138 related articles for article (PubMed ID: 3560154)
1. Thienothiopyran-2-sulfonamides: a novel class of water-soluble carbonic anhydrase inhibitors.
Ponticello GS; Freedman MB; Habecker CN; Lyle PA; Schwam H; Varga SL; Christy ME; Randall WC; Baldwin JJ
J Med Chem; 1987 Apr; 30(4):591-7. PubMed ID: 3560154
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Carbonic anhydrase inhibitors. Water-soluble, topically effective intraocular pressure lowering agents derived from isonicotinic acid and aromatic/heterocyclic sulfonamides: is the tail more important than the ring?
Menabuoni L; Scozzafava A; Mincione F; Briganti F; Mincione G; Supuran CT
J Enzyme Inhib; 1999; 14(6):457-74. PubMed ID: 10536879
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Carbonic anhydrase inhibitors. Part 71. Synthesis and ocular pharmacology of a new class of water-soluble, topically effective intraocular pressure lowering sulfonamides incorporating picolinoyl moieties.
Supuran CT; Scozzafava A; Menabuoni L; Mincione F; Briganti F; Mincione G
Eur J Pharm Sci; 1999 Aug; 8(4):317-28. PubMed ID: 10425382
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Carbonic anhydrase inhibitors - part 78(#). Synthesis of water-soluble sulfonamides incorporating beta-alanyl moieties, possessing long lasting-intraocular pressure lowering properties via the topical route.
Supuran CT; Briganti F; Menabuoni L; Mincione G; Mincione F; Scozzafava A
Eur J Med Chem; 2000 Mar; 35(3):309-21. PubMed ID: 10785557
[TBL] [Abstract][Full Text] [Related]
9. Carbonic anhydrase inhibitors. Part 79. Synthesis of topically acting sulfonamides incorporating GABA moieties in their molecule, with long-lasting intraocular pressure-lowering properties.
Mincione G; Menabuoni L; Briganti F; Mincione F; Scozzafava A; Supuran CT
Eur J Pharm Sci; 1999 Dec; 9(2):185-99. PubMed ID: 10620731
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Synthesis and characterization of metal complexes of heterocyclic sulfonamide as carbonic anhydrase inhibitors.
Büyükkidan N; Bülbül M; Kasimoğullari R; Büyükkidan B
J Enzyme Inhib Med Chem; 2013 Apr; 28(2):311-5. PubMed ID: 22957724
[TBL] [Abstract][Full Text] [Related]
12. Optimization of heterocyclic substituted benzenesulfonamides as novel carbonic anhydrase IX inhibitors and their structure activity relationship.
Gao R; Liao S; Zhang C; Zhu W; Wang L; Huang J; Zhao Z; Li H; Qian X; Xu Y
Eur J Med Chem; 2013 Apr; 62():597-604. PubMed ID: 23429054
[TBL] [Abstract][Full Text] [Related]
13. Carbonic anhydrase inhibitors: water-soluble 4-sulfamoylphenylthioureas as topical intraocular pressure-lowering agents with long-lasting effects.
Casini A; Scozzafava A; Mincione F; Menabuoni L; Ilies MA; Supuran CT
J Med Chem; 2000 Dec; 43(25):4884-92. PubMed ID: 11123998
[TBL] [Abstract][Full Text] [Related]
14. New isomeric classes of topically active ocular hypotensive carbonic anhydrase inhibitors: 5-substituted thieno[2,3-b]thiophene-2-sulfonamides and 5-substituted thieno[3,2-b]thiophene-2-sulfonamides.
Prugh JD; Hartman GD; Mallorga PJ; McKeever BM; Michelson SR; Murcko MA; Schwam H; Smith RL; Sondey JM; Springer JP
J Med Chem; 1991 Jun; 34(6):1805-18. PubMed ID: 2061922
[TBL] [Abstract][Full Text] [Related]
15. Carbonic anhydrase inhibitors. Synthesis of heterocyclic 4-substituted pyridine-3-sulfonamide derivatives and their inhibition of the human cytosolic isozymes I and II and transmembrane tumor-associated isozymes IX and XII.
Sławiński J; Szafrański K; Vullo D; Supuran CT
Eur J Med Chem; 2013 Nov; 69():701-10. PubMed ID: 24095761
[TBL] [Abstract][Full Text] [Related]
16. Carbonic anhydrase inhibitors: synthesis of water soluble sulfonamides incorporating a 4-sulfamoylphenylmethylthiourea scaffold, with potent intraocular pressure lowering properties.
Casini A; Scozzafava A; Mincione F; Menabuoni L; Supuran CT
J Enzyme Inhib Med Chem; 2002 Oct; 17(5):333-43. PubMed ID: 12683750
[TBL] [Abstract][Full Text] [Related]
17. Synthesis of novel sulfonamides under mild conditions with effective inhibitory activity against the carbonic anhydrase isoforms I and II.
Başar E; Tunca E; Bülbül M; Kaya M
J Enzyme Inhib Med Chem; 2016 Dec; 31(6):1356-61. PubMed ID: 27541741
[TBL] [Abstract][Full Text] [Related]
18. Carbonic anhydrase inhibitors: synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma properties.
Scozzafava A; Menabuoni L; Mincione F; Mincione G; Supuran CT
Bioorg Med Chem Lett; 2001 Feb; 11(4):575-82. PubMed ID: 11229775
[TBL] [Abstract][Full Text] [Related]
19. Topical carbonic anhydrase inhibitors: a new perspective in glaucoma therapy.
Hiett JA; Dockter CA
Optom Clin; 1992; 2(4):97-112. PubMed ID: 1286242
[TBL] [Abstract][Full Text] [Related]
20. Design and synthesis of novel 1,3-diaryltriazene-substituted sulfonamides as potent and selective carbonic anhydrase II inhibitors.
Lolak N; Akocak S; Bua S; Koca M; Supuran CT
Bioorg Chem; 2018 Apr; 77():542-547. PubMed ID: 29462772
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
