336 related articles for article (PubMed ID: 15236839)
1. QSAR study on carbonic anhydrase inhibitors: aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties, with topical activity as antiglaucoma agents.
Agrawal VK; Bano S; Supuran CT; Khadikar PV
Eur J Med Chem; 2004 Jul; 39(7):593-600. PubMed ID: 15236839
[TBL] [Abstract][Full Text] [Related]
2. Carbonic anhydrase inhibitors: synthesis and topical intraocular pressure lowering effects of fluorine-containing inhibitors devoid of enhanced reactivity.
de Leval X; Ilies M; Casini A; Dogné JM; Scozzafava A; Masini E; Mincione F; Starnotti M; Supuran CT
J Med Chem; 2004 May; 47(11):2796-804. PubMed ID: 15139757
[TBL] [Abstract][Full Text] [Related]
3. Carbonic anhydrase inhibitors: synthesis of water-soluble, topically effective intraocular pressure lowering aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties: is the tail more important than the ring?
Borras J; Scozzafava A; Menabuoni L; Mincione F; Briganti F; Mincione G; Supuran CT
Bioorg Med Chem; 1999 Nov; 7(11):2397-406. PubMed ID: 10632049
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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?
Scozzafava A; Menabuoni L; Mincione F; Briganti F; Mincione G; Supuran CT
J Med Chem; 1999 Jul; 42(14):2641-50. PubMed ID: 10411484
[TBL] [Abstract][Full Text] [Related]
6. Carbonic anhydrase inhibitors: synthesis of water-soluble, aminoacyl/dipeptidyl sulfonamides possessing long-lasting intraocular pressure-lowering properties via the topical route.
Scozzafava A; Briganti F; Mincione G; Menabuoni L; Mincione F; Supuran CT
J Med Chem; 1999 Sep; 42(18):3690-700. PubMed ID: 10479300
[TBL] [Abstract][Full Text] [Related]
7. Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides derived from 4-isothiocyanato-benzolamide.
Cecchi A; Winum JY; Innocenti A; Vullo D; Montero JL; Scozzafava A; Supuran CT
Bioorg Med Chem Lett; 2004 Dec; 14(23):5775-80. PubMed ID: 15501039
[TBL] [Abstract][Full Text] [Related]
8. Carbonic anhydrase inhibitors. Aromatic/heterocyclic sulfonamides incorporating phenacetyl, pyridylacetyl and thienylacetyl tails act as potent inhibitors of human mitochondrial isoforms VA and VB.
Güzel O; Innocenti A; Scozzafava A; Salman A; Supuran CT
Bioorg Med Chem; 2009 Jul; 17(14):4894-9. PubMed ID: 19539481
[TBL] [Abstract][Full Text] [Related]
9. 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.
Krasavin M; Korsakov M; Dorogov M; Tuccinardi T; Dedeoglu N; Supuran CT
Eur J Med Chem; 2015 Aug; 101():334-47. PubMed ID: 26160114
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I, II, III, VII and XIII with less investigated inorganic anions.
Innocenti A; Scozzafava A; Supuran CT
Bioorg Med Chem Lett; 2009 Apr; 19(7):1855-7. PubMed ID: 19269822
[TBL] [Abstract][Full Text] [Related]
12. Carbonic anhydrase inhibitors: design of thioureido sulfonamides with potent isozyme II and XII inhibitory properties and intraocular pressure lowering activity in a rabbit model of glaucoma.
Mincione F; Starnotti M; Masini E; Bacciottini L; Scrivanti C; Casini A; Vullo D; Scozzafava A; Supuran CT
Bioorg Med Chem Lett; 2005 Sep; 15(17):3821-7. PubMed ID: 16039853
[TBL] [Abstract][Full Text] [Related]
13. QSAR study on topically acting sulfonamides incorporating GABA moieties: a molecular connectivity approach.
Agrawal VK; Singh J; Khadikar PV; Supuran CT
Bioorg Med Chem Lett; 2006 Apr; 16(7):2044-51. PubMed ID: 16458003
[TBL] [Abstract][Full Text] [Related]
14. QSAR study on para-substituted aromatic sulfonamides as carbonic anhydrase II inhibitors using topological information indices.
Melagraki G; Afantitis A; Sarimveis H; Igglessi-Markopoulou O; Supuran CT
Bioorg Med Chem; 2006 Feb; 14(4):1108-14. PubMed ID: 16213737
[TBL] [Abstract][Full Text] [Related]
15. Carbonic anhydrase inhibitors: topically acting antiglaucoma sulfonamides incorporating phthaloyl and phthalimido moieties.
Scozzafava A; Mincione F; Menabuoni L; Supuran CT
Drug Des Discov; 2001; 17(4):337-48. PubMed ID: 11765137
[TBL] [Abstract][Full Text] [Related]
16. Carbonic anhydrase inhibitors: aromatic and heterocyclic sulfonamides incorporating adamantyl moieties with strong anticonvulsant activity.
Ilies MA; Masereel B; Rolin S; Scozzafava A; Câmpeanu G; Cîmpeanu V; Supuran CT
Bioorg Med Chem; 2004 May; 12(10):2717-26. PubMed ID: 15110853
[TBL] [Abstract][Full Text] [Related]
17. Quantum chemical QSAR models to distinguish between inhibitory activities of sulfonamides against human carbonic anhydrases I and II and bovine IV isozymes.
Deeb O; Goodarzi M; Khadikar PV
Chem Biol Drug Des; 2012 Apr; 79(4):514-22. PubMed ID: 22181786
[TBL] [Abstract][Full Text] [Related]
18. A quantitative structure-activity relationship study on some aromatic/heterocyclic sulfonamides and their charged derivatives acting as carbonic anhydrase inhibitors.
Gupta SP; Kumaran S
J Enzyme Inhib Med Chem; 2005 Jun; 20(3):251-9. PubMed ID: 16119196
[TBL] [Abstract][Full Text] [Related]
19. Design, synthesis and anticancer evaluation of novel tetrahydroquinoline derivatives containing sulfonamide moiety.
Ghorab MM; Ragab FA; Hamed MM
Eur J Med Chem; 2009 Oct; 44(10):4211-7. PubMed ID: 19540022
[TBL] [Abstract][Full Text] [Related]
20. Benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulfonamides as inhibitors of carbonic anhydrase.
Dudutiene V; Baranauskiene L; Matulis D
Bioorg Med Chem Lett; 2007 Jun; 17(12):3335-8. PubMed ID: 17442568
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]