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Volumn 16, Issue 14, 2012, Pages 1670-1676

Novel glycomimetics: Anomeric and N-glycosyl sulfonamides

Author keywords

Anomeric sulfonamides; Carbohydrates; Enzyme inhibition; Glycomimetics; N glycosyl sulfonamides

Indexed keywords


EID: 84862749937     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/138527212800840892     Document Type: Article
Times cited : (23)

References (52)
  • 1
    • 68249116079 scopus 로고    scopus 로고
    • From carbohydrate leads to glycomimetic drugs
    • Ernst, B.; Magnani, J. L., From carbohydrate leads to glycomimetic drugs. Nat. Rev. Drug Disc., 2009, 8(8), 661-677.
    • (2009) Nat. Rev. Drug Disc , vol.8 , Issue.8 , pp. 661-677
    • Ernst, B.1    Magnani, J.L.2
  • 2
    • 84862748498 scopus 로고    scopus 로고
    • Note
    • This review will not discuss the Danishefskýs work. His group reported on the reaction of glycals with iodonium disym-collidine perchlorate and benzenesulfonamide to afford stereoselectively 2-β-iodo-1-α- sulfonamidohexoses. This class of glycosylsulfonamides were used for the preparation of oligosaccharides with the 2-aminohexosesubunit. Note.
  • 3
    • 0029739240 scopus 로고    scopus 로고
    • Glycals in organic synthesis: The evolution of comprehensive strategies for the assembly of oligosaccharides and glycoconjugates of biological consequence
    • Danishefsky, S. J.; Bilodeau, M. T., Glycals in organic synthesis: The evolution of comprehensive strategies for the assembly of oligosaccharides and glycoconjugates of biological consequence. Angewandte Chemie (International Edition in English) 1996, 35 (13/14), 1381-1419.
    • (1996) Angewandte Chemie (International Edition In English) , vol.35 , Issue.13-14 , pp. 1381-1419
    • Danishefsky, S.J.1    Bilodeau, M.T.2
  • 4
    • 84862748502 scopus 로고    scopus 로고
    • Also we will not consider the synthesis of glycosidic compounds in which the sulfonamide functionality is not directly linked to the carbohydrate moiety
    • Also we will not consider the synthesis of glycosidic compounds in which the sulfonamide functionality is not directly linked to the carbohydrate moiety.
  • 5
    • 66149131065 scopus 로고    scopus 로고
    • Therapeutic applications of glycosidic carbonic anhydrase inhibitors
    • Winum, J. Y.; Poulsen, S. A.; Supuran, C. T., Therapeutic applications of glycosidic carbonic anhydrase inhibitors. Med. Res. Rev., 2009, 29 (3), 419-435
    • (2009) Med. Res. Rev , vol.29 , Issue.3 , pp. 419-435
    • Winum, J.Y.1    Poulsen, S.A.2    Supuran, C.T.3
  • 6
    • 77349096856 scopus 로고    scopus 로고
    • Synthesis of new sulfonic acid-containing oligosaccharide mimetics of sialyl Lewis A
    • Jakab, Z.; Fekete, A.; Borbás, A.; Lipták, A.; Antus, S., Synthesis of new sulfonic acid-containing oligosaccharide mimetics of sialyl Lewis A. Tetrahedron, 2010, 66 (13), 2404-2414.
    • (2010) Tetrahedron , vol.66 , Issue.13 , pp. 2404-2414
    • Jakab, Z.1    Fekete, A.2    Borbás, A.3    Lipták, A.4    Antus, S.5
  • 7
    • 0347418215 scopus 로고    scopus 로고
    • The first synthesis of secondary sugar sulfonic acids by nucleophilic displacement reactions
    • Lipták, A.; Balla, E.; Jánossy, L.; Sajtos, F.; Szilágyi, L., The first synthesis of secondary sugar sulfonic acids by nucleophilic displacement reactions. Tetrahedron Lett., 2004, 45 (4), 839-842.
    • (2004) Tetrahedron Lett , vol.45 , Issue.4 , pp. 839-842
    • Lipták, A.1    Balla, E.2    Jánossy, L.3    Sajtos, F.4    Szilágyi, L.5
  • 8
    • 33644512737 scopus 로고    scopus 로고
    • New glycomimetics: Anomeric sulfonates, sulfenamides, and sulfonamides
    • Knapp, S.; Darout, E.; Amorelli, B., New glycomimetics: Anomeric sulfonates, sulfenamides, and sulfonamides. J. Org. Chem., 2006, 71 (4), 1380-1389.
    • (2006) J. Org. Chem , vol.71 , Issue.4 , pp. 1380-1389
    • Knapp, S.1    Darout, E.2    Amorelli, B.3
  • 9
    • 59849107600 scopus 로고    scopus 로고
    • Synthesis of anomeric sulfonamides and their behaviour under radical-mediated bromination conditions
    • Czifrák, K.; Somsák, L., Synthesis of anomeric sulfonamides and their behaviour under radical-mediated bromination conditions. Carbohydrate Res., 2009, 344 (3), 269-277.
    • (2009) Carbohydrate Res , vol.344 , Issue.3 , pp. 269-277
    • Czifrák, K.1    Somsák, L.2
  • 10
    • 0029947945 scopus 로고    scopus 로고
    • NAGthiazoline, an N-acetyl-β-hexosaminidase inhibitor that implicates acetamido participation
    • Knapp, S.; Vocadlo, D.; Gao, Z.; Kirk, B.; Lou, J.; Withers, S. G., NAGthiazoline, an N-acetyl-β-hexosaminidase inhibitor that implicates acetamido participation. J. Am. Chem. Soc., 1996, 118 (28), 6804-6805.
    • (1996) J. Am. Chem. Soc , vol.118 , Issue.28 , pp. 6804-6805
    • Knapp, S.1    Vocadlo, D.2    Gao, Z.3    Kirk, B.4    Lou, J.5    Withers, S.G.6
  • 12
    • 64249150644 scopus 로고    scopus 로고
    • Synthesis of Sglycosyl primary sulfonamides
    • Lopez, M.; Drillaud, N.; Bornaghi, L. F.; Poulsen, S. A., Synthesis of Sglycosyl primary sulfonamides. J. Org. Chem., 2009, 74 (7), 2811-2816.
    • (2009) J. Org. Chem , vol.74 , Issue.7 , pp. 2811-2816
    • Lopez, M.1    Drillaud, N.2    Bornaghi, L.F.3    Poulsen, S.A.4
  • 13
    • 77950563961 scopus 로고    scopus 로고
    • Sulfonamide linked neoglycoconjugates-A new class of inhibitors for cancer-associated carbonic anhydrases
    • Lopez, M.; Bornaghi, L. F.; Innocenti, A.; Vullo, D.; Charman, S. A.; Supuran, C. T.; Poulsen, S. A., Sulfonamide linked neoglycoconjugates-A new class of inhibitors for cancer-associated carbonic anhydrases. J. Med. Chem., 2010, 53 (7), 2913-2926.
    • (2010) J. Med. Chem , vol.53 , Issue.7 , pp. 2913-2926
    • Lopez, M.1    Bornaghi, L.F.2    Innocenti, A.3    Vullo, D.4    Charman, S.A.5    Supuran, C.T.6    Poulsen, S.A.7
  • 14
    • 70350072336 scopus 로고    scopus 로고
    • S-glycosyl primary sulfonamides - A new structural class for selective inhibition of cancerassociated carbonic anhydrases
    • Lopez, M.; Paul, B.; Hofmann, A.; Morizzi, J.; Wu, Q. K.; Charman, S. A.; Innocenti, A.; Vullo, D.; Supuran, C. T.; Poulsen, S. A., S-glycosyl primary sulfonamides - A new structural class for selective inhibition of cancerassociated carbonic anhydrases. J. Med. Chem., 2009, 52 (20), 6421-6432.
    • (2009) J. Med. Chem , vol.52 , Issue.20 , pp. 6421-6432
    • Lopez, M.1    Paul, B.2    Hofmann, A.3    Morizzi, J.4    Wu, Q.K.5    Charman, S.A.6    Innocenti, A.7    Vullo, D.8    Supuran, C.T.9    Poulsen, S.A.10
  • 15
    • 80053563164 scopus 로고    scopus 로고
    • Interfering with pH regulation in tumours as a therapeutic strategy
    • Neri, D.; Supuran, C. T., Interfering with pH regulation in tumours as a therapeutic strategy. Nat. Rev. Drug Disc., 2011, 10(10), 767-777.
    • (2011) Nat. Rev. Drug Disc , vol.10 , Issue.10 , pp. 767-777
    • Neri, D.1    Supuran, C.T.2
  • 17
    • 38849143765 scopus 로고    scopus 로고
    • Carbonic anhydrases: Novel therapeutic applications for inhibitors and activators
    • Supuran, C. T., Carbonic anhydrases: Novel therapeutic applications for inhibitors and activators. Nat. Rev. Drug Disc.,2008, 7 (2), 168-181.
    • (2008) Nat. Rev. Drug Disc , vol.7 , Issue.2 , pp. 168-181
    • Supuran, C.T.1
  • 18
    • 84889331040 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors targeting cancer: Therapeutic, immunologic, and diagnostic tools targeting isoforms IX and XI
    • Supuran, C. T.; Winum, J.-Y., Ed.; Wiley: Hoboken
    • Pastoreková, S.; Barathova, M.; Kopacek, J.; Pastorek, J., Carbonic anhydrase inhibitors targeting cancer: Therapeutic, immunologic, and diagnostic tools targeting isoforms IX and XI. Drug Design of Zinc-enzyme Inhibitors; Supuran, C. T.; Winum, J.-Y., Ed.; Wiley: Hoboken 2009; pp. 193-222.
    • (2009) Drug Design of Zinc-enzyme Inhibitors , pp. 193-222
    • Pastoreková, S.1    Barathova, M.2    Kopacek, J.3    Pastorek, J.4
  • 20
    • 0032568397 scopus 로고    scopus 로고
    • Physicochemical high throughput screening: Parallel artificial membrane permeation assay in the description of passive absorption processes
    • Kansy, M.; Senner, F.; Gubernator, K., Physicochemical high throughput screening: Parallel artificial membrane permeation assay in the description of passive absorption processes. J. Med. Chem., 1998, 41 (7), 1007-1010.
    • (1998) J. Med. Chem , vol.41 , Issue.7 , pp. 1007-1010
    • Kansy, M.1    Senner, F.2    Gubernator, K.3
  • 21
    • 79955558727 scopus 로고    scopus 로고
    • Synthesis of sulfonamide- bridged glycomimetics
    • Lopez, M.; Bornaghi, L. F.; Driguez, H.; Poulsen, S. A., Synthesis of sulfonamide- bridged glycomimetics. J. Org. Chem., 2011, 76 (9), 2965-2975.
    • (2011) J. Org. Chem , vol.76 , Issue.9 , pp. 2965-2975
    • Lopez, M.1    Bornaghi, L.F.2    Driguez, H.3    Poulsen, S.A.4
  • 22
    • 0344927809 scopus 로고    scopus 로고
    • A Novel Sulfonamidoglycosylation of Glycals
    • Colinas, P. A.; Bravo, R. D., A Novel Sulfonamidoglycosylation of Glycals. Org. Lett., 2003, 5 (23), 4509-4511.
    • (2003) Org. Lett , vol.5 , Issue.23 , pp. 4509-4511
    • Colinas, P.A.1    Bravo, R.D.2
  • 23
    • 0035936677 scopus 로고    scopus 로고
    • Facile C1 epimerization of β-1-sulfonamidyl-2-deoxy-2-iodoglycopyranosides
    • Owens, J. M.; Yeung, B. K. S.; Hill, D. C.; Petillo, P. A., Facile C1 epimerization of β-1-sulfonamidyl-2-deoxy-2-iodoglycopyranosides. J. Org. Chem., 2001, 66 (4), 1484-1486.
    • (2001) J. Org. Chem. , vol.66 , Issue.4 , pp. 1484-1486
    • Owens, J.M.1    Yeung, B.K.S.2    Hill, D.C.3    Petillo, P.A.4
  • 24
    • 0035864875 scopus 로고    scopus 로고
    • Conformational preferences in glycosylamines. Implications for the exoanomeric effect
    • Batchelor, R. J.; Green, D. F.; Johnston, B. D.; Patrick, B. O.; Pinto, B. M., Conformational preferences in glycosylamines. Implications for the exoanomeric effect. Carbohydrate Res., 2001, 330 (3), 421-426.
    • (2001) Carbohydrate Res , vol.330 , Issue.3 , pp. 421-426
    • Batchelor, R.J.1    Green, D.F.2    Johnston, B.D.3    Patrick, B.O.4    Pinto, B.M.5
  • 25
    • 0035829356 scopus 로고    scopus 로고
    • Synthesis of erythro and threo furanoid glycals from 1- and 2-phenylselenenyl-carbohydrate derivatives
    • Bravo, F.; Kassou, M.; Díaz, Y.; Castillón, S., Synthesis of erythro and threo furanoid glycals from 1- and 2-phenylselenenyl-carbohydrate derivatives. Carbohydrate Res., 2001, 336 (2), 83-97.
    • (2001) Carbohydrate Res , vol.336 , Issue.2 , pp. 83-97
    • Bravo, F.1    Kassou, M.2    Díaz, Y.3    Castillón, S.4
  • 26
    • 13744260946 scopus 로고    scopus 로고
    • Sulfonamidoglycosylation of methyl ribofuranosides: A novel approach to furanosylsulfonamides
    • Colinas, P. A.; Bravo, R. D., Sulfonamidoglycosylation of methyl ribofuranosides: A novel approach to furanosylsulfonamides. Tetrahedron Lett., 2005, 46 (10), 1687-1689.
    • (2005) Tetrahedron Lett , vol.46 , Issue.10 , pp. 1687-1689
    • Colinas, P.A.1    Bravo, R.D.2
  • 27
    • 45949093914 scopus 로고    scopus 로고
    • Sulfonamidoglycosylation of methyl glycosides employing perchloric acid supported on silica gel
    • Colinas, P. A.; Núñez, N. A.; Bravo, R. D., Sulfonamidoglycosylation of methyl glycosides employing perchloric acid supported on silica gel. J. Carbohydrate Chem., 2008, 27 (3), 141-147.
    • (2008) J. Carbohydrate Chem , vol.27 , Issue.3 , pp. 141-147
    • Colinas, P.A.1    Núñez, N.A.2    Bravo, R.D.3
  • 28
    • 77953320381 scopus 로고    scopus 로고
    • Perchloric acid and its salts: Very powerful catalysts in organic chemistry
    • Dalpozzo, R.; Bartoli, G.; Sambri, L.; Melchiorre, P., Perchloric acid and its salts: Very powerful catalysts in organic chemistry. Chemical Rev., 2010, 110 (6), 3501-3551.
    • (2010) Chemical Rev , vol.110 , Issue.6 , pp. 3501-3551
    • Dalpozzo, R.1    Bartoli, G.2    Sambri, L.3    Melchiorre, P.4
  • 29
    • 36148991800 scopus 로고    scopus 로고
    • Synthesis of amides and sulfonamides of β-Dgalactopyranosylamine and β -lactosylamine and evaluation of their interactions with the lectins from Erythrina cristagalli and Ricinus communis
    • Butera, A. P.; De Souza Filho, J. D.; Carvalho, D. T.; Figueiredo, R. C.; De Faria, L. C. A.; Nunes, M. A.; Prado, M. A. F.; Alves, R. J.; De Andrade, M. H. G.; Silva, K. T. S., Synthesis of amides and sulfonamides of β-Dgalactopyranosylamine and β -lactosylamine and evaluation of their interactions with the lectins from Erythrina cristagalli and Ricinus communis. Quim. Nova, 2007, 30 (5), 1267-1274.
    • (2007) Quim. Nova , vol.30 , Issue.5 , pp. 1267-1274
    • Butera, A.P.1    de Souza Filho, J.D.2    Carvalho, D.T.3    Figueiredo, R.C.4    de Faria, L.C.A.5    Nunes, M.A.6    Prado, M.A.F.7    Alves, R.J.8    de Andrade, M.H.G.9    Silva, K.T.S.10
  • 30
    • 70349176081 scopus 로고    scopus 로고
    • Facile synthesis of N-glycosyl amides using a N-glycosyl-2,4-dinitrobenzenesulfonamide and thioacids
    • Talan, R. S.; Sanki, A. K.; Sucheck, S. J., Facile synthesis of N-glycosyl amides using a N-glycosyl-2,4-dinitrobenzenesulfonamide and thioacids. Carbohydrate Res.,2009, 344 (15), 2048-2050.
    • (2009) Carbohydrate Res , vol.344 , Issue.15 , pp. 2048-2050
    • Talan, R.S.1    Sanki, A.K.2    Sucheck, S.J.3
  • 31
    • 0032006361 scopus 로고    scopus 로고
    • Glycotargeting: The preparation of glyco-amino acids and derivatives from unprotected reducing sugars
    • Monsigny, M.; Quétard, C.; Bourgerie, S.; Delay, D.; Pichon, C.; Midoux, P.; Mayer, R.; Roche, A. C., Glycotargeting: The preparation of glyco-amino acids and derivatives from unprotected reducing sugars. Biochimie, 1998, 80 (2), 99-108.
    • (1998) Biochimie , vol.80 , Issue.2 , pp. 99-108
    • Monsigny, M.1    Quétard, C.2    Bourgerie, S.3    Delay, D.4    Pichon, C.5    Midoux, P.6    Mayer, R.7    Roche, A.C.8
  • 32
    • 77958054104 scopus 로고    scopus 로고
    • Stereoselective synthesis of novel N-β-glycosyl sulfonamides by sulfonamidoglycosylation of per-O-acetylated sugars
    • Colinas, P. A.; Témpera, C. A.; Rodriguez, O. M.; Bravo, R. D., Stereoselective synthesis of novel N-β-glycosyl sulfonamides by sulfonamidoglycosylation of per-O-acetylated sugars. Synthesis, 2009, (24), 4143-4148.
    • (2009) Synthesis , vol.24 , pp. 4143-4148
    • Colinas, P.A.1    Témpera, C.A.2    Rodriguez, O.M.3    Bravo, R.D.4
  • 33
    • 79960349940 scopus 로고    scopus 로고
    • N-β-Glycosyl sulfamides are selective inhibitors of the cancer associated carbonic anhydrase isoforms IX and XII
    • Rodríguez, O. M.; Maresca, A.; Témpera, C. A.; Bravo, R. D.; Colinas, P. A.; Supuran, C. T., N-β-Glycosyl sulfamides are selective inhibitors of the cancer associated carbonic anhydrase isoforms IX and XII. Bioorg. Med. Chem., Lett., 2011, 21 (15), 4447-4450.
    • (2011) Bioorg. Med. Chem., Lett , vol.21 , Issue.15 , pp. 4447-4450
    • Rodríguez, O.M.1    Maresca, A.2    Témpera, C.A.3    Bravo, R.D.4    Colinas, P.A.5    Supuran, C.T.6
  • 35
    • 4143104581 scopus 로고    scopus 로고
    • Tris(pentafluorophenyl)borane catalyzed Ferrier azaglycosylation with sulfonamides and carbamates
    • Chandrasekhar, S.; Reddy, C. R.; Chandrashekar, G., Tris(pentafluorophenyl)borane catalyzed Ferrier azaglycosylation with sulfonamides and carbamates. Tetrahedron Lett., 2004, 45 (34), 6481-6484.
    • (2004) Tetrahedron Lett , vol.45 , Issue.34 , pp. 6481-6484
    • Chandrasekhar, S.1    Reddy, C.R.2    Chandrashekar, G.3
  • 36
    • 34548148871 scopus 로고    scopus 로고
    • Ferrier sulfonamidoglycosylation of D-glycals
    • Colinas, P. A.; Bravo, R. D., Ferrier sulfonamidoglycosylation of D-glycals. Carbohydrate Res.,2007, 342 (15), 2297-2302.
    • (2007) Carbohydrate Res , vol.342 , Issue.15 , pp. 2297-2302
    • Colinas, P.A.1    Bravo, R.D.2
  • 37
    • 53849109146 scopus 로고    scopus 로고
    • X-ray crystallographic and high-resolution NMR spectroscopy characterization of 4,6-di-O-acetyl-2,3- dideoxy- β-d-erythro-hex-2-enopyranosyl sulfamide
    • Colinas, P. A.; Bravo, R. D.; Echeverría, G. A., X-ray crystallographic and high-resolution NMR spectroscopy characterization of 4,6-di-O-acetyl-2,3- dideoxy- β-d-erythro-hex-2-enopyranosyl sulfamide. Carbohydrate Res., 2008, 343 (17), 3005-3008.
    • (2008) Carbohydrate Res , vol.343 , Issue.17 , pp. 3005-3008
    • Colinas, P.A.1    Bravo, R.D.2    Echeverría, G.A.3
  • 38
    • 58949097547 scopus 로고    scopus 로고
    • Experimental and theoretical study of the conformational, vibrational and magnetic properties of 4,6-di-Oacetyl- 2,3-dideoxy-D-threo-hex-2-enopyranosyl ethanesulfonamide
    • Alegre, M.L.; Diez, R. P.; Colinas, P. A., Experimental and theoretical study of the conformational, vibrational and magnetic properties of 4,6-di-Oacetyl- 2,3-dideoxy-D-threo-hex-2-enopyranosyl ethanesulfonamide. J. Mol. Struct., 2009, 919 (1/3), 223-226.
    • (2009) J. Mol. Struct , vol.919 , Issue.1-3 , pp. 223-226
    • Alegre, M.L.1    Diez, R.P.2    Colinas, P.A.3
  • 39
    • 79951515664 scopus 로고    scopus 로고
    • A combined theoretical and spectroscopic study of 4,6-di-O-acetyl-2,3-dideoxy-d-erythro-hex-2- enopyranosyl sulfamide: A novel glycosyl carbonic anhydrase IX inhibitor
    • Lavecchia, M. J.; Diez, R. P.; Colinas, P. A., A combined theoretical and spectroscopic study of 4,6-di-O-acetyl-2,3-dideoxy-d-erythro-hex-2- enopyranosyl sulfamide: A novel glycosyl carbonic anhydrase IX inhibitor. Carbohydrate Res., 2011, 346 (3), 442-448.
    • (2011) Carbohydrate Res , vol.346 , Issue.3 , pp. 442-448
    • Lavecchia, M.J.1    Diez, R.P.2    Colinas, P.A.3
  • 40
    • 79960963804 scopus 로고    scopus 로고
    • Efficient synthesis of 2,3- unsaturated sulfonamidoglycosides by Amberlyst 15
    • Témpera, C. A.; Colinas, P. A.; Bravo, R. D., Efficient synthesis of 2,3- unsaturated sulfonamidoglycosides by Amberlyst 15. Tetrahedron Lett., 2010, 51 (41), 5372-5374.
    • (2010) Tetrahedron Lett , vol.51 , Issue.41 , pp. 5372-5374
    • Témpera, C.A.1    Colinas, P.A.2    Bravo, R.D.3
  • 41
    • 1342302272 scopus 로고    scopus 로고
    • Solid Acid Catalysts for Industrial Condensations of Ketones and Aldehydes with Aromatics
    • De Angelis, A.; Ingallina, P.; Perego, C., Solid Acid Catalysts for Industrial Condensations of Ketones and Aldehydes with Aromatics. Indust. Eng. Chem. Res., 2004, 43 (5), 1169-1178.
    • (2004) Indust. Eng. Chem. Res , vol.43 , Issue.5 , pp. 1169-1178
    • de Angelis, A.1    Ingallina, P.2    Perego, C.3
  • 42
    • 33847104634 scopus 로고    scopus 로고
    • Amberlyst 15-catalyzed efficient synthesis of 2,3-unsaturated glycosides via Ferrier rearrangement for glycal
    • Tian, Q.; Zhu, X. M.; Yang, J. S., Amberlyst 15-catalyzed efficient synthesis of 2,3-unsaturated glycosides via Ferrier rearrangement for glycal. Synthetic Comm., 2007, 37 (5), 691-701.
    • (2007) Synthetic Comm , vol.37 , Issue.5 , pp. 691-701
    • Tian, Q.1    Zhu, X.M.2    Yang, J.S.3
  • 43
    • 77953123688 scopus 로고    scopus 로고
    • A mild and efficient synthetic protocol for Ferrier azaglycosylation promoted by ZnCl2/Al2O3
    • Ding, F.; William, R.; Gorityala, B. K.; Ma, J.; Wang, S.; Liu, X. W., A mild and efficient synthetic protocol for Ferrier azaglycosylation promoted by ZnCl2/Al2O3. Tetrahedron Lett., 2010, 51 (23), 3146-3148.
    • (2010) Tetrahedron Lett , vol.51 , Issue.23 , pp. 3146-3148
    • Ding, F.1    William, R.2    Gorityala, B.K.3    Ma, J.4    Wang, S.5    Liu, X.W.6
  • 44
    • 34547890260 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I and II, and extracellular isoforms IV, IX, and XII with sulfamides incorporating sugar moieties
    • Colinas, P. A.; Bravo, R. D.; Vullo, D.; Scozzafava, A.; Supuran, C. T., Carbonic anhydrase inhibitors. Inhibition of cytosolic isoforms I and II, and extracellular isoforms IV, IX, and XII with sulfamides incorporating sugar moieties. Bioorg. Med. Chem. Lett., 2007, 17 (18), 5086-5090.
    • (2007) Bioorg. Med. Chem. Lett , vol.17 , Issue.18 , pp. 5086-5090
    • Colinas, P.A.1    Bravo, R.D.2    Vullo, D.3    Scozzafava, A.4    Supuran, C.T.5
  • 45
    • 84859870939 scopus 로고    scopus 로고
    • Recent developments in targeting carbonic anhydrase IX for cancer therapeutics
    • McDonald, P. C.; Winum, J.-Y.; Supuran, C. T.; Dedhar, S. Recent developments in targeting carbonic anhydrase IX for cancer therapeutics. Oncotarget 2012, 3(1), 84-97.
    • (2012) Oncotarget , vol.3 , Issue.1 , pp. 84-97
    • McDonald, P.C.1    Winum, J.-Y.2    Supuran, C.T.3    Dedhar, S.4
  • 46
    • 1942438028 scopus 로고    scopus 로고
    • Microtubules as a target for anticancer drugs
    • Jordan, M. A.; Wilson, L., Microtubules as a target for anticancer drugs. Nat. Rev. Cancer, 2004, 4 (4), 253-265.
    • (2004) Nat. Rev. Cancer , vol.4 , Issue.4 , pp. 253-265
    • Jordan, M.A.1    Wilson, L.2
  • 48
    • 34247118852 scopus 로고    scopus 로고
    • Selective COX-2 inhibitor, NS-398, suppresses cellular proliferation in human hepatocellular carcinoma cell lines via cell cycle arrest
    • Baek, J. Y.; Hur, W.; Wang, J. S.; Bae, S. H.; Yoon, S. K., Selective COX-2 inhibitor, NS-398, suppresses cellular proliferation in human hepatocellular carcinoma cell lines via cell cycle arrest. World J. Gastroenterol., 2007, 13 (8), 1175-1181.
    • (2007) World J. Gastroenterol , vol.13 , Issue.8 , pp. 1175-1181
    • Baek, J.Y.1    Hur, W.2    Wang, J.S.3    Bae, S.H.4    Yoon, S.K.5
  • 49
    • 33644766747 scopus 로고    scopus 로고
    • Cytotoxicity of a noncyclooxygenase- 2 inhibitory derivative of celecoxib in non-small-cell lung cancer A549 cells
    • Tong, Z.; Wu, X.; Chen, C. S.; Kehrer, J. P., Cytotoxicity of a noncyclooxygenase- 2 inhibitory derivative of celecoxib in non-small-cell lung cancer A549 cells. Lung Cancer, 2006, 52 (1), 117-124.
    • (2006) Lung Cancer , vol.52 , Issue.1 , pp. 117-124
    • Tong, Z.1    Wu, X.2    Chen, C.S.3    Kehrer, J.P.4
  • 50
    • 70450230732 scopus 로고    scopus 로고
    • Recent development and SAR analysis of colchicine binding site inhibitors
    • Chen, J.; Liu, T.; Dong, X.; Hu, Y., Recent development and SAR analysis of colchicine binding site inhibitors. Mini-Reviews in Medicinal Chemistry 2009, 9 (10), 1174-1190.
    • (2009) Mini-Reviews In Medicinal Chemistry , vol.9 , Issue.10 , pp. 1174-1190
    • Chen, J.1    Liu, T.2    Dong, X.3    Hu, Y.4
  • 52
    • 77955336015 scopus 로고    scopus 로고
    • Pteridine-sulfonamide conjugates as dual inhibitors of carbonic anhydrases and dihydrofolate reductase with potential antitumor activity
    • Marques, S. M.; Enyedy, E. A.; Supuran, C. T.; Krupenko, N. I.; Krupenko, S. A.; Amélia Santos, M., Pteridine-sulfonamide conjugates as dual inhibitors of carbonic anhydrases and dihydrofolate reductase with potential antitumor activity. Bioorg. Med. Chem., 2010, 18 (14), 5081-5089.
    • (2010) Bioorg. Med. Chem , vol.18 , Issue.14 , pp. 5081-5089
    • Marques, S.M.1    Enyedy, E.A.2    Supuran, C.T.3    Krupenko, N.I.4    Krupenko, S.A.5    Amélia Santos, M.6


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