ARTICLE;
BINDING AFFINITY;
DRUG DESIGN;
DRUG SELECTIVITY;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
HYDROPHILICITY;
HYDROPHOBICITY;
STRUCTURE ACTIVITY RELATION;
Directed ortho metalation-cross coupling strategies. N-Cumyl arylsulfonamides. Facile deprotection and expedient route to 7- and 4,7-substituted saccharins
Blanchet, J.; Macklin, T.; Ang, P.; Metallinos, C.; Snieckus, V. Directed ortho metalation-cross coupling strategies. N-Cumyl arylsulfonamides. Facile deprotection and expedient route to 7- and 4,7-substituted saccharins J. Org. Chem. 2007, 72, 3199-3206
Advances in the chemistry of saccharins: From synthetic novelties towards biologically active compounds
Jakopin, Z.; Dolenc, M. S. Advances in the chemistry of saccharins: from synthetic novelties towards biologically active compounds Curr. Med. Chem. 2010, 17, 651-671
The inhibition of bovine carbonic anhydrase by saccharin and 2- and 4-carbobenzoxybenzene sulfonamide
Wilson, J. M.; Tanko, Q.; Wendland, M. M.; Meany, J. E.; Nedved, J. F.; Pocker, Y. The inhibition of bovine carbonic anhydrase by saccharin and 2- and 4-carbobenzoxybenzene sulfonamide Physiol. Chem. Phys. Med. NMR 1998, 30, 149-162
Hypoxia activates the capacity of tumor-associated carbonic anhydrase IX to acidify extracellular pH
Svastova, E.; Hulikova, A.; Rafajova, M.; Zatovicova, M.; Gibadulinova, A.; Casini, A.; Cecchi, A.; Scozzafava, A.; Supuran, C. T.; Pastorek, J.; Pastoreková, S. Hypoxia activates the capacity of tumor-associated carbonic anhydrase IX to acidify extracellular pH FEBS Lett. 2004, 577, 439-445
Hypoxia-inducible carbonic anhydrase IX and XII promote tumor cell growth by counteracting acidosis through the regulation of the intracellular pH
Chiche, J.; Ilc, K.; Laferriere, J.; Trottier, E.; Dayan, F.; Mazure, N. M.; Brahimi-Horn, M. C.; Pouyssegur, J. Hypoxia-inducible carbonic anhydrase IX and XII promote tumor cell growth by counteracting acidosis through the regulation of the intracellular pH Cancer Res. 2009, 69, 358-368
The chemistry, physiology and pathology of pH in cancer
Swietach, P.; Vaughan-Jones, R.; Harris, A.; Hulikova, A. The chemistry, physiology and pathology of pH in cancer Philos. Trans R Soc., B 2014, 369, 1638
Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms?
Alterio, V.; Di Fiore, A.; D'Ambrosio, K.; Supuran, C. T.; De Simone, G. Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms? Chem. Rev. 2012, 112, 4421-4468
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, C. T.; De Simone, G. Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of N-substituted benzenesulfonamides to human isoform II Chem. Commun. 2011, 47, 11636-11638
Prediction of chlorine potentials of N-chlorinated organic molecules
Pitman, I. H.; Dawn, H.; Higuchi, T.; Hussain, A. A. Prediction of chlorine potentials of N-chlorinated organic molecules J. Chem. Soc. B 1969, 1230-1232
The preparatation and X-ray crystal structure of a saccharin complex of copper(II)
Ahmed, K. J.; Habib, A.; Haider, S. Z.; Malik, K. M. A.; Hurthouse, M. B. The preparatation and X-ray crystal structure of a saccharin complex of copper(II) Inorg. Chim. Acta 1981, 56, L37
A facile construction of 4-hydroxymethylbenzoisothiazolone-1,1-dioxide
Yeung, K.-S.; Meanwell, N. A.; Li, Y.; Gao, Q. A facile construction of 4-hydroxymethylbenzoisothiazolone-1,1-dioxide Tetrahedron Lett. 1998, 39, 1483-1486
Oxidative cyclization of N -alkyl- o -methyl-arenesulfonamides to biologically important saccharin derivatives
Xu, L.; Shu, H.; Liu, Y.; Zhang, S.; Trudell, M. L. Oxidative cyclization of N -alkyl- o -methyl-arenesulfonamides to biologically important saccharin derivatives Tetrahedron 2006, 62, 7902-7910
A prodrug approach toward cancer-related carbonic anhydrase inhibition
Carroux, C. J.; Rankin, G. M.; Moeker, J.; Bornaghi, L. F.; Katneni, K.; Morizzi, J.; Charman, S. A.; Vullo, D.; Supuran, C. T.; Poulsen, S.-A. A prodrug approach toward cancer-related carbonic anhydrase inhibition J. Med. Chem. 2013, 56, 9623-9634
Moeker J., Teruya K., Rossit S., Wilkinson B.L., Lopez M., Bornaghi L.F., Innocenti A., Supuran C.T., Poulsen S.-A., Design and synthesis of thiourea compounds that inhibit transmembrane anchored carbonic anhydrases.