-
2
-
-
38849143765
-
Carbonic anhydrases: Novel therapeutic applications for inhibitors and activators
-
Supuran CT. Carbonic anhydrases: Novel therapeutic applications for inhibitors and activators. Nat Rev Drug Discov 2008;7:168-81.
-
(2008)
Nat Rev Drug Discov
, vol.7
, pp. 168-181
-
-
Supuran, C.T.1
-
3
-
-
79961070760
-
Carbonic anhydrase inhibitors and activators for novel therapeutic applications
-
Supuran CT. Carbonic anhydrase inhibitors and activators for novel therapeutic applications. Future Med Chem 2011;3:1165-80.
-
(2011)
Future Med Chem
, vol.3
, pp. 1165-1180
-
-
Supuran, C.T.1
-
4
-
-
84863501358
-
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, et al. Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms? Chem Rev 2012;112:4421-68.
-
(2012)
Chem Rev
, vol.112
, pp. 4421-4468
-
-
Alterio, V.1
Di Fiore, A.2
D'Ambrosio, K.3
-
5
-
-
84865850354
-
Structure-based drug discovery of carbonic anhydrase inhibitors
-
Supuran CT. Structure-based drug discovery of carbonic anhydrase inhibitors. J Enzym Inhib Med Chem 2012;27:759-72.
-
(2012)
J Enzym Inhib Med Chem
, vol.27
, pp. 759-772
-
-
Supuran, C.T.1
-
6
-
-
78649857406
-
Carbonic anhydrase inhibition/activation: Trip of a scientist around the world in the search of novel chemotypes and drug targets
-
Supuran CT. Carbonic anhydrase inhibition/activation: Trip of a scientist around the world in the search of novel chemotypes and drug targets. Curr Pharm Design 2010;16:3233-45.
-
(2010)
Curr Pharm Design
, vol.16
, pp. 3233-3245
-
-
Supuran, C.T.1
-
9
-
-
33746934196
-
New zinc binding motifs in the design of selective carbonic anhydrase inhibitors
-
Winum JY, Scozzafava A, Montero JL, Supuran CT. New zinc binding motifs in the design of selective carbonic anhydrase inhibitors. Mini Rev Med Chem 2006;6:921-36.
-
(2006)
Mini Rev Med Chem
, vol.6
, pp. 921-936
-
-
Winum, J.Y.1
Scozzafava, A.2
Montero, J.L.3
Supuran, C.T.4
-
10
-
-
76649098835
-
Carbonic anhydrase inhibitors. Inhibition of transmembrane isoforms IX, XII, and XIV with less investigated anions including trithiocarbonate and dithiocarbamate
-
Innocenti A, Scozzafava A, Supuran CT. Carbonic anhydrase inhibitors. Inhibition of transmembrane isoforms IX, XII, and XIV with less investigated anions including trithiocarbonate and dithiocarbamate. Bioorg Med Chem Lett 2010;20:1548-50.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 1548-1550
-
-
Innocenti, A.1
Scozzafava, A.2
Supuran, C.T.3
-
11
-
-
72249106865
-
Carbonic anhydrase inhibitors. X-ray crystal studies of the carbonic anhydrase IItrithiocarbonate adduct-an inhibitor mimicking the sulfonamide and urea binding to the enzyme
-
Temperini C, Scozzafava A, Supuran CT. Carbonic anhydrase inhibitors. X-ray crystal studies of the carbonic anhydrase IItrithiocarbonate adduct-an inhibitor mimicking the sulfonamide and urea binding to the enzyme. Bioorg Med Chem Lett 2010;20: 474-8.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 474-478
-
-
Temperini, C.1
Scozzafava, A.2
Supuran, C.T.3
-
12
-
-
84857420193
-
Dithiocarbamates strongly inhibit carbonic anhydrases and show antiglaucoma action in vivo
-
Carta F, Aggarwal M, Maresca A, et al. Dithiocarbamates strongly inhibit carbonic anhydrases and show antiglaucoma action in vivo. J Med Chem 2012;55:1721-30.
-
(2012)
J Med Chem
, vol.55
, pp. 1721-1730
-
-
Carta, F.1
Aggarwal, M.2
Maresca, A.3
-
13
-
-
84874604544
-
Dithiocarbamates strongly inhibit the b-class carbonic anhydrases from Mycobacterium tuberculosis
-
Maresca A, Carta F, Vullo D, Supuran CT. Dithiocarbamates strongly inhibit the b-class carbonic anhydrases from Mycobacterium tuberculosis. J Enzyme Inhib Med Chem 2013; 28:407-11.
-
(2013)
J Enzyme Inhib Med Chem
, vol.28
, pp. 407-411
-
-
Maresca, A.1
Carta, F.2
Vullo, D.3
Supuran, C.T.4
-
14
-
-
84855658697
-
Dithiocarbamates are strong inhibitors of the beta-class fungal carbonic anhydrases from Cryptococcus neoformans, Candida albicans and Candida glabrata
-
Monti SM, Maresca A, Viparelli F, et al. Dithiocarbamates are strong inhibitors of the beta-class fungal carbonic anhydrases from Cryptococcus neoformans, Candida albicans and Candida glabrata. Bioorg Med Chem Lett 2012;22:859-62.
-
(2012)
Bioorg Med Chem Lett
, vol.22
, pp. 859-862
-
-
Monti, S.M.1
Maresca, A.2
Viparelli, F.3
-
15
-
-
84855702121
-
Dithiocarbamates: A new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations
-
Carta F, Aggarwal M, Maresca A, et al. Dithiocarbamates: A new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations. Chem Comm 2012;48:1868-70.
-
(2012)
Chem Comm
, vol.48
, pp. 1868-1870
-
-
Carta, F.1
Aggarwal, M.2
Maresca, A.3
-
16
-
-
84879051423
-
Xanthates and trithiocarbonates strongly inhibit carbonic anhydrases and show antiglaucoma effects in vivo
-
Carta F, Akdemir A, Scozzafava A, et al. Xanthates and trithiocarbonates strongly inhibit carbonic anhydrases and show antiglaucoma effects in vivo. J Med Chem 2013;56:4691-700.
-
(2013)
J Med Chem
, vol.56
, pp. 4691-4700
-
-
Carta, F.1
Akdemir, A.2
Scozzafava, A.3
-
17
-
-
0034609778
-
Carbonic anhydrase and matrix metalloproteinase inhibitors: Sulfonylated amino acid hydroxamates with MMP inhibitory properties act as efficient inhibitors of CA isozymes I, II, and IV, and N-hydroxysulfonamides inhibit both these zinc enzymes
-
Scozzafava A, Supuran CT. Carbonic anhydrase and matrix metalloproteinase inhibitors: Sulfonylated amino acid hydroxamates with MMP inhibitory properties act as efficient inhibitors of CA isozymes I, II, and IV, and N-hydroxysulfonamides inhibit both these zinc enzymes. J Med Chem 2000;43:3677-87.
-
(2000)
J Med Chem
, vol.43
, pp. 3677-3687
-
-
Scozzafava, A.1
Supuran, C.T.2
-
18
-
-
33847003058
-
Carbonic anhydrase and matrix metalloproteinase inhibitors. Inhibition of human tumorassociated isozymes IX and cytosolic isozyme i and II with sulfonylated hydroxamates
-
Nuti E, Orlandini E, Nencetti S, et al. Carbonic anhydrase and matrix metalloproteinase inhibitors. Inhibition of human tumorassociated isozymes IX and cytosolic isozyme I and II with sulfonylated hydroxamates. Bioorg Med Chem 2007;15: 2298-311.
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 2298-2311
-
-
Nuti, E.1
Orlandini, E.2
Nencetti, S.3
-
19
-
-
58149086406
-
Dual inhibitors of matrix metalloproteinases and carbonic anhydrases: Iminodiacetyl-based hydroxamate-benzenesulfonamide conjugates
-
Marques SM, Nuti E, Rossello E, et al. Dual inhibitors of matrix metalloproteinases and carbonic anhydrases: iminodiacetyl-based hydroxamate-benzenesulfonamide conjugates. J Med Chem 2008; 51:7968-79.
-
(2008)
J Med Chem
, vol.51
, pp. 7968-7979
-
-
Marques, S.M.1
Nuti, E.2
Rossello, E.3
-
20
-
-
84864690761
-
Hydroxamate represents a versatile zinc binding group for the development of new carbonic anhydrase inhibitors
-
Di Fiore A, Maresca A, Supuran CT, De Simone G. Hydroxamate represents a versatile zinc binding group for the development of new carbonic anhydrase inhibitors. Chem Comm 2012;48:8838-40.
-
(2012)
Chem Comm
, vol.48
, pp. 8838-8840
-
-
Di Fiore, A.1
Maresca, A.2
Supuran, C.T.3
De Simone, G.4
-
21
-
-
84893073618
-
Design, synthesis, and evaluation of hydroxamic Acid derivatives as promising agents for the management of chagas disease
-
Rodrigues GC, Feijó DF, Bozza MT, et al. Design, synthesis, and evaluation of hydroxamic Acid derivatives as promising agents for the management of chagas disease. J Med Chem 2014;57: 298-308.
-
(2014)
J Med Chem
, vol.57
, pp. 298-308
-
-
Rodrigues, G.C.1
Feijó, D.F.2
Bozza, M.T.3
-
22
-
-
84874527057
-
Salicylaldoxime derivatives as new leads for the development of carbonic anhydrase inhibitors
-
Tuccinardi T, Bertini S, Granchi C, et al. Salicylaldoxime derivatives as new leads for the development of carbonic anhydrase inhibitors. Bioorg Med Chem 2013;21:1511-15.
-
(2013)
Bioorg Med Chem
, vol.21
, pp. 1511-1515
-
-
Tuccinardi, T.1
Bertini, S.2
Granchi, C.3
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