-
1
-
-
33947497852
-
Osteoclasts: What do they do and how they do it?
-
Teitelbaum SL. Osteoclasts: what do they do and how they do it? Am J Pathol 2007;170:427-435
-
(2007)
Am J Pathol
, vol.170
, pp. 427-435
-
-
Teitelbaum, S.L.1
-
2
-
-
34249791173
-
Regulation and enzymatic basis of bone resorption by human osteoclasts
-
Fuller K, Kirstein B, Chambers TJ. Regulation and enzymatic basis of bone resorption by human osteoclasts. Clin Sci (Lond) 2007;112:567-575
-
(2007)
Clin Sci (Lond)
, vol.112
, pp. 567-575
-
-
Fuller, K.1
Kirstein, B.2
Chambers, T.J.3
-
3
-
-
0037566322
-
Molecular mechanisms underlying osteoclast formation and activation
-
Troen BR. Molecular mechanisms underlying osteoclast formation and activation. Exp Gerontol 2003;38:605-614
-
(2003)
Exp Gerontol
, vol.38
, pp. 605-614
-
-
Troen, B.R.1
-
4
-
-
33846031926
-
The molecular understanding of osteoclast differentiation
-
Asagiri M, Takayanagi H. The molecular understanding of osteoclast differentiation. Bone 2007;40:251-264
-
(2007)
Bone
, vol.40
, pp. 251-264
-
-
Asagiri, M.1
Takayanagi, H.2
-
7
-
-
0034285013
-
The osteoblast: A sophisticated fibroblast under central surveillance
-
Ducy P, Schinke T, Karsenty G. The osteoblast: a sophisticated fibroblast under central surveillance. Science 2000;289:1501-1504
-
(2000)
Science
, vol.289
, pp. 1501-1504
-
-
Ducy, P.1
Schinke, T.2
Karsenty, G.3
-
8
-
-
6344226562
-
Interaction between osteoblast and osteoclast: Impact on bone disease
-
Phan TC, Xu J, Zheng MH. Interaction between osteoblast and osteoclast: impact on bone disease. Histol Histopathol 2004;19:1325-1344
-
(2004)
Histol Histopathol
, vol.19
, pp. 1325-1344
-
-
Phan, T.C.1
Xu, J.2
Zheng, M.H.3
-
9
-
-
0038725736
-
Generating human osteoclasts from peripheral blood
-
Sabokbar A, Athanasou NS. Generating human osteoclasts from peripheral blood. Methods Mol Med 2003;80:101-111
-
(2003)
Methods Mol Med
, vol.80
, pp. 101-111
-
-
Sabokbar, A.1
Athanasou, N.S.2
-
10
-
-
39649099367
-
Bone disease drug discovery: Examing the interactions between osteoblast and osteoclast
-
Sun S. Bone disease drug discovery: examing the interactions between osteoblast and osteoclast. Expert Opin Ther Targets 2008;12(2):239-251
-
(2008)
Expert Opin Ther Targets
, vol.12
, Issue.2
, pp. 239-251
-
-
Sun, S.1
-
11
-
-
35748967004
-
Zoledronic acid and clinical fractures and mortality after hip fracture
-
Lyles KW, Colon-Emeric CS, Magaziner JS, et al. Zoledronic acid and clinical fractures and mortality after hip fracture. N Engl J Med 2007;357:1799-1809
-
(2007)
N Engl J Med
, vol.357
, pp. 1799-1809
-
-
Lyles, K.W.1
Colon-Emeric, C.S.2
Magaziner, J.S.3
-
12
-
-
0035837553
-
Effect of parathyroid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis
-
Neer RM, Arnaud CD, Zanchetta RJ, et al. Effect of parathyroid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis. N Engl J Med 2001;344:1434-1441
-
(2001)
N Engl J Med
, vol.344
, pp. 1434-1441
-
-
Neer, R.M.1
Arnaud, C.D.2
Zanchetta, R.J.3
-
13
-
-
34548076624
-
Increases in bone mineral density correlate with improvements in bone microarchitecture with teriparatide treatment in postmenopausal women with osteoporosis
-
Chen P, Miller PD, Recker R, et al. Increases in bone mineral density correlate with improvements in bone microarchitecture with teriparatide treatment in postmenopausal women with osteoporosis. J Bone Miner Res 2007;22:1173-1180
-
(2007)
J Bone Miner Res
, vol.22
, pp. 1173-1180
-
-
Chen, P.1
Miller, P.D.2
Recker, R.3
-
14
-
-
34249105908
-
Effects of statins on bone mineral density: A meta-analysis of clinical studies
-
Uzzan B, Cohen R, Nicolas P, et al. Effects of statins on bone mineral density: a meta-analysis of clinical studies. Bone 2007;40:1581-1587
-
(2007)
Bone
, vol.40
, pp. 1581-1587
-
-
Uzzan, B.1
Cohen, R.2
Nicolas, P.3
-
15
-
-
84979134203
-
Acetodiphosphoriga sauer
-
Von Baeyer H, Hofmann KS. Acetodiphosphoriga sauer. Ber 1897;30:1973
-
(1897)
Ber
, vol.30
, pp. 1973
-
-
Von Baeyer, H.1
Hofmann, K.S.2
-
16
-
-
34248369003
-
Historical perspectives on the clinical development of bisphosphonates in the treatment of bone diseases
-
Francis MD, Valent DJ. Historical perspectives on the clinical development of bisphosphonates in the treatment of bone diseases. J Musculoskelet Neuronal Interact 2007;7(1):2-8
-
(2007)
J Musculoskelet Neuronal Interact
, vol.7
, Issue.1
, pp. 2-8
-
-
Francis, M.D.1
Valent, D.J.2
-
17
-
-
0036148405
-
Development of bisphosphonates
-
Fleisch H. Development of bisphosphonates. Breast Cancer Res 2002;4(1):30-34
-
(2002)
Breast Cancer Res
, vol.4
, Issue.1
, pp. 30-34
-
-
Fleisch, H.1
-
18
-
-
0242610812
-
Differentiating the mechanisms of antiresorptive action of nitrogen containing bisphosphonates
-
Van Beek ER, Cohen LH, Leroy IM, et al. Differentiating the mechanisms of antiresorptive action of nitrogen containing bisphosphonates. Bone 2003;33(5):805-811
-
(2003)
Bone
, vol.33
, Issue.5
, pp. 805-811
-
-
Van Beek, E.R.1
Cohen, L.H.2
Leroy, I.M.3
-
19
-
-
67650557310
-
Thermodynamics of bisphosphonates binding to human bone: A two-site model
-
Mukherjee S, Huang C, Oldfield E, et al. Thermodynamics of bisphosphonates binding to human bone: a two-site model. J Am Chem Soc 2009;131:8374-8375
-
(2009)
J Am Chem Soc
, vol.131
, pp. 8374-8375
-
-
Mukherjee, S.1
Huang, C.2
Oldfield, E.3
-
20
-
-
0028036624
-
Bisphosphonates in development for metabolic bone disease
-
Ebetino HF, Sietsema KW. Bisphosphonates in development for metabolic bone disease. Expert Opin Invest Drugs 1994;3(12):1255-1276
-
(1994)
Expert Opin Invest Drugs
, vol.3
, Issue.12
, pp. 1255-1276
-
-
Ebetino, H.F.1
Sietsema, K.W.2
-
27
-
-
33846951516
-
Effects of osteoporosis medications on bone quality
-
Benhamou CL. Effects of osteoporosis medications on bone quality. Joint Bone Spine 2007;74:39-47
-
(2007)
Joint Bone Spine
, vol.74
, pp. 39-47
-
-
Benhamou, C.L.1
-
28
-
-
33747041999
-
Developments in the pharmacotherapeutic management of osteoporosis
-
Close P, Neuprez A, Reginster JY. Developments in the pharmacotherapeutic management of osteoporosis. Expert Opin Pharmacother 2006;7:1603-1615
-
(2006)
Expert Opin Pharmacother
, vol.7
, pp. 1603-1615
-
-
Close, P.1
Neuprez, A.2
Reginster, J.Y.3
-
29
-
-
42949145038
-
Use of alendronate and risk of incident atrial fibrillation in women
-
Heckbert SR, Li G, Cummings SR, et al. Use of alendronate and risk of incident atrial fibrillation in women. Arch Intern Med 2008;168(8):826-831
-
(2008)
Arch Intern Med
, vol.168
, Issue.8
, pp. 826-831
-
-
Heckbert, S.R.1
Li, G.2
Cummings, S.R.3
-
30
-
-
0031760512
-
Studies on novel bone resorption inhibitors. II. Synthesis and pharmcological activities of fused aza-heteroarylbisphosphonate derivatives
-
Takeuchi M, Sakamoto S, Kawamuki K, et al. Studies on novel bone resorption inhibitors. II. Synthesis and pharmacological activities of fused aza-heteroarylbisphosphonate derivatives. Chem Pharm Bull 1998;46(11):1703-1709
-
(1998)
Chem Pharm Bull
, vol.46
, Issue.11
, pp. 1703-1709
-
-
Takeuchi, M.1
Sakamoto, S.2
Kawamuki, K.3
-
31
-
-
67349251553
-
A bouble-blinded head-to-head trial of minodronate and alendronate in women with postmenopausal osteoporosis
-
Hagino H, Nishizaki Y, Sone T, et al. A bouble-blinded head-to-head trial of minodronate and alendronate in women with postmenopausal osteoporosis. Bone 2009;44(6):1078-1084
-
(2009)
Bone
, vol.44
, Issue.6
, pp. 1078-1084
-
-
Hagino, H.1
Nishizaki, Y.2
Sone, T.3
-
32
-
-
67650503125
-
Effect of daily oral minodronate on vertebral fractures in Japanese postmenopausal women with established osteoporosis: A randomized placebo-controlled double-blind study
-
Matsumoto T, Hagino H, Shiraki M, et al. Effect of daily oral minodronate on vertebral fractures in Japanese postmenopausal women with established osteoporosis: a randomized placebo-controlled double-blind study. Osteoporos Int 2009;20(8):1429-1437
-
(2009)
Osteoporos Int
, vol.20
, Issue.8
, pp. 1429-1437
-
-
Matsumoto, T.1
Hagino, H.2
Shiraki, M.3
-
33
-
-
0035866666
-
Bisphosphonates inhibit the growth of trypanosoma brucei, trypanosoma cruzi, leishmania donovani, toxoplasma gondii and plasmodium falciparum: A potential route to chemotherapy
-
Martin MB, Grimley JS, Oldfield E, et al. Bisphosphonates inhibit the growth of trypanosoma brucei, trypanosoma cruzi, leishmania donovani, toxoplasma gondii and plasmodium falciparum: a potential route to chemotherapy. J Med Chem 2001;44:909-916
-
(2001)
J Med Chem
, vol.44
, pp. 909-916
-
-
Martin, M.B.1
Grimley, J.S.2
Oldfield, E.3
-
34
-
-
51449109024
-
Synthesis and biological evaluation of indolyl bisphosphonates as anti-bone resorptive and anti-leishmanial agents
-
Singh US, Shankar R, Hajela K, et al. Synthesis and biological evaluation of indolyl bisphosphonates as anti-bone resorptive and anti-leishmanial agents. Bioorg Med Chem 2008;16:8482-8491
-
(2008)
Bioorg Med Chem
, vol.16
, pp. 8482-8491
-
-
Singh, U.S.1
Shankar, R.2
Hajela, K.3
-
35
-
-
67649326778
-
-
The Board of Trustees of the University of Illinois, WO07109585
-
The Board of Trustees of the University of Illinois. Bisphosphonate compounds and methods. WO07109585; 2007
-
(2007)
Bisphosphonate Compounds and Methods
-
-
-
36
-
-
72849116796
-
Anti-tumour effects of bisphosphonates - What have we learned from in vivo models?
-
Brown HK, Holen I. Anti-tumour effects of bisphosphonates - what have we learned from in vivo models? Curr Cancer Drug Targets 2009;9:807-823
-
(2009)
Curr Cancer Drug Targets
, vol.9
, pp. 807-823
-
-
Brown, H.K.1
Holen, I.2
-
37
-
-
58049191457
-
Novel anti-cancer strategy in bone tumors by targeting molecular and cellular modulators of bone resorption
-
Brounais B, Ruiz VC, Redini F, et al. Novel anti-cancer strategy in bone tumors by targeting molecular and cellular modulators of bone resorption. Recent Pat Anti Cancer Drug Discov 2008;3:178-186
-
(2008)
Recent Pat Anti Cancer Drug Discov
, vol.3
, pp. 178-186
-
-
Brounais, B.1
Ruiz, V.C.2
Redini, F.3
-
38
-
-
54949093656
-
Novel bone cancer drugs: Investigational agents and control paradigms for primary bone sarcomas (Ewing' sarcoma and osteosarcoma
-
Anderson P, Kopp L, Anderson N, et al. Novel bone cancer drugs: investigational agents and control paradigms for primary bone sarcomas (Ewing' sarcoma and osteosarcoma). Expert Opin Investig Drugs 2008;17(11):1703-1715
-
(2008)
Expert Opin Investig Drugs
, vol.17
, Issue.11
, pp. 1703-1715
-
-
Anderson, P.1
Kopp, L.2
Anderson, N.3
-
39
-
-
20444405348
-
Synthesis and biological evaluation of novel bisphosphonates with dual activities on bone in vitro
-
Xie Y, Ding H, Qian L, et al. Synthesis and biological evaluation of novel bisphosphonates with dual activities on bone in vitro. Bioorg Med Chem Lett 2005;15:3267-3270
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 3267-3270
-
-
Xie, Y.1
Ding, H.2
Qian, L.3
-
40
-
-
0242691686
-
3D QSAR investigations of the inhibition of leishmania major farnesyl pyrophosphate synthase by bisphosphonates
-
Sanders JM, Gomez AO, Oldfield E, et al. 3D QSAR investigations of the inhibition of leishmania major farnesyl pyrophosphate synthase by bisphosphonates. J Med Chem 2003;46:5171-5183
-
(2003)
J Med Chem
, vol.46
, pp. 5171-5183
-
-
Sanders, J.M.1
Gomez, A.O.2
Oldfield, E.3
-
41
-
-
0028831635
-
Molecular cloning of human cDNA for cathepsin K: Novel cysteine proteinase predominantly expressed in bone
-
Inaoka T, Bilbe G, Ishibashi O, et al. Molecular cloning of human cDNA for cathepsin K: novel cysteine proteinase predominantly expressed in bone. Biochem Biophys Res Commun 1995;206(1):89-96
-
(1995)
Biochem Biophys Res Commun
, vol.206
, Issue.1
, pp. 89-96
-
-
Inaoka, T.1
Bilbe, G.2
Ishibashi, O.3
-
42
-
-
0033610853
-
The collagenolytic activity of cathepsin K is unique among mammalian proteinases
-
Garnero P, Borel O, Byrjalsen I, et al. The collagenolytic activity of cathepsin K is unique among mammalian proteinases. J Biol Chem 1998;273:32347-32352
-
(1998)
J Biol Chem
, vol.273
, pp. 32347-32352
-
-
Garnero, P.1
Borel, O.2
Byrjalsen, I.3
-
43
-
-
0032506007
-
Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice
-
Saftig P, Hunziker E, Wehmeyer O, et al. Impaired osteoclastic bone resorption leads to osteopetrosis in cathepsin-K-deficient mice. Proc Natl Acad Sci USA 1998;95:13453-13458
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 13453-13458
-
-
Saftig, P.1
Hunziker, E.2
Wehmeyer, O.3
-
44
-
-
13544254618
-
Cathepsin K inhibitors, 2000-2004
-
Cai J, Jamieson C, Moir J, Rankovic Z. Cathepsin K inhibitors, 2000-2004. Expert Opin Ther Pat 2005;15(1):33-48
-
(2005)
Expert Opin Ther Pat
, vol.15
, Issue.1
, pp. 33-48
-
-
Cai, J.1
Jamieson, C.2
Moir, J.3
Rankovic, Z.4
-
45
-
-
0033037118
-
Structural basis of inhibition of cysteine proteases by E-64 and its derivatives
-
Matsumoto K, Mizoue K, Kitamura K, et al. Structural basis of inhibition of cysteine proteases by E-64 and its derivatives. Biopolymers 1999;51(1):99-107
-
(1999)
Biopolymers
, vol.51
, Issue.1
, pp. 99-107
-
-
Matsumoto, K.1
Mizoue, K.2
Kitamura, K.3
-
46
-
-
0034041529
-
Cathepsin K and the design of inhibitiors of cathepsin K
-
Yamashita DS, Dodds RA. Cathepsin K and the design of inhibitiors of cathepsin K. Curr Pharm Des 2000;6(1):1-24
-
(2000)
Curr Pharm des
, vol.6
, Issue.1
, pp. 1-24
-
-
Yamashita, D.S.1
Dodds, R.A.2
-
47
-
-
0019753251
-
Inactivation of thiol proteases with peptidyl diazomethyl ketones
-
Shaw E, Green GD. Inactivation of thiol proteases with peptidyl diazomethyl ketones. J Methods Enzymol 1981;80(Pt C):820-826
-
(1981)
J Methods Enzymol
, vol.80
, Issue.PART C
, pp. 820-826
-
-
Shaw, E.1
Green, G.D.2
-
48
-
-
0021206502
-
The selective inactivation of thiol proteases in vitro and in vivo
-
Shaw E. The selective inactivation of thiol proteases in vitro and in vivo. J Protein Chem 1984;3:109-120
-
(1984)
J Protein Chem
, vol.3
, pp. 109-120
-
-
Shaw, E.1
-
49
-
-
0036882396
-
Irreversible inhibitors of serine, cysteine, and threonine proteases
-
Powers JC, Asgian JL, James KE, et al. Irreversible inhibitors of serine, cysteine, and threonine proteases. Chem Rev 2002;102:4639-4750
-
(2002)
Chem Rev
, vol.102
, pp. 4639-4750
-
-
Powers, J.C.1
Asgian, J.L.2
James, K.E.3
-
50
-
-
0036260967
-
Thiol-dependent enzymes and their inhibitors: A review
-
Leung-Toung R, Li W, Tam TF, et al. Thiol-dependent enzymes and their inhibitors: a review. Curr Med Chem 2002;9:979-1002
-
(2002)
Curr Med Chem
, vol.9
, pp. 979-1002
-
-
Leung-Toung, R.1
Li, W.2
Tam, T.F.3
-
51
-
-
0001920201
-
Small synthetic inhibitors of cysteine proteases
-
Rasnick D. Small synthetic inhibitors of cysteine proteases. Perspect Drug Discov Des 1996;6:47-63
-
(1996)
Perspect Drug Discov des
, vol.6
, pp. 47-63
-
-
Rasnick, D.1
-
52
-
-
0033058811
-
Cysteine protease inhibitors as chemotherapy for parasitic infections
-
McKerrow JH, Engel JC, Caffrey CR. Cysteine protease inhibitors as chemotherapy for parasitic infections. Bioorg Med Chem 1999;7:639-644
-
(1999)
Bioorg Med Chem
, vol.7
, pp. 639-644
-
-
McKerrow, J.H.1
Engel, J.C.2
Caffrey, C.R.3
-
53
-
-
0021260942
-
Vinylogous amino acid esters: A new class of inactivators for thiol proteases
-
Hanzlik RP, Thompson SA. Vinylogous amino acid esters: a new class of inactivators for thiol proteases. J Med Chem 1984;27:711-712
-
(1984)
J Med Chem
, vol.27
, pp. 711-712
-
-
Hanzlik, R.P.1
Thompson, S.A.2
-
54
-
-
0022607084
-
Carbonyl-modified amino acids and peptides as protease inhibitors
-
Thompson SA, Andrews PR, Hanzlik RP. Carbonyl-modified amino acids and peptides as protease inhibitors. J Med Chem 1986;29:104-111
-
(1986)
J Med Chem
, vol.29
, pp. 104-111
-
-
Thompson, S.A.1
Andrews, P.R.2
Hanzlik, R.P.3
-
55
-
-
0032474754
-
Synthesis and evaluation of peptidyl michael acceptors that inactivate human rhinovirus 3C protease and inhibit virus replication
-
Kong J-S, Venkatraman S, Furness K, et al. Synthesis and evaluation of peptidyl michael acceptors that inactivate human rhinovirus 3C protease and inhibit virus replication. J Med Chem 1998;41:2579-2587
-
(1998)
J Med Chem
, vol.41
, pp. 2579-2587
-
-
Kong, J.-S.1
Venkatraman, S.2
Furness, K.3
-
56
-
-
14444272282
-
Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. michael acceptor structure-activity studies
-
Dragovich PS, Webber SE, Babine RE, et al. Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. michael acceptor structure-activity studies. J Med Chem 1998;41:2806-2818
-
(1998)
J Med Chem
, vol.41
, pp. 2806-2818
-
-
Dragovich, P.S.1
Webber, S.E.2
Babine, R.E.3
-
57
-
-
77949901611
-
-
Smithkline Beecham Corp. WO05013909
-
Smithkline Beecham Corp. Novel cathepsin K inhibitors. WO05013909; 2005
-
(2005)
Novel Cathepsin K Inhibitors
-
-
-
58
-
-
33644865031
-
Structure activity relationships of 5-, 6-, and 7-methyl-substituted azepan-3-one cathepsin K inhibitors
-
Yamashita DS, Marquis RW, Xie R, et al. Structure activity relationships of 5-, 6-, and 7-methyl-substituted azepan-3-one cathepsin K inhibitors. J Med Chem 2006;49:1597-1612
-
(2006)
J Med Chem
, vol.49
, pp. 1597-1612
-
-
Yamashita, D.S.1
Marquis, R.W.2
Xie, R.3
-
59
-
-
67649587136
-
Large-scale synthesis of SB-462795, a cathepsin K inhibitor: The RCM-based approaches
-
Wang H, Matsuhashi H, Doan DB, et al. Large-scale synthesis of SB-462795, a cathepsin K inhibitor: the RCM-based approaches. Tetrahedron 2009;65:6291-6303
-
(2009)
Tetrahedron
, vol.65
, pp. 6291-6303
-
-
Wang, H.1
Matsuhashi, H.2
Doan, D.B.3
-
62
-
-
78649994355
-
-
Amura Therapeutics Ltd WO04007501
-
Amura Therapeutics Ltd. Biologically active compounds. WO04007501; 2004
-
(2004)
Biologically Active Compounds
-
-
-
63
-
-
77949879355
-
-
Amura Therapeutics Ltd. WO09087379
-
Amura Therapeutics Ltd. Compounds. WO09087379; 2009
-
(2009)
Compounds
-
-
-
67
-
-
77952519757
-
Effect of one year treatment with the cathepsin-K inhibitor balicatib on bone mineral density (BMD) in postmenopausal woman with osteopenia/osteoporosis
-
Washington DC; 17 September
-
Adami S, et al. Effect of one year treatment with the cathepsin-K inhibitor, balicatib, on bone mineral density (BMD) in postmenopausal woman with osteopenia/osteoporosis. American Society for Bone and Mineral Research, Washington, DC; 17 September 2006
-
(2006)
American Society for Bone and Mineral Research
-
-
Adami, S.1
-
68
-
-
38749144762
-
The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K
-
Gauthier JY, Chauret N, Cromlish W, et al. The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K. Bioorg Med Chem Lett 2008;18:923-928
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 923-928
-
-
Gauthier, J.Y.1
Chauret, N.2
Cromlish, W.3
-
69
-
-
65749102126
-
Cathepsin K - A new molecular target for osteoporosis
-
Rodan SB, Duong LT. Cathepsin K - A new molecular target for osteoporosis. IBMS BoneKEy 2008;5:16-24
-
(2008)
IBMS BoneKEy
, vol.5
, pp. 16-24
-
-
Rodan, S.B.1
Duong, L.T.2
-
70
-
-
67651180563
-
Effect of the cathepsin K inhibitor odanacatib on bone resorption biomarkers in healthy postmenopausal women: Two double-blind, randomized, placebo-controlled phase i studies
-
Stoch SA, Zajic S, Stone J, et al. Effect of the cathepsin K inhibitor odanacatib on bone resorption biomarkers in healthy postmenopausal women: two double-blind, randomized, placebo-controlled phase i studies. Clin Pharmacol Ther 2009;86(2):175-182
-
(2009)
Clin Pharmacol Ther
, vol.86
, Issue.2
, pp. 175-182
-
-
Stoch, S.A.1
Zajic, S.2
Stone, J.3
-
72
-
-
54549088956
-
Identification of a nonbasic, nitrile-containing cathepsin K inhibitor (MK-1256) that is efficausious in a monkey model of osteoporosis
-
Robichaud J, Black WC, Crane SN, et al. Identification of a nonbasic, nitrile-containing cathepsin K inhibitor (MK-1256) that is efficausious in a monkey model of osteoporosis. J Med Chem 2008;51:6410-6420
-
(2008)
J Med Chem
, vol.51
, pp. 6410-6420
-
-
Robichaud, J.1
Black, W.C.2
Crane, S.N.3
-
81
-
-
51849157339
-
Effect of cathepsin K inhibitors on bone resorption
-
Teno N, Masuya K, Ehara T, et al. Effect of cathepsin K inhibitors on bone resorption. J Med Chem 2008;51:5459-5462
-
(2008)
J Med Chem
, vol.51
, pp. 5459-5462
-
-
Teno, N.1
Masuya, K.2
Ehara, T.3
-
88
-
-
77949894903
-
-
Merck Frosst, Axys Pharma Inc and Banyu Pharma Co Ltd. WO01077073
-
Merck Frosst, Axys Pharma, Inc and Banyu Pharma Co, Ltd. Cathepsin cysteine protease inhibitors. WO01077073; 2001
-
(2001)
Cathepsin Cysteine Protease Inhibitors
-
-
-
90
-
-
47149107203
-
Effect of novel N-cyano-tetrahydropyridazine compounds, a class of cathepsin K inhibitors, on the bone resorptive activity of mature osteoclasts
-
Kim SH, Jhon DJ, Kang NS, et al. Effect of novel N-cyano- tetrahydropyridazine compounds, a class of cathepsin K inhibitors, on the bone resorptive activity of mature osteoclasts. Bioorg Med Chem Lett 2008;18:3988-3991
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 3988-3991
-
-
Kim, S.H.1
Jhon, D.J.2
Kang, N.S.3
-
91
-
-
0000102001
-
Integrinmediated signaling in the regulation of osteoclast adhesion and activation
-
Duong LT, Rodan GA. Integrinmediated signaling in the regulation of osteoclast adhesion and activation. Front Biosci 1998;3:d757-68
-
(1998)
Front Biosci
, vol.3
-
-
Duong, L.T.1
Rodan, G.A.2
-
92
-
-
0025880146
-
Arg-Gly-Asp constrained within cyclic pentapoptides Strong and selective inhibitors of cell adhesion to vitronectin and laminin fragment P1
-
Aumailley M, Gurrath M, Muller G, et al. Arg-Gly-Asp constrained within cyclic pentapoptides Strong and selective inhibitors of cell adhesion to vitronectin and laminin fragment P1. FEBS Lett 1991;291:50-54
-
(1991)
FEBS Lett
, vol.291
, pp. 50-54
-
-
Aumailley, M.1
Gurrath, M.2
Muller, G.3
-
93
-
-
0030020835
-
Type II to type i beta-turn swap changes specificity for integrins
-
Bach AC, Espina JR, et al. Type II to type I beta-turn swap changes specificity for integrins. J Am Chem Soc 1996;118:293-294
-
(1996)
J Am Chem Soc
, vol.118
, pp. 293-294
-
-
Bach, A.C.1
Espina, J.R.2
-
94
-
-
0029862394
-
Synthesis and solution conformation of cyclo [RGDRGD]: A cyclic peptide with selectivity for the alphavbeta3 receptor
-
Burgess K, Lim D, Mousa SA. Synthesis and solution conformation of cyclo [RGDRGD]: a cyclic peptide with selectivity for the alphavbeta3 receptor. J Med Chem 1996;39:4520-4526
-
(1996)
J Med Chem
, vol.39
, pp. 4520-4526
-
-
Burgess, K.1
Lim, D.2
Mousa, S.A.3
-
95
-
-
33744827414
-
Novel and selective alphavbeta3 receptor peptide antagonist: Design, synthesis, and biological behavior
-
Gatto AD, Zaccaro L, Grieco P, et al. Novel and selective alphavbeta3 receptor peptide antagonist: design, synthesis, and biological behavior. J Med Chem 2006;49:3416-3420
-
(2006)
J Med Chem
, vol.49
, pp. 3416-3420
-
-
Gatto, A.D.1
Zaccaro, L.2
Grieco, P.3
-
96
-
-
41149130788
-
Discovery of subnanomolar arginineglycine- Aspartate-based alphaVbeta3/ alphaVbeta5 integrin binders embedding 4-aminoproline residues
-
Zanardi F, Burreddu P, Rassu G, et al. Discovery of subnanomolar arginineglycine- aspartate-based alphaVbeta3/ alphaVbeta5 integrin binders embedding 4-aminoproline residues. J Med Chem 2008;51:1771-1782
-
(2008)
J Med Chem
, vol.51
, pp. 1771-1782
-
-
Zanardi, F.1
Burreddu, P.2
Rassu, G.3
-
97
-
-
33750701133
-
NC-100717: A versatile RGD peptide scaffold for angiogenesis imaging
-
Indrevoll B, Kindberg GM, Solbakken M, et al. NC-100717: a versatile RGD peptide scaffold for angiogenesis imaging. Bioorg Med Chem Lett 2006;16:6190-6193
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 6190-6193
-
-
Indrevoll, B.1
Kindberg, G.M.2
Solbakken, M.3
-
98
-
-
33846897471
-
Synthesis and biological evaluation of new conformationally biased integrin ligands based on tetrahydroazoninone scaffold
-
Banfi L, Basso A, Damonte G, et al. Synthesis and biological evaluation of new conformationally biased integrin ligands based on tetrahydroazoninone scaffold. Bioorg Med Chem Lett 2007;17:1341-1345
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 1341-1345
-
-
Banfi, L.1
Basso, A.2
Damonte, G.3
-
102
-
-
0030841977
-
Discovery of potent nonpeptide vitronectin receptor (alphavbeta3) antagonists
-
Keenan RM, Milller WH, Kwon C, et al. Discovery of potent nonpeptide vitronectin receptor (alphavbeta3) antagonists. J Med Chem 1997;40:2289-2292
-
(1997)
J Med Chem
, vol.40
, pp. 2289-2292
-
-
Keenan, R.M.1
Milller, W.H.2
Kwon, C.3
-
103
-
-
18244403789
-
Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective alphavbeta3 antagonists
-
Kling A, Backfisch G, Delzer J, et al. Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective alphavbeta3 antagonists. Bioorg Med Chem Lett 2002;12:441-446
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 441-446
-
-
Kling, A.1
Backfisch, G.2
Delzer, J.3
-
104
-
-
0030924638
-
Solid-phase synthesis of a selective alphavbeta3 integrin antagonist library
-
Corbett JW, Graciani NR, Mousa S, et al. Solid-phase synthesis of a selective alphavbeta3 integrin antagonist library. Bioorg Med Chem Lett 1997;7:1371-1376
-
(1997)
Bioorg Med Chem Lett
, vol.7
, pp. 1371-1376
-
-
Corbett, J.W.1
Graciani, N.R.2
Mousa, S.3
-
105
-
-
0034642555
-
Isoxazolines as potent antagonists of the integrin alphavbeta3
-
Pitts WJ, Wityak J, Smallheer JM, et al. Isoxazolines as potent antagonists of the integrin alphavbeta3. J Med Chem 2000;43:27-40
-
(2000)
J Med Chem
, vol.43
, pp. 27-40
-
-
Pitts, W.J.1
Wityak, J.2
Smallheer, J.M.3
-
106
-
-
33747116507
-
Synthesis of pyrazoles and isoxazoles as potent alphavbeta3 receptor antagonists
-
Penning TD, Khilevich A, Chen BB, et al. Synthesis of pyrazoles and isoxazoles as potent alphavbeta3 receptor antagonists. Bioorg Med Chem Lett 2006;16:3156-3161
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 3156-3161
-
-
Penning, T.D.1
Khilevich, A.2
Chen, B.B.3
-
107
-
-
0034642520
-
Disubstituted indazoles as potent antagonists of the integrin alphavbeta3
-
Batt DG, Petraitis JJ, Houghton GC, et al. Disubstituted indazoles as potent antagonists of the integrin alphavbeta3. J Med Chem 2000;43:41-58
-
(2000)
J Med Chem
, vol.43
, pp. 41-58
-
-
Batt, D.G.1
Petraitis, J.J.2
Houghton, G.C.3
-
108
-
-
0034609772
-
Nonpeptide alphavbeta3 antagonists 1. Transformation of a potent, integrin-selective alphaIIbbeta3 antagonist into a potent alphavbeta3 antagonist
-
Duggan ME, Duong LT, Fisher JE, et al. Nonpeptide alphavbeta3 antagonists. 1. Transformation of a potent, integrin-selective alphaIIbbeta3 antagonist into a potent alphavbeta3 antagonist. J Med Chem 2000;43:3736-3745
-
(2000)
J Med Chem
, vol.43
, pp. 3736-3745
-
-
Duggan, M.E.1
Duong, L.T.2
Fisher, J.E.3
-
109
-
-
0034618228
-
Parallel solid-phase synthesis of vitronectin receptor (alphavbeta3) inhibitors
-
Gopalsamy A, Yang H, Ellingboe JW, et al. Parallel solid-phase synthesis of vitronectin receptor (alphavbeta3) inhibitors. Bioorg Med Chem Lett 2000;10:1715-1718
-
(2000)
Bioorg Med Chem Lett
, vol.10
, pp. 1715-1718
-
-
Gopalsamy, A.1
Yang, H.2
Ellingboe, J.W.3
-
110
-
-
18244390513
-
Nonpeptide alphavbeta3 antagonists. Part 2: Constrained glycyl amides derived from the RGD tripeptide
-
Meissner RS, Perkins JJ, Duong LT, et al. Nonpeptide alphavbeta3 antagonists. Part 2: constrained glycyl amides derived from the RGD tripeptide. Bioorg Med Chem Lett 2002;12:25-29
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 25-29
-
-
Meissner, R.S.1
Perkins, J.J.2
Duong, L.T.3
-
111
-
-
0344064881
-
Non-peptide alphavbeta3 Antagonists: Identification of potent, chain-shortened RGD mimetics that incorporate a central pyrrolidinone constraint
-
Perkins JJ, Duong LT, Fernandez- Metzler C, et al. Non-peptide alphavbeta3 Antagonists: identification of potent, chain-shortened RGD mimetics that incorporate a central pyrrolidinone constraint. Bioorg Med Chem Lett 2003;13:4285-4288
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 4285-4288
-
-
Perkins, J.J.1
Duong, L.T.2
Fernandez-Metzler, C.3
-
112
-
-
0142060908
-
Nonpeptide alphavbeta3 Antagonists. 8 in vitro and in vivo evaluation of a potent alphavbeta3 antagonist for the prevention and treatment of osteoporosis
-
Hutchinson JH, Halczenko W, Brashear KM, et al. Nonpeptide alphavbeta3 Antagonists. 8. In vitro and in vivo evaluation of a potent alphavbeta3 antagonist for the prevention and treatment of osteoporosis. J Med Chem 2003;46:4790-4798
-
(2003)
J Med Chem
, vol.46
, pp. 4790-4798
-
-
Hutchinson, J.H.1
Halczenko, W.2
Brashear, K.M.3
-
113
-
-
4544384606
-
Nonpeptide alphavbeta3 antagonists. part 11: Discovery and preclinical evaluation of potent alphavbeta3 antagonists for the prevention and treatment of osteoporosis
-
Coleman PJ, Brashear KM, Askew BC, et al. Nonpeptide alphavbeta3 antagonists. part 11: discovery and preclinical evaluation of potent alphavbeta3 antagonists for the prevention and treatment of osteoporosis. J Med Chem 2004;47:4829-4837
-
(2004)
J Med Chem
, vol.47
, pp. 4829-4837
-
-
Coleman, P.J.1
Brashear, K.M.2
Askew, B.C.3
-
114
-
-
18344375818
-
Synthesis of highly potent and selective hetaryl ureas as integrin alphavbeta3- Receptor antagonists
-
Lange UEW, Backfisch G, Elzer J, et al. Synthesis of highly potent and selective hetaryl ureas as integrin alphavbeta3- Receptor antagonists. Bioorg Med Chem Lett 2002;12:1379-1382
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 1379-1382
-
-
Lange, U.E.W.1
Backfisch, G.2
Elzer, J.3
-
115
-
-
17944391700
-
T. Highly potent and selective alphaVbeta3-receptor antagonists: Solid-phase synthesis and SAR of 1-substituted 4-amino-1H-pyrimidin- 2-ones
-
Zechel C, Backfisch G, Delzer J, et al. T. Highly potent and selective alphaVbeta3-receptor antagonists: solid-phase synthesis and SAR of 1-substituted 4-amino-1H-pyrimidin- 2-ones. Bioorg Med Chem Lett 2003;13:165-169
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 165-169
-
-
Zechel, C.1
Backfisch, G.2
Delzer, J.3
-
116
-
-
0037147775
-
Biphenyls as potent vitronectin receptor antagonists
-
Urbahns K, Harter M, Albers M, et al. Biphenyls as potent vitronectin receptor antagonists. Bioorg Med Chem Lett 2002;12:205-208
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 205-208
-
-
Urbahns, K.1
Harter, M.2
Albers, M.3
-
117
-
-
35148882994
-
Biphenyls as potent vitronectin receptor antagonists. Part 3: Squaric acid amides
-
Urbahns K, Harter M, Albers M, et al. Biphenyls as potent vitronectin receptor antagonists. Part 3: squaric acid amides. Bioorg Med Chem Lett 2007;17:6151-6154
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 6151-6154
-
-
Urbahns, K.1
Harter, M.2
Albers, M.3
-
118
-
-
38349008476
-
Design and synthesis of novel potent and selective integrin alphavbeta3 antagonists-Novel synthetic routes to isoquinolinone, benzoxazinone, and quinazolinone acetates
-
Seitz W, Geneste H, Backfisch G, et al. Design and synthesis of novel potent and selective integrin alphavbeta3 antagonists-Novel synthetic routes to isoquinolinone, benzoxazinone, and quinazolinone acetates. Bioorg Med Chem Lett 2008;18:527-531
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 527-531
-
-
Seitz, W.1
Geneste, H.2
Backfisch, G.3
-
119
-
-
33847407041
-
Identification of novel short chain 4-substitute indoles as potent alphavbeta3 antagonists using structure based drug design
-
Raboisson P, DesJarlais RL, Reed R, et al. Identification of novel short chain 4-substitute indoles as potent alphavbeta3 antagonists using structure based drug design. Eur J Med Chem 2007;42:334-343
-
(2007)
Eur J Med Chem
, vol.42
, pp. 334-343
-
-
Raboisson, P.1
Desjarlais, R.L.2
Reed, R.3
-
120
-
-
77949907738
-
-
The Government of the United State, As Represented by the Secretary of Health and Human service, National Institutes of Health. WO06015382
-
The Government of the United State, As Represented by the Secretary of Health and Human service, National Institutes of Health. Integrin alphavbeta3 antagonists for use in imaging and therapy. WO06015382; 2006
-
(2006)
Integrin alphavbeta3 Antagonists for Use in Imaging and Therapy
-
-
-
121
-
-
77949891020
-
-
Ube Industries Ltd. WO09063990
-
Ube Industries, Ltd. Benzazepinone compound. WO09063990; 2009
-
(2009)
Benzazepinone Compound
-
-
-
124
-
-
77949907191
-
-
Pharmacia Corporation. WO06043930
-
Pharmacia Corporation. Biphenyl integrin antagonists. WO06043930; 2006
-
(2006)
Biphenyl Integrin Antagonists
-
-
-
125
-
-
33750682652
-
Natural inhibitors targeting osteoclast-mediated bone resorption
-
Zeng G-Z, Tan N-H, Hao X-J, et al. Natural inhibitors targeting osteoclast-mediated bone resorption. Bioorg Med Chem Lett 2006;16:6178-6180
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 6178-6180
-
-
Zeng, G.-Z.1
Tan, N.-H.2
Hao, X.-J.3
-
126
-
-
0033121275
-
The role of Rv integrins during angiogenesis: Insights into potential mechanisms of action and clinical development
-
Eliceiri BP, Cheresh DA. The role of Rv integrins during angiogenesis: insights into potential mechanisms of action and clinical development. J Clin Invest 1999;103:1227-1230
-
(1999)
J Clin Invest
, vol.103
, pp. 1227-1230
-
-
Eliceiri, B.P.1
Cheresh, D.A.2
-
127
-
-
0037318003
-
Integrin alphavbeta3 as a therapeutic target for blocking tumor induced angiogenesis
-
Kumar CC. Integrin alphavbeta3 as a therapeutic target for blocking tumor induced angiogenesis. Curr Drug Targets 2003;4:123-131
-
(2003)
Curr Drug Targets
, vol.4
, pp. 123-131
-
-
Kumar, C.C.1
-
128
-
-
0031813032
-
Recent insights into the role of integrins in cancer metastasis
-
Clezardin P. Recent insights into the role of integrins in cancer metastasis. Cell Mol Life Sci 1998;54:541-548
-
(1998)
Cell Mol Life Sci
, vol.54
, pp. 541-548
-
-
Clezardin, P.1
-
129
-
-
57749118590
-
Synthesis and initial evaluation of novel, non-peptidic antagonists of the alphav-integrins alphavbeta3 and alphavbeta5
-
Letourneau JJ, Liu J, Ohlmeyer MHJ, et al. Synthesis and initial evaluation of novel, non-peptidic antagonists of the alphav-integrins alphavbeta3 and alphavbeta5. Bioorg Med Chem Lett 2009;19:352-355
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 352-355
-
-
Letourneau, J.J.1
Liu, J.2
Ohlmeyer, M.H.J.3
-
131
-
-
39049171041
-
Metalloproteases as potential therapeutic targets in arthritis treatment
-
Rowan AD, Litherland GJ, Hui M, et al. Metalloproteases as potential therapeutic targets in arthritis treatment. Expert Opin Ther Targets 2008;12:1-18
-
(2008)
Expert Opin Ther Targets
, vol.12
, pp. 1-18
-
-
Rowan, A.D.1
Litherland, G.J.2
Hui, M.3
-
132
-
-
34447520043
-
Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases
-
Hu J, Van den Steen PE, Sang Q-X A, Opdenakker G. Matrix metalloproteinase inhibitors as therapy for inflammatory and vascular diseases. Nat Rev Drug Discov 2007;6:480-498
-
(2007)
Nat Rev Drug Discov
, vol.6
, pp. 480-498
-
-
Hu, J.1
Van Den Steen, P.E.2
Sang -X Q, A.3
Opdenakker, G.4
-
133
-
-
44649131333
-
Potential directions for drug development for osteoarthritis
-
Roach HI. Potential directions for drug development for osteoarthritis. Expert Opin Drug Discov 2008;3:475-486
-
(2008)
Expert Opin Drug Discov
, vol.3
, pp. 475-486
-
-
Roach, H.I.1
-
134
-
-
15644374838
-
Discovery of CGS27023A, a nonpeptidic, potent, and orally active stromelysin inhibitor that blocks cartilage degradation in rabbits
-
MacPherson LJ, Bayburt EK, Capparelli MP, et al. Discovery of CGS27023A, a nonpeptidic, potent, and orally active stromelysin inhibitor that blocks cartilage degradation in rabbits. J Med Chem 1997;40:2525-2532
-
(1997)
J Med Chem
, vol.40
, pp. 2525-2532
-
-
MacPherson, L.J.1
Bayburt, E.K.2
Capparelli, M.P.3
-
135
-
-
77949893346
-
Activity of a selective inhibitor of collagenase-3 in models of arthritis
-
San Diego CA December 11-12
-
Walker K. Activity of a selective inhibitor of collagenase-3 in models of arthritis. First Annual International Conference on Orthopaedic Biomaterials, San Diego, CA, December 11-12, 1997.
-
(1997)
First Annual International Conference on Orthopaedic Biomaterials
-
-
Walker, K.1
-
136
-
-
77949905911
-
Discovery of RS-130830, a potent and selective MMP inhibitor for osteoarthritis
-
Book of Abstracts. Washington, DC; MEDI-004
-
Campbell, J. A. Discovery of RS-130830, a potent and selective MMP inhibitor for osteoarthritis. Book of Abstracts, 216th ACS National Meeting; American Chemical Society. Washington, DC, 1998; MEDI-004
-
(1998)
216th ACS National Meeting; American Chemical Society
-
-
Campbell, J.A.1
-
137
-
-
0000781901
-
Inhibition of articular cartilage degradation in dog and guinea pig models of osteoarthritis by the stromelysin inhibitor BAY 12-9566
-
Chau T, Jolly G, Plym JM, et al. Inhibition of articular cartilage degradation in dog and guinea pig models of osteoarthritis by the stromelysin inhibitor BAY 12-9566. Arthritis Rheum 1998;41:S300
-
(1998)
Arthritis Rheum
, vol.41
-
-
Chau, T.1
Jolly, G.2
Plym, J.M.3
-
140
-
-
0006315176
-
AG-334
-
Griffioen AW. AG-334. IDrugs 2000;3:336-345
-
(2000)
IDrugs
, vol.3
, pp. 336-345
-
-
Griffioen, A.W.1
-
141
-
-
4444309926
-
The design and synthesis of aryl hydroxamic acid inhibitors of MMPs and TACE
-
Levin JI. The design and synthesis of aryl hydroxamic acid inhibitors of MMPs and TACE. Curr Top Med Chem 2004;4:1289-1310
-
(2004)
Curr Top Med Chem
, vol.4
, pp. 1289-1310
-
-
Levin, J.I.1
-
142
-
-
2542530041
-
Sultam hydroxamates as novel matrix metalloproteinase inhibitors
-
Cherney RJ, Mo R, Meyer DT, et al. Sultam hydroxamates as novel matrix metalloproteinase inhibitors. J Med Chem 2004;47:2981-2983
-
(2004)
J Med Chem
, vol.47
, pp. 2981-2983
-
-
Cherney, R.J.1
Mo, R.2
Meyer, D.T.3
-
143
-
-
13844324397
-
N-i-Propoxy-Nbiphenylsulfonylaminobutylhydroxamic acids as potent and selective inhibitors of MMP-2 and MT1-MMP
-
Rossello A, Nuti E, Carelli P, et al. N-i-Propoxy- Nbiphenylsulfonylaminobutylhydroxamic acids as potent and selective inhibitors of MMP-2 and MT1-MMP. Bioorg Med Chem Lett 2005;15:1321-1326
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 1321-1326
-
-
Rossello, A.1
Nuti, E.2
Carelli, P.3
-
144
-
-
33845283570
-
Alpha-Biphenylsulfonylamino 2-methylpropyl phosphonates: Enantioselective synthesis and selective inhibition of MMPs
-
Biasone A, Tortorella P, Campestre C, et al. alpha-Biphenylsulfonylamino 2-methylpropyl phosphonates: enantioselective synthesis and selective inhibition of MMPs. Bioorg Med Chem 2007;15:791-799
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 791-799
-
-
Biasone, A.1
Tortorella, P.2
Campestre, C.3
-
145
-
-
34249780518
-
Simultaneous presence of unsaturation and long alkyl chain at P'1 of Ilomastat confers selectivity for gelatinase A (MMP-2) over gelatinase B (MMP-9) inhibition as shown by molecular modelling studies
-
Moroy G, Denhez C, Mourabit HE, et al. Simultaneous presence of unsaturation and long alkyl chain at P'1 of Ilomastat confers selectivity for gelatinase A (MMP-2) over gelatinase B (MMP-9) inhibition as shown by molecular modelling studies. Bioorg Med Chem 2007;15:4753-4766
-
(2007)
Bioorg Med Chem
, vol.15
, pp. 4753-4766
-
-
Moroy, G.1
Denhez, C.2
Mourabit, H.E.3
-
146
-
-
56249124956
-
N-((8-Hydroxy-5-substitutedquinolin- 7-yl)-phenyl)methyl)-2- phenyloxy/amino-acetamide inhibitors of ADAMTS-5 (Aggrecanase-2)
-
Gilbert AM, Bursavich MG, Lombardi S, et al. N-((8-Hydroxy-5- substitutedquinolin- 7-yl)-(phenyl)methyl)-2- phenyloxy/amino-acetamide inhibitors of ADAMTS-5 (Aggrecanase-2). Bioorg Med Chem Lett 2008;18:6454-6457
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 6454-6457
-
-
Gilbert, A.M.1
Bursavich, M.G.2
Lombardi, S.3
-
147
-
-
4444341426
-
The evolution of the matrix metalloproteinase inhibitor drug discovery program at Abbott laboratories
-
Wada CK. The evolution of the matrix metalloproteinase inhibitor drug discovery program at Abbott laboratories. Curr Top Med Chem 2004;4:1255-1267
-
(2004)
Curr Top Med Chem
, vol.4
, pp. 1255-1267
-
-
Wada, C.K.1
-
148
-
-
4444274979
-
Sulfonamide-based acyclic and conformationally constrained MMP inhibitors: From computer-assisted design to nanomolar compounds
-
Hanessiana S, Moitessier N. Sulfonamide-based acyclic and conformationally constrained MMP inhibitors: from computer-assisted design to nanomolar compounds. Curr Top Med Chem 2004;4:1269-1287
-
(2004)
Curr Top Med Chem
, vol.4
, pp. 1269-1287
-
-
Hanessiana, S.1
Moitessier, N.2
-
149
-
-
33646136687
-
Matrix metalloproteinase inhibitors as prospective agents for the prevention and treatment of cardiovascular and neoplastic diseases
-
Sang Q-X A, Jin Y, Newcomer RG, et al. Matrix metalloproteinase inhibitors as prospective agents for the prevention and treatment of cardiovascular and neoplastic diseases. Curr Top Med Chem 2006;6:289-316
-
(2006)
Curr Top Med Chem
, vol.6
, pp. 289-316
-
-
Sang -X Q, A.1
Jin, Y.2
Newcomer, R.G.3
-
153
-
-
39449128920
-
Joint diseases and matrix metalloproteinases: A role for MMP-13
-
Takaishi H, Kimura T, Delal S, et al. Joint diseases and matrix metalloproteinases: a role for MMP-13. Curr Pharm Biotechnol 2008;9:47-54
-
(2008)
Curr Pharm Biotechnol
, vol.9
, pp. 47-54
-
-
Takaishi, H.1
Kimura, T.2
Delal, S.3
-
154
-
-
66749184678
-
Discovery of potent, selective, and orally active carboxylic acid based inhibitors of matrix metalloproteinase-13
-
Monovich LG, Tommasi RA, Fujimoto RA, et al. Discovery of potent, selective, and orally active carboxylic acid based inhibitors of matrix metalloproteinase-13. J Med Chem 2009;52:3523-3538
-
(2009)
J Med Chem
, vol.52
, pp. 3523-3538
-
-
Monovich, L.G.1
Tommasi, R.A.2
Fujimoto, R.A.3
-
155
-
-
33749233835
-
Potent, selective pyrimidinetrionebased inhibitors of MMP-13
-
Reiter LA, Freeman-Cook KD, Jones CS, et al. Potent, selective pyrimidinetrionebased inhibitors of MMP-13. Bioorg Med Chem Lett 2006;16:5822-5826
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 5822-5826
-
-
Reiter, L.A.1
Freeman-Cook, K.D.2
Jones, C.S.3
-
156
-
-
25844469594
-
Synthesis and SAR of highly selective MMP-13 inhibitors
-
Li J, Rush TS III, Li W, et al. Synthesis and SAR of highly selective MMP-13 inhibitors. Bioorg Med Chem Lett 2005;15:4961-4966
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 4961-4966
-
-
Li, J.1
Rush Ts, I.I.I.2
Li, W.3
-
157
-
-
21144437429
-
Discovery of 3,3-dimethyl-5- hydroxypipecolic hydroxamate-based inhibitors of aggrecanase and MMP-13
-
Noe MC, Natarajan V, Snow SL, et al. Discovery of 3,3-dimethyl-5- hydroxypipecolic hydroxamate-based inhibitors of aggrecanase and MMP-13. Bioorg Med Chem Lett 2005;15:2808-2811
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 2808-2811
-
-
Noe, M.C.1
Natarajan, V.2
Snow, S.L.3
-
163
-
-
33748416303
-
MMP-9 antisense oligodeoxynucleotide exerts an inhibitory effect on osteoclastic bone resorption by suppressing cell migration
-
Ishibashi O, Niwa S, Kadoyama K, et al. MMP-9 antisense oligodeoxynucleotide exerts an inhibitory effect on osteoclastic bone resorption by suppressing cell migration. Life Sci 2006;79:1657-1660
-
(2006)
Life Sci
, vol.79
, pp. 1657-1660
-
-
Ishibashi, O.1
Niwa, S.2
Kadoyama, K.3
-
164
-
-
0029002420
-
A targeted mutation at the known collagenase cleavage site in mouse type i collagen impairs tissue remodelling
-
Liu X, Wu H, Byrne M, et al. A targeted mutation at the known collagenase cleavage site in mouse type I collagen impairs tissue remodelling. J Cell Biol 1995;130:227-237
-
(1995)
J Cell Biol
, vol.130
, pp. 227-237
-
-
Liu, X.1
Wu, H.2
Byrne, M.3
-
165
-
-
15544382811
-
The hyalectan degrading ADAMTS-1 enzyme is expressed by osteoblasts and upregulated at regions of new bone formation
-
Lind T, McKie N, Wendel M, et al. The hyalectan degrading ADAMTS-1 enzyme is expressed by osteoblasts and upregulated at regions of new bone formation. Bone 2005;36:408-417
-
(2005)
Bone
, vol.36
, pp. 408-417
-
-
Lind, T.1
McKie, N.2
Wendel, M.3
-
166
-
-
0032823306
-
Prostanoid receptors: Structures, properties, and functions
-
Narumiya S, Sugimoto Y, Ushikubi F. Prostanoid receptors: structures, properties, and functions. Physiol Rev 1999;79:1193-1226
-
(1999)
Physiol Rev
, vol.79
, pp. 1193-1226
-
-
Narumiya, S.1
Sugimoto, Y.2
Ushikubi, F.3
-
167
-
-
0032590075
-
EP4 receptor mediation of prostaglandin E2-stimulated mucus secretion by rabbit gastric epithelial cells
-
Takahashi S, Takeuchi K, Okabe S. EP4 receptor mediation of prostaglandin E2-stimulated mucus secretion by rabbit gastric epithelial cells. Biochem Pharmacol 1999;58:1997-2002
-
(1999)
Biochem Pharmacol
, vol.58
, pp. 1997-2002
-
-
Takahashi, S.1
Takeuchi, K.2
Okabe, S.3
-
168
-
-
67649616236
-
Prostaglandin EP2 and EP4 receptor agonists in bone formation and bone healing:In vivo and in vitro evidence
-
Graham S, Gamie Z, Polyzois I, et al. Prostaglandin EP2 and EP4 receptor agonists in bone formation and bone healing: In vivo and in vitro evidence. Expert Opin Investig Drugs 2009;18:749-766
-
(2009)
Expert Opin Investig Drugs
, vol.18
, pp. 749-766
-
-
Graham, S.1
Gamie, Z.2
Polyzois, I.3
-
169
-
-
0036009875
-
Design and synthesis of a selective EP-4 receptor agonists Part 13: 16- Phenyl-5-thiaPGE1 and 9-beta-halo derivatives with improved stability
-
Maruyama T, Asada M, Shiraishi T, et al. Design and synthesis of a selective EP-4 receptor agonists. Part 13: 16- Phenyl-5-thiaPGE1 and 9-beta-halo derivatives with improved stability. Bioorg Med Chem 2002;10:1743-1759
-
(2002)
Bioorg Med Chem
, vol.10
, pp. 1743-1759
-
-
Maruyama, T.1
Asada, M.2
Shiraishi, T.3
-
170
-
-
0037007077
-
Stimulation of bone formation and prevention of bone loss by prostaglandin e E4 receptor activation
-
Yoshida K, Oida H, Kobayashi T, et al. Stimulation of bone formation and prevention of bone loss by prostaglandin E E4 receptor activation. Proc Natl Acad Sci USA 2000;99:4580-4585
-
(2000)
Proc Natl Acad Sci USA
, vol.99
, pp. 4580-4585
-
-
Yoshida, K.1
Oida, H.2
Kobayashi, T.3
-
171
-
-
15544382810
-
Effect of a selective agonist for prostaglandin e receptor subtype EP4 (ONO-4819) on the cortical bone response to mechanical loading
-
Hagino H, Kuraoka M, Kameyama Y, et al. Effect of a selective agonist for prostaglandin E receptor subtype EP4 (ONO-4819) on the cortical bone response to mechanical loading. Bone 2005;36:444-453
-
(2005)
Bone
, vol.36
, pp. 444-453
-
-
Hagino, H.1
Kuraoka, M.2
Kameyama, Y.3
-
172
-
-
24944446761
-
Augmentation of bone morphogenetic protein-induced bone mass by local delivery of a prostaglandin e EP4 receptor agonist
-
Toyoda H, Terai H, Sasaoka R, et al. Augmentation of bone morphogenetic protein-induced bone mass by local delivery of a prostaglandin E EP4 receptor agonist. Bone 2005;37:555-562
-
(2005)
Bone
, vol.37
, pp. 555-562
-
-
Toyoda, H.1
Terai, H.2
Sasaoka, R.3
-
173
-
-
34548532872
-
Prostaglandin E2 EP4 agonist (ONO- 4819) accelerates BMP-induced osteoblastic differentiation
-
Nakagawa K, Imai Y, Ohta Y, et al. Prostaglandin E2 EP4 agonist (ONO- 4819) accelerates BMP-induced osteoblastic differentiation. Bone 2007;41:543-548
-
(2007)
Bone
, vol.41
, pp. 543-548
-
-
Nakagawa, K.1
Imai, Y.2
Ohta, Y.3
-
175
-
-
9744245978
-
Lactams as EP4 prostanoid receptor agonists 3. Discovery of N-ethylbenzoic acid 2-pyrrolidines as subtype selective agents
-
Elworthy TR, Brill ER, Chiou S-S, et al. Lactams as EP4 prostanoid receptor agonists. 3. Discovery of N-ethylbenzoic acid 2-pyrrolidines as subtype selective agents. J Med Chem 2004;47:6124-6127
-
(2004)
J Med Chem
, vol.47
, pp. 6124-6127
-
-
Elworthy, T.R.1
Brill, E.R.2
Chiou, S.-S.3
-
176
-
-
6044271282
-
Lactams as EP4 prostanoid receptor subtype selective agonists Part 1: 2- Pyrrolidinones-stereochemical and lower side-chain optimization
-
Elworthy TR, Kertesz DJ, Kim W, et al. Lactams as EP4 prostanoid receptor subtype selective agonists. Part 1: 2- Pyrrolidinones-stereochemical and lower side-chain optimization. Bioorg Med Chem Lett 2004;14:1655-1659
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 1655-1659
-
-
Elworthy, T.R.1
Kertesz, D.J.2
Kim, W.3
-
177
-
-
18144430970
-
Lactams as prostanoid receptor ligands Part 4: 2-Piperidones as selective EP4 receptor agonists
-
Elworthy TR, Brill ER, Caires CC, et al. Lactams as prostanoid receptor ligands. Part 4: 2-Piperidones as selective EP4 receptor agonists. Bioorg Med Chem Lett 2005;15:2523-2526
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 2523-2526
-
-
Elworthy, T.R.1
Brill, E.R.2
Caires, C.C.3
-
178
-
-
33144478325
-
Discovery of highly selective EP4 receptor agonists that stimulate new bone formation and restore bone mass in ovariectomized rats
-
Cameron KO, Lefker BA, Chu-Moyer MY, et al. Discovery of highly selective EP4 receptor agonists that stimulate new bone formation and restore bone mass in ovariectomized rats. Bioorg Med Chem Lett 2006;16:1799-1802
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 1799-1802
-
-
Cameron, K.O.1
Lefker, B.A.2
Chu-Moyer, M.Y.3
-
179
-
-
34347403843
-
Discovery of novel prostaglandin analogs of PGE2 as potent and selective EP2 and EP4 receptor agonists
-
Xiao Y, Araldi GL, Zhao Z, et al. Discovery of novel prostaglandin analogs of PGE2 as potent and selective EP2 and EP4 receptor agonists. Bioorg Med Chem Lett 2007;17:4323-4327
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 4323-4327
-
-
Xiao, Y.1
Araldi, G.L.2
Zhao, Z.3
-
180
-
-
38149041705
-
Synthesis and evaluation of a gammalactam as a highly selective EP2 and EP4 receptor agonist
-
Xiao Y, Araldi GL, Zhao Z, et al. Synthesis and evaluation of a gammalactam as a highly selective EP2 and EP4 receptor agonist. Bioorg Med Chem Lett 2008;18:821-824
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 821-824
-
-
Xiao, Y.1
Araldi, G.L.2
Zhao, Z.3
-
181
-
-
38149041705
-
Synthesis and evaluation of a gamma-lactam as a highly selective EP2 and EP4 receptor agonist
-
Xiao Y, Araldi GL, et al. Synthesis and evaluation of a gamma-lactam as a highly selective EP2 and EP4 receptor agonist. Bioorg Med Chem Lett 2008;18:821-824
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 821-824
-
-
Xiao, Y.1
Araldi, G.L.2
-
189
-
-
0011913143
-
Bafilomycine: A class of inhibitors of membrane ATPase from microorganism, animal cells, and plant cells
-
Bowmann EJ, Siebers A, Altendorf K. Bafilomycine: a class of inhibitors of membrane ATPase from microorganism, animal cells, and plant cells. Proc Natl Acad Sci USA 1988;85:7972-7976
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 7972-7976
-
-
Bowmann, E.J.1
Siebers, A.2
Altendorf, K.3
-
190
-
-
0027322674
-
Inhibitory effect of modified bafilomycins and concanamycins on Pand V-type adenosinetriphosphatases
-
Drose S, Bindseil KU, Bowman EJ, et al. Inhibitory effect of modified bafilomycins and concanamycins on Pand V-type adenosinetriphosphatases. Biochemistry 1993;32:3902-3906
-
(1993)
Biochemistry
, vol.32
, pp. 3902-3906
-
-
Drose, S.1
Bindseil, K.U.2
Bowman, E.J.3
-
191
-
-
0025317797
-
Inhibition of osteoclast proton transport by bafilomycin A1 abolishes bone resorption
-
Sundquist K, Lakkakorpi P, Wallmark B, et al. Inhibition of osteoclast proton transport by bafilomycin A1 abolishes bone resorption. Biochem Biophys Res Commun 1990;168:309-313
-
(1990)
Biochem Biophys Res Commun
, vol.168
, pp. 309-313
-
-
Sundquist, K.1
Lakkakorpi, P.2
Wallmark, B.3
-
192
-
-
0032951939
-
Selective inhibitors of vacuolar H+-ATPase of osteoclasts with bone antiresorptive activity
-
Farina C, Gagliardi S. Selective inhibitors of vacuolar H+-ATPase of osteoclasts with bone antiresorptive activity. Exp Opin Ther Patents 1999;9:157-168
-
(1999)
Exp Opin Ther Patents
, vol.9
, pp. 157-168
-
-
Farina, C.1
Gagliardi, S.2
-
193
-
-
0027207229
-
Effect of omeprazole, an inhibitor of H+, K+-ATPase, on bone resorption in humans
-
Mizunashi K, Furukawa Y, Katano K, et al. Effect of omeprazole, an inhibitor of H+, K+-ATPase, on bone resorption in humans. Calcif Tissue 1993;53:21-25
-
(1993)
Calcif Tissue
, vol.53
, pp. 21-25
-
-
Mizunashi, K.1
Furukawa, Y.2
Katano, K.3
-
194
-
-
0037262045
-
Novel marine and microbial natural product inhibitors of vacuolar ATPase
-
Beutler AJ, Mckee TC. Novel marine and microbial natural product inhibitors of vacuolar ATPase. Curr Med Chem 2003;10:787-796
-
(2003)
Curr Med Chem
, vol.10
, pp. 787-796
-
-
Beutler, A.J.1
McKee, T.C.2
-
198
-
-
0034611326
-
Solid phase synthesis of diamines as potential bone resorption inhibitors
-
Edvinsson KM, Herslof M, Holm P, et al. Solid phase synthesis of diamines as potential bone resorption inhibitors. Bioorg Med Chem Lett 2000;10:503-507
-
(2000)
Bioorg Med Chem Lett
, vol.10
, pp. 503-507
-
-
Edvinsson, K.M.1
Herslof, M.2
Holm, P.3
-
200
-
-
33847727477
-
FR177995, a novel vacuolar ATPase inhibitor, exerts not only an inhibitory effect on bone destruction but also anti-immunoinflammatory effects in adjuvant-induced arthritic rats
-
Niikura K, Nakajima S, Takano M, et al. FR177995, a novel vacuolar ATPase inhibitor, exerts not only an inhibitory effect on bone destruction but also anti-immunoinflammatory effects in adjuvant-induced arthritic rats. Bone 2007;40:888-894
-
(2007)
Bone
, vol.40
, pp. 888-894
-
-
Niikura, K.1
Nakajima, S.2
Takano, M.3
-
201
-
-
0034644703
-
The amino-terminal domain of the B subunit of vacuolar H+-ATPase contains a filamentous actin binding site
-
Holliday LS, Lu M, Lee BS, et al. The amino-terminal domain of the B subunit of vacuolar H+-ATPase contains a filamentous actin binding site. J Biol Chem 2000;275:32331-32337
-
(2000)
J Biol Chem
, vol.275
, pp. 32331-32337
-
-
Holliday, L.S.1
Lu, M.2
Lee, B.S.3
-
202
-
-
10744233422
-
Vacuolar H+-ATPase binding to microfilaments: Regulation in response to phosphatidylinositol 3-kinase activity and detailed characterization of the actinbinding site in subunit B
-
Chen SH, Bubb MR, Yarmola EG, et al. Vacuolar H+-ATPase binding to microfilaments: regulation in response to phosphatidylinositol 3-kinase activity and detailed characterization of the actinbinding site in subunit B. J Biol Chem 2004;279:7988-7998
-
(2004)
J Biol Chem
, vol.279
, pp. 7988-7998
-
-
Chen, S.H.1
Bubb, M.R.2
Yarmola, E.G.3
-
203
-
-
69049093857
-
Identification of enoxacin as an inhibitor of osteoclast formation and bone resorption by structure-based virtual screening
-
Ostrov DA, Magis AT, Wronski TJ, et al. Identification of enoxacin as an inhibitor of osteoclast formation and bone resorption by structure-based virtual screening. J Med Chem 2009;52:5144-5151
-
(2009)
J Med Chem
, vol.52
, pp. 5144-5151
-
-
Ostrov, D.A.1
Magis, A.T.2
Wronski, T.J.3
-
204
-
-
0034727078
-
An LDL-receptor-related protein mediates Wnt signalling in mice
-
Pinson KI, Brennan J, Monkley S, et al. An LDL-receptor-related protein mediates Wnt signalling in mice. Nature 2000;407:535-538
-
(2000)
Nature
, vol.407
, pp. 535-538
-
-
Pinson, K.I.1
Brennan, J.2
Monkley, S.3
-
205
-
-
1242272029
-
Murine frizzled-1 behaves as an antagonist of the canonical Wnt/bcatenin signaling
-
Roman-Roman S, Shi D-L, Stiot V, et al. Murine frizzled-1 behaves as an antagonist of the canonical Wnt/bcatenin signaling. J Biol Chem 2004;279:5725-5733
-
(2004)
J Biol Chem
, vol.279
, pp. 5725-5733
-
-
Roman-Roman, S.1
Shi, D.-L.2
Stiot, V.3
-
206
-
-
27944444857
-
The Wnt antagonist secreted frizzledrelated protein-1 controls osteoblast and osteocyte apoptosis
-
Bodine PVN, Billiard J, Moran RA, et al. The Wnt antagonist secreted frizzledrelated protein-1 controls osteoblast and osteocyte apoptosis. J Cell Biochem 2005;96:1212-1230
-
(2005)
J Cell Biochem
, vol.96
, pp. 1212-1230
-
-
Bodine, P.V.N.1
Billiard, J.2
Moran, R.A.3
-
207
-
-
2342529836
-
The Wnt antagonist secreted frizzled-related protein-1 is a negative regulator of trabecular bone formation in adult mice
-
Bodine PVN, Zhao W, Kharode YP, et al. The Wnt antagonist secreted frizzled-related protein-1 is a negative regulator of trabecular bone formation in adult mice. Mol Endocrinol 2004;18:1222-1237
-
(2004)
Mol Endocrinol
, vol.18
, pp. 1222-1237
-
-
Bodine, P.V.N.1
Zhao, W.2
Kharode, Y.P.3
-
208
-
-
0035837553
-
Effect of parathyroid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis
-
Neer RM, Arnaud CD, Zanchetta JR, et al. Effect of parathyroid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis. N Engl J Med 2001;344:1434-1441
-
(2001)
N Engl J Med
, Issue.344
, pp. 1434-1441
-
-
Neer, R.M.1
Arnaud, C.D.2
Zanchetta, J.R.3
-
210
-
-
33845665838
-
Bone anabolic effects of parathyroid hormone are blunted by deletion of the Wnt antagonist secreted frizzled-related protein-1
-
Bodine PVN, Seestaller-Wehr L, Kharode YP, et al. Bone anabolic effects of parathyroid hormone are blunted by deletion of the Wnt antagonist secreted frizzled-related protein-1. J Cell Phys 2007;210:352-357
-
(2007)
J Cell Phys
, vol.210
, pp. 352-357
-
-
Bodine, P.V.N.1
Seestaller-Wehr, L.2
Kharode, Y.P.3
-
211
-
-
58149092256
-
Identification of diarylsulfone sulfonamides as secreted Frizzled Related Protein-1 (sFRP-1) inhibitors
-
Gopalsamy A, Shi M, Stauffe B, et al. Identification of diarylsulfone
-
(2008)
J Med Chem
, vol.51
, pp. 7670-7672
-
-
Gopalsamy, A.1
Shi, M.2
Stauffe, B.3
-
212
-
-
59449102727
-
Modulation of Wnt signaling through inhibition of secreted Frizzled-Related Protein i (sFRP-1) with N-substituted piperidinyl diphenylsulfonyl sulfonamides
-
Moore WJ, Kern JC, Bhat R, et al. Modulation of Wnt signaling through inhibition of secreted Frizzled-Related Protein I (sFRP-1) with N-substituted piperidinyl diphenylsulfonyl sulfonamides. J Med Chem 2009;52:105-116
-
(2009)
J Med Chem
, vol.52
, pp. 105-116
-
-
Moore, W.J.1
Kern, J.C.2
Bhat, R.3
-
218
-
-
33749017931
-
Cysteine cathepsins: Multifunctional enzymes in cancer
-
Mohamed MM, Sloane BF. Cysteine cathepsins: multifunctional enzymes in cancer. Nat Rev Cancer 2006;6:764-775
-
(2006)
Nat Rev Cancer
, vol.6
, pp. 764-775
-
-
Mohamed, M.M.1
Sloane, B.F.2
-
219
-
-
35448959223
-
Cathepsin K inhibitor reduces breast cancer-induced osteolysis and skeletal tumor burden
-
Gall CL, Bellahcene A, Bonnelye E, et al. Cathepsin K inhibitor reduces breast cancer-induced osteolysis and skeletal tumor burden. Cancer Res 2007;67:9894-9902
-
(2007)
Cancer Res
, vol.67
, pp. 9894-9902
-
-
Gall, C.L.1
Bellahcene, A.2
Bonnelye, E.3
-
220
-
-
0036763816
-
Clinical profiles of celecoxib and rofecoxib in the rheumatic diseases
-
Gibofsky A. Clinical profiles of celecoxib and rofecoxib in the rheumatic diseases. J Hypertens 2002;20:S25-30
-
(2002)
J Hypertens
, vol.20
-
-
Gibofsky, A.1
-
221
-
-
0033601089
-
Anti-inflammatory and upper gastrointestinal effects of celecoxib in rheumatoid arthritis: A randomized controlled trial
-
Simon LS, Weaver AL, Graham DY, et al. Anti-inflammatory and upper gastrointestinal effects of celecoxib in rheumatoid arthritis: a randomized controlled trial. JAMA 1999;282:1921-1928
-
(1999)
JAMA
, vol.282
, pp. 1921-1928
-
-
Simon, L.S.1
Weaver, A.L.2
Graham, D.Y.3
-
222
-
-
34147113829
-
NO-Donor COX-2 inhibitors. New nitrooxy-substituted 1,5-diarylimidazoles endowed with COX-2 inhibitory and vasodilator properties
-
Konstantin C, Loretta L, Paolo T, et al. NO-Donor COX-2 inhibitors. New nitrooxy-substituted 1,5-diarylimidazoles endowed with COX-2 inhibitory and vasodilator properties. J Med Chem 2007;50:1449-1457
-
(2007)
J Med Chem
, vol.50
, pp. 1449-1457
-
-
Konstantin, C.1
Loretta, L.2
Paolo, T.3
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