-
1
-
-
0033043693
-
Characterization of the tumour necrosis factor alpha converting enzyme, TACE/ADAM17
-
Cerretti DP. Characterization of the tumour necrosis factor alpha converting enzyme, TACE/ADAM17. Biochem Soc Trans 1999;27:219-223
-
(1999)
Biochem Soc Trans
, vol.27
, pp. 219-223
-
-
Cerretti, D.P.1
-
2
-
-
0026717674
-
The pathophysiology of tumor necrosis factors
-
Vassalli P. The pathophysiology of tumor necrosis factors. Annu Rev Immunol 1992;10:411-452
-
(1992)
Annu Rev Immunol
, vol.10
, pp. 411-452
-
-
Vassalli, P.1
-
4
-
-
0032961923
-
The therapeutic potential of small molecule TACE inhibitors
-
Nelson FC, Zask A. The therapeutic potential of small molecule TACE inhibitors. Exp Opin Invest Drugs 1999;8:383-392
-
(1999)
Exp Opin Invest Drugs
, vol.8
, pp. 383-392
-
-
Nelson, F.C.1
Zask, A.2
-
5
-
-
0035986907
-
TACE inhibition a new approach to treating inflammation
-
Doggrell SA. TACE inhibition a new approach to treating inflammation. Exp Opin Invest Drugs 2002;11:1003-1006
-
(2002)
Exp Opin Invest Drugs
, vol.11
, pp. 1003-1006
-
-
Doggrell, S.A.1
-
6
-
-
0035352672
-
Modifying TNF alpha for therapeutic use: A perspective on the TNF receptor system
-
Hasegawa A, Takasaki W, Greene MI, Murali R. Modifying TNF alpha for therapeutic use: a perspective on the TNF receptor system. Mini Rev Med Chem 2001;1:5-16
-
(2001)
Mini Rev Med Chem
, vol.1
, pp. 5-16
-
-
Hasegawa, A.1
Takasaki, W.2
Greene, M.I.3
Murali, R.4
-
7
-
-
44849120587
-
Drug Insight tumor necrosis factor-converting enzyme as a pharmaceutical target for rheumatoid arthritis
-
Moss ML, Tavron LS, Nedelman R. Drug Insight: tumor necrosis factor-converting enzyme as a pharmaceutical target for rheumatoid arthritis. Nat Clin Prac Rheum 2008;4:300-309
-
(2008)
Nat Clin Prac Rheum
, vol.4
, pp. 300-309
-
-
Moss, M.L.1
Tavron, L.S.2
Nedelman, R.3
-
8
-
-
0024281428
-
A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: Ramifications for the complex physiology of TNF
-
Kriegler M, Perez C, DeFay K, et al. A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: ramifications for the complex physiology of TNF. Cell 1988;53:45-53
-
(1988)
Cell
, vol.53
, pp. 45-53
-
-
Kriegler, M.1
Perez, C.2
Defay, K.3
-
9
-
-
8044257704
-
A metalloproteinase disintegrin that releases tumour necrosis factor-alpha from cells
-
Black RA, Rauch CT, Kozlosky CJ, et al. A metalloproteinase disintegrin that releases tumour necrosis factor-alpha from cells. Nature 1997;385:729-733
-
(1997)
Nature
, vol.385
, pp. 729-733
-
-
Black, R.A.1
Rauch, C.T.2
Kozlosky, C.J.3
-
10
-
-
8044250278
-
Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor- alpha
-
Moss ML, Jin SL, Milla ME, et al. Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor- alpha. Nature 1997;385:733-736
-
(1997)
Nature
, vol.385
, pp. 733-736
-
-
Moss, M.L.1
Jin, S.L.2
Milla, M.E.3
-
14
-
-
0033168031
-
Therapeutic potential and strategies for inhibiting tumor necrosis factor-alpha
-
Newton RC, Decicco CP. Therapeutic potential and strategies for inhibiting tumor necrosis factor-alpha. J Med Chem 1999;42:2295-2314
-
(1999)
J Med Chem
, vol.42
, pp. 2295-2314
-
-
Newton, R.C.1
Decicco, C.P.2
-
15
-
-
0344019404
-
Crystal structure of the catalytic domain of human tumor necrosis factor-alpha-converting enzyme
-
Maskos K, Fernandez-Catalan C, Huber R, et al. Crystal structure of the catalytic domain of human tumor necrosis factor-alpha-converting enzyme. Proc Natl Acad Sci USA 1998;95:3408-3412
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 3408-3412
-
-
Maskos, K.1
Fernandez-Catalan, C.2
Huber, R.3
-
16
-
-
40449129841
-
3D-Quantitative structure-activity relationship studies on benzothiadiazepine hydroxamates as inhibitors of tumor necrosis factor-alpha converting enzyme
-
Murumkar PR, Giridhar R, Yadav MR. 3D-Quantitative structure-activity relationship studies on benzothiadiazepine hydroxamates as inhibitors of tumor necrosis factor-alpha converting enzyme. Chem Biol Drug Des 2008;71:363-373
-
(2008)
Chem Biol Drug des
, vol.71
, pp. 363-373
-
-
Murumkar, P.R.1
Giridhar, R.2
Yadav, M.R.3
-
17
-
-
58149102483
-
Development of predictive 3D-QSAR CoMFA and CoMSIA models for-aminohydroxamic acid-derived tumor necrosis factor-alpha converting enzyme inhibitors
-
Murumkar PR, Dasgupta SD, Zambre VP, et al. Development of predictive 3D-QSAR CoMFA and CoMSIA models for-aminohydroxamic acid-derived tumor necrosis factor-alpha converting enzyme inhibitors. Chem Biol Drug Des 2009;73:97-107
-
(2009)
Chem Biol Drug des
, vol.73
, pp. 97-107
-
-
Murumkar, P.R.1
Dasgupta, S.D.2
Zambre, V.P.3
-
18
-
-
65449150196
-
Studies on novel 2-imidazolidinones and tetrahydropyrimidin-2(1H)-ones as potential TACE inhibitors: Design, synthesis, molecular modeling, and preliminary biological evaluation
-
Dasgupta S, Murumkar PR, Giridhar R, Yadav MR. Studies on novel 2-imidazolidinones and tetrahydropyrimidin-2(1H)-ones as potential TACE inhibitors: design, synthesis, molecular modeling, and preliminary biological evaluation. Bioorg Med Chem 2009;17:3604-3617
-
(2009)
Bioorg Med Chem
, vol.17
, pp. 3604-3617
-
-
Dasgupta, S.1
Murumkar, P.R.2
Giridhar, R.3
Yadav, M.R.4
-
19
-
-
73649093532
-
Development of predictive pharmacophore model for in silico screening and 3D-QSAR CoMFA and CoMSIA studies for lead optimization for designing of potent tumor necrosis factor alpha converting enzyme inhibitors
-
Communicated (in press)
-
Murumkar PR, Dasgupta SD, Zambre VP, et al. Development of predictive pharmacophore model for in silico screening and 3D-QSAR CoMFA and CoMSIA studies for lead optimization for designing of potent tumor necrosis factor alpha converting enzyme inhibitors. J Comp Mol Design 2009; Communicated (in press)
-
(2009)
J Comp Mol Design
-
-
Murumkar, P.R.1
Dasgupta, S.D.2
Zambre, V.P.3
-
20
-
-
0028466705
-
Protection against a lethal dose of endotoxin by an inhibitor of tumour necrosis factor processing
-
Mohler KM, Sleath PR, Fitzner JN, et al. Protection against a lethal dose of endotoxin by an inhibitor of tumour necrosis factor processing. Nature 1994;370:218-220
-
(1994)
Nature
, vol.370
, pp. 218-220
-
-
Mohler, K.M.1
Sleath, P.R.2
Fitzner, J.N.3
-
21
-
-
0028483534
-
Regulation of tumour necrosis factor-alpha processing by a metalloproteinase inhibitor
-
McGeehan GM, Becherer JD, Bast RC Jr, et al. Regulation of tumour necrosis factor-alpha processing by a metalloproteinase inhibitor. Nature 1994;370:558-561
-
(1994)
Nature
, vol.370
, pp. 558-561
-
-
McGeehan, G.M.1
Becherer, J.D.2
Bast Jr, R.C.3
-
22
-
-
0034628448
-
Protease inhibitors: Current status and future prospectus
-
Leung D, Giovanni A, Fairlie DP. Protease inhibitors: current status and future prospectus. J Med Chem 2000;43:305-341
-
(2000)
J Med Chem
, vol.43
, pp. 305-341
-
-
Leung, D.1
Giovanni, A.2
Fairlie, D.P.3
-
23
-
-
34447529140
-
Chronic obstructive pulmonary disease: Role of matrix mettaloprotease and future challenge of drug therapy
-
Shrivastava PK, Dastidar SG, Ray A. Chronic obstructive pulmonary disease: role of matrix mettaloprotease and future challenge of drug therapy. Exp Opin Invest Drugs 2007;16:1069-1078
-
(2007)
Exp Opin Invest Drugs
, vol.16
, pp. 1069-1078
-
-
Shrivastava, P.K.1
Dastidar, S.G.2
Ray, A.3
-
32
-
-
65549102504
-
Synthesis and activity of tryptophan sulphonamide derivatives as novel non-hydroxamate TNF-alpha converting enzyme (TACE) inhibitors
-
Park K, Gopalsamy A, Aplasca A, et al. Synthesis and activity of tryptophan sulphonamide derivatives as novel non-hydroxamate TNF-alpha converting enzyme (TACE) inhibitors. Bioorg Med Chem 2009;17(11):3857-3865
-
(2009)
Bioorg Med Chem
, vol.17
, Issue.11
, pp. 3857-3865
-
-
Park, K.1
Gopalsamy, A.2
Aplasca, A.3
-
45
-
-
0035806101
-
Arylsulphonyl hydroxamic acids: Potent and selective matrix metalloproteinase inhibitors
-
Baxter AD, Bhogal R, Bird J. Arylsulphonyl hydroxamic acids: potent and selective matrix metalloproteinase inhibitors. Bioorg Med Chem Lett 2001;11:1465-1468
-
(2001)
Bioorg Med Chem Lett
, vol.11
, pp. 1465-1468
-
-
Baxter, A.D.1
Bhogal, R.2
Bird, J.3
-
46
-
-
0037147984
-
An enantioselective synthesis of sulphonamide hydroxamic acids as matrix metalloprotease inhibitors
-
Watson RJ, Batty D, Baxter AD, et al. An enantioselective synthesis of sulphonamide hydroxamic acids as matrix metalloprotease inhibitors. Tetrahedron Lett 2002;43:683-685
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 683-685
-
-
Watson, R.J.1
Batty, D.2
Baxter, A.D.3
-
49
-
-
0742299372
-
TNF inhibitors: A review of the recent patent literature
-
Watson B. TNF inhibitors: a review of the recent patent literature. I Drugs 2002;5:1151-1162
-
(2002)
I Drugs
, vol.5
, pp. 1151-1162
-
-
Watson, B.1
-
55
-
-
33845612218
-
Discovery of low nanomolar non-hydroxamate inhibitors of tumor necrosis factor-α converting enzyme (TACE)
-
DOI 10.1016/j.bmcl.2006.09.048, PII S0960894X06011073
-
Duan J, Chen L, Lu Z, et al. Discovery of low nanomolar non-hydroxamate inhibitors of tumor necrosis factor-alpha converting enzyme (TACE). Bioorg Med Chem Lett 2007;17:266-271 (Pubitemid 44959953)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.1
, pp. 266-271
-
-
Duan, J.J.-W.1
Chen, L.2
Lu, Z.3
Jiang, B.4
Asakawa, N.5
Sheppeck II, J.E.6
Liu, R.-Q.7
Covington, M.B.8
Pitts, W.9
Kim, S.-H.10
Decicco, C.P.11
-
58
-
-
34247326550
-
Hydantoins, triazolones, and imidazolones as selective non-hydroxamate inhibitors of tumor necrosis factor-α converting enzyme (TACE)
-
DOI 10.1016/j.bmcl.2007.02.076, PII S0960894X07002764
-
Sheppeck J, Gilmore J, Tebben A, et al. Hydantoins, triazolones, and imidazolones as selective non-hydroxamate inhibitors of tumor necrosis factor-a converting enzyme (TACE) Bioorg Med Chem Lett 2007;17:2769-2774 (Pubitemid 46636261)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.10
, pp. 2769-2774
-
-
Sheppeck II, J.E.1
Gilmore, J.L.2
Tebben, A.3
Xue, C.-B.4
Liu, R.-Q.5
Decicco, C.P.6
Duan, J.J.-W.7
-
61
-
-
33846895737
-
Discovery of novel hydantoins as selective non-hydroxamate inhibitors of tumor necrosis factor-α converting enzyme (TACE)
-
DOI 10.1016/j.bmcl.2006.11.089, PII S0960894X06013734
-
Sheppeck J, Gilmore J, Yang A, et al. Discovery of novel hydantoins as selective non-hydroxamate inhibitors of tumor necrosis factor-alpha converting enzyme (TACE ) Bioorg Med Chem Lett 2007;17:1413-1417 (Pubitemid 46240831)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.5
, pp. 1413-1417
-
-
Sheppeck II, J.E.1
Gilmore, J.L.2
Yang, A.3
Chen, X.-T.4
Xue, C.-B.5
Roderick, J.6
Liu, R.-Q.7
Covington, M.B.8
Decicco, C.P.9
Duan, J.J.-W.10
-
66
-
-
33847636782
-
A new 4-(2-methylquinolin-4-ylmethyl) phenyl P1 group for the beta-amino hydroxamic acid derived TACE inhibitors
-
Chen X, Ghavimi B, Corbett R, et al. A new 4-(2-methylquinolin-4- ylmethyl) phenyl P1 group for the beta-amino hydroxamic acid derived TACE inhibitors. Bioorg Med Chem Lett 2007;17:1865-1870
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 1865-1870
-
-
Chen, X.1
Ghavimi, B.2
Corbett, R.3
-
68
-
-
38949095681
-
Alpha, beta-Cyclic-beta-benzamido hydroxamic acids: Novel oxaspiro[4.4]nonane templates for the discovery of potent, selective, orally bioavailable inhibitors of tumor necrosis factor- alpha converting enzyme (TACE)
-
Ott G, Asakawa N, Liu R, et al. alpha, beta-Cyclic-beta-benzamido hydroxamic acids: Novel oxaspiro[4.4]nonane templates for the discovery of potent, selective, orally bioavailable inhibitors of tumor necrosis factor- alpha converting enzyme (TACE). Bioorg Med Chem Lett 2008;18:1288-1292
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 1288-1292
-
-
Ott, G.1
Asakawa, N.2
Liu, R.3
-
72
-
-
34447322020
-
Synthesis and structure-activity relationship of a novel, non-hydroxamate series of TNF-a converting enzyme inhibitors
-
Gilmore J, King B, Asakawa N, et al. Synthesis and structure-activity relationship of a novel, non-hydroxamate series of TNF-a converting enzyme inhibitors. Bioorg Med Chem Lett 2007;17:4678-4682
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 4678-4682
-
-
Gilmore, J.1
King, B.2
Asakawa, N.3
-
73
-
-
73649101069
-
-
Pfizer limited. EP 1104412
-
Pfizer limited. TACE inhibitors. EP 1104412; 2005
-
(2005)
TACE Inhibitors
-
-
-
80
-
-
73649144318
-
-
Vertex Pharmaceuticals, Inc. US7485664
-
Vertex Pharmaceuticals, Inc. Inhibitors of TACE. US7485664; 2009
-
(2009)
Inhibitors of TACE
-
-
-
81
-
-
33947591481
-
Novel thiol-based TACE inhibitors: Rational design, synthesis, and SAR of thiol-containing aryl sulphonamides
-
Rao B, Bandarage U, Wang T, et al. Novel thiol-based TACE inhibitors: rational design, synthesis, and SAR of thiol-containing aryl sulphonamides. Bioorg Med Chem Lett 2007;17:2250-2253
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 2250-2253
-
-
Rao, B.1
Bandarage, U.2
Wang, T.3
-
83
-
-
0033863530
-
Ongoing trials with matrix metalloproteinase inhibitors
-
Brown PD. Ongoing trials with matrix metalloproteinase inhibitors.Exp Opin Invest Drugs 2000;9:2167-2177
-
(2000)
Exp Opin Invest Drugs
, vol.9
, pp. 2167-2177
-
-
Brown, P.D.1
-
84
-
-
0033946952
-
Metalloproteinase inhibitors-New opportunities for the treatment of rheumatoid arthritis and osteoarthriris
-
Shaw T, Nixon JS, Bottomley KM. Metalloproteinase inhibitors-New opportunities for the treatment of rheumatoid arthritis and osteoarthriris. Exp Opin Invest Drugs 2000;9:1469-1478
-
(2000)
Exp Opin Invest Drugs
, vol.9
, pp. 1469-1478
-
-
Shaw, T.1
Nixon, J.S.2
Bottomley, K.M.3
-
85
-
-
0035056510
-
The clinical potential of matrix metalloproteinase inhibitors in the rheumatic disorder
-
Elliot S, Cawston T. The clinical potential of matrix metalloproteinase inhibitors in the rheumatic disorder. Drugs Aging 2001;18:87-99
-
(2001)
Drugs Aging
, vol.18
, pp. 87-99
-
-
Elliot, S.1
Cawston, T.2
-
86
-
-
12444273714
-
Synthesis and structure - Activity relationship of N-substituted 4-arylsulfonylpiperidine-4-hydroxamic acids as novel, orally active matrix metalloproteinase inhibitors for the treatment of osteoarthritis
-
DOI 10.1021/jm0205550
-
Aranapakam V, Davis JM, Grosu GT, et al. Synthesis and structure-activity relationship of N-substituted 4-arylsulfonylpiperidine-4-hydroxamic acids as novel, orally active matrix metalloproteinase inhibitors for the treatment of osteoarthritis. J Med Chem 2003;46:2376-2396 (Pubitemid 36637922)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.12
, pp. 2376-2396
-
-
Aranapakam, V.1
Davis, J.M.2
Grosu, G.T.3
Baker, J.4
Ellingboe, J.5
Zask, A.6
Levin, J.I.7
Sandanayaka, V.P.8
Du, M.9
Skotnicki, J.S.10
DiJoseph, J.F.11
Sung, A.12
Sharr, M.A.13
Killar, L.M.14
Walter, T.15
Jin, G.16
Cowling, R.17
Tillett, J.18
Zhao, W.19
McDevitt, J.20
Xu, Z.B.21
more..
-
87
-
-
4444348543
-
-
Greenwald RA, Zucker S, Golub LM, editors. The New York Academy of Sciences: NY
-
Yocum SA, Lopresti-Monow L, Reeves LM, Mitchell PG. Inhibition of matrix metalloproteinases: therapeutic applications. In: Greenwald RA, Zucker S, Golub LM, editors. The New York Academy of Sciences: NY; 1999. p. 583-586
-
(1999)
Inhibition of Matrix Metalloproteinases: Therapeutic Applications
, pp. 583-586
-
-
Yocum, S.A.1
Lopresti-Monow, L.2
Reeves, L.M.3
Mitchell, P.G.4
-
88
-
-
0034775522
-
Biology of TACE inhibition
-
Newton, RC, Solomon KA, et al. Biology of TACE inhibition. Ann Rheum Dis 2001;60(Suppl 3):iii25-32
-
(2001)
Ann Rheum Dis
, vol.60
, Issue.SUPPL. 3
-
-
Newton, R.C.1
Solomon, K.A.2
-
89
-
-
2342564528
-
Reverse hydroxamate based selective TACE inhibitors
-
Kamei N, Tanaka T, Kawai K, et al. Reverse hydroxamate based selective TACE inhibitors. Bioorg Med Chem Lett 2004;14(11):2897-2900
-
(2004)
Bioorg Med Chem Lett
, vol.14
, Issue.11
, pp. 2897-2900
-
-
Kamei, N.1
Tanaka, T.2
Kawai, K.3
-
90
-
-
0034883069
-
Inhibition of tumor necrosis factor alpha production and arthritis in rat by GW3333, a dual inhibitor of TNF-A converting enzyme and matrix metalloproteinases
-
Conway JG, Andrews RC, Beaudet B, et al. Inhibition of tumor necrosis factor alpha production and arthritis in rat by GW3333, a dual inhibitor of TNF-A converting enzyme and matrix metalloproteinases. J Pharm Exp Ther 2001;298(3):900-908
-
(2001)
J Pharm Exp Ther
, vol.298
, Issue.3
, pp. 900-908
-
-
Conway, J.G.1
Andrews, R.C.2
Beaudet, B.3
-
91
-
-
17944389351
-
Structure based design and synthesis of a potent matrix metalloproteinase-13 inhibitor based on a pyrrolidinone scaffold
-
Robinson RP, Laird ER, Blake JF, et al. Structure based design and synthesis of a potent matrix metalloproteinase-13 inhibitor based on a pyrrolidinone scaffold. J Med Chem 2000;43:2293-2296
-
(2000)
J Med Chem
, vol.43
, pp. 2293-2296
-
-
Robinson, R.P.1
Laird, E.R.2
Blake, J.F.3
-
92
-
-
17944371861
-
N-hydroxyformamide peptidomimetics as TACE/matrix metalloprotease inhibitors: Oral activity via P1 isobutyl substitution
-
Musso DL, Anderson MW, Andrews RC, et al. N-hydroxyformamide peptidomimetics as TACE/matrix metalloprotease inhibitors: oral activity via P1 isobutyl substitution. Bioorg Med Chem Lett 2001;11:2147-2151
-
(2001)
Bioorg Med Chem Lett
, vol.11
, pp. 2147-2151
-
-
Musso, D.L.1
Anderson, M.W.2
Andrews, R.C.3
-
93
-
-
9744249418
-
Synthesis and structure-activity relationships of 4-alkynyloxy phenyl sulfanyl, sulfinyl and sulfonyl alkyl hydroxamates as tumor necrosis factor-alpha converting enzyme and matrix metalloproteinase inhibitors
-
Venkatesan AM, Davis JM, Grosu GT, et al. Synthesis and structure-activity relationships of 4-alkynyloxy phenyl sulfanyl, sulfinyl and sulfonyl alkyl hydroxamates as tumor necrosis factor-alpha converting enzyme and matrix metalloproteinase inhibitors. J Med Chem 2004;47(25):6255-6269
-
(2004)
J Med Chem
, vol.47
, Issue.25
, pp. 6255-6269
-
-
Venkatesan, A.M.1
Davis, J.M.2
Grosu, G.T.3
-
94
-
-
12144287462
-
Identification & characterisation of 4-[[4-(2-Butynyloxy) phenyl]sulfonyl]-N-hydroxy-2,2- dimethyl-(3S)-thiomorphol- in carboxamide (TMI-1), a novel dual tumor necrosis factor-alpha converting enzyme/ matrix metalloprotease inhibitor for the treatment of rheumatoid arthritis
-
Zhang Y, Xu J, Levin J, et al. Identification & characterisation of 4-[[4-(2-Butynyloxy) phenyl]sulfonyl]-N-hydroxy-2,2- dimethyl-(3S)-thiomorphol- in carboxamide (TMI-1), a novel dual tumor necrosis factor-alpha converting enzyme/ matrix metalloprotease inhibitor for the treatment of rheumatoid arthritis. J Pharmacol Exp Ther 2004;309:348-355
-
(2004)
J Pharmacol Exp Ther
, vol.309
, pp. 348-355
-
-
Zhang, Y.1
Xu, J.2
Levin, J.3
-
95
-
-
0037038311
-
Inhibition of potent and selective TACE inhibitors via the S1 pocket
-
Duan JJW, Chen L, Wasserman ZR, et al. Inhibition of potent and selective TACE inhibitors via the S1 pocket. J Med Chem 2002;45:4954-4957
-
(2002)
J Med Chem
, vol.45
, pp. 4954-4957
-
-
Duan, J.J.W.1
Chen, L.2
Wasserman, Z.R.3
-
96
-
-
0037352018
-
Identification of a selectivity determinant for the inhibition of tumor necrosis factor-alpha converting enzyme by comparative modelling
-
Wasserman ZR, Duan JJW, Voss ME, et al. Identification of a selectivity determinant for the inhibition of tumor necrosis factor-alpha converting enzyme by comparative modelling. Chem Biol 2003;10:215-223
-
(2003)
Chem Biol
, vol.10
, pp. 215-223
-
-
Wasserman, Z.R.1
Duan, J.J.W.2
Voss, M.E.3
-
97
-
-
0033526103
-
Discovery of novel series of selective matrix metalloproteinase inhibitors: Identification of the gamma-sulfone thiols
-
Freskos JN, Mischke BV, Decrescenzo GA, et al. Discovery of novel series of selective matrix metalloproteinase inhibitors: identification of the gamma-sulfone thiols. Bio Med Chem Lett 1999;9:943-948
-
(1999)
Bio Med Chem Lett
, vol.9
, pp. 943-948
-
-
Freskos, J.N.1
Mischke, B.V.2
Decrescenzo, G.A.3
-
98
-
-
33846817495
-
Targeting TACE dependent EGFR ligand shedding in breast cancer
-
Kenny PA, Bissell MJ. Targeting TACE dependent EGFR ligand shedding in breast cancer. J Clin Invest 2007;117:337-345
-
(2007)
J Clin Invest
, vol.117
, pp. 337-345
-
-
Kenny, P.A.1
Bissell, M.J.2
-
99
-
-
35348962179
-
Tackling EGFR signaling with TACE antagonist: A rational target for metalloprotease inhibitors in cancer
-
Kenny PA. Tackling EGFR signaling with TACE antagonist: a rational target for metalloprotease inhibitors in cancer. Exp Opin Ther Targets 2007;11:1287-1298
-
(2007)
Exp Opin Ther Targets
, vol.11
, pp. 1287-1298
-
-
Kenny, P.A.1
-
100
-
-
36048938454
-
TACE: A new target in epidermal growth factor receptor dependent tumors
-
Kenny PA. TACE: a new target in epidermal growth factor receptor dependent tumors. Differentiation 2007;75:800-808
-
(2007)
Differentiation
, vol.75
, pp. 800-808
-
-
Kenny, P.A.1
|