efficient inhibitors of CA isozymes I, II, and IV, and N-hydroxysulfonamides inhibit both these zinc enzymes.	Universita Degli Studi