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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 9825306)

  • 1. Carbonic anhydrase inhibitors: novel compounds containing S-NH moieties: sulfenamido-sulfonamides, sulfenimido-sulfonamides and their interaction with isozymes I, II and IV.
    Scozzafava A; Supuran CT
    J Enzyme Inhib; 1998 Sep; 13(6):419-42. PubMed ID: 9825306
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sulfenamido-sulfonamides as inhibitors of carbonic anhydrase isozymes I, II and IV.
    Supuran CT; Briganti F; Scozzafava A
    J Enzyme Inhib; 1997 Aug; 12(3):175-90. PubMed ID: 9314114
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Carbonic anhydrase inhibitors: perfluoroalkyl/aryl-substituted derivatives of aromatic/heterocyclic sulfonamides as topical intraocular pressure-lowering agents with prolonged duration of action.
    Scozzafava A; Menabuoni L; Mincione F; Briganti F; Mincione G; Supuran CT
    J Med Chem; 2000 Nov; 43(23):4542-51. PubMed ID: 11087579
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Carbonic anhydrase inhibitors: topical sulfonamide antiglaucoma agents incorporating secondary amine moieties.
    Renzi G; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2000 Apr; 10(7):673-6. PubMed ID: 10762051
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Carbonic anhydrase inhibitors: synthesis of sulfonamides incorporating 2,4,6-trisubstituted-pyridinium-ethylcarboxamido moieties possessing membrane-impermeability and in vivo selectivity for the membrane-bound (CA IV) versus the cytosolic (CA I and CA II) isozymes.
    Supuran CT; Scozzafava A; Ilies MA; Briganti F
    J Enzyme Inhib; 2000; 15(4):381-401. PubMed ID: 10995069
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Carbonic anhydrase inhibitors. Arylsulfonylureido- and arylureido-substituted aromatic and heterocyclic sulfonamides: towards selective inhibitors of carbonic anhydrase isozyme I.
    Scozzafava A; Supuran CT
    J Enzyme Inhib; 1999; 14(5):343-63. PubMed ID: 10488246
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Carbonic anhydrase inhibitors: inhibition of isozymes I, II and IV with N-hydroxysulfonamides--a novel class of intraocular pressure lowering agents.
    Mincione F; Menabuoni L; Briganti F; Mincione G; Scozzafava A; Supuran CT
    J Enzyme Inhib; 1998 Jul; 13(4):267-84. PubMed ID: 9795865
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Carbonic anhydrase inhibitors: novel sulfonamides incorporating 1,3,5-triazine moieties as inhibitors of the cytosolic and tumour-associated carbonic anhydrase isozymes I, II and IX.
    Garaj V; Puccetti L; Fasolis G; Winum JY; Montero JL; Scozzafava A; Vullo D; Innocenti A; Supuran CT
    Bioorg Med Chem Lett; 2005 Jun; 15(12):3102-8. PubMed ID: 15905091
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel aromatic/heterocyclic sulfonamides and their metal complexes as inhibitors of carbonic anhydrase isozymes I, II and IV.
    Supuran CT; Scozzafava A
    J Enzyme Inhib; 1997 Apr; 12(1):37-51. PubMed ID: 9204381
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Carbonic anhydrase inhibitors: synthesis and inhibition against isozymes I, II and IV of topically acting antiglaucoma sulfonamides incorporating cis-5-norbornene-endo-3-carboxy-2-carboxamido moieties.
    Casini A; Mincione F; Ilies MA; Menabuoni L; Scozzafava A; Supuran CT
    J Enzyme Inhib; 2001; 16(2):113-23. PubMed ID: 11342280
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Carbonic anhydrase inhibitors: synthesis of N-morpholylthiocarbonylsulfenylamino aromatic/heterocyclic sulfonamides and their interaction with isozymes I, II and IV.
    Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2000 May; 10(10):1117-20. PubMed ID: 10843231
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Carbonic anhydrase inhibitors. Synthesis of topically effective intraocular pressure lowering agents derived from 5-(omega-aminoalkylcarboxamido)-1,3,4-thiadiazole-2-sulfonamide.
    Barboiu M; Supuran CT; Menabuoni L; Scozzafava A; Mincione F; Briganti F; Mincione G
    J Enzyme Inhib; 2000; 15(1):23-46. PubMed ID: 10850953
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carbonic anhydrase inhibitors: sulfonamides as antitumor agents?
    Supuran CT; Briganti F; Tilli S; Chegwidden WR; Scozzafava A
    Bioorg Med Chem; 2001 Mar; 9(3):703-14. PubMed ID: 11310605
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.