메뉴 건너뛰기




Volumn 6, Issue 3, 2015, Pages 292-295

α-carbonic anhydrases possess thioesterase activity

Author keywords

Carbonic anhydrase; inhibitors; prodrugs; thioesterase

Indexed keywords

ALPHA CARBONIC ANHYDRASE; BENZENESULFONAMIDE DERIVATIVE; CARBONATE DEHYDRATASE; DITHIOCARBAMATE ESTER; DITHIOCARBAMIC ACID DERIVATIVE; ENZYME INHIBITOR; METHANETHIOL; PRODRUG; THIOL ESTER HYDROLASE; UNCLASSIFIED DRUG;

EID: 84924744865     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml500470b     Document Type: Article
Times cited : (42)

References (30)
  • 1
    • 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 Discovery 2008, 7, 168-181
    • (2008) Nat. Rev. Drug Discovery , vol.7 , pp. 168-181
    • Supuran, C.T.1
  • 2
    • 84863501358 scopus 로고    scopus 로고
    • Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms?
    • Alterio, V.; Di Fiore, A.; DAmbrosio, 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
    • (2012) Chem. Rev. , vol.112 , pp. 4421-4468
    • Alterio, V.1    Di Fiore, A.2    Dambrosio, K.3    Supuran, C.T.4    De Simone, G.5
  • 4
    • 84865850354 scopus 로고    scopus 로고
    • Structure-based drug discovery of carbonic anhydrase inhibitors
    • Supuran, C. T. Structure-based drug discovery of carbonic anhydrase inhibitors J. Enzyme Inhib. Med. Chem. 2012, 27, 759-772
    • (2012) J. Enzyme Inhib. Med. Chem. , vol.27 , pp. 759-772
    • Supuran, C.T.1
  • 6
    • 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 Discovery 2011, 10, 767-777
    • (2011) Nat. Rev. Drug Discovery , vol.10 , pp. 767-777
    • Neri, D.1    Supuran, C.T.2
  • 7
    • 84858420920 scopus 로고    scopus 로고
    • (In)organic anions as carbonic anhydrase inhibitors
    • De Simone, G.; Supuran, C. T. (In)organic anions as carbonic anhydrase inhibitors J. Inorg. Biochem. 2012, 111, 117-129
    • (2012) J. Inorg. Biochem. , vol.111 , pp. 117-129
    • De Simone, G.1    Supuran, C.T.2
  • 9
    • 84879037030 scopus 로고    scopus 로고
    • Secondary/tertiary benzenesulfonamides with inhibitory action against the cytosolic human carbonic anhydrase isoforms i and II
    • Alp, C.; Maresca, A.; Alp, N. A.; Gültekin, M. S.; Ekinci, D.; Scozzafava, A.; Supuran, C. T. Secondary/tertiary benzenesulfonamides with inhibitory action against the cytosolic human carbonic anhydrase isoforms I and II J. Enzyme Inhib. Med. Chem. 2013, 28, 294-298
    • (2013) J. Enzyme Inhib. Med. Chem. , vol.28 , pp. 294-298
    • Alp, C.1    Maresca, A.2    Alp, N.A.3    Gültekin, M.S.4    Ekinci, D.5    Scozzafava, A.6    Supuran, C.T.7
  • 10
    • 0013843449 scopus 로고
    • The catalytic versatility of erythrocyte carbonic anhydrase the enzyme-catalyzed hydrolysis of para-nitrophenyl acetate
    • Pocker, Y.; Stone, J. T. The catalytic versatility of erythrocyte carbonic anhydrase. The enzyme-catalyzed hydrolysis of para-nitrophenyl acetate J. Am. Chem. Soc. 1965, 87, 5497-5498
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 5497-5498
    • Pocker, Y.1    Stone, J.T.2
  • 12
    • 84870560662 scopus 로고    scopus 로고
    • Simple methanesulfonates are hydrolyzed by the sulfatase carbonic anhydrase activity
    • Kazančlu, E. A.; Güney, M.; Şentürk, M.; Supuran, C. T. Simple methanesulfonates are hydrolyzed by the sulfatase carbonic anhydrase activity J. Enzyme Inhib. Med. Chem. 2012, 27, 880-885
    • (2012) J. Enzyme Inhib. Med. Chem. , vol.27 , pp. 880-885
    • Kazančlu, E.A.1    Güney, M.2    Şentürk, M.3    Supuran, C.T.4
  • 13
    • 77957876033 scopus 로고    scopus 로고
    • Paraoxon, 4-nitrophenyl phosphate and acetate are substrates of α- But not of β-, γ- And ζ-carbonic anhydrases
    • Innocenti, A.; Supuran, C. T. Paraoxon, 4-nitrophenyl phosphate and acetate are substrates of α- but not of β-, γ- and ζ-carbonic anhydrases Bioorg. Med. Chem. Lett. 2010, 20, 6208-6212
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 6208-6212
    • Innocenti, A.1    Supuran, C.T.2
  • 14
    • 41149141063 scopus 로고    scopus 로고
    • Investigations of the esterase, phosphatase, and sulfatase activities of the cytosolic mammalian carbonic anhydrase isoforms I, II, and XIII with 4-nitrophenyl esters as substrates
    • Innocenti, A.; Scozzafava, A.; Parkkila, S.; Puccetti, L.; De Simone, G.; Supuran, C. T. Investigations of the esterase, phosphatase, and sulfatase activities of the cytosolic mammalian carbonic anhydrase isoforms I, II, and XIII with 4-nitrophenyl esters as substrates Bioorg. Med. Chem. Lett. 2008, 18, 2267-2271
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 2267-2271
    • Innocenti, A.1    Scozzafava, A.2    Parkkila, S.3    Puccetti, L.4    De Simone, G.5    Supuran, C.T.6
  • 17
    • 0032708011 scopus 로고    scopus 로고
    • Carbonic anhydrase catalyzes cyanamide hydration to urea: Is it mimicking the physiological reaction?
    • Briganti, F.; Mangani, S.; Scozzafava, A.; Vernaglione, G.; Supuran, C. T. Carbonic anhydrase catalyzes cyanamide hydration to urea: is it mimicking the physiological reaction? J. Biol. Inorg. Chem. 1999, 4, 528-536
    • (1999) J. Biol. Inorg. Chem. , vol.4 , pp. 528-536
    • Briganti, F.1    Mangani, S.2    Scozzafava, A.3    Vernaglione, G.4    Supuran, C.T.5
  • 18
    • 0007530501 scopus 로고
    • The catalytic versatility of carbonic anhydrase fro erythrocytes the enzymatic catalyzed hydration of acetaldehyde
    • Pocker, Y.; Meany, J. E. The catalytic versatility of carbonic anhydrase fro erythrocytes. The enzymatic catalyzed hydration of acetaldehyde J. Am. Chem. Soc. 1965, 87, 1809-1811
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 1809-1811
    • Pocker, Y.1    Meany, J.E.2
  • 20
    • 74849118851 scopus 로고    scopus 로고
    • Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins
    • Maresca, A.; Temperini, C.; Pochet, L.; Masereel, B.; Scozzafava, A.; Supuran, C. T. Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins J. Med. Chem. 2010, 53, 335-344
    • (2010) J. Med. Chem. , vol.53 , pp. 335-344
    • Maresca, A.1    Temperini, C.2    Pochet, L.3    Masereel, B.4    Scozzafava, A.5    Supuran, C.T.6
  • 21
    • 84858288806 scopus 로고    scopus 로고
    • Novel coumarins and 2-thioxo-coumarins as inhibitors of the tumor-associated carbonic anhydrases IX and XII
    • Carta, F.; Maresca, A.; Scozzafava, A.; Supuran, C. T. Novel coumarins and 2-thioxo-coumarins as inhibitors of the tumor-associated carbonic anhydrases IX and XII Bioorg. Med. Chem. 2012, 20, 2266-2273
    • (2012) Bioorg. Med. Chem. , vol.20 , pp. 2266-2273
    • Carta, F.1    Maresca, A.2    Scozzafava, A.3    Supuran, C.T.4
  • 22
    • 0017107411 scopus 로고
    • Interaction of cobalt-bovine carbonic anhydrase with the acetate ion
    • Bertini, I.; Luchinat, C.; Scozzafava, A. Interaction of cobalt-bovine carbonic anhydrase with the acetate ion Biochim. Biophys. Acta 1976, 452, 239-244
    • (1976) Biochim. Biophys. Acta , vol.452 , pp. 239-244
    • Bertini, I.1    Luchinat, C.2    Scozzafava, A.3
  • 23
    • 0015239422 scopus 로고
    • The carbon dioxide hydration activity of carbonic anhydrase
    • Khalifah, R. J. The carbon dioxide hydration activity of carbonic anhydrase J. Biol. Chem. 1971, 246, 2561-2573
    • (1971) J. Biol. Chem. , vol.246 , pp. 2561-2573
    • Khalifah, R.J.1
  • 24
    • 0029904689 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors. Part 37. Novel classes of isozyme i and II inhibitors and their mechanism of action. Kinetic and spectroscopic investigations on native and cobalt-substituted enzymes
    • Briganti, F.; Pierattelli, R.; Scozzafava, A.; Supuran, C. T. Carbonic anhydrase inhibitors. Part 37. Novel classes of isozyme I and II inhibitors and their mechanism of action. Kinetic and spectroscopic investigations on native and cobalt-substituted enzymes Eur. J. Med. Chem. 1996, 31, 1001-1010
    • (1996) Eur. J. Med. Chem. , vol.31 , pp. 1001-1010
    • Briganti, F.1    Pierattelli, R.2    Scozzafava, A.3    Supuran, C.T.4
  • 25
    • 0346252639 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibitors: X ray crystallographic structure of the adduct of human isozyme II with a EMATE, a dual inhibitor of carbonic anhydrases and steroid sulfatase
    • Abbate, F.; Winum, J. Y.; Potter, B. V.; Casini, A.; Montero, J. L.; Scozzafava, A.; Supuran, C. T. Carbonic anhydrase inhibitors: X ray crystallographic structure of the adduct of human isozyme II with a EMATE, a dual inhibitor of carbonic anhydrases and steroid sulfatase Bioorg. Med. Chem. Lett. 2004, 14, 231-234
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 231-234
    • Abbate, F.1    Winum, J.Y.2    Potter, B.V.3    Casini, A.4    Montero, J.L.5    Scozzafava, A.6    Supuran, C.T.7
  • 26
    • 77954011231 scopus 로고    scopus 로고
    • Thioesterases: A new prespective based on their primary and tertiary structures
    • Cantu, D. C.; Chen, Y.; Reilly, P. J. Thioesterases: A new prespective based on their primary and tertiary structures Protein Sci. 2010, 19, 1281-1295
    • (2010) Protein Sci. , vol.19 , pp. 1281-1295
    • Cantu, D.C.1    Chen, Y.2    Reilly, P.J.3
  • 27
    • 84921473930 scopus 로고    scopus 로고
    • Repositioning proton pump inhibitors as anti-cancer drugs by targeting the thioesterase domain of human fatty acid synthase
    • Fako, V.; Wu, X.; Pflug, B.; Liu, J. Y.; Zhang, J. T. Repositioning proton pump inhibitors as anti-cancer drugs by targeting the thioesterase domain of human fatty acid synthase J. Med. Chem. 2014, 10.1021/jm501543u
    • (2014) J. Med. Chem.
    • Fako, V.1    Wu, X.2    Pflug, B.3    Liu, J.Y.4    Zhang, J.T.5
  • 30
    • 84879407175 scopus 로고    scopus 로고
    • Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors
    • De Simone, G.; Alterio, V.; Supuran, C. T. Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors Expert Opin. Drug Discovery 2013, 8, 793-810
    • (2013) Expert Opin. Drug Discovery , vol.8 , pp. 793-810
    • De Simone, G.1    Alterio, V.2    Supuran, C.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.