49 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
26498394	105	Inhibition of mammalian carbonic anhydrase isoforms I-XIV with a series of phenolic acid esters.	Universit£
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
23490152	15	Structural effect of phenyl ring compared to thiadiazole based adamantyl-sulfonamides on carbonic anhydrase inhibition.	University of Florida
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£
22487176	109	Flavones and structurally related 4-chromenones inhibit carbonic anhydrases by a different mechanism of action compared to coumarins.	Universit£
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
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
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£
19186056	60	A thiabendazole sulfonamide shows potent inhibitory activity against mammalian and nematode alpha-carbonic anhydrases.	Universit£
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£
17826101	41	Carbonic anhydrase inhibitors: cloning, characterization, and inhibition studies of the cytosolic isozyme III with sulfonamides.	Kochi Medical School
17228881	141	Carbonic anhydrase inhibitors. DNA cloning, characterization, and inhibition studies of the human secretory isoform VI, a new target for sulfonamide and sulfamate inhibitors.	Kochi Medical School
15686895	112	Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides.	Universit£
16039848	93	Carbonic anhydrase inhibitors: inhibition of the transmembrane isozyme XIV with sulfonamides.	Kochi Medical School
22365761	144	New chemotypes acting as isozyme-selective carbonic anhydrase inhibitors with low affinity for the offtarget cytosolic isoform II.	Universit£
22277279	9	Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors.	Istituto Di Biostrutture E Bioimmagini-Cnr
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
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
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
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
30553625	761	Pyrrolidinone-bearing methylated and halogenated benzenesulfonamides as inhibitors of carbonic anhydrases.	Kaunas University of Technology
26525863	71	Anion and sulfonamide inhibition studies of an ?-carbonic anhydrase from the Antarctic hemoglobinless fish Chionodraco hamatus.	Universit£
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£
30344913	24	Famotidine, an Antiulcer Agent, Strongly Inhibits	University of Florence
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
28277280	43	Bortezomib inhibits mammalian carbonic anhydrases.	Universit£
10945872	14	Pharmacological actions of a novel, high-affinity, and selective human dopamine D(3) receptor antagonist, SB-277011-A.	Smithkline Beecham Pharmaceuticals
7815325	65	Cloning and pharmacological characterization of human alpha-1 adrenergic receptors: sequence corrections and direct comparison with other species homologues.	Duke University
3130534	3	7-[3-(4-[2,3-Dimethylphenyl]piperazinyl)propoxy]-2(1H)-quinolinone (OPC-4392), a presynaptic dopamine autoreceptor agonist and postsynaptic D2 receptor antagonist.	Tokushima Research Institute
2664084	17	Detection of a novel serotonin receptor subtype (5-HT1E) in human brain: interaction with a GTP-binding protein.	Albany Medical College
2547939	11	Characterization of the striatal M2 muscarinic receptor mediating inhibition of cyclic AMP using selective antagonists: a comparison with the brainstem M2 receptor.	Abbott Laboratories
2537406	2	Pharmacological characterization of the M1 muscarinic receptors expressed in murine fibroblast B82 cells.	University of Arizona