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 *

126 related articles for article (PubMed ID: 14642579)

  • 1. Quantitative structure-activity relationship study on sulfanilamide schiff's bases: carbonic anhydrase (CA) inhibitors.
    Agrawal VK; Srivastava S; Khadikar PV; Supuran CT
    Bioorg Med Chem; 2003 Dec; 11(24):5353-62. PubMed ID: 14642579
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inhibition of carbonic anhydrase isoforms I, II, IX and XII with Schiff's bases incorporating iminoureido moieties.
    Singasane N; Kharkar PS; Ceruso M; Supuran CT; Toraskar MP
    J Enzyme Inhib Med Chem; 2015 Dec; 30(6):901-7. PubMed ID: 25744513
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Carbonic anhydrase inhibitors: Schiff's bases of aromatic and heterocyclic sulfonamides and their metal complexes.
    Mahmood-Ul-Hassan ; Chohan ZH; Scozzafava A; Supuran CT
    J Enzyme Inhib Med Chem; 2004 Jun; 19(3):263-7. PubMed ID: 15499998
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Carbonic anhydrase inhibitors. Inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, IX, and XII with Schiff's bases incorporating chromone and aromatic sulfonamide moieties, and their zinc complexes.
    Puccetti L; Fasolis G; Vullo D; Chohan ZH; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2005 Jun; 15(12):3096-101. PubMed ID: 15908204
    [TBL] [Abstract][Full Text] [Related]  

  • 5. QSAR study using topological indices for inhibition of carbonic anhydrase II by sulfanilamides and Schiff bases.
    Balaban AT; Basak SC; Beteringhe A; Mills D; Supuran CT
    Mol Divers; 2004; 8(4):401-12. PubMed ID: 15612644
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Carbonic anhydrase II-induced selection of inhibitors from a dynamic combinatorial library of Schiff's bases.
    Nasr G; Petit E; Supuran CT; Winum JY; Barboiu M
    Bioorg Med Chem Lett; 2009 Nov; 19(21):6014-7. PubMed ID: 19796939
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Carbonic anhydrase inhibitors: inhibition of cytosolic carbonic anhydrase isozymes II and VII with simple aromatic sulfonamides and some azo dyes.
    Carta F; Pothen B; Maresca A; Tiwari M; Singh V; Supuran CT
    Chem Biol Drug Des; 2009 Aug; 74(2):196-202. PubMed ID: 19549076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Orbital symmetry in QSAR: some Schiff's base inhibitors of carbonic anhydrase.
    Supuran CT; Clare BW
    SAR QSAR Environ Res; 2001; 12(1-2):17-29. PubMed ID: 11697055
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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.
    Sarikaya B; Ceruso M; Carta F; Supuran CT
    Bioorg Med Chem; 2014 Nov; 22(21):5883-90. PubMed ID: 25267005
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Carbonic anhydrase inhibitors. Inhibition of human cytosolic isoforms I and II with (reduced) Schiff's bases incorporating sulfonamide, carboxylate and carboxymethyl moieties.
    Nasr G; Cristian A; Barboiu M; Vullo D; Winum JY; Supuran CT
    Bioorg Med Chem; 2014 May; 22(10):2867-74. PubMed ID: 24746465
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis and biological evaluation of novel aromatic and heterocyclic bis-sulfonamide Schiff bases as carbonic anhydrase I, II, VII and IX inhibitors.
    Akocak S; Lolak N; Nocentini A; Karakoc G; Tufan A; Supuran CT
    Bioorg Med Chem; 2017 Jun; 25(12):3093-3097. PubMed ID: 28400084
    [TBL] [Abstract][Full Text] [Related]  

  • 13. QSAR studies on benzene sulfonamide carbonic anhydrase inhibitors: need of hydrophobic parameter for topological modeling of binding constants of sulfonamides to human CA-II.
    Khadikar PV; Sharma V; Karmarkar S; Supuran CT
    Bioorg Med Chem Lett; 2005 Feb; 15(4):923-30. PubMed ID: 15686888
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Schiff bases and their amines: Synthesis and discovery of carbonic anhydrase and acetylcholinesterase enzymes inhibitors.
    Yiğit B; Yiğit M; Taslimi P; Gök Y; Gülçin İ
    Arch Pharm (Weinheim); 2018 Sep; 351(9):e1800146. PubMed ID: 30033646
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inhibition studies of bacterial, fungal and protozoan β-class carbonic anhydrases with Schiff bases incorporating sulfonamide moieties.
    Ceruso M; Carta F; Osman SM; Alothman Z; Monti SM; Supuran CT
    Bioorg Med Chem; 2015 Aug; 23(15):4181-4187. PubMed ID: 26145821
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Carbonic anhydrase inhibitors: metal complexes of a sulfanilamide derived Schiff base and their interaction with isozymes I, II and IV.
    Ul-Hassan M; Scozzafava A; Chohan ZH; Supuran CT
    J Enzyme Inhib; 2001 Dec; 16(6):499-505. PubMed ID: 12164389
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthesis and evaluation of N-heteroarylsubstituted triazolosulfonamides as carbonic anhydrase inhibitors.
    Balci A; Arslan M; Nixha AR; Bilen C; Ergun A; Gençer N
    J Enzyme Inhib Med Chem; 2015 Jun; 30(3):377-82. PubMed ID: 25068730
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 3D-QSAR study of benzene sulfonamide analogs as carbonic anhydrase II inhibitors.
    Sethi KK; Verma SM; Prasanthi N; Sahoo SK; Parhi RN; Suresh P
    Bioorg Med Chem Lett; 2010 May; 20(10):3089-93. PubMed ID: 20443227
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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.
    Congiu C; Onnis V; Balboni G; Supuran CT
    Bioorg Med Chem Lett; 2014 Apr; 24(7):1776-9. PubMed ID: 24589511
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis of 4-sulfamoylphenyl-benzylamine derivatives with inhibitory activity against human carbonic anhydrase isoforms I, II, IX and XII.
    Durgun M; Turkmen H; Ceruso M; Supuran CT
    Bioorg Med Chem; 2016 Mar; 24(5):982-8. PubMed ID: 26803577
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.