72 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 34358123 | Synthesis and Human Carbonic Anhydrase I, II, IX, and XII Inhibition Studies of Sulphonamides Incorporating Mono-, Bi- and Tricyclic Imide Moieties. | 2021 Jul 19 | 1 |
2 | 31718943 | Synthesis, biological and molecular dynamics investigations with a series of triazolopyrimidine/triazole-based benzenesulfonamides as novel carbonic anhydrase inhibitors. | 2020 Jan 1 | 3 |
3 | 31813300 | Novel sulphonamides incorporating triazene moieties show powerful carbonic anhydrase I and II inhibitory properties. | 2020 Dec | 1 |
4 | 31914827 | Synthesis and human carbonic anhydrase I, II, VA, and XII inhibition with novel amino acid-sulphonamide conjugates. | 2020 Dec | 2 |
5 | 32058104 | Synthesis, structure elucidation, and in vitro pharmacological evaluation of novel polyfluoro substituted pyrazoline type sulfonamides as multi-target agents for inhibition of acetylcholinesterase and carbonic anhydrase I and II enzymes. | 2020 Mar | 2 |
6 | 32748253 | Evaluation of some thiophene-based sulfonamides as potent inhibitors of carbonic anhydrase I and II isoenzymes isolated from human erythrocytes by kinetic and molecular modelling studies. | 2020 Dec | 2 |
7 | 32891000 | Pyridinium derivatives of 3-aminobenzenesulfonamide are nanomolar-potent inhibitors of tumor-expressed carbonic anhydrase isozymes CA IX and CA XII. | 2020 Oct | 1 |
8 | 32926233 | Native mass spectrometry of human carbonic anhydrase I and its inhibitor complexes. | 2020 Oct | 2 |
9 | 30312867 | 3-Aminobenzenesulfonamides incorporating acylthiourea moieties selectively inhibit the tumor-associated carbonic anhydrase isoform IX over the off-target isoforms I, II and IV. | 2019 Feb | 1 |
10 | 30594030 | Continued exploration of 1,2,4-oxadiazole periphery for carbonic anhydrase-targeting primary arene sulfonamides: Discovery of subnanomolar inhibitors of membrane-bound hCA IX isoform that selectively kill cancer cells in hypoxic environment. | 2019 Feb 15 | 1 |
11 | 30811749 | Investigation of the effects of some sulfonamides on acetylcholinesterase and carbonic anhydrase enzymes. | 2019 May | 1 |
12 | 30978604 | Novel synthesized SLC-0111 thiazole and thiadiazole analogues: Determination of their carbonic anhydrase inhibitory activity and molecular modeling studies. | 2019 Jun | 1 |
13 | 31374520 | Sulfonamides incorporating piperazine bioisosteres as potent human carbonic anhydrase I, II, IV and IX inhibitors. | 2019 Oct | 1 |
14 | 31419777 | Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells. | 2019 Nov 15 | 1 |
15 | 31515058 | Synthesis and exploration of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives for their effects against carbonic anhydrase I, II, IX and XII isoforms as a non-sulfonamide class of inhibitors. | 2019 Nov 1 | 2 |
16 | 29271264 | Inhibition studies of Brucella suis β-carbonic anhydrases with a series of 4-substituted pyridine-3-sulphonamides. | 2018 Dec | 1 |
17 | 29324250 | Novel sulfonamide incorporating piperazine, aminoalcohol and 1,3,5-triazine structural motifs with carbonic anhydrase I, II and IX inhibitory action. | 2018 Apr | 1 |
18 | 28024887 | 5-Substituted-benzylsulfanyl-thiophene-2-sulfonamides with effective carbonic anhydrase inhibitory activity: Solution and crystallographic investigations. | 2017 Feb 1 | 1 |
19 | 28161252 | Synthesis and biological evaluation of cyclic imides incorporating benzenesulfonamide moieties as carbonic anhydrase I, II, IV and IX inhibitors. | 2017 Mar 1 | 2 |
20 | 28256371 | 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. | 2017 Apr 1 | 1 |
21 | 28318894 | Synthesis and human/bacterial carbonic anhydrase inhibition with a series of sulfonamides incorporating phthalimido moieties. | 2017 Apr 15 | 1 |
22 | 28802125 | 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. | 2017 Oct 20 | 1 |
23 | 26741028 | 4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic Studies. | 2016 Jan 28 | 1 |
24 | 26744900 | Synthesis and evaluation of sulfonamide-bearing thiazole as carbonic anhydrase isoforms hCA I and hCA II. | 2016 Dec | 2 |
25 | 27234893 | Synthesis of 4-(thiazol-2-ylamino)-benzenesulfonamides with carbonic anhydrase I, II and IX inhibitory activity and cytotoxic effects against breast cancer cell lines. | 2016 Jul 1 | 2 |
26 | 27353698 | A class of sulfonamides as carbonic anhydrase I and II inhibitors. | 2016 | 1 |
27 | 27396930 | Synthesis 4-[2-(2-mercapto-4-oxo-4H-quinazolin-3-yl)-ethyl]-benzenesulfonamides with subnanomolar carbonic anhydrase II and XII inhibitory properties. | 2016 Sep 15 | 1 |
28 | 27435177 | Synthesis and carbonic anhydrase inhibitory activities of new thienyl-substituted pyrazoline benzenesulfonamides. | 2016 | 1 |
29 | 24666294 | Inhibition of human carbonic anhydrase isozymes I, II, IX and XII with a new series of sulfonamides incorporating aroylhydrazone-, [1,2,4]triazolo[3,4-b][1,3,4]thiadiazinyl- or 2-(cyanophenylmethylene)-1,3,4-thiadiazol-3(2H)-yl moieties. | 2015 Feb | 1 |
30 | 24758348 | Intrinsic thermodynamics of sulfonamide inhibitor binding to human carbonic anhydrases I and II. | 2015 Apr | 1 |
31 | 25089707 | New series of sulfonamides containing amino acid moiety act as effective and selective inhibitors of tumor-associated carbonic anhydrase XII. | 2015 Jun | 1 |
32 | 25912674 | Synthesis, carbonic anhydrase inhibition and cytotoxic activity of novel chromone-based sulfonamide derivatives. | 2015 | 1 |
33 | 26160114 | Probing the 'bipolar' nature of the carbonic anhydrase active site: aromatic sulfonamides containing 1,3-oxazol-5-yl moiety as picomolar inhibitors of cytosolic CA I and CA II isoforms. | 2015 Aug 28 | 1 |
34 | 26233435 | Synthesis of sulfonamides incorporating piperazinyl-ureido moieties and their carbonic anhydrase I, II, IX and XII inhibitory activity. | 2015 Sep 15 | 1 |
35 | 26276436 | Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms. | 2015 Sep 18 | 1 |
36 | 26639945 | Benzenesulfonamides incorporating bulky aromatic/heterocyclic tails with potent carbonic anhydrase inhibitory activity. | 2015 Dec 15 | 1 |
37 | 24589511 | Synthesis and carbonic anhydrase I, II, IX and XII inhibition studies of 4-N,N-disubstituted sulfanilamides incorporating 4,4,4-trifluoro-3-oxo-but-1-enyl, phenacylthiourea and imidazol-2(3H)-one/thione moieties. | 2014 Apr 1 | 1 |
38 | 25267005 | Inhibition of carbonic anhydrase isoforms I, II, IX and XII with novel Schiff bases: identification of selective inhibitors for the tumor-associated isoforms over the cytosolic ones. | 2014 Nov 1 | 1 |
39 | 22146078 | Docking, CoMFA and CoMSIA studies of a series of sulfonamides derivatives as carbonic anhydrase I inhibitors. | 2013 Apr | 1 |
40 | 23352754 | o-Benzenedisulfonimido-sulfonamides are potent inhibitors of the tumor-associated carbonic anhydrase isoforms CA IX and CA XII. | 2013 Mar 15 | 1 |
41 | 23859774 | 5-Substituted-(1,2,3-triazol-4-yl)thiophene-2-sulfonamides strongly inhibit human carbonic anhydrases I, II, IX and XII: solution and X-ray crystallographic studies. | 2013 Sep 1 | 1 |
42 | 22181786 | Quantum chemical QSAR models to distinguish between inhibitory activities of sulfonamides against human carbonic anhydrases I and II and bovine IV isozymes. | 2012 Apr | 1 |
43 | 22733110 | Polypharmacology of sulfonamides: pazopanib, a multitargeted receptor tyrosine kinase inhibitor in clinical use, potently inhibits several mammalian carbonic anhydrases. | 2012 Aug 25 | 1 |
44 | 23067387 | Tricyclic sulfonamides incorporating benzothiopyrano[4,3-c]pyrazole and pyridothiopyrano[4,3-c]pyrazole effectively inhibit α- and β-carbonic anhydrase: X-ray crystallography and solution investigations on 15 isoforms. | 2012 Nov 26 | 1 |
45 | 21549597 | Synthesis and crystallographic analysis of new sulfonamides incorporating NO-donating moieties with potent antiglaucoma action. | 2011 Jun 1 | 1 |
46 | 20166929 | Drug design studies of the novel antitumor targets carbonic anhydrase IX and XII. | 2010 | 1 |
47 | 20299219 | Carbonic anhydrase inhibitors. The beta-carbonic anhydrases from the fungal pathogens Cryptococcus neoformans and Candida albicans are strongly inhibited by substituted-phenyl-1H-indole-5-sulfonamides. | 2010 Apr 15 | 1 |
48 | 20624682 | Mutation of Phe91 to Asn in human carbonic anhydrase I unexpectedly enhanced both catalytic activity and affinity for sulfonamide inhibitors. | 2010 Aug 1 | 2 |
49 | 19193158 | Cloning, expression, post-translational modifications and inhibition studies on the latest mammalian carbonic anhydrase isoform, CA XV. | 2009 Feb 12 | 1 |
50 | 19201197 | Carbonic anhydrase inhibitors. The nematode alpha-carbonic anhydrase of Caenorhabditis elegans CAH-4b is highly inhibited by 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides. | 2009 Apr 15 | 1 |