-
1
-
-
70450181696
-
Selective matrix metalloproteinase inhibitors for cancer
-
Li, N. G.; Shi, Z.-H.; Tang, Y. P.; Duan, J. A. Selective matrix metalloproteinase inhibitors for cancer Curr. Med. Chem. 2009, 16, 3805-3827
-
(2009)
Curr. Med. Chem.
, vol.16
, pp. 3805-3827
-
-
Li, N.G.1
Shi, Z.-H.2
Tang, Y.P.3
Duan, J.A.4
-
2
-
-
67651112138
-
Control of melanoma invasiveness by anticollagenolytic agents: A reappraisal of an old concept
-
Bourguet, E.; Sapi, J.; Emonard, H.; Hornebeck, W. Control of melanoma invasiveness by anticollagenolytic agents: A reappraisal of an old concept Anti-Cancer Ag. Med. Chem. 2009, 9, 576-597
-
(2009)
Anti-Cancer Ag. Med. Chem.
, vol.9
, pp. 576-597
-
-
Bourguet, E.1
Sapi, J.2
Emonard, H.3
Hornebeck, W.4
-
3
-
-
54749146365
-
The role of proteases in individual and collective cancer cell invasion
-
Friedl, P.; Wolf, K.; Travel, T. The role of proteases in individual and collective cancer cell invasion Cancer Res. 2008, 68, 7247-7249
-
(2008)
Cancer Res.
, vol.68
, pp. 7247-7249
-
-
Friedl, P.1
Wolf, K.2
Travel, T.3
-
4
-
-
34447520043
-
Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases
-
DOI 10.1038/nrd2308, PII NRD2308
-
Hu, J.; Van den Steen, P. E.; Sang, Q.-X.; Opdenakker, G. Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases Nat. Rev. Drug Discovery 2007, 6, 480-498 (Pubitemid 47064570)
-
(2007)
Nature Reviews Drug Discovery
, vol.6
, Issue.6
, pp. 480-498
-
-
Hu, J.1
Van Den Steen, P.E.2
Sang, Q.-X.A.3
Opdenakker, G.4
-
5
-
-
0029790101
-
Expression of matrix metalloproteinase 9 (96-kd gelatinase B) in human rheumatoid arthritis
-
Ahrens, D.; Koch, A. E.; Pope, R. M.; Steinpicarella, M.; Niedbala, M. J. Expression of matrix metalloproteinase 9 (96-kd gelatinase B) in human rheumatoid arthritis Arthritis Rheumatism 1996, 39, 1576
-
(1996)
Arthritis Rheumatism
, vol.39
, pp. 1576
-
-
Ahrens, D.1
Koch, A.E.2
Pope, R.M.3
Steinpicarella, M.4
Niedbala, M.J.5
-
6
-
-
0040708902
-
Determination of metalloproteinases, plasminogen-activators and their inhibitors in the synovial fluids of patients with rheumatoid arthritis during chemical synoviorthesis
-
DOI 10.1016/0009-8981(95)06172-X
-
Blaser, J.; Triebel, S.; Maasjosthusmann, U.; Romisch, J.; Krahlmateblowski, U.; Freudenberg, W.; Fricke, R.; Tschesche, H. Determination of metalloproteinases, plasminogen-activators and their inhibitors in the synovial fluids of patients with rheumatoid arthritis during chemical synoviorthesis Clin. Chim. Acta 1996, 244, 17-33 (Pubitemid 26053175)
-
(1996)
Clinica Chimica Acta
, vol.244
, Issue.1
, pp. 17-33
-
-
Blaser, J.1
Triebel, S.2
Maasjosthusmann, U.3
Romisch, J.4
Krahl-Mateblowski, U.5
Freudenberg, W.6
Fricke, R.7
Tschesche, H.8
-
7
-
-
0031799439
-
Matrix metalloproteinase inhibitors in arthritis
-
Bottomley, K. M.; Johnson, W. H.; Walter, D. S. Matrix metalloproteinase inhibitors in arthritis J. Enzyme Inhibit. 1998, 13, 79-101 (Pubitemid 28230676)
-
(1998)
Journal of Enzyme Inhibition
, vol.13
, Issue.2
, pp. 79-101
-
-
Bottomley, K.M.1
Johnson, W.H.2
Walter, D.S.3
-
8
-
-
0028123480
-
Molecular cloning of a possible cysteine proteinase predominantly expressed in osteoclasts
-
Tezuka, K.; Nemato, K.; Tezuka, Y.; Sato, T.; Ikeda, Y.; Kobori, M.; Kawashima, H.; Eguchi, H.; Hakeda, Y.; Kumegawa, M. Molecular cloning of a possible cysteine proteinase predominantly expressed in osteoclasts J. Biol. Chem. 1994, 269, 1106
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 1106
-
-
Tezuka, K.1
Nemato, K.2
Tezuka, Y.3
Sato, T.4
Ikeda, Y.5
Kobori, M.6
Kawashima, H.7
Eguchi, H.8
Hakeda, Y.9
Kumegawa, M.10
-
9
-
-
0028999498
-
H-31 human breast cancer cells stimulate type i collagenase production in osteoblast-like cells and induce bone resorption
-
Ohishi, K.; Fujita, N.; Morinaga, Y.; Tsuruo, T. H-31 human breast cancer cells stimulate type I collagenase production in osteoblast-like cells and induce bone resorption Clin. Exp. Metastasis 1995, 13, 287-295
-
(1995)
Clin. Exp. Metastasis
, vol.13
, pp. 287-295
-
-
Ohishi, K.1
Fujita, N.2
Morinaga, Y.3
Tsuruo, T.4
-
10
-
-
0030024108
-
Parathyroid hormone-induced resorption in fetal rat limb bones is associated with production of the metalloproteinases collagenase and gelatinase B
-
Witty, J. P.; Foster, S. A.; Stricklin, G. P.; Matrisian, L. M.; Stern, P. H. Parathyroid hormone-induced resorption in fetal rat limb bones is associated with production of the metalloproteinases collagenase and gelatinase B J. Bone Mineral Res. 1996, 11, 72-78 (Pubitemid 26026746)
-
(1996)
Journal of Bone and Mineral Research
, vol.11
, Issue.1
, pp. 72-78
-
-
Witty, J.P.1
Foster, S.A.2
Stricklin, G.P.3
Matrisian, L.M.4
Stern, P.H.5
-
11
-
-
0028625739
-
The family of matrix metalloproteinases
-
Woessner, J. F., Jr. The family of matrix metalloproteinases Ann. N. Y. Acad. Sci. 1994, 732, 11-21
-
(1994)
Ann. N. Y. Acad. Sci.
, vol.732
, pp. 11-21
-
-
Woessner, Jr.J.F.1
-
12
-
-
0030831896
-
Matrix metalloproteinases and coronary artery disease: A novel therapeutic target
-
Celentano, D. C.; Frishman, W. H. Matrix metalloproteinases and coronary artery disease: a novel therapeutic target J. Clin. Pharmacol. 1997, 37, 991-1000 (Pubitemid 27524557)
-
(1997)
Journal of Clinical Pharmacology
, vol.37
, Issue.11
, pp. 991-1000
-
-
Celentano, D.C.1
Frishman, W.H.2
-
13
-
-
0031723106
-
Matrix metalloproteinases contribute to the blood-brain barrier disruption during bacterial meningitis
-
Lorenzl, P. R.; Koedel, S.; Sporer, U.; Vogel, B.; Frosch, U.; Pfister, M. Matrix metalloproteinases contribute to the blood-brain barrier disruption during bacterial meningitis Ann. Neurol. 1998, 44, 592-600
-
(1998)
Ann. Neurol.
, vol.44
, pp. 592-600
-
-
Lorenzl, P.R.1
Koedel, S.2
Sporer, U.3
Vogel, B.4
Frosch, U.5
Pfister, M.6
-
14
-
-
0030994326
-
Emerging therapeutic advances for the development of second generation matrix metalloproteinase inhibitors
-
White, A. D.; Bocan, T. M.A.; Boxer, P, A.; Peterson, J. T.; Schrier, D., Emerging therapeutic advances for the generation matrix metalloproteinase inhibitors Curr. Pharm. Design 1997, 3, 45-58 (Pubitemid 27215887)
-
(1997)
Current Pharmaceutical Design
, vol.3
, Issue.1
, pp. 45-58
-
-
White, A.D.1
Bocan, T.M.A.2
Boxer, P.A.3
Peterson, J.T.4
Schrier, D.5
-
15
-
-
0028323297
-
Structural remodelling in heart failure: Gelatinase induction
-
Armstrong, P. W.; Moe, G. W.; Howard, R. J.; Grima, E. A.; Cruz, T. F. Structural remodelling in heart failure: gelatinase induction Can. J. Cardiol. 1994, 10, 214
-
(1994)
Can. J. Cardiol.
, vol.10
, pp. 214
-
-
Armstrong, P.W.1
Moe, G.W.2
Howard, R.J.3
Grima, E.A.4
Cruz, T.F.5
-
16
-
-
1842451934
-
Matrix metalloproteinases in the Pathogenesis of asthma and COPD: Implications for therapy
-
DOI 10.2165/00151829-200403010-00003
-
Suzuki, R.; Miyazaki, Y.; Takagi, K.; Torii, K.; Taniguchi, H. Matrix metalloproteinases in the pathogenesis of asthma and COPD: implications for therapy Treat. Respir. Med. 2004, 3, 17-27 (Pubitemid 38444328)
-
(2004)
Treatments in Respiratory Medicine
, vol.3
, Issue.1
, pp. 17-27
-
-
Suzuki, R.1
Miyazaki, Y.2
Takagi, K.3
Torii, K.4
Taniguchi, H.5
-
17
-
-
84866315807
-
Serum levels of TIMP-2 and MMP-2 in patients with liver disease
-
Fukuda, E. M.; Nakano, Y.; Katano, I.; Fujimoto, Y.; Hayakawa, N. Serum levels of TIMP-2 and MMP-2 in patients with liver disease Liver 1997, 17, 293-299
-
(1997)
Liver
, vol.17
, pp. 293-299
-
-
Fukuda, E.M.1
Nakano, Y.2
Katano, I.3
Fujimoto, Y.4
Hayakawa, N.5
-
18
-
-
0031959973
-
Matrix metalloproteinase expression increases after cerebral focal ischemia in rats: Inhibition of matrix metalloproteinase-9 reduces infarct size
-
Romanic, A. M.; White, R. F.; Arleth, A. J.; Ohlstein, E. H.; Barone, F. C. Matrix metalloproteinase expression increases after cerebral focal ischemia in rats: inhibition of matrix metalloproteinase-9 reduces infarct size Stroke 1998, 29, 1020-1030 (Pubitemid 28228167)
-
(1998)
Stroke
, vol.29
, Issue.5
, pp. 1020-1030
-
-
Romanic, A.M.1
White, R.F.2
Arleth, A.J.3
Ohlstein, E.H.4
Barone, F.C.5
-
19
-
-
43049142648
-
Matrix metalloproteinase inhibitors as anticancer agents
-
Konstantinopoulos, P. A.; Karamouzis, M. V.; Papatsoris, A. G.; Papavassiliou, A. G. Matrix metalloproteinase inhibitors as anticancer agents Int. J. Biochem. Cell Biol. 2008, 40, 1156-1168
-
(2008)
Int. J. Biochem. Cell Biol.
, vol.40
, pp. 1156-1168
-
-
Konstantinopoulos, P.A.1
Karamouzis, M.V.2
Papatsoris, A.G.3
Papavassiliou, A.G.4
-
20
-
-
33646136687
-
Matrix metalloproteinase inhibitors as prospective agents for the prevention and treatment of cardiovascular and neoplastic diseases
-
Sang, Q.-X. A.; Jin, Y.; Newcomer, R. G.; Monroe, S. C.; Fang, X.; Hurst, D. R.; Lee, S.; Cao, Q.; Schwartz, M. A. Matrix metalloproteinase inhibitors as prospective agents for the prevention and treatment of cardiovascular and neoplastic diseases Curr. Topics Med. Chem 2006, 6, 289-316
-
(2006)
Curr. Topics Med. Chem
, vol.6
, pp. 289-316
-
-
Sang, Q.-X.A.1
Jin, Y.2
Newcomer, R.G.3
Monroe, S.C.4
Fang, X.5
Hurst, D.R.6
Lee, S.7
Cao, Q.8
Schwartz, M.A.9
-
21
-
-
77249129690
-
Avoiding spam in the proteolytic internet: Future strategies for anti-metastatic MMP inhibition
-
Krüger, A.; Kates, R. E.; Edwards, D. R. Avoiding spam in the proteolytic internet: Future strategies for anti-metastatic MMP inhibition Biochim. Biophys. Acta 2010, 1803, 95-102
-
(2010)
Biochim. Biophys. Acta
, vol.1803
, pp. 95-102
-
-
Krüger, A.1
Kates, R.E.2
Edwards, D.R.3
-
22
-
-
14144252682
-
Structural basis for the highly selective inhibition of MMP-13
-
DOI 10.1016/j.chembiol.2004.11.014
-
Engel, C. K.; Pirard, B.; Schimanski, S.; Kirsch, R.; Habermann, J.; Klingler, O.; Schlotte, V.; Weithmann, K. U.; Wendt, K. U. Structural basis for the highly selective inhibition of MMP-13 Chem. Biol. 2005, 12, 181-189 (Pubitemid 40281325)
-
(2005)
Chemistry and Biology
, vol.12
, Issue.2
, pp. 181-189
-
-
Engel, C.K.1
Pirard, B.2
Schimanski, S.3
Kirsch, R.4
Habermann, J.5
Klingler, O.6
Schlotte, V.7
Weithmann, K.U.8
Wendt, K.U.9
-
23
-
-
64349106309
-
Extra binding region induced by non-zinc chelating inhibitors into the S1′ subsite of matrix metalloproteinase 8 (MMP-8)
-
Pochetti, G.; Montanari, R.; Gege, C.; Chevrier, C.; Taveras, A. G.; Mazza, F. Extra binding region induced by non-zinc chelating inhibitors into the S1′ subsite of matrix metalloproteinase 8 (MMP-8) J. Med. Chem. 2009, 52, 1040-1049
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1040-1049
-
-
Pochetti, G.1
Montanari, R.2
Gege, C.3
Chevrier, C.4
Taveras, A.G.5
Mazza, F.6
-
24
-
-
33646804364
-
Development of selective inhibitors and substrate of matrix metalloproteinase-12
-
DOI 10.1074/jbc.M600222200
-
Devel, L.; Rogakos, V.; David, A.; Makaritis, A.; Beau, F.; Cuniasse, P.; Yiotakis, A.; Dive, V. Development of selective inhibitors and substrate of matrix metalloproteinase-12 J. Biol. Chem. 2006, 281, 11152-11160 (Pubitemid 43855540)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.16
, pp. 11152-11160
-
-
Devel, L.1
Rogakos, V.2
David, A.3
Makaritis, A.4
Beau, F.5
Cuniasse, P.6
Yiotakis, A.7
Dive, V.8
-
25
-
-
77956614709
-
Phosphorus based inhibitors of matrix metalloproteinases
-
Veerendhar, A.; Reich, R.; Breuer, E. Phosphorus based inhibitors of matrix metalloproteinases C. R. Chimie 2010, 13, 1191-1202
-
(2010)
C. R. Chimie
, vol.13
, pp. 1191-1202
-
-
Veerendhar, A.1
Reich, R.2
Breuer, E.3
-
26
-
-
34648815810
-
Emerging roles of proteases in tumour suppression
-
DOI 10.1038/nrc2228, PII NRC2228
-
López-Otín, C.; Matrisian, L. M. Emerging roles of proteases in tumour suppression Nat. Rev. Cancer 2007, 7, 800-808 (Pubitemid 47463671)
-
(2007)
Nature Reviews Cancer
, vol.7
, Issue.10
, pp. 800-808
-
-
Lopez-Otin, C.1
Matrisian, L.M.2
-
27
-
-
70349335653
-
Matrix metalloproteinase proteomics: Substrates, targets, and therapy
-
Morrison, C. J.; Butler, G. S.; Rodriguez, D.; Overall, C. M. Matrix metalloproteinase proteomics: substrates, targets, and therapy Curr. Opin. Cell Biol. 2009, 21, 645-653
-
(2009)
Curr. Opin. Cell Biol.
, vol.21
, pp. 645-653
-
-
Morrison, C.J.1
Butler, G.S.2
Rodriguez, D.3
Overall, C.M.4
-
28
-
-
2342624494
-
Carbamoylphosphonate-based matrix metalloproteinase inhibitor metal complexes: Solution studies and stability constants. Towards a zinc-selective binding group
-
DOI 10.1007/s00775-004-0524-5
-
Farkas, E.; Katz, Y.; Bhusare, S.; Reich, R.; Röschenthaler, G.-V.; Königsmann, M.; Breuer, E. Carbamoylphosphonate Based Matrix Metalloproteinase (MMP) Inhibitor Metal Complexes-Solution Studies and Stability Constants. Towards a Zinc Selective Binding Group J. Biol. Inorg. Chem. 2004, 9, 307-315 (Pubitemid 38595915)
-
(2004)
Journal of Biological Inorganic Chemistry
, vol.9
, Issue.3
, pp. 307-315
-
-
Farkas, E.1
Katz, Y.2
Bhusare, S.3
Reich, R.4
Roschenthaler, G.-V.5
Konigsmann, M.6
Breuer, E.7
-
29
-
-
2442713986
-
Carbamoylphosphonates, a new class of in vivo active matrix metalloproteinase inhibitors. 1. Alkyl- and cycloalkylcarbamoylphosphonic acids
-
DOI 10.1021/jm030386z
-
Breuer, E.; Salomon, C. J.; Katz, Y.; Chen, W.; Lu, S.; Röschenthaler, G.-V.; Hadar, R.; Reich, R. Carbamoylphosphonates-A New Class of In Vivo Active Matrix Metalloproteinase Inhibitors 1. Alkyl- and Cycloalkylcarbamoylphosphonic acids J. Med. Chem. 2004, 47, 2826-2832 (Pubitemid 38656735)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.11
, pp. 2826-2832
-
-
Breuer, E.1
Salomon, C.J.2
Katz, Y.3
Chen, W.4
Lu, S.5
Roschenthaler, G.-V.6
Hadar, R.7
Reich, R.8
-
30
-
-
18844424018
-
Carbamoylphosphonate matrix metalloproteinase inhibitors 3: In vivo evaluation of cyclopentylcarbamoylphosphonic acid in experimental metastasis and angiogenesis
-
DOI 10.1158/1078-0432.CCR-04-1985
-
Reich, R.; Katz, Y.; Hadar, R.; Breuer, E. Carbamoylphosphonate MMP inhibitors 3. In vivo evaluation of cyclopentylcarbamoylphosphonic acid, CPCPA, in experimental metastasis and angiogenesis Clin. Cancer Res. 2005, 11, 3925-3929 (Pubitemid 40685614)
-
(2005)
Clinical Cancer Research
, vol.11
, Issue.10
, pp. 3925-3929
-
-
Reich, R.1
Katz, Y.2
Hadar, R.3
Breuer, E.4
-
31
-
-
4143137943
-
Carbamoylphosphonate MMP inhibitors. Part 4: The influence of chirality and geometrical isomerism on the potency and selectivity of inhibition
-
DOI 10.1016/j.tetasy.2004.07.002, PII S0957416604004860
-
Breuer, E.; Katz, Y.; Hadar, R.; Reich, R. Carbamoylphosphonate MMP Inhibitors 4. The influence of chirality and geometrical isomerism on the potency and selectivity of inhibition Tetrahedron: Asymmetry 2004, 15, 2415-2420 (Pubitemid 39092300)
-
(2004)
Tetrahedron Asymmetry
, vol.15
, Issue.15
, pp. 2415-2420
-
-
Breuer, E.1
Katz, Y.2
Hadar, R.3
Reich, R.4
-
32
-
-
41349106390
-
Carbamoylphosphonate matrix metalloproteinase inhibitors 6: Cis-2-aminocyclohexylcarbamoylphosphonic acid, a novel orally active antimetastatic matrix metalloproteinase-2 selective inhibitor-synthesis and pharmacodynamic and pharmacokinetic analysis
-
DOI 10.1021/jm701087n
-
Hoffman, A.; Qadri, B.; Frant, J.; Katz, Y.; Bhusare, S.; Breuer, E.; Hadar, R.; Reich, R. Carbamoylphosphonate Matrix Metalloproteinase Inhibitors 6. cis -2-Aminocyclohexylcarbamoyl phosphonic Acid. A Novel Orally Active Antimetastatic Matrix Metalloproteinase-2 Selective Inhibitor -Synthesis, and Pharmacodynamic and Pharmacokinetic Analysis J. Med. Chem. 2008, 51, 1406-1414 (Pubitemid 351480402)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.5
, pp. 1406-1414
-
-
Hoffman, A.1
Qadri, B.2
Frant, J.3
Katz, Y.4
Bhusare, S.R.5
Breuer, E.6
Hadar, R.7
Reich, R.8
-
33
-
-
79960694567
-
Carbamoylphosphonates 9 - Orally active, antimetastatic, non-toxic, diphenyl ether-derived carbamoylphosphonate matrix metalloproteinase inhibitors
-
Frant, J.; Veerendhar, A.; Chernilovsky, T.; Nedvetzki, S.; Vaksman, O.; Hoffman, A.; Breuer, E.; Reich, R. Carbamoylphosphonates 9-Orally active, antimetastatic, non-toxic, diphenyl ether-derived carbamoylphosphonate matrix metalloproteinase inhibitors ChemMedChem 2011, 6, 1471-1477
-
(2011)
ChemMedChem
, vol.6
, pp. 1471-1477
-
-
Frant, J.1
Veerendhar, A.2
Chernilovsky, T.3
Nedvetzki, S.4
Vaksman, O.5
Hoffman, A.6
Breuer, E.7
Reich, R.8
-
34
-
-
38849143765
-
Carbonic anhydrases: Novel therapeutic applications for inhibitors and activators
-
DOI 10.1038/nrd2467, PII NRD2467
-
Supuran, C. T. Carbonic anhydrases: novel therapeutic applications for inhibitors and activators Nat. Rev. Drug Discovery 2008, 7, 168-181 (Pubitemid 351194064)
-
(2008)
Nature Reviews Drug Discovery
, vol.7
, Issue.2
, pp. 168-181
-
-
Supuran, C.T.1
-
35
-
-
84889385876
-
Carbonic anhydrases as drug targets - General presentation
-
In, Supuran, C. T. Winum, J.-Y. Wiley: Hoboken
-
Supuran, C. T. Carbonic anhydrases as drug targets - general presentation. In Drug Design of Zinc-Enzyme Inhibitors: Functional, Structural, and Disease Applications, Supuran, C. T.; Winum, J.-Y., Eds.; Wiley: Hoboken, 2009; pp 15-38.
-
(2009)
Drug Design of Zinc-Enzyme Inhibitors: Functional, Structural, and Disease Applications
, pp. 15-38
-
-
Supuran, C.T.1
-
36
-
-
77949344262
-
Zinc binding functions in the design of carbonic anhydrase inhibitors
-
In, Supuran, C. T. Winum, J.-Y. Wiley: Hoboken
-
Winum, J.-Y.; Montero, J.-L.; Scozzafava, A.; Supuran, C. T. Zinc binding functions in the design of carbonic anhydrase inhibitors. In Drug Design of Zinc-Enzyme Inhibitors: Functional, Structural, and Disease Applications, Supuran, C. T.; Winum, J.-Y., Eds.; Wiley: Hoboken, 2009; pp 39-72.
-
(2009)
Drug Design of Zinc-Enzyme Inhibitors: Functional, Structural, and Disease Applications
, pp. 39-72
-
-
Winum, J.-Y.1
Montero, J.-L.2
Scozzafava, A.3
Supuran, C.T.4
-
37
-
-
84889476926
-
X-Ray crystallography of CA inhibitors and its importance in drug design
-
In, Supuran, C. T. Winum, J.-Y. Wiley: Hoboken
-
Alterio, V.; Di Fiore, A.; D'Ambrosio, K.; Supuran, C. T.; De Simone, G. X-Ray crystallography of CA inhibitors and its importance in drug design. In Drug Design of Zinc-Enzyme Inhibitors: Functional, Structural, and Disease Applications, Supuran, C. T.; Winum, J.-Y., Eds.; Wiley: Hoboken, 2009; pp 73-138.
-
(2009)
Drug Design of Zinc-Enzyme Inhibitors: Functional, Structural, and Disease Applications
, pp. 73-138
-
-
Alterio, V.1
Di Fiore, A.2
D'Ambrosio, K.3
Supuran, C.T.4
De Simone, G.5
-
38
-
-
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
-
39
-
-
8844249356
-
Hypoxia activates the capacity of tumor-associated carbonic anhydrase IX to acidify extracellular pH
-
DOI 10.1016/j.febslet.2004.10.043, PII S0014579304012943
-
Svastová, E.; Hulíková, A.; Rafajová, M.; Zat'ovicová, M.; Gibadulinová, 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 (Pubitemid 39535327)
-
(2004)
FEBS Letters
, vol.577
, Issue.3
, pp. 439-445
-
-
Svastova, E.1
Hulikova, A.2
Rafajova, M.3
Zat'Ovicova, M.4
Gibadulinova, A.5
Casini, A.6
Cecchi, A.7
Scozzafava, A.8
Supuran, C.T.9
Pastorek, J.10
Pastorekova, S.11
-
40
-
-
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
-
41
-
-
84859870939
-
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, 84-97
-
(2012)
Oncotarget
, vol.3
, pp. 84-97
-
-
McDonald, P.C.1
Winum, J.-Y.2
Supuran, C.T.3
Dedhar, S.4
-
42
-
-
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, 3364-76
-
(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..
-
43
-
-
84861762712
-
Carbonic anhydrase IX promotes tumor growth and necrosis in vivo and inhibition enhances anti-VEGF therapy
-
McIntyre, A.; Patiar, S.; Wigfield, S.; Li, J. L.; Ledaki, I.; Turley, H.; Leek, R.; Snell, C.; Gatter, K.; Sly, W. S.; Vaughan-Jones, R. D.; Swietach, P.; Harris, A. L. Carbonic anhydrase IX promotes tumor growth and necrosis in vivo and inhibition enhances anti-VEGF therapy Clin. Cancer Res. 2012, 18, 3100-11
-
(2012)
Clin. Cancer Res.
, vol.18
, pp. 3100-3111
-
-
McIntyre, A.1
Patiar, S.2
Wigfield, S.3
Li, J.L.4
Ledaki, I.5
Turley, H.6
Leek, R.7
Snell, C.8
Gatter, K.9
Sly, W.S.10
Vaughan-Jones, R.D.11
Swietach, P.12
Harris, A.L.13
-
44
-
-
0034504075
-
Long-chain functional bisphosphonates: Synthesis, anticalcification, and antiresorption activity
-
DOI 10.1002/1098-1071(20 00)11:7<470::AID-HC 5>3.0.CO;2-P
-
Chen, R.; Schlossman, A.; Breuer, E.; Hägele, G.; Tillmann, C.; Van Gelder, J. M.; Golomb, G. Long-Chain Functional Bisphosphonates: Synthesis, Anticalcification, and Antiresorption Activity Heteroatom Chem. 2000, 11, 470-479 (Pubitemid 32074837)
-
(2000)
Heteroatom Chemistry
, vol.11
, Issue.7
, pp. 470-479
-
-
Chen, R.1
Schlossman, A.2
Breuer, E.3
Hagele, G.4
Tillmann, C.5
Van Gelder, J.M.6
Golomb, G.7
-
45
-
-
77958056213
-
Aminoalkylcarbamoylphosphonates reduce TNFa release from activated immune cells
-
Harel, E.; Rubinstein, A.; Chen, W.; Breuer, E.; Tirosh, B. Aminoalkylcarbamoylphosphonates reduce TNFa release from activated immune cells Bioorg. Med. Chem. Lett. 2010, 20, 6518-6523
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 6518-6523
-
-
Harel, E.1
Rubinstein, A.2
Chen, W.3
Breuer, E.4
Tirosh, B.5
-
46
-
-
84866313999
-
-
Ph.D. Thesis; Hebrew University of Jerusalem
-
Frant, J. Ph.D. Thesis; Hebrew University of Jerusalem, 2010.
-
(2010)
-
-
Frant, J.1
-
47
-
-
22744446294
-
Carbonic anhydrase inhibitors. Design of fluorescent sulfonamides as probes of tumor-associated carbonic anhydrase IX that inhibit isozyme IX-mediated acidification of hypoxic tumors
-
DOI 10.1021/jm0501073
-
Cecchi, A.; Hulikova, A.; Pastorek, J.; Pastoreková, S.; Scozzafava, A.; Winum, J. Y.; Montero, J. L.; Supuran, C. T. Carbonic anhydrase inhibitors. Design of fluorescent sulfonamides as probes of tumor-associated carbonic anhydrase IX that inhibit isozyme IX-mediated acidification of hypoxic tumors J. Med. Chem. 2005, 48, 4834-4841 (Pubitemid 41033126)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.15
, pp. 4834-4841
-
-
Cecchi, A.1
Hulikova, A.2
Pastorek, J.3
Pastorekova, S.4
Scozzafava, A.5
Winum, J.-Y.6
Montero, J.-L.7
Supuran, C.T.8
-
48
-
-
1242303231
-
-
in Supuran, C. T. CRC Press: Boca Raton
-
Pastorekova, S.; Pastorek, J. in Carbonic Anhydrase-Its Inhibitors and Activators, Supuran, C. T., Ed.; CRC Press: Boca Raton, 2004; pp 255-281.
-
(2004)
Carbonic Anhydrase - Its Inhibitors and Activators
, pp. 255-281
-
-
Pastorekova, S.1
Pastorek, J.2
-
49
-
-
0028957571
-
Role of phospholipase D in laminin-induced production of gelatinase A (MMP-2) in metastatic cells
-
Reich, R.; Blumenthal, M.; Liscovitch, M. Role of phospholipase D in laminin-induced production of gelatinase A (MMP-2) in metastatic cells Clin. Exp. Metastasis 1995, 13, 134-140
-
(1995)
Clin. Exp. Metastasis
, vol.13
, pp. 134-140
-
-
Reich, R.1
Blumenthal, M.2
Liscovitch, M.3
-
50
-
-
0024434199
-
Two different laminin domains mediate the differentiation of human endothelial cells into capillary-like structures in vitro
-
DOI 10.1016/0092-8674(89)90945-8
-
Grant, D. S.; Tashiro, K.; Segui-Real, B.; Yamada, Y.; Martin, G. R.; Kleinman, H. K. Two different laminin domains mediate the differentiation of human endothelial cells into capillary-like structures in vitro Cell 1989, 58, 933-943 (Pubitemid 19227901)
-
(1989)
Cell
, vol.58
, Issue.5
, pp. 933-943
-
-
Grant, D.S.1
Tashiro, K.-I.2
Segui-Real, B.3
Yamada, Y.4
Martin, G.R.5
Kleinman, H.K.6
-
51
-
-
33751011581
-
Proteomic analysis of plasma membrane from hypoxia-adapted malignant melanoma
-
DOI 10.1021/pr0601739
-
Stockwin, L. H.; Blonder, J.; Bumke, M. A.; Lucas, D. A.; Chan, K. C.; Conrads, T. P.; Issaq, H. J.; Veenstra, T. D.; Newton, D. L.; Rybak, S. M. Proteomic Analysis of Plasma Membrane from Hypoxia-Adapted Malignant Melanoma J. Proteome Res. 2006, 5, 2996-3007 (Pubitemid 44749218)
-
(2006)
Journal of Proteome Research
, vol.5
, Issue.11
, pp. 2996-3007
-
-
Stockwin, L.H.1
Blonder, J.2
Bumke, M.A.3
Lucas, D.A.4
Chan, K.C.5
Conrads, T.P.6
Issaq, H.J.7
Veenstra, T.D.8
Newton, D.L.9
Rybak, S.M.10
-
52
-
-
7044239365
-
Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with phosphates, carbamoyl phosphate, and the phosphonate antiviral drug foscarnet
-
DOI 10.1016/j.bmcl.2004.09.064, PII S0960894X04011874
-
Rusconi, S.; Innocenti, A.; Vullo, D.; Mastrolorenzo, A.; Scozzafava, A.; Supuran, C. T. Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with phosphates, carbamoyl phosphate, and the phosphonate antiviral drug foscarnet Bioorg. Med. Chem. Lett. 2004, 14, 5763-5767 (Pubitemid 39421516)
-
(2004)
Bioorganic and Medicinal Chemistry Letters
, vol.14
, Issue.23
, pp. 5763-5767
-
-
Rusconi, S.1
Innocenti, A.2
Vullo, D.3
Mastrolorenzo, A.4
Scozzafava, A.5
Supuran, C.T.6
-
53
-
-
14644437644
-
Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with organic phosphates and phosphonates
-
DOI 10.1016/j.bmcl.2005.01.049
-
Winum, J.-Y.; Innocenti, A.; Gagnard, V.; Montero, J.-L.; Scozzafava, A.; Vullo, D.; Supuran, C. T. Carbonic anhydrase inhibitors. Interaction of isozymes I, II, IV, V, and IX with organic phosphates and phosphonates Bioorg. Med. Chem. Lett. 2005, 15, 1683-1686 (Pubitemid 40312552)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.6
, pp. 1683-1686
-
-
Winum, J.-Y.1
Innocenti, A.2
Gagnard, V.3
Montero, J.-L.4
Scozzafava, A.5
Vullo, D.6
Supuran, C.T.7
-
54
-
-
33947690287
-
Phosph(on)ate as a zinc-binding group in metalloenzyme inhibitors: X-ray crystal structure of the antiviral drug foscarnet complexed to human carbonic anhydrase I
-
DOI 10.1016/j.bmcl.2007.01.113, PII S0960894X07001709
-
Temperini, C.; Innocenti, A.; Guerri, A.; Scozzafava, A.; Rusconi, S.; Supuran, C. T. Phosph(on)ate as a zinc-binding group in metalloenzyme inhibitors: X-ray crystal structure of the antiviral drug foscarnet complexed to human carbonic anhydrase Bioorg. Med. Chem. Lett. 2007, 17, 2210-2215 (Pubitemid 46501767)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.8
, pp. 2210-2215
-
-
Temperini, C.1
Innocenti, A.2
Guerri, A.3
Scozzafava, A.4
Rusconi, S.5
Supuran, C.T.6
-
55
-
-
84858420920
-
(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
-
56
-
-
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, C. T. 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, 3677-3687
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3677-3687
-
-
Scozzafava, A.1
Supuran, C.T.2
-
57
-
-
77954244965
-
New hydroxypyrimidinone-containing sulfonamides as carbonic anhydrase inhibitors also acting as MMP inhibitors
-
Esteves, M. A.; Ortet, O.; Capelo, A.; Supuran, C. T.; Marques, S. M.; Santos, M. A. New hydroxypyrimidinone-containing sulfonamides as carbonic anhydrase inhibitors also acting as MMP inhibitors Bioorg. Med. Chem. Lett. 2010, 20, 3623-3627
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 3623-3627
-
-
Esteves, M.A.1
Ortet, O.2
Capelo, A.3
Supuran, C.T.4
Marques, S.M.5
Santos, M.A.6
-
58
-
-
0037975559
-
Broad-spectrum matrix metalloproteinase inhibitor marimastat-induced musculoskeletal side effects in rats
-
DOI 10.1002/art.11030
-
Renkiewicz, R.; Qiu, L.; Lesch, C.; Sun, X.; Devalaraja, R.; Cody, T.; Kaldjian, E.; Welgus, H.; Baragi, V. Broad-spectrum matrix metalloproteinase inhibitor marimastat-induced musculoskeletal side effects in rats Arthritis Rheum. 2003, 48, 1742-1749 (Pubitemid 36682383)
-
(2003)
Arthritis and Rheumatism
, vol.48
, Issue.6
, pp. 1742-1749
-
-
Renkiewicz, R.1
Qiu, L.2
Lesch, C.3
Sun, X.4
Devalaraja, R.5
Cody, T.6
Kaldjian, E.7
Welgus, H.8
Baragi, V.9
-
59
-
-
0034732648
-
2Sha, a model for a peroxidase-inhibitor complex
-
DOI 10.1016/S0162-0134(99)00245-7, PII S0162013499002457
-
O'Brien, E. C.; Farkas, E.; Gil, M. J.; Fitzgerald, D.; Castineras, A.; Nolan, K. B. Metal complexes of salicylhydroxamic acid (H(2)Sha), anthranilic hydroxamic acid and benzohydroxamic acid. Crystal and molecular structure of [Cu(phen)(2)(Cl)] Cl center dot H(2)Sha, a model for a peroxidase-inhibitor complex J. Inorg. Biochem. 2000, 79, 47-51 (Pubitemid 30628711)
-
(2000)
Journal of Inorganic Biochemistry
, vol.79
, Issue.1-4
, pp. 47-51
-
-
O'Brien, E.C.1
Farkas, E.2
Gil, M.J.3
Fitzgerald, D.4
Castineras, A.5
Nolan, K.B.6
-
60
-
-
15544373919
-
Recent non-hydroxamate matrix metalloproteinase inhibitors
-
DOI 10.1517/13543776.15.3.253
-
Breuer, E.; Frant, J.; Reich, R. Recent Non Hydroxamate Matrix Metalloproteinase Inhibitors Expert Opin. Ther. Patents 2005, 15, 253-269 (Pubitemid 40403380)
-
(2005)
Expert Opinion on Therapeutic Patents
, vol.15
, Issue.3
, pp. 253-269
-
-
Breuer, E.1
Frant, J.2
Reich, R.3
-
61
-
-
0000603473
-
Biomolecules and Nanotechnology
-
Goodsell, D. S. Biomolecules and Nanotechnology American Scientist 2000, 88, 230
-
(2000)
American Scientist
, vol.88
, pp. 230
-
-
Goodsell, D.S.1
-
62
-
-
43049158125
-
Designing transient binding drugs: A new concept for drug discovery
-
Ohlson, S. Designing transient binding drugs: A new concept for drug discovery Drug Discovery Today 2008, 13, 433-439
-
(2008)
Drug Discovery Today
, vol.13
, pp. 433-439
-
-
Ohlson, S.1
-
63
-
-
33846122993
-
Dimethyl sulfoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug
-
DOI 10.1038/nbt1272, PII NBT1272
-
It has been pointed out by the authors of the following paper that vorinostat was better than its numerous higher potency analogs, which had unacceptable side effects and, therefore, had to be discontinued: Marks, P. A.; Breslow, R. Dimethyl sulfoxide to vorinostat: Development of this histone deacetylase inhibitor as an anticancer drug Nat. Biotechnol. 2007, 25, 84-90 (Pubitemid 46087907)
-
(2007)
Nature Biotechnology
, vol.25
, Issue.1
, pp. 84-90
-
-
Marks, P.A.1
Breslow, R.2
-
64
-
-
77951685290
-
An in vitro assay to measure targeted drug delivery to bone mineral
-
Jahnke, W.; Henry, C. An in vitro assay to measure targeted drug delivery to bone mineral ChemMedChem 2010, 5, 770-776
-
(2010)
ChemMedChem
, vol.5
, pp. 770-776
-
-
Jahnke, W.1
Henry, C.2
-
65
-
-
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, 3057-3062
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 3057-3062
-
-
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
-
66
-
-
0037093669
-
Neuroprotective effects of carnosine and homocarnosine on pheochromocytoma PC12 cells exposed to ischemia
-
DOI 10.1002/jnr.10228
-
Tabakman, R.; Lazarovici, P.; Kohen, R. Neuroprotective effects of carnosine and homocarnosine on pheochromocytoma PC12 cells exposed to ischemia J. Neurosci. Res. 2002, 68, 463-469 (Pubitemid 34461577)
-
(2002)
Journal of Neuroscience Research
, vol.68
, Issue.4
, pp. 463-469
-
-
Tabakman, R.1
Lazarovici, P.2
Kohen, R.3
|