-
1
-
-
84872343989
-
Sulfocoumarins (1,2-benzoxathiine-2,2-dioxides): a class of potent and isoform-selective inhibitors of tumor-associated carbonic anhydrases
-
Tars, K.; Vullo, D.; Kazaks, A.; Leitans, J.; Lends, A.; Grandane, A.; Zalubovskis, R.; Scozzafava, A.; Supuran, C. T. Sulfocoumarins (1,2-benzoxathiine-2,2-dioxides): a class of potent and isoform-selective inhibitors of tumor-associated carbonic anhydrases J. Med. Chem. 2013, 56, 293-300
-
(2013)
J. Med. Chem.
, vol.56
, pp. 293-300
-
-
Tars, K.1
Vullo, D.2
Kazaks, A.3
Leitans, J.4
Lends, A.5
Grandane, A.6
Zalubovskis, R.7
Scozzafava, A.8
Supuran, C.T.9
-
2
-
-
67749116253
-
Non-zinc mediated inhibition of carbonic anhydrases: Coumarins are a new class of suicide inhibitors
-
Maresca, A.; Temperini, C.; Vu, H.; Pham, N. B.; Poulsen, S. A.; Scozzafava, A.; Quinn, R. J.; Supuran, C. T. Non-zinc mediated inhibition of carbonic anhydrases: Coumarins are a new class of suicide inhibitors J. Am. Chem. Soc. 2009, 131, 3057-62
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 3057-62
-
-
Maresca, A.1
Temperini, C.2
Vu, H.3
Pham, N.B.4
Poulsen, S.A.5
Scozzafava, A.6
Quinn, R.J.7
Supuran, C.T.8
-
3
-
-
74849118851
-
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
-
4
-
-
78449303755
-
7,8-Disubstituted- but not 6,7-disubstituted coumarins selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and II in the low nanomolar/subnanomolar range
-
Maresca, A.; Scozzafava, A.; Supuran, C. T. 7,8-Disubstituted- but not 6,7-disubstituted coumarins selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic ones I and II in the low nanomolar/subnanomolar range Bioorg. Med. Chem. Lett. 2010, 20, 7255-7258
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 7255-7258
-
-
Maresca, A.1
Scozzafava, A.2
Supuran, C.T.3
-
5
-
-
84055176334
-
Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors
-
Touisni, N.; Maresca, A.; McDonald, P. C.; Lou, Y.; Scozzafava, A.; Dedhar, S.; Winum, J. Y.; Supuran, C. T. Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors J. Med. Chem. 2011, 54, 8271-8277
-
(2011)
J. Med. Chem.
, vol.54
, pp. 8271-8277
-
-
Touisni, N.1
Maresca, A.2
McDonald, P.C.3
Lou, Y.4
Scozzafava, A.5
Dedhar, S.6
Winum, J.Y.7
Supuran, C.T.8
-
6
-
-
84879662265
-
Metronidazole-coumarin conjugates and 3-cyano-7-hydroxy-coumarin act as isoform-selective carbonic anhydrase inhibitors
-
Bonneau, A.; Maresca, A.; Winum, J. Y.; Supuran, C. T. Metronidazole-coumarin conjugates and 3-cyano-7-hydroxy-coumarin act as isoform-selective carbonic anhydrase inhibitors J. Enzyme Inhib. Med. Chem. 2013, 28, 397-401
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 397-401
-
-
Bonneau, A.1
Maresca, A.2
Winum, J.Y.3
Supuran, C.T.4
-
7
-
-
84655175049
-
5- And 6-membered (thio)lactones are prodrug type carbonic anhydrase inhibitors
-
Carta, F.; Maresca, A.; Scozzafava, A.; Supuran, C. T. 5- And 6-membered (thio)lactones are prodrug type carbonic anhydrase inhibitors Bioorg. Med. Chem. Lett. 2012, 22, 267-270
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 267-270
-
-
Carta, F.1
Maresca, A.2
Scozzafava, A.3
Supuran, C.T.4
-
8
-
-
84905506909
-
Sulfonamides and their isosters as carbonic anhydrase inhibitors
-
Carta, F.; Supuran, C. T.; Scozzafava, A. Sulfonamides and their isosters as carbonic anhydrase inhibitors Future Med. Chem. 2014, 10, 1149-1165
-
(2014)
Future Med. Chem.
, vol.10
, pp. 1149-1165
-
-
Carta, F.1
Supuran, C.T.2
Scozzafava, A.3
-
9
-
-
84878089506
-
Carbonic anhydrases: from biomedical applications of the inhibitors and activators to biotechnologic use for CO2 capture
-
Supuran, C. T. Carbonic anhydrases: from biomedical applications of the inhibitors and activators to biotechnologic use for CO2 capture J. Enzyme Inhib. Med. Chem. 2013, 28, 229-230
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 229-230
-
-
Supuran, C.T.1
-
10
-
-
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.; 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
D'Ambrosio, K.3
Supuran, C.T.4
De Simone, G.5
-
11
-
-
38849143765
-
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
-
12
-
-
80053563164
-
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
-
13
-
-
84874526048
-
Insights towards sulfonamide drug specificity in α-carbonic anhydrases
-
Aggarwal, M.; Kondeti, B.; McKenna, R. Insights towards sulfonamide drug specificity in α-carbonic anhydrases Bioorg. Med. Chem. 2013, 21, 1526-1533
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 1526-1533
-
-
Aggarwal, M.1
Kondeti, B.2
McKenna, R.3
-
14
-
-
84864247302
-
Update on carbonic anhydrase inhibitors: a patent review (2008-2011)
-
Aggarwal, M.; McKenna, R. Update on carbonic anhydrase inhibitors: a patent review (2008-2011) Expert. Opin. Ther. Pat. 2012, 22, 903-915
-
(2012)
Expert. Opin. Ther. Pat.
, vol.22
, pp. 903-915
-
-
Aggarwal, M.1
McKenna, R.2
-
15
-
-
84865850354
-
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
-
16
-
-
0037369153
-
Carbonic anhydrase inhibitors
-
Supuran, C. T.; Scozzafava, A.; Casini, A. Carbonic anhydrase inhibitors Med. Res. Rev. 2003, 23, 146-189
-
(2003)
Med. Res. Rev.
, vol.23
, pp. 146-189
-
-
Supuran, C.T.1
Scozzafava, A.2
Casini, A.3
-
17
-
-
3442883664
-
Carbonic anhydrases: current state of the art, therapeutic applications and future prospects
-
Pastorekova, S.; Parkkila, S.; Pastorek, J.; Supuran, C. T. Carbonic anhydrases: current state of the art, therapeutic applications and future prospects J. Enzyme Inhib. Med. Chem. 2004, 19, 199-229
-
(2004)
J. Enzyme Inhib. Med. Chem.
, vol.19
, pp. 199-229
-
-
Pastorekova, S.1
Parkkila, S.2
Pastorek, J.3
Supuran, C.T.4
-
18
-
-
5144224910
-
Development of sulfonamide carbonic anhydrase inhibitors (CAIs)
-
Supuran, C.T. Scozzafava, A. Conway, J. CRC Press: Boca Raton, FL
-
Supuran, C. T.; Scozzafava, A.; Casini, A. Development of sulfonamide carbonic anhydrase inhibitors (CAIs). In Carbonic Anhydrase-Its Inhibitors and Activators; Supuran, C.T.; Scozzafava, A.; Conway, J., Eds.; CRC Press: Boca Raton, FL, 2004; pp 67-147.
-
(2004)
Carbonic Anhydrase - Its Inhibitors and Activators
, pp. 67-147
-
-
Supuran, C.T.1
Scozzafava, A.2
Casini, A.3
-
19
-
-
77954218410
-
Carbonic anhydrase inhibitors
-
Supuran, C. T. Carbonic anhydrase inhibitors Bioorg. Med. Chem. Lett. 2010, 20, 3467-3474
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 3467-3474
-
-
Supuran, C.T.1
-
20
-
-
79961070760
-
Carbonic anhydrase inhibitors and activators for novel therapeutic applications
-
Supuran, C. T. Carbonic anhydrase inhibitors and activators for novel therapeutic applications Future Med. Chem. 2011, 3, 1165-1180
-
(2011)
Future Med. Chem.
, vol.3
, pp. 1165-1180
-
-
Supuran, C.T.1
-
21
-
-
84875720899
-
Structural annotation of human carbonic anhydrases
-
Aggarwal, M.; Boone, C. D.; Kondeti, B.; McKenna, R. Structural annotation of human carbonic anhydrases J. Enzyme Inhib. Med. Chem. 2013, 28, 267-277
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 267-277
-
-
Aggarwal, M.1
Boone, C.D.2
Kondeti, B.3
McKenna, R.4
-
22
-
-
0027936228
-
Identification of two hydrophobic patches in the active-site cavity of human carbonic anhydrase II by solution-phase and solid-state studies and their use in the development of tight-binding inhibitors
-
Jain, A.; Whitesides, G. M.; Alexander, R. S.; Christianson, D. W. Identification of two hydrophobic patches in the active-site cavity of human carbonic anhydrase II by solution-phase and solid-state studies and their use in the development of tight-binding inhibitors J. Med. Chem. 1994, 37, 2100-2105
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2100-2105
-
-
Jain, A.1
Whitesides, G.M.2
Alexander, R.S.3
Christianson, D.W.4
-
23
-
-
84887843075
-
Synthesis of aminocyanopyrazoles via a multi-component reaction and anti-carbonic anhydrase inhibitory activity of their sulfamide derivatives against cytosolic and transmembrane isoforms
-
Allouche, F.; Chabchoub, F.; Carta, F.; Supuran, C. T. Synthesis of aminocyanopyrazoles via a multi-component reaction and anti-carbonic anhydrase inhibitory activity of their sulfamide derivatives against cytosolic and transmembrane isoforms J. Enzyme Inhib. Med. Chem. 2013, 28, 343-349
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 343-349
-
-
Allouche, F.1
Chabchoub, F.2
Carta, F.3
Supuran, C.T.4
-
24
-
-
84874638714
-
Inhibition of the alpha- and beta-carbonic anhydrases from the gastric pathogen Helycobacter pylori with anions
-
Maresca, A.; Vullo, D.; Scozzafava, A.; Supuran, C. T. Inhibition of the alpha- and beta-carbonic anhydrases from the gastric pathogen Helycobacter pylori with anions J. Enzyme Inhib. Med. Chem. 2013, 28, 388-391
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 388-391
-
-
Maresca, A.1
Vullo, D.2
Scozzafava, A.3
Supuran, C.T.4
-
25
-
-
84890292269
-
Three new aromatic sulfonamide inhibitors of carbonic anhydrases I, II, IV and XII
-
Supuran, C. T.; Maresca, A.; Gregáň, F.; Remko, M. Three new aromatic sulfonamide inhibitors of carbonic anhydrases I, II, IV and XII J. Enzyme Inhib. Med. Chem. 2013, 28, 289-293
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 289-293
-
-
Supuran, C.T.1
Maresca, A.2
Gregáň, F.3
Remko, M.4
-
26
-
-
84866091339
-
QSARs on human carbonic anhydrase VA and VB inhibitors of some new not yet synthesized, substituted aromatic/heterocyclic sulphonamides as anti-obesity agent
-
Singh, S.; Supuran, C. T. QSARs on human carbonic anhydrase VA and VB inhibitors of some new not yet synthesized, substituted aromatic/heterocyclic sulphonamides as anti-obesity agent J. Enzyme Inhib. Med. Chem. 2012, 27, 666-672
-
(2012)
J. Enzyme Inhib. Med. Chem.
, vol.27
, pp. 666-672
-
-
Singh, S.1
Supuran, C.T.2
-
28
-
-
8844249356
-
Hypoxia activates the capacity of tumor-associated carbonic anhydrase IX to acidify extracellular pH
-
Svastova, E.; Hulíkova, A.; Rafajova, M.; Zatovicova, M.; Gibadulinova, A.; Casini, A.; Cecchi, A.; Scozzafava, A.; Supuran, C. T.; Pastorek, J.; Pastorekova, S. Hypoxia activates the capacity of tumor-associated carbonic anhydrase IX to acidify extracellular pH FEBS Lett. 2004, 577, 439-445
-
(2004)
FEBS Lett.
, vol.577
, pp. 439-445
-
-
Svastova, E.1
Hulíkova, A.2
Rafajova, M.3
Zatovicova, M.4
Gibadulinova, A.5
Casini, A.6
Cecchi, A.7
Scozzafava, A.8
Supuran, C.T.9
Pastorek, J.10
Pastorekova, S.11
-
29
-
-
33750082400
-
Targeting tumor-associated carbonic anhydrase IX in cancer therapy
-
Thiry, A.; Dogné, J. M.; Masereel, B.; Supuran, C. T. Targeting tumor-associated carbonic anhydrase IX in cancer therapy Trends Pharmacol. Sci. 2006, 27, 566-573
-
(2006)
Trends Pharmacol. Sci.
, vol.27
, pp. 566-573
-
-
Thiry, A.1
Dogné, J.M.2
Masereel, B.3
Supuran, C.T.4
-
30
-
-
70349490906
-
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX
-
Alterio, V.; Hilvo, M.; Di Fiore, A.; Supuran, C. T.; Pan, P.; Parkkila, S.; Scaloni, A.; Pastorek, J.; Pastorekova, S.; Pedone, C.; Scozzafava, A.; Monti, S. M.; De Simone, G. Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX Proc. Natl. Acad. Sci. U.S.A. 2009, 106, 16233-16238
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 16233-16238
-
-
Alterio, V.1
Hilvo, M.2
Di Fiore, A.3
Supuran, C.T.4
Pan, P.5
Parkkila, S.6
Scaloni, A.7
Pastorek, J.8
Pastorekova, S.9
Pedone, C.10
Scozzafava, A.11
Monti, S.M.12
De Simone, G.13
-
31
-
-
67651091693
-
In vivo targeting of tumor-associated carbonic anhydrases using acetazolamide derivatives
-
Ahlskog, J. K.; Schliemann, C.; MaÌŠrlind, J.; Qureshi, U.; Ammar, A.; Pedleym, R. B.; Neri, D. In vivo targeting of tumor-associated carbonic anhydrases using acetazolamide derivatives Bioorg. Med. Chem. Lett. 2009, 19, 4851-4856
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 4851-4856
-
-
Ahlskog, J.K.1
Schliemann, C.2
Maìšrlind, J.3
Qureshi, U.4
Ammar, A.5
Pedleym, R.B.6
Neri, D.7
-
32
-
-
84873136745
-
Signaling pathways of ESE-16, an antimitotic and anticarbonic anhydrase estradiol analog, in breast cancer cells
-
Stander, B. A.; Joubert, F.; Tu, C.; Sippel, K. H.; McKenna, R.; Joubert, A. M. Signaling pathways of ESE-16, an antimitotic and anticarbonic anhydrase estradiol analog, in breast cancer cells PLoS One 2013, 8, e53853
-
(2013)
PLoS One
, vol.8
-
-
Stander, B.A.1
Joubert, F.2
Tu, C.3
Sippel, K.H.4
McKenna, R.5
Joubert, A.M.6
-
33
-
-
79952808077
-
Ureido-substituted benzenesulfonamides potently inhibit carbonic anhydrase IX and show antimetastatic activity in a model of breast cancer metastasis
-
Pacchiano, F.; Carta, F.; McDonald, P. C.; Lou, Y.; Vullo, D.; Scozzafava, A.; Dedhar, S.; Supuran, C. T. Ureido-substituted benzenesulfonamides potently inhibit carbonic anhydrase IX and show antimetastatic activity in a model of breast cancer metastasis J. Med. Chem. 2011, 54, 1896-1902
-
(2011)
J. Med. Chem.
, vol.54
, pp. 1896-1902
-
-
Pacchiano, F.1
Carta, F.2
McDonald, P.C.3
Lou, Y.4
Vullo, D.5
Scozzafava, A.6
Dedhar, S.7
Supuran, C.T.8
-
34
-
-
79955490807
-
Targeting tumor hypoxia: suppression of breast tumor growth and metastasis by novel carbonic anhydrase IX inhibitors
-
Lou, Y.; McDonald, P. C.; Oloumi, A.; Chia, S. K.; Ostlund, C.; Ahmadi, A.; Kyle, A.; Auf dem Keller, U.; Leung, S.; Huntsman, D. G.; Clarke, B.; Sutherland, B. W.; Waterhouse, D.; Bally, M. B.; Roskelley, C. D.; Overall, C. M.; Minchinton, A.; Pacchiano, F.; Carta, F.; Scozzafava, A.; Touisni, N.; Winum, J. Y.; Supuran, C. T.; Dedhar, S. Targeting tumor hypoxia: suppression of breast tumor growth and metastasis by novel carbonic anhydrase IX inhibitors Cancer Res. 2011, 71, 3364-3376
-
(2011)
Cancer Res.
, vol.71
, pp. 3364-3376
-
-
Lou, Y.1
McDonald, P.C.2
Oloumi, A.3
Chia, S.K.4
Ostlund, C.5
Ahmadi, A.6
Kyle, A.7
Auf Dem Keller, U.8
Leung, S.9
Huntsman, D.G.10
Clarke, B.11
Sutherland, B.W.12
Waterhouse, D.13
Bally, M.B.14
Roskelley, C.D.15
Overall, C.M.16
Minchinton, A.17
Pacchiano, F.18
Carta, F.19
Scozzafava, A.20
Touisni, N.21
Winum, J.Y.22
Supuran, C.T.23
Dedhar, S.24
more..
-
35
-
-
78049375982
-
Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency
-
Pacchiano, F.; Aggarwal, M.; Avvaru, B. S.; Robbins, A. H.; Scozzafava, A.; McKenna, R.; Supuran, C. T. Selective hydrophobic pocket binding observed within the carbonic anhydrase II active site accommodate different 4-substituted-ureido-benzenesulfonamides and correlate to inhibitor potency Chem. Commun. 2010, 46, 8371-8373
-
(2010)
Chem. Commun.
, vol.46
, pp. 8371-8373
-
-
Pacchiano, F.1
Aggarwal, M.2
Avvaru, B.S.3
Robbins, A.H.4
Scozzafava, A.5
McKenna, R.6
Supuran, C.T.7
-
36
-
-
77955391402
-
Polyamines inhibit carbonic anhydrases by anchoring to the zinc-coordinated water molecule
-
Carta, F.; Temperini, C.; Innocenti, A.; Scozzafava, A.; Kaila, K.; Supuran, C. T. Polyamines inhibit carbonic anhydrases by anchoring to the zinc-coordinated water molecule J. Med. Chem. 2010, 53, 5511-5522
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5511-5522
-
-
Carta, F.1
Temperini, C.2
Innocenti, A.3
Scozzafava, A.4
Kaila, K.5
Supuran, C.T.6
-
37
-
-
40049101317
-
Carbonic anhydrase inhibitors: interactions of phenols with the 12 catalytically active mammalian isoforms (CA I-XIV)
-
Innocenti, A.; Vullo, D.; Scozzafava, A.; Supuran, C. T. Carbonic anhydrase inhibitors: interactions of phenols with the 12 catalytically active mammalian isoforms (CA I-XIV) Bioorg. Med. Chem. Lett. 2008, 18, 1583-1587
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 1583-1587
-
-
Innocenti, A.1
Vullo, D.2
Scozzafava, A.3
Supuran, C.T.4
-
38
-
-
48449106536
-
Carbonic anhydrase inhibitors: inhibition of mammalian isoforms I-XIV with a series of substituted phenols including paracetamol and salicylic acid
-
Innocenti, A.; Vullo, D.; Scozzafava, A.; Supuran, C. T. Carbonic anhydrase inhibitors: inhibition of mammalian isoforms I-XIV with a series of substituted phenols including paracetamol and salicylic acid Bioorg. Med. Chem. 2008, 16, 7424-7428
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 7424-7428
-
-
Innocenti, A.1
Vullo, D.2
Scozzafava, A.3
Supuran, C.T.4
-
39
-
-
72049112279
-
Carbonic anhydrase inhibitors. Identification of selective inhibitors of the human mitochondrial isozymes VA and VB over the cytosolic isozymes I and II from a natural product-based phenolic library
-
Davis, R. A.; Innocenti, A.; Poulsen, S. A.; Supuran, C. T. Carbonic anhydrase inhibitors. Identification of selective inhibitors of the human mitochondrial isozymes VA and VB over the cytosolic isozymes I and II from a natural product-based phenolic library Bioorg. Med. Chem. 2010, 18, 14-18
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 14-18
-
-
Davis, R.A.1
Innocenti, A.2
Poulsen, S.A.3
Supuran, C.T.4
-
40
-
-
79952786687
-
Natural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrases
-
Davis, R. A.; Hofmann, A.; Osman, A.; Hall, R. A.; Mühlschlegel, F. A.; Vullo, D.; Innocenti, A.; Supuran, C. T.; Poulsen, S. A. Natural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrases J. Med. Chem. 2011, 54, 1682-1692
-
(2011)
J. Med. Chem.
, vol.54
, pp. 1682-1692
-
-
Davis, R.A.1
Hofmann, A.2
Osman, A.3
Hall, R.A.4
Mühlschlegel, F.A.5
Vullo, D.6
Innocenti, A.7
Supuran, C.T.8
Poulsen, S.A.9
-
41
-
-
84855702121
-
Dithiocarbamates: a new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations
-
Carta, F.; Aggarwal, M.; Maresca, A.; Scozzafava, A.; McKenna, R.; Supuran, C. T. Dithiocarbamates: a new class of carbonic anhydrase inhibitors. Crystallographic and kinetic investigations Chem. Commun. 2012, 48, 1868-1870
-
(2012)
Chem. Commun.
, vol.48
, pp. 1868-1870
-
-
Carta, F.1
Aggarwal, M.2
Maresca, A.3
Scozzafava, A.4
McKenna, R.5
Supuran, C.T.6
-
42
-
-
84874604544
-
Dithiocarbamates strongly inhibit the β-class carbonic anhydrases from Mycobacterium tuberculosis
-
Maresca, A.; Carta, F.; Vullo, D.; Supuran, C. T. Dithiocarbamates strongly inhibit the β-class carbonic anhydrases from Mycobacterium tuberculosis J. Enzyme Inhib. Med. Chem. 2013, 28, 407-411
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 407-411
-
-
Maresca, A.1
Carta, F.2
Vullo, D.3
Supuran, C.T.4
-
43
-
-
84855658697
-
Dithiocarbamates are strong inhibitors of the beta-class fungal carbonic anhydrases from Cryptococcus neoformans, Candida albicans and Candida glabrata
-
Monti, S. M.; Maresca, A.; Carta, F.; De Simone, G.; Mühlschlegel, F. A.; Scozzafava, A.; Supuran, C. T. 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, 859-862
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 859-862
-
-
Monti, S.M.1
Maresca, A.2
Carta, F.3
De Simone, G.4
Mühlschlegel, F.A.5
Scozzafava, A.6
Supuran, C.T.7
-
44
-
-
84857420193
-
Dithiocarbamates strongly inhibit carbonic anhydrases and show antiglaucoma action in vivo
-
Carta, F.; Aggarwal, M.; Maresca, A.; Scozzafava, A.; McKenna, R.; Masini, E.; Supuran, C. T. Dithiocarbamates strongly inhibit carbonic anhydrases and show antiglaucoma action in vivo J. Med. Chem. 2012, 55, 1721-1730
-
(2012)
J. Med. Chem.
, vol.55
, pp. 1721-1730
-
-
Carta, F.1
Aggarwal, M.2
Maresca, A.3
Scozzafava, A.4
McKenna, R.5
Masini, E.6
Supuran, C.T.7
-
45
-
-
84879051423
-
Xanthates and trithiocarbonates strongly inhibit carbonic anhydrases and show antiglaucoma effects in vivo
-
Carta, F.; Akdemir, A.; Scozzafava, A.; Masini, E.; Supuran, C. T. Xanthates and trithiocarbonates strongly inhibit carbonic anhydrases and show antiglaucoma effects in vivo J. Med. Chem. 2013, 56, 4691-4700
-
(2013)
J. Med. Chem.
, vol.56
, pp. 4691-4700
-
-
Carta, F.1
Akdemir, A.2
Scozzafava, A.3
Masini, E.4
Supuran, C.T.5
-
46
-
-
84857918967
-
New chemotypes acting as isozyme-selective carbonic anhydrase inhibitors with low affinity for the offtarget cytosolic isoform II
-
Carta, F.; Vullo, D.; Maresca, A.; Scozzafava, A.; Supuran, C. T. New chemotypes acting as isozyme-selective carbonic anhydrase inhibitors with low affinity for the offtarget cytosolic isoform II Bioorg. Med. Chem. Lett. 2012, 22, 2182-2185
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 2182-2185
-
-
Carta, F.1
Vullo, D.2
Maresca, A.3
Scozzafava, A.4
Supuran, C.T.5
-
47
-
-
84858288806
-
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
-
48
-
-
84874530114
-
Natural product coumarins that inhibit human carbonic anhydrases
-
Davis, R. A.; Vullo, D.; Maresca, A.; Supuran, C. T.; Poulsen, S. A. Natural product coumarins that inhibit human carbonic anhydrases Bioorg. Med. Chem. 2013, 21, 1539-1543
-
(2013)
Bioorg. Med. Chem.
, vol.21
, pp. 1539-1543
-
-
Davis, R.A.1
Vullo, D.2
Maresca, A.3
Supuran, C.T.4
Poulsen, S.A.5
-
49
-
-
84879642740
-
7-Substituted-sulfocoumarins are isoform-selective, potent carbonic anhydrase II inhibitors
-
Tanc, M.; Carta, F.; Bozdag, M.; Scozzafava, A.; Supuran, C. T. 7-Substituted-sulfocoumarins are isoform-selective, potent carbonic anhydrase II inhibitors Bioorg. Med. Chem. 2013, 15, 4502-4510
-
(2013)
Bioorg. Med. Chem.
, vol.15
, pp. 4502-4510
-
-
Tanc, M.1
Carta, F.2
Bozdag, M.3
Scozzafava, A.4
Supuran, C.T.5
-
50
-
-
84894567311
-
6-Triazolyl-substituted sulfocoumarins are potent, selective inhibitors of the tumor-associated carbonic anhydrases IX and XII
-
Grandane, A.; Tanc, M.; Zalubovskis, R.; Supuran, C. T. 6-Triazolyl-substituted sulfocoumarins are potent, selective inhibitors of the tumor-associated carbonic anhydrases IX and XII Bioorg. Med. Chem. Lett. 2014, 5, 1256-1260
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 1256-1260
-
-
Grandane, A.1
Tanc, M.2
Zalubovskis, R.3
Supuran, C.T.4
-
51
-
-
84896697813
-
Synthesis of 6-tetrazolyl-substituted sulfocoumarins acting as highly potent and selective inhibitors of the tumor-associated carbonic anhydrase isoforms IX and XII
-
Grandane, A.; Tanc, M.; Zalubovskis, R.; Supuran, C. T. Synthesis of 6-tetrazolyl-substituted sulfocoumarins acting as highly potent and selective inhibitors of the tumor-associated carbonic anhydrase isoforms IX and XII Bioorg. Med. Chem. 2014, 5, 1522-1528
-
(2014)
Bioorg. Med. Chem.
, vol.5
, pp. 1522-1528
-
-
Grandane, A.1
Tanc, M.2
Zalubovskis, R.3
Supuran, C.T.4
-
52
-
-
84862004700
-
Facile synthesis of coumarin bioisosteres 1,2-benzoxathiine 2,2-dioxides
-
Grandane, A.; Belyakov, S.; Trapencieris, P.; Zalubovskis, R. Facile synthesis of coumarin bioisosteres 1,2-benzoxathiine 2,2-dioxides Tetrahedron 2012, 68, 5541-5546
-
(2012)
Tetrahedron
, vol.68
, pp. 5541-5546
-
-
Grandane, A.1
Belyakov, S.2
Trapencieris, P.3
Zalubovskis, R.4
-
53
-
-
34250322126
-
Imaging the hypoxia surrogate marker CA IX requires expression and catalytic activity for binding fluorescent sulfonamide inhibitors
-
Dubois, L.; Douma, K.; Supuran, C. T.; Chiu, R. K.; van Zandvoort, M. A. M.; Pastoreková, S.; Scozzafava, A.; Wouters, B. G.; Lambin, P. Imaging the hypoxia surrogate marker CA IX requires expression and catalytic activity for binding fluorescent sulfonamide inhibitors Radiother. Oncol. 2007, 83, 367-373
-
(2007)
Radiother. Oncol.
, vol.83
, pp. 367-373
-
-
Dubois, L.1
Douma, K.2
Supuran, C.T.3
Chiu, R.K.4
Van Zandvoort, M.A.M.5
Pastoreková, S.6
Scozzafava, A.7
Wouters, B.G.8
Lambin, P.9
-
54
-
-
69949128698
-
Imaging of CA IX with fluorescent labelled sulfonamides distinguishes hypoxic and (re)-oxygenated cells in a xenograft tumour model
-
Dubois, L.; Lieuwes, N. G.; Maresca, A.; Thiry, A.; Supuran, C. T.; Scozzafava, A.; Wouters, B. G.; Lambin, P. Imaging of CA IX with fluorescent labelled sulfonamides distinguishes hypoxic and (re)-oxygenated cells in a xenograft tumour model Radiother. Oncol. 2009, 92, 423-428
-
(2009)
Radiother. Oncol.
, vol.92
, pp. 423-428
-
-
Dubois, L.1
Lieuwes, N.G.2
Maresca, A.3
Thiry, A.4
Supuran, C.T.5
Scozzafava, A.6
Wouters, B.G.7
Lambin, P.8
-
55
-
-
77953807572
-
Synthesis and biological evaluation of a 99mTc-labelled sulfonamide conjugate for in vivo visualization of carbonic anhydrase IX expression in tumor hypoxia
-
Akurathi, V.; Dubois, L.; Lieuwes, N. G.; Chitneni, S. K.; Cleynhens, B. J.; Vullo, D.; Supuran, C. T.; Verbruggen, A. M.; Lambin, P.; Bormans, G. M. Synthesis and biological evaluation of a 99mTc-labelled sulfonamide conjugate for in vivo visualization of carbonic anhydrase IX expression in tumor hypoxia Nuclear Med. Biol. 2010, 37, 557-564
-
(2010)
Nuclear Med. Biol.
, vol.37
, pp. 557-564
-
-
Akurathi, V.1
Dubois, L.2
Lieuwes, N.G.3
Chitneni, S.K.4
Cleynhens, B.J.5
Vullo, D.6
Supuran, C.T.7
Verbruggen, A.M.8
Lambin, P.9
Bormans, G.M.10
-
56
-
-
79960359073
-
Specific inhibition of CA IX activity enhances the therapeutic effect of tumor irradiation
-
Dubois, L.; Peeters, S.; Lieuwes, N. G.; Geusens, N.; Thiry, A.; Carta, F.; Scozzafava, A.; Dogné, J. M.; Supuran, C. T.; Harris, A. L.; Masereel, B.; Lambin, P. Specific inhibition of CA IX activity enhances the therapeutic effect of tumor irradiation Radiother. Oncol. 2011, 99, 424-431
-
(2011)
Radiother. Oncol.
, vol.99
, pp. 424-431
-
-
Dubois, L.1
Peeters, S.2
Lieuwes, N.G.3
Geusens, N.4
Thiry, A.5
Carta, F.6
Scozzafava, A.7
Dogné, J.M.8
Supuran, C.T.9
Harris, A.L.10
Masereel, B.11
Lambin, P.12
-
57
-
-
84655176328
-
Synthesis and evaluation of near-infrared fluorescent sulfonamide derivatives for imaging of hypoxia-induced carbonic anhydrase IX expression in tumors
-
Groves, K.; Bao, B.; Zhang, J.; Handy, E.; Kennedy, P.; Cuneo, G.; Supuran, C. T.; Yared, W.; Peterson, J. D.; Rajopadhye, M. Synthesis and evaluation of near-infrared fluorescent sulfonamide derivatives for imaging of hypoxia-induced carbonic anhydrase IX expression in tumors Bioorg. Med. Chem. Lett. 2012, 22, 653-657
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 653-657
-
-
Groves, K.1
Bao, B.2
Zhang, J.3
Handy, E.4
Kennedy, P.5
Cuneo, G.6
Supuran, C.T.7
Yared, W.8
Peterson, J.D.9
Rajopadhye, M.10
-
58
-
-
0015239422
-
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
-
59
-
-
84899779537
-
Carbonic anhydrase inhibitors drug design
-
McKenna, R. Frost, S. Springer Verlag: Heidelberg
-
Supuran, C. T.; McKenna, R. Carbonic anhydrase inhibitors drug design. In Carbonic Anhydrase: Mechanism, Regulation, Links to Disease, and Industrial Applications; McKenna, R.; Frost, S., Eds.; Springer Verlag: Heidelberg, 2014; pp 291-323.
-
(2014)
Carbonic Anhydrase: Mechanism, Regulation, Links to Disease, and Industrial Applications
, pp. 291-323
-
-
Supuran, C.T.1
McKenna, R.2
-
60
-
-
84899779537
-
-
(Subcell. Biochem. 2014, 75, 291.)
-
(2014)
Subcell. Biochem.
, vol.75
, pp. 291
-
-
-
61
-
-
84874640228
-
Inhibition of the β-class carbonic anhydrases from Mycobacterium tuberculosis with carboxylic acids
-
Maresca, A.; Vullo, D.; Scozzafava, A.; Manole, G.; Supuran, C. T. Inhibition of the β-class carbonic anhydrases from Mycobacterium tuberculosis with carboxylic acids J. Enzyme Inhib. Med. Chem. 2013, 28, 392-396
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 392-396
-
-
Maresca, A.1
Vullo, D.2
Scozzafava, A.3
Manole, G.4
Supuran, C.T.5
-
62
-
-
84874626003
-
Dihalogenated sulfanilamides and benzolamides are effective inhibitors of the three β-class carbonic anhydrases from Mycobacterium tuberculosis
-
Maresca, A.; Scozzafava, A.; Vullo, D.; Supuran, C. T. Dihalogenated sulfanilamides and benzolamides are effective inhibitors of the three β-class carbonic anhydrases from Mycobacterium tuberculosis J. Enzyme Inhib. Med. Chem. 2013, 28, 384-387
-
(2013)
J. Enzyme Inhib. Med. Chem.
, vol.28
, pp. 384-387
-
-
Maresca, A.1
Scozzafava, A.2
Vullo, D.3
Supuran, C.T.4
-
63
-
-
0035952224
-
Carbonic anhydrase inhibitors. Synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma properties
-
Scozzafava, A.; Menabuoni, L.; Mincione, F.; Mincione, G.; Supuran, C. T. Carbonic anhydrase inhibitors. Synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma properties Bioorg. Med. Chem. Lett. 2001, 11, 575-582
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 575-582
-
-
Scozzafava, A.1
Menabuoni, L.2
Mincione, F.3
Mincione, G.4
Supuran, C.T.5
-
64
-
-
60449084598
-
Carbonic anhydrase inhibitors: two-prong versus mono-prong inhibitors of isoforms I, II, IX, and XII exemplified by photochromic cis -1,2-α-dithienylethene derivatives
-
Vomasta, D.; Innocenti, A.; König, B.; Supuran, C. T. Carbonic anhydrase inhibitors: two-prong versus mono-prong inhibitors of isoforms I, II, IX, and XII exemplified by photochromic cis -1,2-α-dithienylethene derivatives Bioorg. Med. Chem. Lett. 2009, 19, 1283-1286
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 1283-1286
-
-
Vomasta, D.1
Innocenti, A.2
König, B.3
Supuran, C.T.4
|