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 *

192 related articles for article (PubMed ID: 34340630)

  • 21. Novel indolin-2-one-based sulfonamides as carbonic anhydrase inhibitors: Synthesis, in vitro biological evaluation against carbonic anhydrases isoforms I, II, IV and VII and molecular docking studies.
    Eldehna WM; Al-Ansary GH; Bua S; Nocentini A; Gratteri P; Altoukhy A; Ghabbour H; Ahmed HY; Supuran CT
    Eur J Med Chem; 2017 Feb; 127():521-530. PubMed ID: 28109946
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Carbonic anhydrase inhibitors: synthesis and inhibition studies against mammalian isoforms I-XV with a series of 2-(hydrazinocarbonyl)-3-substituted-phenyl-1H-indole-5-sulfonamides.
    Güzel O; Innocenti A; Scozzafava A; Salman A; Parkkila S; Hilvo M; Supuran CT
    Bioorg Med Chem; 2008 Oct; 16(20):9113-20. PubMed ID: 18819811
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Carbonic anhydrase activation and the drug design.
    Temperini C; Scozzafava A; Supuran CT
    Curr Pharm Des; 2008; 14(7):708-15. PubMed ID: 18336317
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Five- and Six-Membered Nitrogen-Containing Compounds as Selective Carbonic Anhydrase Activators.
    Mollica A; Macedonio G; Stefanucci A; Carradori S; Akdemir A; Angeli A; Supuran CT
    Molecules; 2017 Dec; 22(12):. PubMed ID: 29232847
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Carbonic anhydrase inhibitors: synthesis and inhibition of the human carbonic anhydrase isoforms I, II, VII, IX and XII with benzene sulfonamides incorporating 4,5,6,7-tetrabromophthalimide moiety.
    Sethi KK; Vullo D; Verma SM; Tanç M; Carta F; Supuran CT
    Bioorg Med Chem; 2013 Oct; 21(19):5973-82. PubMed ID: 23965175
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Structure-activity relationships for the interaction of 5,10-dihydroindeno[1,2-b]indole derivatives with human and bovine carbonic anhydrase isoforms I, II, III, IV and VI.
    Ekinci D; Cavdar H; Durdagi S; Talaz O; Sentürk M; Supuran CT
    Eur J Med Chem; 2012 Mar; 49():68-73. PubMed ID: 22245047
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Carbonic anhydrase activators: gold nanoparticles coated with derivatized histamine, histidine, and carnosine show enhanced activatory effects on several mammalian isoforms.
    Saada MC; Montero JL; Vullo D; Scozzafava A; Winum JY; Supuran CT
    J Med Chem; 2011 Mar; 54(5):1170-7. PubMed ID: 21291238
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Carbonic anhydrase activators - part 21. Novel activators of isozymes I, II and IV incorporating carboxamido and ureido histamine moieties.
    Scozzafava A; Supuran CT
    Eur J Med Chem; 2000 Jan; 35(1):31-9. PubMed ID: 10733601
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Carbonic anhydrase activators: activation of isozyme XIII with amino acids and amines.
    Parkkila S; Vullo D; Puccetti L; Parkkila AK; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2006 Aug; 16(15):3955-9. PubMed ID: 16730978
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Synthesis and inhibitory properties of some carbamates on carbonic anhydrase and acetylcholine esterase.
    Yılmaz S; Akbaba Y; Özgeriş B; Köse LP; Göksu S; Gülçin İ; Alwasel SH; Supuran CT
    J Enzyme Inhib Med Chem; 2016 Dec; 31(6):1484-91. PubMed ID: 26985691
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A class of carbonic anhydrase I - selective activators.
    Licsandru E; Tanc M; Kocsis I; Barboiu M; Supuran CT
    J Enzyme Inhib Med Chem; 2017 Dec; 32(1):37-46. PubMed ID: 27798977
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Carbonic anhydrase activators: activation of human isozymes I, II and IX with phenylsulfonylhydrazido l-histidine derivatives.
    Abdo MR; Vullo D; Saada MC; Montero JL; Scozzafava A; Winum JY; Supuran CT
    Bioorg Med Chem Lett; 2009 May; 19(9):2440-3. PubMed ID: 19345095
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Evaluation of selenide, diselenide and selenoheterocycle derivatives as carbonic anhydrase I, II, IV, VII and IX inhibitors.
    Angeli A; Tanini D; Viglianisi C; Panzella L; Capperucci A; Menichetti S; Supuran CT
    Bioorg Med Chem; 2017 Apr; 25(8):2518-2523. PubMed ID: 28302505
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pyridinium derivatives of histamine are potent activators of cytosolic carbonic anhydrase isoforms I, II and VII.
    Dave K; Scozzafava A; Vullo D; Supuran CT; Ilies MA
    Org Biomol Chem; 2011 Apr; 9(8):2790-800. PubMed ID: 21369613
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Synthesis of bulky-tailed sulfonamides incorporating pyrido[2,3-d][1,2,4]triazolo[4,3-a]pyrimidin-1(5H)-yl) moieties and evaluation of their carbonic anhydrases I, II, IV and IX inhibitory effects.
    Fares M; Eladwy RA; Nocentini A; El Hadi SRA; Ghabbour HA; Abdel-Megeed A; Eldehna WM; Abdel-Aziz HA; Supuran CT
    Bioorg Med Chem; 2017 Apr; 25(7):2210-2217. PubMed ID: 28256371
    [TBL] [Abstract][Full Text] [Related]  

  • 36. State of the Art on Carbonic Anhydrase Modulators for Biomedical Purposes.
    Bozdag M; Altamimi ASA; Vullo D; Supuran CT; Carta F
    Curr Med Chem; 2019; 26(15):2558-2573. PubMed ID: 29932025
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Carbonic anhydrase inhibitors: inhibition of the human isozymes I, II, VA, and IX with a library of substituted difluoromethanesulfonamides.
    Cecchi A; Taylor SD; Liu Y; Hill B; Vullo D; Scozzafava A; Supuran CT
    Bioorg Med Chem Lett; 2005 Dec; 15(23):5192-6. PubMed ID: 16203142
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel 2-(2-arylmethylthio-4-chloro-5-methylbenzenesulfonyl)-1-(1,3,5-triazin-2-ylamino)guanidine derivatives: Inhibition of human carbonic anhydrase cytosolic isozymes I and II and the transmembrane tumor-associated isozymes IX and XII, anticancer activity, and molecular modeling studies.
    Żołnowska B; Sławiński J; Szafrański K; Angeli A; Supuran CT; Kawiak A; Wieczór M; Zielińska J; Bączek T; Bartoszewska S
    Eur J Med Chem; 2018 Jan; 143():1931-1941. PubMed ID: 29146134
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Carbonic anhydrase inhibitors. Phenacetyl-, pyridylacetyl- and thienylacetyl-substituted aromatic sulfonamides act as potent and selective isoform VII inhibitors.
    Güzel O; Innocenti A; Scozzafava A; Salman A; Supuran CT
    Bioorg Med Chem Lett; 2009 Jun; 19(12):3170-3. PubMed ID: 19435663
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mono- and di-halogenated histamine, histidine and carnosine derivatives are potent carbonic anhydrase I, II, VII, XII and XIV activators.
    Saada MC; Vullo D; Montero JL; Scozzafava A; Supuran CT; Winum JY
    Bioorg Med Chem; 2014 Sep; 22(17):4752-8. PubMed ID: 25082511
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.