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 *

176 related articles for article (PubMed ID: 32230853)

  • 1. The Influence of Varying Fluorination Patterns on the Thermodynamics and Kinetics of Benzenesulfonamide Binding to Human Carbonic Anhydrase II.
    Glöckner S; Ngo K; Wagner B; Heine A; Klebe G
    Biomolecules; 2020 Mar; 10(4):. PubMed ID: 32230853
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Conformational Changes in Alkyl Chains Determine the Thermodynamic and Kinetic Binding Profiles of Carbonic Anhydrase Inhibitors.
    Glöckner S; Ngo K; Sager CP; Hüfner-Wulsdorf T; Heine A; Klebe G
    ACS Chem Biol; 2020 Mar; 15(3):675-685. PubMed ID: 32027480
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Thermodynamic parameters for the association of fluorinated benzenesulfonamides with bovine carbonic anhydrase II.
    Krishnamurthy VM; Bohall BR; Kim CY; Moustakas DT; Christianson DW; Whitesides GM
    Chem Asian J; 2007 Jan; 2(1):94-105. PubMed ID: 17441142
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the "hydrophobic wall" of carbonic anhydrase.
    Mecinović J; Snyder PW; Mirica KA; Bai S; Mack ET; Kwant RL; Moustakas DT; Héroux A; Whitesides GM
    J Am Chem Soc; 2011 Sep; 133(35):14017-26. PubMed ID: 21790183
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Intrinsic Thermodynamics and Structures of 2,4- and 3,4-Substituted Fluorinated Benzenesulfonamides Binding to Carbonic Anhydrases.
    Zubrienė A; Smirnov A; Dudutienė V; Timm DD; Matulienė J; Michailovienė V; Zakšauskas A; Manakova E; Gražulis S; Matulis D
    ChemMedChem; 2017 Jan; 12(2):161-176. PubMed ID: 28001003
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Kinetic and Structural Insights into the Mechanism of Binding of Sulfonamides to Human Carbonic Anhydrase by Computational and Experimental Studies.
    Gaspari R; Rechlin C; Heine A; Bottegoni G; Rocchia W; Schwarz D; Bomke J; Gerber HD; Klebe G; Cavalli A
    J Med Chem; 2016 May; 59(9):4245-56. PubMed ID: 26700575
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Superacid synthesis of halogen containing N-substituted-4-aminobenzene sulfonamides: new selective tumor-associated carbonic anhydrase inhibitors.
    Compain G; Martin-Mingot A; Maresca A; Thibaudeau S; Supuran CT
    Bioorg Med Chem; 2013 Mar; 21(6):1555-63. PubMed ID: 22705188
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Residual ligand entropy in the binding of p-substituted benzenesulfonamide ligands to bovine carbonic anhydrase II.
    Stöckmann H; Bronowska A; Syme NR; Thompson GS; Kalverda AP; Warriner SL; Homans SW
    J Am Chem Soc; 2008 Sep; 130(37):12420-6. PubMed ID: 18717559
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Thermodynamic, kinetic, and structural parameterization of human carbonic anhydrase interactions toward enhanced inhibitor design.
    Linkuvienė V; Zubrienė A; Manakova E; Petrauskas V; Baranauskienė L; Zakšauskas A; Smirnov A; Gražulis S; Ladbury JE; Matulis D
    Q Rev Biophys; 2018 Jan; 51():e10. PubMed ID: 30912486
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Binding affinity of substituted ureido-benzenesulfonamide ligands to the carbonic anhydrase receptor: a theoretical study of enzyme inhibition.
    Sahu C; Sen K; Pakhira S; Mondal B; Das AK
    J Comput Chem; 2013 Aug; 34(22):1907-16. PubMed ID: 23712937
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural study of interaction between brinzolamide and dorzolamide inhibition of human carbonic anhydrases.
    Pinard MA; Boone CD; Rife BD; Supuran CT; McKenna R
    Bioorg Med Chem; 2013 Nov; 21(22):7210-5. PubMed ID: 24090602
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency.
    Pacchiano F; Aggarwal M; Avvaru BS; Robbins AH; Scozzafava A; McKenna R; Supuran CT
    Chem Commun (Camb); 2010 Nov; 46(44):8371-3. PubMed ID: 20922253
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structural analysis of charge discrimination in the binding of inhibitors to human carbonic anhydrases I and II.
    Srivastava DK; Jude KM; Banerjee AL; Haldar M; Manokaran S; Kooren J; Mallik S; Christianson DW
    J Am Chem Soc; 2007 May; 129(17):5528-37. PubMed ID: 17407288
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 5-Substituted-(1,2,3-triazol-4-yl)thiophene-2-sulfonamides strongly inhibit human carbonic anhydrases I, II, IX and XII: solution and X-ray crystallographic studies.
    Leitans J; Sprudza A; Tanc M; Vozny I; Zalubovskis R; Tars K; Supuran CT
    Bioorg Med Chem; 2013 Sep; 21(17):5130-8. PubMed ID: 23859774
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Pairwise decomposition of residue interaction energies using semiempirical quantum mechanical methods in studies of protein-ligand interaction.
    Raha K; van der Vaart AJ; Riley KE; Peters MB; Westerhoff LM; Kim H; Merz KM
    J Am Chem Soc; 2005 May; 127(18):6583-94. PubMed ID: 15869279
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of N-substituted benzenesulfonamides to human isoform II.
    Di Fiore A; Maresca A; Alterio V; Supuran CT; De Simone G
    Chem Commun (Camb); 2011 Nov; 47(42):11636-8. PubMed ID: 21952494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spectroscopic and molecular modeling studies on binding of dorzolamide to bovine and human carbonic anhydrase II.
    Bijari N; Ghobadi S; Mahdiuni H; Khodarahmi R; Ghadami SA
    Int J Biol Macromol; 2015 Sep; 80():189-99. PubMed ID: 26093313
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fluorinated pyrrolidines and piperidines incorporating tertiary benzenesulfonamide moieties are selective carbonic anhydrase II inhibitors.
    Le Darz A; Mingot A; Bouazza F; Castelli U; Karam O; Tanc M; Supuran CT; Thibaudeau S
    J Enzyme Inhib Med Chem; 2015; 30(5):737-45. PubMed ID: 25431145
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inhibition and binding studies of carbonic anhydrase isozymes I, II and IX with benzimidazo[1,2-c][1,2,3]thiadiazole-7-sulphonamides.
    Baranauskienė L; Hilvo M; Matulienė J; Golovenko D; Manakova E; Dudutienė V; Michailovienė V; Torresan J; Jachno J; Parkkila S; Maresca A; Supuran CT; Gražulis S; Matulis D
    J Enzyme Inhib Med Chem; 2010 Dec; 25(6):863-70. PubMed ID: 20166809
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Protein surface-assisted enhancement in the binding affinity of an inhibitor for recombinant human carbonic anhydrase-II.
    Banerjee AL; Swanson M; Roy BC; Jia X; Haldar MK; Mallik S; Srivastava DK
    J Am Chem Soc; 2004 Sep; 126(35):10875-83. PubMed ID: 15339172
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.