24 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£
23685174	6	Natural product hybrid and its superacid synthesized analogues: dodoneine and its derivatives show selective inhibition of carbonic anhydrase isoforms I, III, XIII and XIV.	Superacid Group In Organic Synthesis Team-Universit£
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
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£
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£
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£
15686895	112	Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides.	Universit£
15454240	57	Carbonic anhydrase inhibitors. Inhibition of the newly isolated murine isozyme XIII with anions.	Universit£
15203157	68	Carbonic anhydrase inhibitors. Inhibition of cytosolic isozyme XIII with aromatic and heterocyclic sulfonamides: a novel target for the drug design.	University Of Tampere
20833546	6	Paraoxon, 4-nitrophenyl phosphate and acetate are substrates ofa- but not ofß-,¿- and¿-carbonic anhydrases.	Università
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
18353640	6	Investigations of the esterase, phosphatase, and sulfatase activities of the cytosolic mammalian carbonic anhydrase isoforms I, II, and XIII with 4-nitrophenyl esters as substrates.	Universita Degli Studi Di Firenze
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
19900813	12	Optimization of (4,4-difluoro-1,2,3,4-tetrahydro-5H-1-benzazepine-5-ylidene)acetamide derivatives as arginine vasopressin V2 receptor agonists and discussion of their binding modes.	Astellas Pharma