These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
128 related articles for article (PubMed ID: 22443141)
1. Synthesis, structure-activity relationship studies, and X-ray crystallographic analysis of arylsulfonamides as potent carbonic anhydrase inhibitors. Gitto R; Damiano FM; Mader P; De Luca L; Ferro S; Supuran CT; Vullo D; Brynda J; Rezáčová P; Chimirri A J Med Chem; 2012 Apr; 55(8):3891-9. PubMed ID: 22443141 [TBL] [Abstract][Full Text] [Related]
2. Carbonic anhydrase inhibitors. Synthesis, molecular structures, and inhibition of the human cytosolic isozymes I and II and transmembrane isozymes IX, XII (cancer-associated) and XIV with novel 3-pyridinesulfonamide derivatives. Brzozowski Z; Sławiński J; Gdaniec M; Innocenti A; Supuran CT Eur J Med Chem; 2011 Sep; 46(9):4403-10. PubMed ID: 21820216 [TBL] [Abstract][Full Text] [Related]
3. Carbonic anhydrase inhibitors. Inhibition of isoforms I, II, IV, VA, VII, IX, and XIV with sulfonamides incorporating fructopyranose-thioureido tails. Winum JY; Thiry A; Cheikh KE; Dogné JM; Montero JL; Vullo D; Scozzafava A; Masereel B; Supuran CT Bioorg Med Chem Lett; 2007 May; 17(10):2685-91. PubMed ID: 17376683 [TBL] [Abstract][Full Text] [Related]
4. Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms. Buemi MR; De Luca L; Ferro S; Bruno E; Ceruso M; Supuran CT; Pospíšilová K; Brynda J; Řezáčová P; Gitto R Eur J Med Chem; 2015 Sep; 102():223-32. PubMed ID: 26276436 [TBL] [Abstract][Full Text] [Related]
5. 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. Carta F; Garaj V; Maresca A; Wagner J; Avvaru BS; Robbins AH; Scozzafava A; McKenna R; Supuran CT Bioorg Med Chem; 2011 May; 19(10):3105-19. PubMed ID: 21515057 [TBL] [Abstract][Full Text] [Related]
6. Identification of 3,4-Dihydroisoquinoline-2(1H)-sulfonamides as potent carbonic anhydrase inhibitors: synthesis, biological evaluation, and enzyme--ligand X-ray studies. Gitto R; Agnello S; Ferro S; De Luca L; Vullo D; Brynda J; Mader P; Supuran CT; Chimirri A J Med Chem; 2010 Mar; 53(6):2401-8. PubMed ID: 20170095 [TBL] [Abstract][Full Text] [Related]
7. 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. Güzel O; Innocenti A; Scozzafava A; Salman A; Parkkila S; Hilvo M; Supuran CT Bioorg Med Chem; 2008 Oct; 16(20):9113-20. PubMed ID: 18819811 [TBL] [Abstract][Full Text] [Related]
8. Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides. Vullo D; Voipio J; Innocenti A; Rivera C; Ranki H; Scozzafava A; Kaila K; Supuran CT Bioorg Med Chem Lett; 2005 Feb; 15(4):971-6. PubMed ID: 15686895 [TBL] [Abstract][Full Text] [Related]
9. Carbonic anhydrase inhibitors: inhibition of isozymes I, II, and IX with triazole-linked O-glycosides of benzene sulfonamides. Wilkinson BL; Bornaghi LF; Houston TA; Innocenti A; Vullo D; Supuran CT; Poulsen SA J Med Chem; 2007 Apr; 50(7):1651-7. PubMed ID: 17343373 [TBL] [Abstract][Full Text] [Related]
10. Carbonic anhydrase inhibitors. Interaction of 2-(hydrazinocarbonyl)-3-phenyl-1H-indole-5-sulfonamide with 12 mammalian isoforms: kinetic and X-ray crystallographic studies. Güzel O; Temperini C; Innocenti A; Scozzafava A; Salman A; Supuran CT Bioorg Med Chem Lett; 2008 Jan; 18(1):152-8. PubMed ID: 18024029 [TBL] [Abstract][Full Text] [Related]
11. Carbonic anhydrase inhibitors. DNA cloning, characterization, and inhibition studies of the human secretory isoform VI, a new target for sulfonamide and sulfamate inhibitors. Nishimori I; Minakuchi T; Onishi S; Vullo D; Scozzafava A; Supuran CT J Med Chem; 2007 Jan; 50(2):381-8. PubMed ID: 17228881 [TBL] [Abstract][Full Text] [Related]
12. Carbonic anhydrase inhibitors: inhibition of human cytosolic isozymes I and II and tumor-associated isozymes IX and XII with S-substituted 4-chloro-2-mercapto-5-methyl-benzenesulfonamides. Saczewski F; Innocenti A; Sławiński J; Kornicka A; Brzozowski Z; Pomarnacka E; Scozzafava A; Temperini C; Supuran CT Bioorg Med Chem; 2008 Apr; 16(7):3933-40. PubMed ID: 18242998 [TBL] [Abstract][Full Text] [Related]
13. Carbonic anhydrase inhibitors. Phenacetyl-, pyridylacetyl- and thienylacetyl-substituted aromatic sulfonamides act as potent and selective isoform VII inhibitors. Güzel O; Innocenti A; Scozzafava A; Salman A; Supuran CT Bioorg Med Chem Lett; 2009 Jun; 19(12):3170-3. PubMed ID: 19435663 [TBL] [Abstract][Full Text] [Related]
14. Inhibition of membrane-associated carbonic anhydrase isozymes IX, XII and XIV with a library of glycoconjugate benzenesulfonamides. Wilkinson BL; Bornaghi LF; Houston TA; Innocenti A; Vullo D; Supuran CT; Poulsen SA Bioorg Med Chem Lett; 2007 Feb; 17(4):987-92. PubMed ID: 17157501 [TBL] [Abstract][Full Text] [Related]
15. 4-[N-(substituted 4-pyrimidinyl)amino]benzenesulfonamides as inhibitors of carbonic anhydrase isozymes I, II, VII, and XIII. Sūdžius J; Baranauskienė L; Golovenko D; Matulienė J; Michailovienė V; Torresan J; Jachno J; Sukackaitė R; Manakova E; Gražulis S; Tumkevičius S; Matulis D Bioorg Med Chem; 2010 Nov; 18(21):7413-21. PubMed ID: 20889345 [TBL] [Abstract][Full Text] [Related]
16. Facile synthesis and characterization of novel pyrazole-sulfonamides and their inhibition effects on human carbonic anhydrase isoenzymes. Balseven H; Mustafa İşgör M; Mert S; Alım Z; Beydemir S; Ok S; Kasımoğulları R Bioorg Med Chem; 2013 Jan; 21(1):21-7. PubMed ID: 23218470 [TBL] [Abstract][Full Text] [Related]
17. Carbonic anhydrase inhibitors: inhibition of human cytosolic isozyme II and mitochondrial isozyme V with a series of benzene sulfonamide derivatives. Innocenti A; Antel J; Wurl M; Scozzafava A; Supuran CT Bioorg Med Chem Lett; 2004 Nov; 14(22):5703-7. PubMed ID: 15482952 [TBL] [Abstract][Full Text] [Related]
18. Synthesis and biological profile of new 1,2,3,4-tetrahydroisoquinolines as selective carbonic anhydrase inhibitors. Gitto R; Damiano FM; De Luca L; Ferro S; Vullo D; Supuran CT; Chimirri A Bioorg Med Chem; 2011 Dec; 19(23):7003-7. PubMed ID: 22041171 [TBL] [Abstract][Full Text] [Related]
19. Conformational variability of different sulfonamide inhibitors with thienyl-acetamido moieties attributes to differential binding in the active site of cytosolic human carbonic anhydrase isoforms. Biswas S; Aggarwal M; Güzel Ö; Scozzafava A; McKenna R; Supuran CT Bioorg Med Chem; 2011 Jun; 19(12):3732-8. PubMed ID: 21620713 [TBL] [Abstract][Full Text] [Related]
20. Carbonic anhydrase inhibitors. Interaction of the antiepileptic drug sulthiame with twelve mammalian isoforms: kinetic and X-ray crystallographic studies. Temperini C; Innocenti A; Mastrolorenzo A; Scozzafava A; Supuran CT Bioorg Med Chem Lett; 2007 Sep; 17(17):4866-72. PubMed ID: 17588751 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]