-
1
-
-
0842324615
-
Chemokines: Multiple levels of leukocyte migration control
-
Moser, B.; Wolf, M.; Walz, A.; Loetscher, P. Chemokines: multiple levels of leukocyte migration control. Trends Immunol., 2004, 25(2), 75-84.
-
(2004)
Trends Immunol
, vol.25
, Issue.2
, pp. 75-84
-
-
Moser, B.1
Wolf, M.2
Walz, A.3
Loetscher, P.4
-
2
-
-
0030816336
-
Neutrophil receptors for interleukin-8 and related CXC chemokines
-
Murphy, P. M. Neutrophil receptors for interleukin-8 and related CXC chemokines. Semin. Hematol., 1997, 34(4), 311-318.
-
(1997)
Semin. Hematol
, vol.34
, Issue.4
, pp. 311-318
-
-
Murphy, P.M.1
-
3
-
-
0026095795
-
Structure and functional expression of a human interleukin-8 receptor
-
Holmes, W. E.; Lee, J.; Kuang, W. J.; Rice, G. C.; Wood, W. I. Structure and functional expression of a human interleukin-8 receptor. Science, 1991, 253(5025), 1278-1280.
-
(1991)
Science
, vol.253
, Issue.5025
, pp. 1278-1280
-
-
Holmes, W.E.1
Lee, J.2
Kuang, W.J.3
Rice, G.C.4
Wood, W.I.5
-
4
-
-
0026018108
-
Cloning of complementary DNA encoding a functional human interleukin receptor
-
Murphy, P. M.; Tiffany, H. L. Cloning of complementary DNA encoding a functional human interleukin receptor. Science, 1991, 253(5025), 1280-1282.
-
(1991)
Science
, vol.253
, Issue.5025
, pp. 1280-1282
-
-
Murphy, P.M.1
Tiffany, H.L.2
-
5
-
-
0037377567
-
Pathophysiological roles of interleukin-8/CXCL8 in pulmonary diseases
-
Mukaida, N. Pathophysiological roles of interleukin-8/CXCL8 in pulmonary diseases. Am. J. Physiol. Lung Cell Mol. Physiol., 2002, 284(10), L566-L577.
-
(2002)
Am. J. Physiol. Lung Cell Mol. Physiol
, vol.284
, Issue.10
, pp. L566-L577
-
-
Mukaida, N.1
-
6
-
-
3442895601
-
Specific CXC but not CC chemokines cause elevated monocyte migration in COPD: A role for CXCR2
-
Traves, S.; Smith, S. J.; Barnes, P. J.; Donnelly, L. E. Specific CXC but not CC chemokines cause elevated monocyte migration in COPD: a role for CXCR2. J. Leukoc. Biol. 2004, 76(12), 441-450.
-
(2004)
J. Leukoc. Biol
, vol.76
, Issue.12
, pp. 441-450
-
-
Traves, S.1
Smith, S.J.2
Barnes, P.J.3
Donnelly, L.E.4
-
7
-
-
33644642974
-
Critical role of endothelial CXCR2 in LPS-induced neutrophil migration into the lung
-
Reutershan, J.; Morris, M. A.; Burcin, T. L.; Smith, D. F.; Chang, D.; Saprito, M. S.; Ley, K. Critical role of endothelial CXCR2 in LPS-induced neutrophil migration into the lung. J. Clin. Invest., 2006, 116(3), 695-702.
-
(2006)
J. Clin. Invest
, vol.116
, Issue.3
, pp. 695-702
-
-
Reutershan, J.1
Morris, M.A.2
Burcin, T.L.3
Smith, D.F.4
Chang, D.5
Saprito, M.S.6
Ley, K.7
-
8
-
-
0025888267
-
Structure and neutrophil-activating properties of a novel inflammatory peptide (ENA-78) with homology to interleukin-8
-
Walz, A.; Burgener, R.; Carr, B.; Baggiolini, M.; Kunkel, S. L.; Strieter, R. M. Structure and neutrophil-activating properties of a novel inflammatory peptide (ENA-78) with homology to interleukin-8. J. Exp. Med., 1991, 174(6), 1355-1362.
-
(1991)
J. Exp. Med
, vol.174
, Issue.6
, pp. 1355-1362
-
-
Walz, A.1
Burgener, R.2
Carr, B.3
Baggiolini, M.4
Kunkel, S.L.5
Strieter, R.M.6
-
9
-
-
0031964175
-
Granulocyte chemotactic protein 2 act via both IL-8 receptors, CXCR1 and CXCR2
-
Wolf, M.; Delgado, M. B.; Jones, S. A.; Dewald, B.; Clark-Lewis, B.; Baggiolini, M. Granulocyte chemotactic protein 2 act via both IL-8 receptors, CXCR1 and CXCR2. Eur. J. Immunol., 1998, 28(1), 164-170.
-
(1998)
Eur. J. Immunol
, vol.28
, Issue.1
, pp. 164-170
-
-
Wolf, M.1
Delgado, M.B.2
Jones, S.A.3
Dewald, B.4
Clark-Lewis, B.5
Baggiolini, M.6
-
10
-
-
0028052968
-
Interleukin-8 and related chemotactic cytokines CXC and CC chemokines
-
Baggiolini, M.; Dewald, B.; Moser, B. Interleukin-8 and related chemotactic cytokines CXC and CC chemokines. Adv. Immunol., 1994, 55, 97-179.
-
(1994)
Adv. Immunol
, vol.55
, pp. 97-179
-
-
Baggiolini, M.1
Dewald, B.2
Moser, B.3
-
11
-
-
0032562614
-
Identification of a potent, selective non-peptide antagonist that inhibits interleukin-8-induced neutrophil migration
-
White, J. R.; Lee, J. M.; Young, P. R.; Hertzberg, R. P.; Jurewicz, A. J.; Chaikin, M. A.; Widdowson, K. L.; Foley, J. J.; Martin, L. D.; Griswold, D. E.; Sarau, H. M. Identification of a potent, selective non-peptide antagonist that inhibits interleukin-8-induced neutrophil migration. J. Biol. Chem., 1998, 273(17), 10095-10098.
-
(1998)
J. Biol. Chem
, vol.273
, Issue.17
, pp. 10095-10098
-
-
White, J.R.1
Lee, J.M.2
Young, P.R.3
Hertzberg, R.P.4
Jurewicz, A.J.5
Chaikin, M.A.6
Widdowson, K.L.7
Foley, J.J.8
Martin, L.D.9
Griswold, D.E.10
Sarau, H.M.11
-
12
-
-
0028372188
-
The immunopathology of chemotactic cytokines: The role of interleukin-8 and monocyte chemoattractant protein-1
-
Strieter, R. M., Koch, A. E.; Antony, V. B.; Fick, R. B. Jr.; Standiford, T. J.; Kunkel, S. L. The immunopathology of chemotactic cytokines: The role of interleukin-8 and monocyte chemoattractant protein-1. J. Lab. Clin. Med., 1994, 123(2), 183-197.
-
(1994)
J. Lab. Clin. Med
, vol.123
, Issue.2
, pp. 183-197
-
-
Strieter, R.M.1
Koch, A.E.2
Antony, V.B.3
Fick, R.B.4
Standiford, T.J.5
Kunkel, S.L.6
-
13
-
-
0024831225
-
Effects of the neutrophil-activating peptide NAP-2, platelet basic protein, connective tissue-activating peptide III and platelet factor 4 on human neutrophils
-
Walz, A.; Dewald, B.; von Tscharner, V.; Baggiolini, M. Effects of the neutrophil-activating peptide NAP-2, platelet basic protein, connective tissue-activating peptide III and platelet factor 4 on human neutrophils. J. Exp. Med., 1989, 170(5), 1745-1750.
-
(1989)
J. Exp. Med
, vol.170
, Issue.5
, pp. 1745-1750
-
-
Walz, A.1
Dewald, B.2
von Tscharner, V.3
Baggiolini, M.4
-
14
-
-
0023749502
-
Mechanism of neutrophil activation by NAF, a novel monocytederived peptide agonist
-
Thelen, M.; Peveri, P.; von Tsharaner. V.; Walz, A.; Baggiolini, M. Mechanism of neutrophil activation by NAF, a novel monocytederived peptide agonist. FASEB J., 1988, 2(11), 2702-2706.
-
(1988)
FASEB J
, vol.2
, Issue.11
, pp. 2702-2706
-
-
Thelen, M.1
Peveri, P.2
von Tsharaner, V.3
Walz, A.4
Baggiolini, M.5
-
15
-
-
0023940237
-
A novel neutrophil-activating factor produced by human mononuclear phagocytes
-
Peveri, P.; Walz, A.; Dewald, B.; Baggiolini, M. A novel neutrophil-activating factor produced by human mononuclear phagocytes. J. Exp. Med., 1988, 167(5), 1547-1559.
-
(1988)
J. Exp. Med
, vol.167
, Issue.5
, pp. 1547-1559
-
-
Peveri, P.1
Walz, A.2
Dewald, B.3
Baggiolini, M.4
-
16
-
-
0025726941
-
Neutrophil recruitment by intradermally injected neutrophil attractant/activation protein-1
-
Leonard, E. J.; Yoshimura, T.; Tanaka, S.; Raffeld, M. Neutrophil recruitment by intradermally injected neutrophil attractant/activation protein-1. J. Invest. Dermatol., 1991, 96(5), 690-694.
-
(1991)
J. Invest. Dermatol
, vol.96
, Issue.5
, pp. 690-694
-
-
Leonard, E.J.1
Yoshimura, T.2
Tanaka, S.3
Raffeld, M.4
-
17
-
-
0031843169
-
Inflammatory cells and mediators in bronchial lavage of patients with chronic obstructive pulmonary disease
-
Pesci, A.; Balbi, B.; Majori, M.; Cacciani, G.; Bertacco, S.; Alciato, P.; Donner, C. F. Inflammatory cells and mediators in bronchial lavage of patients with chronic obstructive pulmonary disease. Eur. Respir. J. 1998, 12(2), 380-386.
-
(1998)
Eur. Respir. J
, vol.12
, Issue.2
, pp. 380-386
-
-
Pesci, A.1
Balbi, B.2
Majori, M.3
Cacciani, G.4
Bertacco, S.5
Alciato, P.6
Donner, C.F.7
-
18
-
-
0030071687
-
Differences in interleukin-8 and tumor necrosis factor-888in induced sputum from patients with chronic obstructive pulmonary disease or asthma
-
Keatings, V. M.; Collins, R. D.; Scott, D. M. Differences in interleukin-8 and tumor necrosis factor-888in induced sputum from patients with chronic obstructive pulmonary disease or asthma. J. Am. J. Respir. Crit. Care Med., 1996, 153(2), 530-534.
-
(1996)
J. Am. J. Respir. Crit. Care Med
, vol.153
, Issue.2
, pp. 530-534
-
-
Keatings, V.M.1
Collins, R.D.2
Scott, D.M.3
-
19
-
-
0042387838
-
The role of interleukin-8 and its receptors in inflammatory lung disease: Implications for therapy
-
Pease, J. E.; Sabroe, I. The role of interleukin-8 and its receptors in inflammatory lung disease: implications for therapy. Am. J. Respir. Med. 2002, 1(1), 19-25.
-
(2002)
Am. J. Respir. Med
, vol.1
, Issue.1
, pp. 19-25
-
-
Pease, J.E.1
Sabroe, I.2
-
20
-
-
21044433754
-
The Role of CXCR2/CXCR2 Ligands in Acute Lung Injury
-
Strieter, R. M.; Keane, M. P.; Burdick, M. D.; Sakkour, A.; Murray, L. A.; Belperio, J. A. The Role of CXCR2/CXCR2 Ligands in Acute Lung Injury. Curr. Drug Targ-Inflamm. Allergy, 2005, 4(3), 299-303.
-
(2005)
Curr. Drug Targ-Inflamm. Allergy
, vol.4
, Issue.3
, pp. 299-303
-
-
Strieter, R.M.1
Keane, M.P.2
Burdick, M.D.3
Sakkour, A.4
Murray, L.A.5
Belperio, J.A.6
-
21
-
-
0029823833
-
Cystic Fibrosis
-
Davis, P. B.; Drumm, M.; Konstan, M. W. Cystic Fibrosis. Am. J. Respir. Crit. Care Med., 1996, 154(5), 1229-1256.
-
(1996)
Am. J. Respir. Crit. Care Med
, vol.154
, Issue.5
, pp. 1229-1256
-
-
Davis, P.B.1
Drumm, M.2
Konstan, M.W.3
-
22
-
-
27144517061
-
CXC chemokines in angiogenesis
-
Strieter, R. M., Burdick, M. D., Gomperts, B. N., Belperio, J. A., Keane, M. P. CXC chemokines in angiogenesis. Cytok. Growth Fact. Rev., 2005, 16(6), 593-609.
-
(2005)
Cytok. Growth Fact. Rev
, vol.16
, Issue.6
, pp. 593-609
-
-
Strieter, R.M.1
Burdick, M.D.2
Gomperts, B.N.3
Belperio, J.A.4
Keane, M.P.5
-
23
-
-
77955612605
-
IL-8 receptor antagonist: Basic research and clinical utility. In
-
Moser, B.; Letts, G.L.; Neote, K.; Eds.; Birkhaeuser Verlag: Basel
-
White, J. R.; Sarau, H. M. IL-8 receptor antagonist: basic research and clinical utility. In: Chemokine Biology-Basic Research and Clinical Application; Moser, B.; Letts, G. L.; Neote, K.; Eds.; Birkhaeuser Verlag: Basel, 2007; Vol. 2, pp. 89-102.
-
(2007)
Chemokine Biology-Basic Research and Clinical Application
, vol.2
, pp. 89-102
-
-
White, J.R.1
Sarau, H.M.2
-
24
-
-
57749100072
-
CXCR2 antagonists for the treatment of pulmonary disease
-
Chapman, R. W.; Phillips, J. E.; Hipkin, R. W.; Curran, A. K.; Lundell, D.; Fine, J. S. CXCR2 antagonists for the treatment of pulmonary disease. Pharmacol Therap., 2009, 121(1), 55-68.
-
(2009)
Pharmacol Therap
, vol.121
, Issue.1
, pp. 55-68
-
-
Chapman, R.W.1
Phillips, J.E.2
Hipkin, R.W.3
Curran, A.K.4
Lundell, D.5
Fine, J.S.6
-
25
-
-
84898875335
-
The CXCL8/IL-8 chemokine family and its receptors in inflammatory diseases
-
Russo, R. C.; Garcia, C. C.; Teixeira, M. M.; Amara, F. A. The CXCL8/IL-8 chemokine family and its receptors in inflammatory diseases. Expert Rev. Clin. Immunol., 2014, 10(5), 593-619.
-
(2014)
Expert Rev. Clin. Immunol
, vol.10
, Issue.5
, pp. 593-619
-
-
Russo, R.C.1
Garcia, C.C.2
Teixeira, M.M.3
Amara, F.A.4
-
26
-
-
0028067339
-
Neutrophil and B cell expansion in mice that lack the murine IL-8 receptor homolog
-
Cacalano, G.; Lee, J; Kikly, K.; et al. Neutrophil and B cell expansion in mice that lack the murine IL-8 receptor homolog. Science 1994, 265(5172), 682-684.
-
(1994)
Science
, vol.265
, Issue.5172
, pp. 682-684
-
-
Cacalano, G.1
Lee, J.2
Kikly, K.3
-
27
-
-
84862183490
-
Current status of chemokine receptor inhibitors in development
-
Allegretti, M.; Cesta, M. C.; Garin, A.; et al. Current status of chemokine receptor inhibitors in development. Immunol. Lett., 2012, 145(1-2), 68-78.
-
(2012)
Immunol. Lett
, vol.145
, Issue.1-2
, pp. 68-78
-
-
Allegretti, M.1
Cesta, M.C.2
Garin, A.3
-
28
-
-
84873086545
-
Therapeutic targeting of chemokine receptors by small molecules
-
Wijtmans, M.; Scholten, D. J.; de Esch, I. J. P.; et al. Therapeutic targeting of chemokine receptors by small molecules. Drug Disc. Today Tech., 2012, 9(4), e229-e236.
-
(2012)
Drug Disc. Today Tech
, vol.9
, Issue.4
, pp. e229-e236
-
-
Wijtmans, M.1
Scholten, D.J.2
de Esch, I.J.P.3
-
29
-
-
84952989976
-
Chemokine receptor CXCR2 antagonism to prevent airways inflammation
-
Donnelly, L. E.; Barnes, P. J. Chemokine receptor CXCR2 antagonism to prevent airways inflammation. Drugs of the Future, 2011, 36(6), 465-472.
-
(2011)
Drugs of the Future
, vol.36
, Issue.6
, pp. 465-472
-
-
Donnelly, L.E.1
Barnes, P.J.2
-
30
-
-
33746582271
-
Small molecule antagonists of the CXCR2 and CXCR1 chemokine receptors as therapeutic agents for the treatment of inflammatory diseases
-
Busch-Peterson, J. Small molecule antagonists of the CXCR2 and CXCR1 chemokine receptors as therapeutic agents for the treatment of inflammatory diseases. Curr. Top. Med. Chem., 2006, 6(13), 1354-1362.
-
(2006)
Curr. Top. Med. Chem
, vol.6
, Issue.13
, pp. 1354-1362
-
-
Busch-Peterson, J.1
-
31
-
-
33748142935
-
ELR+ CXC chemokines and their receptors (CXC chemokine receptor 1 and CXC chemokine receptor 2) as therapeutic targets
-
Bizzarri, C.; Beccari, A. R.; Bertini, R.; Cavicchia, M. R.; Giorgini, S.; Allegretti, M. ELR+ CXC chemokines and their receptors (CXC chemokine receptor 1 and CXC chemokine receptor 2) as therapeutic targets. Pharmacol. Ther., 2006, 112(1), 139-149.
-
(2006)
Pharmacol. Ther
, vol.112
, Issue.1
, pp. 139-149
-
-
Bizzarri, C.1
Beccari, A.R.2
Bertini, R.3
Cavicchia, M.R.4
Giorgini, S.5
Allegretti, M.6
-
32
-
-
77955609137
-
Discovery of 3, 4-diaminocyclobut-3-ene-1, 2-dione-based CXCR2 receptor antagonists for the treatment of inflammatory disorders
-
Dwyer. M. P.; Biju, P. Discovery of 3, 4-diaminocyclobut-3-ene-1, 2-dione-based CXCR2 receptor antagonists for the treatment of inflammatory disorders. Curr. Top. Med. Chem., 2010, 10(13), 1339-1350.
-
(2010)
Curr. Top. Med. Chem
, vol.10
, Issue.13
, pp. 1339-1350
-
-
Dwyer, M.P.1
Biju, P.2
-
33
-
-
84898939951
-
Low molecular weight CXCR2 antagonists as promising therapeutics
-
Smit, M.J.; Lira, S.A.; Leurs, R.; Eds.; Wiley-VCG Verlag GmbH & KgaA: Weinheim
-
Mihara, K.; Wijkmans, J. Low molecular weight CXCR2 antagonists as promising therapeutics. In: Chemokine Receptor as Drug Targets; Smit, M. J.; Lira, S. A.; Leurs, R.; Eds.; Wiley-VCG Verlag GmbH & KgaA: Weinheim, 2011; Vol. 46, pp. 279-299.
-
(2011)
Chemokine Receptor as Drug Targets
, vol.46
, pp. 279-299
-
-
Mihara, K.1
Wijkmans, J.2
-
34
-
-
46849120181
-
Phenol-containing antagonists of the CXCR2 receptor
-
Busch-Petersen, J.; Wang, Y. Phenol-containing antagonists of the CXCR2 receptor. Expert Opin. Ther. Patents, 2008, 18(6), 629-637.
-
(2008)
Expert Opin. Ther. Patents
, vol.18
, Issue.6
, pp. 629-637
-
-
Busch-Petersen, J.1
Wang, Y.2
-
35
-
-
84898934029
-
CXCR2 modulators: A patent review (2009-2013)
-
Dwyer, M. P.; Yu, Y. CXCR2 modulators: a patent review (2009-2013). Expert Opin. Ther. Patents, 2014, 24(5), 519-534.
-
(2014)
Expert Opin. Ther. Patents
, vol.24
, Issue.5
, pp. 519-534
-
-
Dwyer, M.P.1
Yu, Y.2
-
36
-
-
0037913735
-
The role of the anionic groups in the receptor binding or interleukin-8 antagonists
-
Widdowson, K.; Nie, H.; Jurewicz, A. J.; Hertzberg, R. P.; Sarau, H. M.; Foley, J. J.; Lee, J.; White, J. R.; Veber, D. F. The role of the anionic groups in the receptor binding or interleukin-8 antagonists. Lett. Peptide Sci., 1998, 5(2-3), 235-239.
-
(1998)
Lett. Peptide Sci
, vol.5
, Issue.2-3
, pp. 235-239
-
-
Widdowson, K.1
Nie, H.2
Jurewicz, A.J.3
Hertzberg, R.P.4
Sarau, H.M.5
Foley, J.J.6
Lee, J.7
White, J.R.8
Veber, D.F.9
-
37
-
-
33746609900
-
Discovery and characterization of potent, small molecule interleukin-8B receptor antagonists
-
Ramage, R.; Epton, R.; Eds.; Mayflower Scientific: Kingswinford
-
Widdowson, K.; Veber, D. F.; Jurewicz, A. J.; Nie, H.; Hertzberg, R. P.; Holl, W.; Sarau, H. M. Discovery and characterization of potent, small molecule interleukin-8B receptor antagonists. In Peptides 1996; Ramage, R.; Epton, R.; Eds.; Mayflower Scientific: Kingswinford, 1998; pp. 87-90.
-
(1998)
Peptides 1996
, pp. 87-90
-
-
Widdowson, K.1
Veber, D.F.2
Jurewicz, A.J.3
Nie, H.4
Hertzberg, R.P.5
Holl, W.6
Sarau, H.M.7
-
38
-
-
3843087497
-
Discovery of potent and orally bioavailable N, N'-diarylurea antagonists for the CXCR2 chemokine receptor
-
Jin, Q.; Nie, H.; McCleland, B. W.; Widdowson, K. L.; Palovich, M. R.; Elliott, J. D.; Goodman, R. M.; Burman, M.; Sarau, H. M.; Ward, K. W.; Nord, M.; Orr, B. M.; Gorycki, P. D.; Busch-Petersen, J. Discovery of potent and orally bioavailable N, N'-diarylurea antagonists for the CXCR2 chemokine receptor. Bioorg. Med. Chem. Lett., 2004, 14(17), 4375-4378.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, Issue.17
, pp. 4375-4378
-
-
Jin, Q.1
Nie, H.2
McCleland, B.W.3
Widdowson, K.L.4
Palovich, M.R.5
Elliott, J.D.6
Goodman, R.M.7
Burman, M.8
Sarau, H.M.9
Ward, K.W.10
Nord, M.11
Orr, B.M.12
Gorycki, P.D.13
Busch-Petersen, J.14
-
39
-
-
0042375056
-
Interleukin-8 receptor (CXCR2) antagonists
-
Sarau, H. M.; Widdowson, K. L.; Palovich, M. R.; White, J. R.; Underwood, D. D; Griswold, D. E. Interleukin-8 receptor (CXCR2) antagonists. Prog. Respir. Res., 2001, 31, 293-296.
-
(2001)
Prog. Respir. Res
, vol.31
, pp. 293-296
-
-
Sarau, H.M.1
Widdowson, K.L.2
Palovich, M.R.3
White, J.R.4
Underwood, D.D.5
Griswold, D.E.6
-
40
-
-
0034802186
-
Nonpeptide CXCR2 antagonist prevents neutrophil accumulation in hyperoxia-exposed newborn rats
-
Auten, R. L.; Richardson, R. M.; White, J. R.; Mason, S. N.; Vozzelli, M. A.; Whorton, M. H. Nonpeptide CXCR2 antagonist prevents neutrophil accumulation in hyperoxia-exposed newborn rats. J. Pharmcol. Exp. Ther., 2001, 299(1), 90-95.
-
(2001)
J. Pharmcol. Exp. Ther
, vol.299
, Issue.1
, pp. 90-95
-
-
Auten, R.L.1
Richardson, R.M.2
White, J.R.3
Mason, S.N.4
Vozzelli, M.A.5
Whorton, M.H.6
-
41
-
-
69249222632
-
SB265610 is an allosteric, inverse agonist at the human CXCR2 receptor
-
Bradley, M. E.; Bond, M. E.; Brown, Z.; Charlton, S. J. SB265610 is an allosteric, inverse agonist at the human CXCR2 receptor. Brit. J. Pharmacol., 2009, 158(1), 328-338.
-
(2009)
Brit. J. Pharmacol
, vol.158
, Issue.1
, pp. 328-338
-
-
Bradley, M.E.1
Bond, M.E.2
Brown, Z.3
Charlton, S.J.4
-
42
-
-
12144291157
-
Evaluation of Potent and Selective Small-Molecule Antagonists for the CXCR2 Chemokine Receptor
-
Widdowson, K. L.; Elliott, J. D.; Veber, D. F.; Nie, H.; Rutledge, M. C.; McCleland, B. W.; Xiang, J.-N.; Jurewicz, A. J.; Hertzberg, R. P.; Foley, J. J.; Griswold, D. E.; Martin, L.; Lee, J. M.; White, J. R.; Sarau, H. M. Evaluation of Potent and Selective Small-Molecule Antagonists for the CXCR2 Chemokine Receptor. J. Med. Chem., 2004, 47(6), 1319-1321.
-
(2004)
J. Med. Chem
, vol.47
, Issue.6
, pp. 1319-1321
-
-
Widdowson, K.L.1
Elliott, J.D.2
Veber, D.F.3
Nie, H.4
Rutledge, M.C.5
McCleland, B.W.6
Xiang, J.-N.7
Jurewicz, A.J.8
Hertzberg, R.P.9
Foley, J.J.10
Griswold, D.E.11
Martin, L.12
Lee, J.M.13
White, J.R.14
Sarau, H.M.15
-
43
-
-
0036884730
-
A potent and selective nonpeptide antagonist of CXCR2 inhibits acute and chronic models of arthritis in the rabbit
-
Podolin, P. L.; Bolognese, B. J.; Foley, J. J.; Schmidt, D. B.; Buckley, P. T.; Widdowson, K. L.; Jin, Q.; White, J. R.; Lee, J. M., Goodman, R. B.; Hagen, T. R.; Kajikawa, O.; Marshall, L. A.; Hay, D. W. P.; Sarau, H. M. A potent and selective nonpeptide antagonist of CXCR2 inhibits acute and chronic models of arthritis in the rabbit. J. Immunol., 2002, 16(11), 6435-6444.
-
(2002)
J. Immunol
, vol.16
, Issue.11
, pp. 6435-6444
-
-
Podolin, P.L.1
Bolognese, B.J.2
Foley, J.J.3
Schmidt, D.B.4
Buckley, P.T.5
Widdowson, K.L.6
Jin, Q.7
White, J.R.8
Lee, J.M.9
Goodman, R.B.10
Hagen, T.R.11
Kajikawa, O.12
Marshall, L.A.13
Hay, D.W.P.14
Sarau, H.M.15
-
44
-
-
33746621022
-
A CXCR2 antagonist, SB-332235, reduces artherosclerosis in LDL receptor deficient mice
-
Benson, G. M.; Grimsditch, D. C.; Piercy, V.; Vidgeon-Hart, M.; Groot, P. H. E.; Suckling, K.; Sarau, H. M.; Foley, J. J.; Jin, Q.; Palovich, M.; Widdowson, K. L. A CXCR2 antagonist, SB-332235, reduces artherosclerosis in LDL receptor deficient mice. Artherosclerosis, 2005, 181, 419.
-
(2005)
Artherosclerosis
, vol.181
, pp. 419
-
-
Benson, G.M.1
Grimsditch, D.C.2
Piercy, V.3
Vidgeon-Hart, M.4
Groot, P.H.E.5
Suckling, K.6
Sarau, H.M.7
Foley, J.J.8
Jin, Q.9
Palovich, M.10
Widdowson, K.L.11
-
45
-
-
13644267621
-
Characterization of cigarette smoke-induced inflammatory and mucus hypersecretory changes in rat lung and the role of CXCR2 ligands in mediating this effect
-
Stevenson, C. S.; Coote, K.; Webster, R.; Johnston, H.; Atherton, H. C.; Nicholls, A.; Giddings, J.; Sugar, R.; Jackson, A.; Press, N. J.; Brown, Z.; Butler, K.; Danahay, H. Characterization of cigarette smoke-induced inflammatory and mucus hypersecretory changes in rat lung and the role of CXCR2 ligands in mediating this effect. Am. J. Physiol. Lung Cell Mol. Physiol., 2005, 288(3, pt1), L514-L522.
-
(2005)
Am. J. Physiol. Lung Cell Mol. Physiol
, vol.288
, Issue.3
, pp. L514-L522
-
-
Stevenson, C.S.1
Coote, K.2
Webster, R.3
Johnston, H.4
Atherton, H.C.5
Nicholls, A.6
Giddings, J.7
Sugar, R.8
Jackson, A.9
Press, N.J.10
Brown, Z.11
Butler, K.12
Danahay, H.13
-
46
-
-
13844302201
-
The selective CXCR2 receptor antagonist SB-656933 inhibits CXCL1-induced neutrophil CD11b expression in human whole blood. Eur. Resp. Symp., September 2004
-
Carpenter, D. C.; Rumsey, W. M.; Busch-Peterson, J.; Sarau, H. M.; Salmon, M. The selective CXCR2 receptor antagonist SB-656933 inhibits CXCL1-induced neutrophil CD11b expression in human whole blood. Eur. Resp. Symp., September 2004. Eur. Resp. J., 2004, 24(suppl 48), 218s.
-
(2004)
Eur. Resp. J
, vol.24
-
-
Carpenter, D.C.1
Rumsey, W.M.2
Busch-Peterson, J.3
Sarau, H.M.4
Salmon, M.5
-
47
-
-
33750490450
-
A novel flow cytometric assay of human whole blood neutrophil and monocyte CD11b levels: Upregulation by chemokines is related to receptor expression, comparison of neutrophil shape change, and effects of a chemokine receptor (CXCR2) antagonist
-
Nicholson, G. C.; Tennant, R. C.; Carpenter, D. C.; Sarau, H. M.; Kon, O. M.; Barnes, P. J.; Salmon, M.; Vessey, R. S.; Tal-Singer, R.; Hansel, T. T. A novel flow cytometric assay of human whole blood neutrophil and monocyte CD11b levels: Upregulation by chemokines is related to receptor expression, comparison of neutrophil shape change, and effects of a chemokine receptor (CXCR2) antagonist. Pulmon. Pharm. Ther. 2007, 20(1), 52-59.
-
(2007)
Pulmon. Pharm. Ther
, vol.20
, Issue.1
, pp. 52-59
-
-
Nicholson, G.C.1
Tennant, R.C.2
Carpenter, D.C.3
Sarau, H.M.4
Kon, O.M.5
Barnes, P.J.6
Salmon, M.7
Vessey, R.S.8
Tal-Singer, R.9
Hansel, T.T.10
-
48
-
-
13844294668
-
Inhibition of LPS-induced neutrophil recruitment in the lung correlates with modulation of neutrophil CD11b expression using the selective CXCR2 receptor antagonist SB-656933. Eur. Resp. Symp., September 2004
-
Salmon, M.; Carpenter, C. J.; DeHaas, C. J.; Tal-Singer, R.; Sarau, H. M.; Underwood, D. C. Inhibition of LPS-induced neutrophil recruitment in the lung correlates with modulation of neutrophil CD11b expression using the selective CXCR2 receptor antagonist SB-656933. Eur. Resp. Symp., September 2004. Eur. Resp. J. 2004, 24(suppl 48), 218s.
-
(2004)
Eur. Resp. J
, vol.24
-
-
Salmon, M.1
Carpenter, C.J.2
DeHaas, C.J.3
Tal-Singer, R.4
Sarau, H.M.5
Underwood, D.C.6
-
49
-
-
85067755776
-
A selective CXCR2 receptor antagonist, SB656933-AAA reduces disease symptomology and ulceration in a DNBS rat model of colitis
-
May 20 (Abs S1603)
-
Kruidenier, L.; Lione, L. A.; McCleary, S.; Vidgeon-Hart, P. M.; Stretton, J. G.; Ashmeade, X.; Lee, K.; Busch-Petersen, J.; Schwartz, S. I.; McLean, P. G. A selective CXCR2 receptor antagonist, SB656933-AAA reduces disease symptomology and ulceration in a DNBS rat model of colitis. Digestive Disease Weekly 2007, May 20 (Abs S1603).
-
(2007)
Digestive Disease Weekly
-
-
Kruidenier, L.1
Lione, L.A.2
McCleary, S.3
Vidgeon-Hart, P.M.4
Stretton, J.G.5
Ashmeade, X.6
Lee, K.7
Busch-Petersen, J.8
Schwartz, S.I.9
McLean, P.G.10
-
50
-
-
58149178530
-
Chemokine receptor antagonists: Overcoming development hurdles
-
Horuk, R. Chemokine receptor antagonists: overcoming development hurdles. Nat. Rev. Drug Discov., 2009, 8, 23-33.
-
(2009)
Nat. Rev. Drug Discov
, vol.8
, pp. 23-33
-
-
Horuk, R.1
-
51
-
-
79959340752
-
SB-656933, a novel CXCR2 selective antagonist, inhibits ex vivo neutrophil activation and ozone-induced airway inflammation in humans
-
Lazaar, A. L.; Sweeney, L. E.; MacDonald, A. J.; Alexis, N. E.; Chen, C.; Tal-Singer, R. SB-656933, a novel CXCR2 selective antagonist, inhibits ex vivo neutrophil activation and ozone-induced airway inflammation in humans. Br. J. Clin. Pharmacol., 2011, 72(2), 282-293.
-
(2011)
Br. J. Clin. Pharmacol
, vol.72
, Issue.2
, pp. 282-293
-
-
Lazaar, A.L.1
Sweeney, L.E.2
McDonald, A.J.3
Alexis, N.E.4
Chen, C.5
Tal-Singer, R.6
-
52
-
-
84876987955
-
Safety and early treatment effects of the CXCR2 receptor antagonist SB-656933 in patients with cystic fibrosis
-
Moss, R. B.; Mistry S. J.; Konstan M. W.; Pilewski, J. M.; Kerem, E.; Tal-Singer, R.; Lazaar, A. L. Safety and early treatment effects of the CXCR2 receptor antagonist SB-656933 in patients with cystic fibrosis. J. Cystic Fibr., 2013, 12(3), 241-248.
-
(2013)
J. Cystic Fibr
, vol.12
, Issue.3
, pp. 241-248
-
-
Moss, R.B.1
Mistry, S.J.2
Konstan, M.W.3
Pilewski, J.M.4
Kerem, E.5
Tal-Singer, R.6
Lazaar, A.L.7
-
53
-
-
84872246395
-
Assessment of potential drug interactions by characterization of human drug metabolism pathways using non-invasive bile sampling
-
Bloomer, J. C.; Nash, M.; Webb, A.; Miller, B. E.; Lazaar, A. L.; Beaumont, C.; Guiney, W. J. Assessment of potential drug interactions by characterization of human drug metabolism pathways using non-invasive bile sampling. Br. J. Pharmacol., 2012, 75(2), 488-496.
-
(2012)
Br. J. Pharmacol
, vol.75
, Issue.2
, pp. 488-496
-
-
Bloomer, J.C.1
Nash, M.2
Webb, A.3
Miller, B.E.4
Lazaar, A.L.5
Beaumont, C.6
Guiney, W.J.7
-
54
-
-
84893186080
-
The pharmacokinetics of conventional and bioenhanced tablet formulations of danirixin (GSK1325756) following oral administration in healthy, elderly, human volunteers
-
Miller, B. E.; Smart, K.; Mistry, S.; Ambery, C. L.; Bloomer, J. C.; Connolly, P.; Sanderson, D.; Shreeves, T.; Smith, R.; Lazaar, A. L. The pharmacokinetics of conventional and bioenhanced tablet formulations of danirixin (GSK1325756) following oral administration in healthy, elderly, human volunteers. Eur. J. Drug Metab. Pharmocokinet. 2014, 39(3), 173-181.
-
(2014)
Eur. J. Drug Metab. Pharmocokinet
, vol.39
, Issue.3
, pp. 173-181
-
-
Miller, B.E.1
Smart, K.2
Mistry, S.3
Ambery, C.L.4
Bloomer, J.C.5
Connolly, P.6
Sanderson, D.7
Shreeves, T.8
Smith, R.9
Lazaar, A.L.10
-
55
-
-
85067745770
-
-
[Accessed May 25, 2014]
-
Investigation of safety, tolerability, pharmacokinetics, pharmacodynamics, and clinical efficacy of oral danirixin in symptomatic COPD subjects with mild to moderate airflow limitation at risk for exacerbations (NCT02130193). http://clinicaltrials. gov/, [Accessed May 25, 2014].
-
Investigation of safety, tolerability, pharmacokinetics, pharmacodynamics, and clinical efficacy of oral danirixin in symptomatic COPD subjects with mild to moderate airflow limitation at risk for exacerbations (NCT02130193)
-
-
-
56
-
-
33745135836
-
Synthesis and structure-activity relationships of 3, 4-diaminocyclobut-3-ene-1, 2-dione CXCR2 antagonists
-
Merritt, J. R.; Rokosz, L. L.; Nelson, K. H.; Kaiser, B.; Wang, W.; Stauffer, T. M.; Ozgur, L. E.; Li, G.; Baldwin, J. J.; Dwyer, M. P.; Chao, J.; Taveras, A. Synthesis and structure-activity relationships of 3, 4-diaminocyclobut-3-ene-1, 2-dione CXCR2 antagonists. Bioorg. Med. Chem. Lett., 2006, 16(15), 4107-4110.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, Issue.15
, pp. 4107-4110
-
-
Merritt, J.R.1
Rokosz, L.L.2
Nelson, K.H.3
Kaiser, B.4
Wang, W.5
Stauffer, T.M.6
Ozgur, L.E.7
Li, G.8
Baldwin, J.J.9
Dwyer, M.P.10
Chao, J.11
Taveras, A.12
-
57
-
-
33746597153
-
Synthesis and characterization of a novel nonurea series of potent CXCR2 antagonists
-
New Orleans, LA, United States, March 23-27
-
McCleland, B. W.; Elliott, J. D.; Palovich, M. R.; Schmidt, D. M.; Sarau, H. M.; Foley, J. J.; Burman, M., Widdowson, K. Synthesis and characterization of a novel nonurea series of potent CXCR2 antagonists. 225th ACS National Meeting, New Orleans, LA, United States, March 23-27, 2003.
-
(2003)
225th ACS National Meeting
-
-
McCleland, B.W.1
Elliott, J.D.2
Palovich, M.R.3
Schmidt, D.M.4
Sarau, H.M.5
Foley, J.J.6
Burman, M.7
Widdowson, K.8
-
58
-
-
33847015952
-
Comparison of N, N'-diarylsquaramides and N, N'-diarylureas as antagonists of the CXCR2 chemokine receptor
-
McCleland, B. W.; Davis, R. S.; Palovich, M. R.; Widdowson, K. L.; Werner, M. L.; Burman, M.; Foley, J. J.; Schmidt, D. B.; Sarau, H. M.; Rogers, M.; Salyers, K. L.; Gorycki, P. D.; Roethke, T. J.; Stelman, G. J.; Azzarano, L. M.; Ward, K. W.; Busch-Petersen, J. Comparison of N, N'-diarylsquaramides and N, N'-diarylureas as antagonists of the CXCR2 chemokine receptor. Bioorg. Med. Chem. Lett., 2007, 17(6), 1713-1717.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, Issue.6
, pp. 1713-1717
-
-
McCleland, B.W.1
Davis, R.S.2
Palovich, M.R.3
Widdowson, K.L.4
Werner, M.L.5
Burman, M.6
Foley, J.J.7
Schmidt, D.B.8
Sarau, H.M.9
Rogers, M.10
Salyers, K.L.11
Gorycki, P.D.12
Roethke, T.J.13
Stelman, G.J.14
Azzarano, L.M.15
Ward, K.W.16
Busch-Petersen, J.17
-
59
-
-
33845963398
-
Discovery of 2-Hydroxy-N, N-dimethyl-3-{2-[[(R)-1-(5-methylfuran-2-yl)propyl]amino]-3, 4-dioxo-cyclobut-1-enylamino}benzamide (SCH 527123): A Potent, Orally Bioavailable CXCR2/CXCR1 Receptor Antagonist
-
Dwyer, M. P.; Yu, Y.; Chao, J.; Aki, C.; Chao, J.; Biju, P.; Girijavallabhan, V.; Rindgen, D.; Bond, R.; Mayer-Ezel, R.; Jakway, J.; Hipkin, R. W.; Fossetta, J.; Gonsiorek, W.; Bian, H.; Fan, X.; Terminelli, C.; Fine, J.; Lundell, D.; Merritt, J. R.; Rokosz, L. L.; Kaiser, B.; Li, G.; Wang, W.; Stauffer, T. M.; Ozgur. L. E.; Taveras, A. G. Discovery of 2-Hydroxy-N, N-dimethyl-3-{2-[[(R)-1-(5-methylfuran-2-yl)propyl]amino]-3, 4-dioxo-cyclobut-1-enylamino}benzamide (SCH 527123): A Potent, Orally Bioavailable CXCR2/CXCR1 Receptor Antagonist J. Med. Chem., 2006, 49(26), 7603-7603.
-
(2006)
J. Med. Chem
, vol.49
, Issue.26
, pp. 7603
-
-
Dwyer, M.P.1
Yu, Y.2
Chao, J.3
Aki, C.4
Chao, J.5
Biju, P.6
Girijavallabhan, V.7
Rindgen, D.8
Bond, R.9
Mayer-Ezel, R.10
Jakway, J.11
Hipkin, R.W.12
Fossetta, J.13
Gonsiorek, W.14
Bian, H.15
Fan, X.16
Terminelli, C.17
Fine, J.18
Lundell, D.19
Merritt, J.R.20
Rokosz, L.L.21
Kaiser, B.22
Li, G.23
Wang, W.24
Stauffer, T.M.25
Ozgur, L.E.26
Taveras, A.G.27
more..
-
60
-
-
34547114011
-
Pharmacological Characterization of Sch 527123, a Potent Allosteric CXCR1/CXCR2 Antagonist
-
Gonsiorek, W.; Fan, X.; Hesk, D.; Fossetta, J.; Qiu, H.; Jakway, J.; Billah, M.; Dwyer, M.; Chao, J.; Deno, G.; Taveras, A.; Lundell, D. J.; Hipkin, R. W. Pharmacological Characterization of Sch 527123, a Potent Allosteric CXCR1/CXCR2 Antagonist. J. Pharm. Exp. Ther., 2007, 322(2), 477-485.
-
(2007)
J. Pharm. Exp. Ther
, vol.322
, Issue.2
, pp. 477-485
-
-
Gonsiorek, W.1
Fan, X.2
Hesk, D.3
Fossetta, J.4
Qiu, H.5
Jakway, J.6
Billah, M.7
Dwyer, M.8
Chao, J.9
Deno, G.10
Taveras, A.11
Lundell, D.J.12
Hipkin, R.W.13
-
61
-
-
34547122884
-
A Novel, Orally Active CXCR1/CXCR2 Receptor Antagonist, Sch527123, Inhibits Neutrophil Recruitment, Mucus Production, and Goblet Cell Hyperplasia in Animal Models of Pulmonary Inflammation
-
Chapman, R. W.; Minnicozzi, M.; Celly, C. S.; Phillips, J. E.; Kung, T. T.; Hipkin, R. W.; Fan, X.; Rindgen, D.; Deno, G.; Bond, R.; Gonsiorek, W.; Billah, M. M.; Fine, J. S.; Hey, J. A. A Novel, Orally Active CXCR1/CXCR2 Receptor Antagonist, Sch527123, Inhibits Neutrophil Recruitment, Mucus Production, and Goblet Cell Hyperplasia in Animal Models of Pulmonary Inflammation. J. Pharm. Exp. Ther., 2007, 322(2), 486-493.
-
(2007)
J. Pharm. Exp. Ther
, vol.322
, Issue.2
, pp. 486-493
-
-
Chapman, R.W.1
Minnicozzi, M.2
Celly, C.S.3
Phillips, J.E.4
Kung, T.T.5
Hipkin, R.W.6
Fan, X.7
Rindgen, D.8
Deno, G.9
Bond, R.10
Gonsiorek, W.11
Billah, M.M.12
Fine, J.S.13
Hey, J.A.14
-
62
-
-
22444450887
-
Role of CXCR2 in cigarette smoke-induced inflammation
-
Thatcher, T. H.; McHugh, N. A.; Egan, R. W.; Chapman, R. W.; Hey, J. A.; Turner, C. K.; Redonnet, M. R.; Seweryniak, K. E.; Sime, P. J.; Phipps, R. P. Role of CXCR2 in cigarette smoke-induced inflammation. Am. J. Physiol. Lung Cell Mol. Physiol. 2005, 289(10), L322-L328.
-
(2005)
Am. J. Physiol. Lung Cell Mol. Physiol
, vol.289
, Issue.10
, pp. L322-L328
-
-
Thatcher, T.H.1
McHugh, N.A.2
Egan, R.W.3
Chapman, R.W.4
Hey, J.A.5
Turner, C.K.6
Redonnet, M.R.7
Seweryniak, K.E.8
Sime, P.J.9
Phipps, R.P.10
-
63
-
-
85067765594
-
-
WO 080053A1
-
Taveras, A. G.; Billah, M.; Lundell, D.; Kreutner, W.; Jakway, J.; Bober, L. A.; Chao, J.; Biju, P., Yu, Y. Combination treatments for chemokine-mediate diseases. WO 080053A1, 2003.
-
(2003)
Combination treatments for chemokine-mediate diseases
-
-
Taveras, A.G.1
Billah, M.2
Lundell, D.3
Kreutner, W.4
Jakway, J.5
Bober, L.A.6
Chao, J.7
Biju, P.8
Yu, Y.9
-
64
-
-
77951165310
-
SCH 527123, a novel CXCR2 antagonist, inhibits ozone-induced neutrophilia in healthy subjects
-
Holz, O.; Khalilieh, S.; Ludwig-Sengpiel, A.; Watz, H.; Stryszak, P.; Soni, P.; Tsai, M.; Sadeh, J.; Magnussen, H. SCH 527123, a novel CXCR2 antagonist, inhibits ozone-induced neutrophilia in healthy subjects. Eur. Respir. J., 2010, 35(3), 564-570.
-
(2010)
Eur. Respir. J
, vol.35
, Issue.3
, pp. 564-570
-
-
Holz, O.1
Khalilieh, S.2
Ludwig-Sengpiel, A.3
Watz, H.4
Stryszak, P.5
Soni, P.6
Tsai, M.7
Sadeh, J.8
Magnussen, H.9
-
65
-
-
20944448534
-
Validation of the human ozone challenge model as a tool for assessing anti-inflammatory drugs in early development
-
Holz, O.; Tal-Singer, R.; Kanniess, F.; Simpson, K. J.; Gibson, A.; Vessey, R. S. J.; Janicki, S.; Magnussen, H.; Jorres, R. A.; Richter, K. Validation of the human ozone challenge model as a tool for assessing anti-inflammatory drugs in early development. J. Clin. Pharm., 2005, 45(5), 498-503.
-
(2005)
J. Clin. Pharm
, vol.45
, Issue.5
, pp. 498-503
-
-
Holz, O.1
Tal-Singer, R.2
Kanniess, F.3
Simpson, K.J.4
Gibson, A.5
Vessey, R.S.J.6
Janicki, S.7
Magnussen, H.8
Jorres, R.A.9
Richter, K.10
-
66
-
-
84862519263
-
Safety and efficacy of a CXCR2 antagonist in patients with severe asthma and sputum neutrophils: A randomized, placebo-controlled clinical trial
-
Nair, P.; Gaga, M.; Zervas, E.; Alagha, K.; Hargreave, F. E.; O'Byrne, P. M.; Stryszak, P.; Gann, L.; Sadeh, J.; Chanez, P. Safety and efficacy of a CXCR2 antagonist in patients with severe asthma and sputum neutrophils: a randomized, placebo-controlled clinical trial. Clin. Exp. Allergy, 2012, 42(7), 1097-1103.
-
(2012)
Clin. Exp. Allergy
, vol.42
, Issue.7
, pp. 1097-1103
-
-
Nair, P.1
Gaga, M.2
Zervas, E.3
Alagha, K.4
Hargreave, F.E.5
O'Byrne, P.M.6
Stryszak, P.7
Gann, L.8
Sadeh, J.9
Chanez, P.10
-
67
-
-
84881521258
-
Humoral immunity and delayed hypersensitivity in healthy subjects treated for 30 days with MK-7123, a selective CXCR2 antagonist
-
Seiberling, M.; Kamtchoua, T.; Strysak, P; Ma, Y.; Langdon, R. B.; Khalilieh, S. Humoral immunity and delayed hypersensitivity in healthy subjects treated for 30 days with MK-7123, a selective CXCR2 antagonist. Int. Immunopharm., 2013, 17(2), 178-183.
-
(2013)
Int. Immunopharm
, vol.17
, Issue.2
, pp. 178-183
-
-
Seiberling, M.1
Kamtchoua, T.2
Strysak, P.3
Ma, Y.4
Langdon, R.B.5
Khalilieh, S.6
-
69
-
-
65249183876
-
Small-molecule antagonists for CXCR2 and CXCR1 inhibit human melanoma growth by decreasing tumor cell proliferation, survival, and angiogenesis
-
Singh, S.; Sadanandam, A.; Nannuru, K. C.; Varney, M. L.; Mayer-Ezell, R.; Bond, R.; Singh, R. K. Small-molecule antagonists for CXCR2 and CXCR1 inhibit human melanoma growth by decreasing tumor cell proliferation, survival, and angiogenesis. Clin. Cancer Res., 2009, 15(7), 2380-2386.
-
(2009)
Clin. Cancer Res
, vol.15
, Issue.7
, pp. 2380-2386
-
-
Singh, S.1
Sadanandam, A.2
Nannuru, K.C.3
Varney, M.L.4
Mayer-Ezell, R.5
Bond, R.6
Singh, R.K.7
-
70
-
-
78649630055
-
Small molecule antagonists for CXCR2 and CXCR1 inhibit human colon cancer liver metastases
-
Varney, M. L.; Singh, S.; Li, A.; Mayer-Ezell, R.; Bond, R.; Singh, R. K. Small molecule antagonists for CXCR2 and CXCR1 inhibit human colon cancer liver metastases Cancer Lett., 2011, 300(2), 180-188.
-
(2011)
Cancer Lett
, vol.300
, Issue.2
, pp. 180-188
-
-
Varney, M.L.1
Singh, S.2
Li, A.3
Mayer-Ezell, R.4
Bond, R.5
Singh, R.K.6
-
71
-
-
84860249964
-
The CXCR2 antagonist, SCH 527123, shows antitumor activity and sensitizes cells to oxaliplatin in preclinical colon cancer models
-
Ning, Y.; Labonte, M. J.; Zhang, W.; Bohanes, P. O.; Gerger, A.; Yang, D.; Benhaim, L.; Paez, D.; Rosenberg, D. O.; Nagulapalli Venkata, K. C.; Louie, S. G.; Petasis, N. A.; Ladner, R. D; Lenz, H.-J. The CXCR2 antagonist, SCH 527123, shows antitumor activity and sensitizes cells to oxaliplatin in preclinical colon cancer models. Mol. Cancer. Ther., 2012, 11(6), 1353-1364.
-
(2012)
Mol. Cancer. Ther
, vol.11
, Issue.6
, pp. 1353-1364
-
-
Ning, Y.1
Labonte, M.J.2
Zhang, W.3
Bohanes, P.O.4
Gerger, A.5
Yang, D.6
Benhaim, L.7
Paez, D.8
Rosenberg, D.O.9
Nagulapalli Venkata, K.C.10
Louie, S.G.11
Petasis, N.A.12
Ladner, R.D.13
Lenz, H.-J.14
-
72
-
-
34250197581
-
C(4)-Alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists
-
Chao, J.; Taveras, A. G.; Chao, J.; Aki, C.; Dwyer, M.; Yu, Y.; Purakkattle, B.; Rindgen, D.; Jakway, J.; Hipkin, W.; Fosetta, J.; Fan, X.; Lundell, D.; Fine, J.; Minnicozzi, M.; Phillips, J.; Merritt, J. R. C(4)-Alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists. Bioorg. Med. Chem. Lett., 2007, 17(13), 3778-3783.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, Issue.13
, pp. 3778-3783
-
-
Chao, J.1
Taveras, A.G.2
Chao, J.3
Aki, C.4
Dwyer, M.5
Yu, Y.6
Purakkattle, B.7
Rindgen, D.8
Jakway, J.9
Hipkin, W.10
Fosetta, J.11
Fan, X.12
Lundell, D.13
Fine, J.14
Minnicozzi, M.15
Phillips, J.16
Merritt, J.R.17
-
73
-
-
72949103055
-
Pharmacological targeting reveals distinct roles for CXCR2/CXCR1 and CCR2 in a mouse model of arthritis
-
Min, S. H.; Wang, Y.; Gonsiorek, W.; Anilkumar, G.; Kozlowski, J.; Lundell, D.; Fine, J. S.; Grant, E. P. Pharmacological targeting reveals distinct roles for CXCR2/CXCR1 and CCR2 in a mouse model of arthritis. Biochem. Biophys. Res. Comm., 2010, 391(1), 1080-1086.
-
(2010)
Biochem. Biophys. Res. Comm
, vol.391
, Issue.1
, pp. 1080-1086
-
-
Min, S.H.1
Wang, Y.2
Gonsiorek, W.3
Anilkumar, G.4
Kozlowski, J.5
Lundell, D.6
Fine, J.S.7
Grant, E.P.8
-
74
-
-
38949192884
-
Synthesis and structure-activity relationships of heteroaryl substituted-3, 4-diamino-3-cyclobut-3-ene-1, 2-dione CXCR2/CXCR1 receptor antagonists
-
Yu, Y.; Dwyer, M. P.; Chao, J.; Aki, C.; Chao, J.; Purakkattle, B.; Rindgen, D.; Bond, R.; Mayer-Ezel, R.; Jakway, J.; Qiu, H.; Hipkin, R. W.; Fossetta, J.; Gonsiorek, W.; Bian, H.; Fan, X.; Terminelli, C.; Fine, J.; Lundell, D.; Merritt, J. R.; He, Z.; Lai, G.; Wu, M.; Taveras, A. G. Synthesis and structure-activity relationships of heteroaryl substituted-3, 4-diamino-3-cyclobut-3-ene-1, 2-dione CXCR2/CXCR1 receptor antagonists. Bioorg. Med. Chem. Lett., 2008, 18(4), 1318-1322.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, Issue.4
, pp. 1318-1322
-
-
Yu, Y.1
Dwyer, M.P.2
Chao, J.3
Aki, C.4
Chao, J.5
Purakkattle, B.6
Rindgen, D.7
Bond, R.8
Mayer-Ezel, R.9
Jakway, J.10
Qiu, H.11
Hipkin, R.W.12
Fossetta, J.13
Gonsiorek, W.14
Bian, H.15
Fan, X.16
Terminelli, C.17
Fine, J.18
Lundell, D.19
Merritt, J.R.20
He, Z.21
Lai, G.22
Wu, M.23
Taveras, A.G.24
more..
-
75
-
-
40849126299
-
Synthesis and structure-activity relationships or new disubstituted phenylcontaining 3, 4-diamino-3-cyclobutene-1, 2-diones as CXCR2 receptor antagonists
-
Lai, G.; Merritt, J. R.; He, Z.; Feng, D.; Chao, J.; Czarniecki, M. F.; Rokosz, L. L.; Stauffer, T. M.; Rindgen, D.; Taveras, A. G. Synthesis and structure-activity relationships or new disubstituted phenylcontaining 3, 4-diamino-3-cyclobutene-1, 2-diones as CXCR2 receptor antagonists. Bioorg. Med. Chem. Lett., 2008, 18(6), 1864-1868.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, Issue.6
, pp. 1864-1868
-
-
Lai, G.1
Merritt, J.R.2
He, Z.3
Feng, D.4
Chao, J.5
Czarniecki, M.F.6
Rokosz, L.L.7
Stauffer, T.M.8
Rindgen, D.9
Taveras, A.G.10
-
76
-
-
60449110305
-
Fluoroalkyl RR-side chain containing 3, 4-diamino-cyclobutenediones as potent and orally bioavailable CXCR2-CXCR1 dual antagonists
-
Biju, P.; Taveras, A. G.; Dwyer, M. P.; Yu, Y.; Chao, J.; Hipkin, R. W.; Fan, X.; Rindgen, D.; Fine, J.; Lundell, D. Fluoroalkyl RR-side chain containing 3, 4-diamino-cyclobutenediones as potent and orally bioavailable CXCR2-CXCR1 dual antagonists. Bioorg. Med. Chem. Lett., 2009, 19(5), 1431-1433.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.5
, pp. 1431-1433
-
-
Biju, P.1
Taveras, A.G.2
Dwyer, M.P.3
Yu, Y.4
Chao, J.5
Hipkin, R.W.6
Fan, X.7
Rindgen, D.8
Fine, J.9
Lundell, D.10
-
77
-
-
69949177611
-
Design, synthesis, and evaluation of novel 3-amino-4-hydrazine-cyclobut-3-ene-1, 2-diones as potent and selective CXCR2 chemokine receptor antagonists
-
Liu, S.; Liu, Y; Wang, H.; Ding, Y.; Wu, H.; Dong, J.; Wong, A.; Chen, S.-H.; Li, G.; Chan, M.; Sawyer, N.; Gervais, F. G.; Henault, M.; Kargman, S.; Bedard, L. L.; Han, Y.; Friesen, R.; Lobell, R. B.; Stout, D. M. Design, synthesis, and evaluation of novel 3-amino-4-hydrazine-cyclobut-3-ene-1, 2-diones as potent and selective CXCR2 chemokine receptor antagonists. Bioorg. Med. Chem. Lett., 2009, 19(19), 5741-5745.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.19
, pp. 5741-5745
-
-
Liu, S.1
Liu, Y.2
Wang, H.3
Ding, Y.4
Wu, H.5
Dong, J.6
Wong, A.7
Chen, S.-H.8
Li, G.9
Chan, M.10
Sawyer, N.11
Gervais, F.G.12
Henault, M.13
Kargman, S.14
Bedard, L.L.15
Han, Y.16
Friesen, R.17
Lobell, R.B.18
Stout, D.M.19
-
78
-
-
67649909861
-
Diaminocyclobutenediones as potent and orally bioavailable CXCR2 receptor antagonists: SAR in the phenolic amide region
-
Aki, C.; Chao, J.; Ferreira, J. A.; Dwyer, M. P.; Yu, Y.; Chao, J.; Merritt, J. R.; He, Z.; Lai, G.; Wu, M.; Hipkin, R. W.; Fan, X.; Gonsiorek, W.; Fossetta, J.; Rindgen, D.; Fine, J.; Lundell, D.; Taveras, A. G.; Biju, P. Diaminocyclobutenediones as potent and orally bioavailable CXCR2 receptor antagonists: SAR in the phenolic amide region. Bioorg. Med. Chem. Lett., 2009, 19(15), 4446-4449.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.15
, pp. 4446-4449
-
-
Aki, C.1
Chao, J.2
Ferreira, J.A.3
Dwyer, M.P.4
Yu, Y.5
Chao, J.6
Merritt, J.R.7
He, Z.8
Lai, G.9
Wu, M.10
Hipkin, R.W.11
Fan, X.12
Gonsiorek, W.13
Fossetta, J.14
Rindgen, D.15
Fine, J.16
Lundell, D.17
Taveras, A.G.18
Biju, P.19
-
79
-
-
67650084297
-
Synthesis of functionalized hydroxyl-thiophene motifs as amido-and sulfonamide-phenol bioisosteres
-
Chao, J.; Taveras, A. G.; Aki, C. J. Synthesis of functionalized hydroxyl-thiophene motifs as amido-and sulfonamide-phenol bioisosteres. Tett. Lett., 2009, 50(35), 5005-5008.
-
(2009)
Tett. Lett
, vol.50
, Issue.35
, pp. 5005-5008
-
-
Chao, J.1
Taveras, A.G.2
Aki, C.J.3
-
80
-
-
33748792863
-
N, N'-Diarylcyanoguanidines as antagonists of the CXCR2 and CXCR1 chemokine receptors
-
Nie, H.; Widdowson, K. L.; Palovich, M. R.; Fu, W.; Elliott, J. D.; Bryan, D. L.; Burman, M.; Schmidt, D. B.; Foley, J. J.; Sarau, H. M.; Busch-Petersen, J. N, N'-Diarylcyanoguanidines as antagonists of the CXCR2 and CXCR1 chemokine receptors. Bioorg. Med. Chem. Lett., 2006, 16(21), 5513-5516.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, Issue.21
, pp. 5513-5516
-
-
Nie, H.1
Widdowson, K.L.2
Palovich, M.R.3
Fu, W.4
Elliott, J.D.5
Bryan, D.L.6
Burman, M.7
Schmidt, D.B.8
Foley, J.J.9
Sarau, H.M.10
Busch-Petersen, J.11
-
81
-
-
34250317293
-
3-Arylamino-2H-1, 2, 4-benzothiadiazin-5-ol 1, 1-dioxides as novel and selective CXCR2 antagonists
-
Wang, Y.; Busch-Petersen, J.; Wang, F.; Ma, L.; Fu, W.; Kerns, J. K.; Jin, J.; Palovich, M. R.; Shen, J.-K.; Burman, M.; Foley, J. J.; Schmidt, D. B.; Hunsberger, G. E.; Sarau, H. M.; Widdowson, K. L. 3-Arylamino-2H-1, 2, 4-benzothiadiazin-5-ol 1, 1-dioxides as novel and selective CXCR2 antagonists. Bioorg. Med. Chem. Lett., 2007, 17(14), 3864-3867.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, Issue.14
, pp. 3864-3867
-
-
Wang, Y.1
Busch-Petersen, J.2
Wang, F.3
Ma, L.4
Fu, W.5
Kerns, J.K.6
Jin, J.7
Palovich, M.R.8
Shen, J.-K.9
Burman, M.10
Foley, J.J.11
Schmidt, D.B.12
Hunsberger, G.E.13
Sarau, H.M.14
Widdowson, K.L.15
-
82
-
-
37549040581
-
3, 4-Diamino-2, 5-thiadiazole-1-oxides as potent CXCR2/CXCR1 antagonists
-
Biju, P.; Taveras, A.; Yu, Y.; Zheng, J.; Chao, J.; Rindgen, D.; Jakway, J.; Hipkin, R. W.; Fossetta, J.; Fan, X.; Fine, J.; Qiu, H.; Merritt, J. R.; Baldwin, J. J. 3, 4-Diamino-2, 5-thiadiazole-1-oxides as potent CXCR2/CXCR1 antagonists. Bioorg. Med. Chem. Lett., 2008, 18(1), 228-231.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, Issue.1
, pp. 228-231
-
-
Biju, P.1
Taveras, A.2
Yu, Y.3
Zheng, J.4
Chao, J.5
Rindgen, D.6
Jakway, J.7
Hipkin, R.W.8
Fossetta, J.9
Fan, X.10
Fine, J.11
Qiu, H.12
Merritt, J.R.13
Baldwin, J.J.14
-
83
-
-
77955638630
-
Synthesis and SAR investigation of 3, 4-diamino derivatives of thiadiazole-1-oxides as CXCR1-CXCR2 dual antagonists. Abstracts of Papers
-
Boston, MA, United States, August 19-23
-
Biju, P.; Yu, Y.; Aki, C.; Zheng, J.; Chao, J.; Dwyer, M. P.; Rindgen, D.; Bond, R.; Jakway, J.; Qiu, Hongchen; Hipkin, R. W.; Fossetta, J.; Gonsiorek, W.; Bian, H.; Fan, X.; Terminelli, C.; Fine, J.; Merritt, J. R.; He, Z.; Lai, G.; Wu, M.; Taveras, A. Synthesis and SAR investigation of 3, 4-diamino derivatives of thiadiazole-1-oxides as CXCR1-CXCR2 dual antagonists. Abstracts of Papers, 234th ACS National Meeting, Boston, MA, United States, August 19-23, 2007.
-
(2007)
234th ACS National Meeting
-
-
Biju, P.1
Yu, Y.2
Aki, C.3
Zheng, J.4
Chao, J.5
Dwyer, M.P.6
Rindgen, D.7
Bond, R.8
Jakway, J.9
Qiu, H.10
Hipkin, R.W.11
Fossetta, J.12
Gonsiorek, W.13
Bian, H.14
Fan, X.15
Terminelli, C.16
Fine, J.17
Merritt, J.R.18
He, Z.19
Lai, G.20
Wu, M.21
Taveras, A.22
more..
-
84
-
-
60449084221
-
3, 4-Diamino-1, 2, 5-thiadiazole as potent and selective CXCR2 antagonists
-
Biju, P.; Taveras, A. G.; Yu, Y.; Zheng, J.; Hipkin, R. W.; Fossetta, J.; Fan, X.; Fine, J.; Lundell, D. 3, 4-Diamino-1, 2, 5-thiadiazole as potent and selective CXCR2 antagonists. Bioorg. Med. Chem. Lett., 2009, 19(5), 1434-1437.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.5
, pp. 1434-1437
-
-
Biju, P.1
Taveras, A.G.2
Yu, Y.3
Zheng, J.4
Hipkin, R.W.5
Fossetta, J.6
Fan, X.7
Fine, J.8
Lundell, D.9
-
85
-
-
5744249662
-
Novel Pyrimidine-based CXCR2 antagonists
-
Anon. Novel Pyrimidine-based CXCR2 antagonists. Exp. Opin. Ther. Pat., 2004, 14(10), 1507-1510.
-
(2004)
Exp. Opin. Ther. Pat
, vol.14
, Issue.10
, pp. 1507-1510
-
-
Anon1
-
86
-
-
30344436368
-
Hit-to-Lead studies: The discovery of potent, orally bioavailable thiazolopyrimidine CXCR2 receptor antagonists
-
Baxter, A.; Cooper, A.; Kinchin, E.; Moakes, K.; Unitt, J.; Wallace, A. Hit-to-Lead studies: The discovery of potent, orally bioavailable thiazolopyrimidine CXCR2 receptor antagonists. Bioorg. Med. Chem. Lett., 2006, 16(4), 960-963.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, Issue.4
, pp. 960-963
-
-
Baxter, A.1
Cooper, A.2
Kinchin, E.3
Moakes, K.4
Unitt, J.5
Wallace, A.6
-
87
-
-
34247366027
-
SAR studies on thiazolo[4, 5-d]pyrimidine based CXCR2 antagonists involving a novel tandem displacement reaction
-
Hunt, F.; Austin, C.; Austin, R.; Bonnert, R.; Cage, P.; Christie, J.; Christie, M.; Dixon, C.; Hill, S.; Jewell, R.; Martin, I.; Robinson, D.; Willis, P. SAR studies on thiazolo[4, 5-d]pyrimidine based CXCR2 antagonists involving a novel tandem displacement reaction. Bioorg. Med. Chem. Lett., 2007, 17(10), 2731-2734.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, Issue.10
, pp. 2731-2734
-
-
Hunt, F.1
Austin, C.2
Austin, R.3
Bonnert, R.4
Cage, P.5
Christie, J.6
Christie, M.7
Dixon, C.8
Hill, S.9
Jewell, R.10
Martin, I.11
Robinson, D.12
Willis, P.13
-
88
-
-
85067779159
-
Structure activity relationships of a series of thiazolopyrimidine based CXCR2 antagonists with additional CCR2b activity. Abstracts of Papers
-
Boston, MA, United States, August 19-23
-
Walters, Iain A. S. Structure activity relationships of a series of thiazolopyrimidine based CXCR2 antagonists with additional CCR2b activity. Abstracts of Papers, 234th ACS National Meeting, Boston, MA, United States, August 19-23, 2007.
-
(2007)
234th ACS National Meeting
-
-
Walters, I.A.S.1
-
89
-
-
38349018273
-
Evaluation of a series of bicyclic CXCR2 antagonists
-
Walters, I.; Austin, C.; Austin, R.; Bonnert, R.; Cage, P.; Christie, M.; Ebden, M.; Gardiner, S.; Grahames, C.; Hill, S.; Hunt, F.; Jewell, R.; Lewis, S.; Martin, I.; Nicholls, D.; Robinson, D. Evaluation of a series of bicyclic CXCR2 antagonists. Bioorg. Med. Chem. Lett., 2008, 18(2), 798-803.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, Issue.2
, pp. 798-803
-
-
Walters, I.1
Austin, C.2
Austin, R.3
Bonnert, R.4
Cage, P.5
Christie, M.6
Ebden, M.7
Gardiner, S.8
Grahames, C.9
Hill, S.10
Hunt, F.11
Jewell, R.12
Lewis, S.13
Martin, I.14
Nicholls, D.15
Robinson, D.16
-
90
-
-
54349117013
-
Identification of a putative intracellular allosteric antagonist binding-site in the CXC chemokines receptors 1 and 2
-
Nicholls, D. J.; Tomkinson, N. P.; Wiley, K. E.; Brammel, A.; Bowers, L.; Grahames, C.; Gaw, A.; Meghani, P.; Shelton, P.; Wright, T. J.; Mallinder, P. R. Identification of a putative intracellular allosteric antagonist binding-site in the CXC chemokines receptors 1 and 2. Mol. Pharmacol., 2008, 74(5), 1193-1202.
-
(2008)
Mol. Pharmacol
, vol.74
, Issue.5
, pp. 1193-1202
-
-
Nicholls, D.J.1
Tomkinson, N.P.2
Wiley, K.E.3
Brammel, A.4
Bowers, L.5
Grahames, C.6
Gaw, A.7
Meghani, P.8
Shelton, P.9
Wright, T.J.10
Mallinder, P.R.11
-
91
-
-
16344389787
-
Drugs in Clinical Development for Chronic Obstructive Pulmonary Disease
-
Molfino, N. A. Drugs in Clinical Development for Chronic Obstructive Pulmonary Disease. Respiration, 2005, 72(1), 105-112.
-
(2005)
Respiration
, vol.72
, Issue.1
, pp. 105-112
-
-
Molfino, N.A.1
-
92
-
-
34249045684
-
Emerging trends in the therapy of COPD: Novel anti-inflammatory agents in clinical development
-
Fitzgerald, M. F.; Fox, J. C. Emerging trends in the therapy of COPD: novel anti-inflammatory agents in clinical development. Drug Disc. Today 2007, 12(11-12), 479-486.
-
(2007)
Drug Disc. Today
, vol.12
, Issue.11-12
, pp. 479-486
-
-
Fitzgerald, M.F.1
Fox, J.C.2
-
93
-
-
32644452768
-
Inhaled endotoxin in healthy human subjects: A dose-related study on systemic effects and peripheral CD4+ and CD8+ T cells
-
Loh, L. C.; Vyas, B.; Kanabar, V.; Kemeny, D. M.; O'Connor, B. J. Inhaled endotoxin in healthy human subjects: A dose-related study on systemic effects and peripheral CD4+ and CD8+ T cells. Respir. Med., 2006, 100(3), 519-528.
-
(2006)
Respir. Med
, vol.100
, Issue.3
, pp. 519-528
-
-
Loh, L.C.1
Vyas, B.2
Kanabar, V.3
Kemeny, D.M.4
O'Connor, B.J.5
-
94
-
-
84858333080
-
Airway inflammation evaluated in a human nasal lipopolysaccharide challenge model by investigating the effect of a CXCR2 inhibitor
-
Virtala, R.; Ekman, A. K.; Jansson, L; Westin, U.; Cardell, L. O. Airway inflammation evaluated in a human nasal lipopolysaccharide challenge model by investigating the effect of a CXCR2 inhibitor. Clin. Exp. Allergy, 2011, 42(4), 590-596.
-
(2011)
Clin. Exp. Allergy
, vol.42
, Issue.4
, pp. 590-596
-
-
Virtala, R.1
Ekman, A.K.2
Jansson, L.3
Westin, U.4
Cardell, L.O.5
-
95
-
-
84890290253
-
Inhibition of LPSinduced airway neutrophilic inflammation in healthy volunteers with an oral CXCR2 antagonist
-
Leaker, B. R.; Barnes, P. J.; O'Connor, B. Inhibition of LPSinduced airway neutrophilic inflammation in healthy volunteers with an oral CXCR2 antagonist. Respiratory Res., 2013, 14, 137/1-137/9.
-
(2013)
Respiratory Res
, vol.14
, pp. 137/1-137/9
-
-
Leaker, B.R.1
Barnes, P.J.2
O'Connor, B.3
-
96
-
-
84871500153
-
Evidence on the identity of the CXCR2 antagonist AZD-5069
-
Norman P. Evidence on the identity of the CXCR2 antagonist AZD-5069. Expert Opin. Ther. Patents, 2013, 23(1), 113-117.
-
(2013)
Expert Opin. Ther. Patents
, vol.23
, Issue.1
, pp. 113-117
-
-
Norman, P.1
-
97
-
-
85067769519
-
-
(NCT01704495, NIMBUS)., [Accessed May 25, 2014]
-
A phase II study to evaluate the efficacy, safety, and tolerability of AZD5069 in patients with uncontrolled persistent asthma (NCT01704495, NIMBUS). http://clinicaltrials. gov/, [Accessed May 25, 2014].
-
A phase II study to evaluate the efficacy, safety, and tolerability of AZD5069 in patients with uncontrolled persistent asthma
-
-
-
98
-
-
84891482449
-
The discovery of potent, orally bioavailable pyrazolo and triazolopyrimidine CXCR2 receptor antagonists
-
Porter, D. W.; Bradley, M.; Brown, Z.; Canova, R.; Charlton, S.; Cox, B.; Hunt, P.; Lolarik, D.; Lewis, S.; O'Connor, D.; Reilly, J.; Spanka, C.; Tedaldi, L.; Watson, S. J.; Watson, S. J.; Wermuth, R.; Press, N. J. The discovery of potent, orally bioavailable pyrazolo and triazolopyrimidine CXCR2 receptor antagonists. Bioorg. Med. Chem. Lett., 2014, 24(1), 72-76.
-
(2014)
Bioorg. Med. Chem. Lett
, vol.24
, Issue.1
, pp. 72-76
-
-
Porter, D.W.1
Bradley, M.2
Brown, Z.3
Canova, R.4
Charlton, S.5
Cox, B.6
Hunt, P.7
Lolarik, D.8
Lewis, S.9
O'Connor, D.10
Reilly, J.11
Spanka, C.12
Tedaldi, L.13
Watson, S.J.14
Watson, S.J.15
Wermuth, R.16
Press, N.J.17
-
99
-
-
84904055279
-
The discovery of potent, orally bioavailable pyrimidine-5-carbonitrile-6-alkyl CXCR2 receptor antagonists
-
Porter, D. W.; Bradley, M.; Brown, Z.; Charlton, S. J.; Cox, B.; Hunt, P.; Janus, D.; Lewis, S.; Oakley, P.; O'Connor, D.; Reilly, J.; Smith, N.; Press, N. J. The discovery of potent, orally bioavailable pyrimidine-5-carbonitrile-6-alkyl CXCR2 receptor antagonists. Bioorg. Med. Chem. Lett. 2014, 24(15), 3285-3290.
-
(2014)
Bioorg. Med. Chem. Lett
, vol.24
, Issue.15
, pp. 3285-3290
-
-
Porter, D.W.1
Bradley, M.2
Brown, Z.3
Charlton, S.J.4
Cox, B.5
Hunt, P.6
Janus, D.7
Lewis, S.8
Oakley, P.9
O'Connor, D.10
Reilly, J.11
Smith, N.12
Press, N.J.13
-
100
-
-
77949861512
-
A common intracellular allosteric binding site for antagonists of the CXCR2 receptor
-
Salchow, K.; Bond, M. E.; Evans, S. C.; Press, N. J.; Charlton, S. J.; Hunt, P. A.; Bradley, M. E. A common intracellular allosteric binding site for antagonists of the CXCR2 receptor. Br. J. Pharm. 2010, 159(7), 1429-1439.
-
(2010)
Br. J. Pharm
, vol.159
, Issue.7
, pp. 1429-1439
-
-
Salchow, K.1
Bond, M.E.2
Evans, S.C.3
Press, N.J.4
Charlton, S.J.5
Hunt, P.A.6
Bradley, M.E.7
-
101
-
-
80055086869
-
Attenuation of leukocyte recruitment via CXCR1/2 inhibition stops the progression of PAH in mice with genetic ablation of endothelial BMPR-II
-
Burton, V. J.; Holmes, A. M.; Ciuclan, L. I.; Robinson, A.; Roger, J. S.; Jarai, G.; Pearce, A. C.; Budd, D. C. Attenuation of leukocyte recruitment via CXCR1/2 inhibition stops the progression of PAH in mice with genetic ablation of endothelial BMPR-II. Blood, 2011, 118(17), 4750-4758.
-
(2011)
Blood
, vol.118
, Issue.17
, pp. 4750-4758
-
-
Burton, V.J.1
Holmes, A.M.2
Ciuclan, L.I.3
Robinson, A.4
Roger, J.S.5
Jarai, G.6
Pearce, A.C.7
Budd, D.C.8
-
102
-
-
33645885315
-
Imidazolylpyrimidine based CXCR2 chemokine receptor antagonists
-
Ho, K.-K.; Auld, D. S.; Bohnstedt, A. C.; Conti, P.; Dokter, W.; Erickson, S.; Feng, D.; Inglese, J.; Kingsbury, C.; Kultgen, S. G.; Liu, R.-Q.; Masterson, C. M.; Ohlmeyer, M.; Rong, Y.; Rooseboom, M.; Roughton, A.; Samama, P.; Smit, M.-J.; Son, E.; Van der Louw, J.; Vogel, G.; Webb, M.; Wijkmans, J.; You, M. Imidazolylpyrimidine based CXCR2 chemokine receptor antagonists. Bioorg. Med. Chem. Lett., 2006, 16(10), 2724-2728.
-
(2006)
Bioorg. Med. Chem. Lett
, vol.16
, Issue.10
, pp. 2724-2728
-
-
Ho, K.-K.1
Auld, D.S.2
Bohnstedt, A.C.3
Conti, P.4
Dokter, W.5
Erickson, S.6
Feng, D.7
Inglese, J.8
Kingsbury, C.9
Kultgen, S.G.10
Liu, R.-Q.11
Masterson, C.M.12
Ohlmeyer, M.13
Rong, Y.14
Rooseboom, M.15
Roughton, A.16
Samama, P.17
Smit, M.-J.18
Son, E.19
Van der Louw, J.20
Vogel, G.21
Webb, M.22
Wijkmans, J.23
You, M.24
more..
-
103
-
-
65649101821
-
Nonpetidergic allosteric antagonists differently bind to the CXCR2 receptor
-
Kruijf, P.; Heteren, J.; Lim, H. D.; Conti, P. G. M.; Van der Lee, M. M. C.; Bosch, L.; Ho, K.-K.; Auld, D.; Ohlmeyer, M.; Smit, M. J.; Wijkmans, J. C. H. M.; Zaman, G. J. R.; Smit, M. J.; Leurs, R. Nonpetidergic allosteric antagonists differently bind to the CXCR2 receptor. J. Pharmacol. Exp. Ther., 2009, 329(2), 783-790.
-
(2009)
J. Pharmacol. Exp. Ther
, vol.329
, Issue.2
, pp. 783-790
-
-
Kruijf, P.1
Heteren, J.2
Lim, H.D.3
Conti, P.G.M.4
Van der Lee, M.M.C.5
Bosch, L.6
Ho, K.-K.7
Auld, D.8
Ohlmeyer, M.9
Smit, M.J.10
Wijkmans, J.C.H.M.11
Zaman, G.J.R.12
Smit, M.J.13
Leurs, R.14
-
104
-
-
81555222803
-
Identification of a novel allosteric binding site in the CXCR2 chemokine receptor
-
Kruijf, P.; Lim, H. D.; Roumen, L.; Renjaan, V. A.; Zhao, J.; Webb. M. L.; Auld, D. S.; Wijkmans, J. C. H. M.; Zaman, G. J. R.; Smit, M. J.; de Graaf, C.; Leurs, R. Identification of a novel allosteric binding site in the CXCR2 chemokine receptor. Mol. Pharmacol., 2011, 80(6), 1108-1118.
-
(2011)
Mol. Pharmacol
, vol.80
, Issue.6
, pp. 1108-1118
-
-
Kruijf, P.1
Lim, H.D.2
Roumen, L.3
Renjaan, V.A.4
Zhao, J.5
Webb, M.L.6
Auld, D.S.7
Wijkmans, J.C.H.M.8
Zaman, G.J.R.9
Smit, M.J.10
de Graaf, C.11
Leurs, R.12
-
105
-
-
0035371366
-
More here Selective inhibition of interleukin-8-induced neutrophil chemotaxis by ketoprofen isomers
-
Bizzarri, C.; Pagliei, S.; Brandolini, L.; more here Selective inhibition of interleukin-8-induced neutrophil chemotaxis by ketoprofen isomers. Biochem. Pharmacol., 2001, 61(11), 1429-1437.
-
(2001)
Biochem. Pharmacol
, vol.61
, Issue.11
, pp. 1429-1437
-
-
Bizzarri, C.1
Pagliei, S.2
Brandolini, L.3
-
106
-
-
21244454119
-
2-Arylpropionic CXC Chemokine Receptor 1 (CXCR1) Ligands as Novel Noncompetitive CXCL8 Inhibitors
-
Allegretti, M.; Bertini, R.; Cesta, M. C.; Bizzarri, C.; Bitondo, R. D.; Cioccio, V. D.; Galliera, E.; Berdini, V.; Topai, A.; Zampella, G.; Russo, V.; Bello, N. D.; Nano, G.; Nicolini, L.; Locati, M.; Fantucci, P.; Florio, S.; Colotta, F. 2-Arylpropionic CXC Chemokine Receptor 1 (CXCR1) Ligands as Novel Noncompetitive CXCL8 Inhibitors. J. Med. Chem. 2005, 48(13), 4312-4331.
-
(2005)
J. Med. Chem
, vol.48
, Issue.13
, pp. 4312-4331
-
-
Allegretti, M.1
Bertini, R.2
Cesta, M.C.3
Bizzarri, C.4
Bitondo, R.D.5
Cioccio, V.D.6
Galliera, E.7
Berdini, V.8
Topai, A.9
Zampella, G.10
Russo, V.11
Bello, N.D.12
Nano, G.13
Nicolini, L.14
Locati, M.15
Fantucci, P.16
Florio, S.17
Colotta, F.18
-
107
-
-
4143050328
-
Noncompetitive allosteric inhibitors of the inflammatory chemokine receptors CXCR1 and CXCR2: Prevention of reperfusion injury
-
Bertini, R.; Allegretti, M.; Bizzarri, C.; Moriconi, A.; Locati, M.; Zampella, G.; Cervellera, M. N.; Di Cioccio, V.; Cesta, M. C.; Galliera, E.; Martinez, F. O.; Di Bitondo, R.; Troiani, G.; Sabbatini, V.; D'Anniballe, G.; Anacardio, R.; Cutrin, J. C.; Cavalieri, B.; Mainiero, F.; Strippoli, R.; Villa, P.; Di Girolamo, M.; Martin, F.; Gentile, M.; Santoni, A.; Corda, D.; Poli, G.; Mantovani, A.; Ghezzi, P.; Colotta, F. Noncompetitive allosteric inhibitors of the inflammatory chemokine receptors CXCR1 and CXCR2: prevention of reperfusion injury. Proc. Natl. Acad. Sci. USA, 2004, 101(24), 11791-11796.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, Issue.24
, pp. 11791-11796
-
-
Bertini, R.1
Allegretti, M.2
Bizzarri, C.3
Moriconi, A.4
Locati, M.5
Zampella, G.6
Cervellera, M.N.7
Di Cioccio, V.8
Cesta, M.C.9
Galliera, E.10
Martinez, F.O.11
Di Bitondo, R.12
Troiani, G.13
Sabbatini, V.14
D'Anniballe, G.15
Anacardio, R.16
Cutrin, J.C.17
Cavalieri, B.18
Mainiero, F.19
Strippoli, R.20
Villa, P.21
Di Girolamo, M.22
Martin, F.23
Gentile, M.24
Santoni, A.25
Corda, D.26
Poli, G.27
Mantovani, A.28
Ghezzi, P.29
Colotta, F.30
more..
-
108
-
-
19944429545
-
Inhibition of interleukin-8 (CXCL8/IL-8) responses by repertaxin, a new inhibitor of the chemokine receptors CXCR1 and CXCR2
-
Casilli, F.; Bianchini, A.; Gloaguen, I.; Biordi, L.; Alesse, E.; Festuccia, C.; Cavalieri, B.; Strippoli, R.; Cervellera, M. N.; Di Bitondo, R.; Ferretti, E.; Mainiero, F.; Bizzarri, C.; Colotta, F.; Bertini, R. Inhibition of interleukin-8 (CXCL8/IL-8) responses by repertaxin, a new inhibitor of the chemokine receptors CXCR1 and CXCR2. Biochem. Pharmacol. 2005, 69(3), 385-394.
-
(2005)
Biochem. Pharmacol
, vol.69
, Issue.3
, pp. 385-394
-
-
Casilli, F.1
Bianchini, A.2
Gloaguen, I.3
Biordi, L.4
Alesse, E.5
Festuccia, C.6
Cavalieri, B.7
Strippoli, R.8
Cervellera, M.N.9
Di Bitondo, R.10
Ferretti, E.11
Mainiero, F.12
Bizzarri, C.13
Colotta, F.14
Bertini, R.15
-
109
-
-
27444442682
-
Neutrophil recruitment in the reperfused-injured rat liver was effectively attenuated by repertaxin, a novel allosteric non-competitive inhibitor of CXCL8 receptors: A therapeutic approach for the treatment of post-ischemic hepatic syndromes
-
Cavalieri, B.; Mosca, M.; Ramadori, P.; Perrelli, M.-G.; De Simone, L.; Colotta, F. Bertini, R.; Poli, G.; Cutrin, J. C. Neutrophil recruitment in the reperfused-injured rat liver was effectively attenuated by repertaxin, a novel allosteric non-competitive inhibitor of CXCL8 receptors: A therapeutic approach for the treatment of post-ischemic hepatic syndromes. Int. J. Immunopath. Pharm., 2005, 18(3), 475-486.
-
(2005)
Int. J. Immunopath. Pharm
, vol.18
, Issue.3
, pp. 475-486
-
-
Cavalieri, B.1
Mosca, M.2
Ramadori, P.3
Perrelli, M.-G.4
De Simone, L.5
Colotta, F.6
Bertini, R.7
Poli, G.8
Cutrin, J.C.9
-
110
-
-
17744382390
-
Inhibition of the chemokine receptor CXCR2 prevents kidney graft function deterioration due to ischemia/reperfusion
-
Cugini, D.; Azzollini, N.; Gagliardini, E.; Cassis, P.; Bertini, R.; Colotta, F.; Noris, M.; Remuzzi, G.; Benigni, A. Inhibition of the chemokine receptor CXCR2 prevents kidney graft function deterioration due to ischemia/reperfusion. Kidney Int., 2005, 67(5), 1753-1761.
-
(2005)
Kidney Int
, vol.67
, Issue.5
, pp. 1753-1761
-
-
Cugini, D.1
Azzollini, N.2
Gagliardini, E.3
Cassis, P.4
Bertini, R.5
Colotta, F.6
Noris, M.7
Remuzzi, G.8
Benigni, A.9
-
111
-
-
17044427879
-
Neuroprotection with the CXCL8 inhibitor repertaxin in transient brain ischemia
-
Garau, A.; Bertini, R.; Colotta, F.; Casilli, F.; Bigini, P.; Cagnotto, A.; Mennini, T.; Ghezzi, P.; Villa, P. Neuroprotection with the CXCL8 inhibitor repertaxin in transient brain ischemia. Cytokine 2005, 30(3), 125-131.
-
(2005)
Cytokine
, vol.30
, Issue.3
, pp. 125-131
-
-
Garau, A.1
Bertini, R.2
Colotta, F.3
Casilli, F.4
Bigini, P.5
Cagnotto, A.6
Mennini, T.7
Ghezzi, P.8
Villa, P.9
-
112
-
-
4644280675
-
Repertaxin, a novel inhibitor of rat CXCR2 function, inhibits inflammatory responses that follow intestinal ischaemia and reperfusion injury
-
Souza, D. G.; Bertini, R.; Vieira, A. T.; Cunha, F. Q.; Poole, S.; Allegretti, M.; Colotta, F.; Teixeira, M. M. Repertaxin, a novel inhibitor of rat CXCR2 function, inhibits inflammatory responses that follow intestinal ischaemia and reperfusion injury. Br. J. Pharmacol., 2004, 143(1), 132-142.
-
(2004)
Br. J. Pharmacol
, vol.143
, Issue.1
, pp. 132-142
-
-
Souza, D.G.1
Bertini, R.2
Vieira, A.T.3
Cunha, F.Q.4
Poole, S.5
Allegretti, M.6
Colotta, F.7
Teixeira, M.M.8
-
113
-
-
34548082787
-
Reparixin, an inhibitor of CXCR2 function, attenuates inflammatory responses and promotes recovery of function after traumatic lesion to the spinal cord
-
Gorio, A.; Madaschi, L.; Zadra, G.; Marfia, G.; Cavalieri, B.; Bertini, R.; Di Giulio, A. M. Reparixin, an inhibitor of CXCR2 function, attenuates inflammatory responses and promotes recovery of function after traumatic lesion to the spinal cord. J. Pharmacol. Exp. Ther., 2007, 322(3), 973-981.
-
(2007)
J. Pharmacol. Exp. Ther
, vol.322
, Issue.3
, pp. 973-981
-
-
Gorio, A.1
Madaschi, L.2
Zadra, G.3
Marfia, G.4
Cavalieri, B.5
Bertini, R.6
Di Giulio, A.M.7
-
114
-
-
33947717211
-
Reparixin, a specific interleukin-8 inhibitor, has no effects on inflammation during endotoxemia
-
Leitner, J. M.; Mayr, F. B.; Firbas, C.; Spiel, A. O.; Steinlechner, B.; Novellini, R.; Jilma, B. Reparixin, a specific interleukin-8 inhibitor, has no effects on inflammation during endotoxemia. Int. J. Immunopath. Pharmacol., 2007, 20(1), 25-36.
-
(2007)
Int. J. Immunopath. Pharmacol
, vol.20
, Issue.1
, pp. 25-36
-
-
Leitner, J.M.1
Mayr, F.B.2
Firbas, C.3
Spiel, A.O.4
Steinlechner, B.5
Novellini, R.6
Jilma, B.7
-
117
-
-
34548133600
-
Design of noncompetitive interleukin-8 inhibitors acting on CXCR1 and CXCR2
-
Moriconi, A.; Cesta, M. C.; Cervellera, M. N.; Aramini, A.; Coniglio, S.; Colagioia, S.; Beccari, A. R.; Bizzarri, C.; Cavicchia, M. R.; Locati, M.; Galliera, E.; Di Benedetto, P.; Vigilante, P.; Bertini, R.; Allegretti, M. Design of noncompetitive interleukin-8 inhibitors acting on CXCR1 and CXCR2. J. Med. Chem., 2007, 50(15), 3984-4002.
-
(2007)
J. Med. Chem
, vol.50
, Issue.15
, pp. 3984-4002
-
-
Moriconi, A.1
Cesta, M.C.2
Cervellera, M.N.3
Aramini, A.4
Coniglio, S.5
Colagioia, S.6
Beccari, A.R.7
Bizzarri, C.8
Cavicchia, M.R.9
Locati, M.10
Galliera, E.11
Di Benedetto, P.12
Vigilante, P.13
Bertini, R.14
Allegretti, M.15
-
118
-
-
67650155472
-
Structure-activity relationship of novel phenylacetic CXCR1 inhibitors
-
Sablone, M. R.; Cesta, M. C.; Moriconi, A.; Aramini, A.; Bizzarri, C.; Di Giacinto, C.; Di Bitondo, R.; Gloaguen, I.; Aschi, M.; Crucianelli, M.; Bertini, R.; Allegretti, M. Structure-activity relationship of novel phenylacetic CXCR1 inhibitors. Bioorg. Med. Chem. Lett., 2009, 19(15), 4026-4030.
-
(2009)
Bioorg. Med. Chem. Lett
, vol.19
, Issue.15
, pp. 4026-4030
-
-
Sablone, M.R.1
Cesta, M.C.2
Moriconi, A.3
Aramini, A.4
Bizzarri, C.5
Di Giacinto, C.6
Di Bitondo, R.7
Gloaguen, I.8
Aschi, M.9
Crucianelli, M.10
Bertini, R.11
Allegretti, M.12
-
119
-
-
80054718887
-
Aryltriflates as a neglected moiety in medicinal chemistry: A case study from a lead optimization of CXCL8 inhibitors
-
Moriconi, A.; Bigogno, C; Bianchini, G; Caligiuri, A.; Resconi, A.; Dondio, M. G.; D'Annibelle, G.; Allegretti, M. Aryltriflates as a neglected moiety in medicinal chemistry: A case study from a lead optimization of CXCL8 inhibitors. ACS Med. Chem. Lett., 2011, 2(10), 768-773.
-
(2011)
ACS Med. Chem. Lett
, vol.2
, Issue.10
, pp. 768-773
-
-
Moriconi, A.1
Bigogno, C.2
Bianchini, G.3
Caligiuri, A.4
Resconi, A.5
Dondio, M.G.6
D'Annibelle, G.7
Allegretti, M.8
-
120
-
-
83755220076
-
Receptor binding mode and pharmacological characterization of a potent and selective dual CXCR1/CXCR2 non-competitive allosteric inhibitor
-
Bertini, R.; Barcelos, L. S.; Beccari, A. R.; Cavalieri, B.; Moriconi, A.; Bizzarri, C.; Di Benedetto, P.; Di Giacinto, C.; Gloaguen, I.; Galliera, E.; Corsi, M. M.; Russo, R. C.; Andrade, S. P.; Cesta, M. C.; Nano, G.; Aramini, A.; Cutrin, J. C.; Locati, M.; Allegretti, M.; Texixeira, M. M. Receptor binding mode and pharmacological characterization of a potent and selective dual CXCR1/CXCR2 non-competitive allosteric inhibitor. Brit. J. Pharm., 2012, 165(2), 436-454.
-
(2012)
Brit. J. Pharm
, vol.165
, Issue.2
, pp. 436-454
-
-
Bertini, R.1
Barcelos, L.S.2
Beccari, A.R.3
Cavalieri, B.4
Moriconi, A.5
Bizzarri, C.6
Di Benedetto, P.7
Di Giacinto, C.8
Gloaguen, I.9
Galliera, E.10
Corsi, M.M.11
Russo, R.C.12
Andrade, S.P.13
Cesta, M.C.14
Nano, G.15
Aramini, A.16
Cutrin, J.C.17
Locati, M.18
Allegretti, M.19
Texixeira, M.M.20
more..
-
121
-
-
0035939346
-
Nicotinamide N-oxides as CXCR2 antagonists
-
Cutshall, N. S.; Ursino, R.; Kucera, K. A.; Latham, J.; Ihle, N. C. Nicotinamide N-oxides as CXCR2 antagonists. Bioorg. Med. Chem. Lett. 2001, 11(14), 1951-1954.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, Issue.14
, pp. 1951-1954
-
-
Cutshall, N.S.1
Ursino, R.2
Kucera, K.A.3
Latham, J.4
Ihle, N.C.5
-
122
-
-
0037013434
-
Nicotinanilides as inhibitors of neutrophil chemotaxis
-
Cutshall, N. S.; Kucera, K. A.; Ursino, R.; Latham, J.; Ihle, N. C. Nicotinanilides as inhibitors of neutrophil chemotaxis. Bioorg. Med. Chem. Lett., 2002, 12(11), 1951-1954.
-
(2002)
Bioorg. Med. Chem. Lett
, vol.12
, Issue.11
, pp. 1951-1954
-
-
Cutshall, N.S.1
Kucera, K.A.2
Ursino, R.3
Latham, J.4
Ihle, N.C.5
-
123
-
-
73949152536
-
Nicotinamide glycolates antagonize CXCR2 activity through and intracellular mechanism
-
Maeda, D. Y.; Quinn, M. T.; Schepetkin, I. A.; Kirpotina, L. N.; Zebala, J. A. Nicotinamide glycolates antagonize CXCR2 activity through and intracellular mechanism. J. Pharmacol. Exp. Ther. 2010, 332(1), 145-152.
-
(2010)
J. Pharmacol. Exp. Ther
, vol.332
, Issue.1
, pp. 145-152
-
-
Maeda, D.Y.1
Quinn, M.T.2
Schepetkin, I.A.3
Kirpotina, L.N.4
Zebala, J.A.5
-
124
-
-
12444257004
-
Synthesis and structureactivity relationship of 2-amino-3-heteroaryl-quinoxalines as nonpeptide, small molecule antagonists for interleukin-8 receptor
-
Li, J. J.; Carson, K. G.; Trivedi, B. K.; Yue, W. S; Ye, Q.; Glynn, R. A.; Miller, S. R.; Connor, D. T.; Roth, B. D.; Luly, J. R.; Low, J. E.; Heilig, D. J.; Yang, W.; Qin, S.; Hunt, S. Synthesis and structureactivity relationship of 2-amino-3-heteroaryl-quinoxalines as nonpeptide, small molecule antagonists for interleukin-8 receptor. Bioorg. Med. Chem., 2003, 11(17), 3777-3790.
-
(2003)
Bioorg. Med. Chem
, vol.11
, Issue.17
, pp. 3777-3790
-
-
Li, J.J.1
Carson, K.G.2
Trivedi, B.K.3
Yue, W.S.4
Ye, Q.5
Glynn, R.A.6
Miller, S.R.7
Connor, D.T.8
Roth, B.D.9
Luly, J.R.10
Low, J.E.11
Heilig, D.J.12
Yang, W.13
Qin, S.14
Hunt, S.15
-
125
-
-
12444266409
-
Hit-to-lead studies: The discovery of potent, orally bioavailable triazolethiol CXCR2 receptor antagonists
-
Baxter, A.; Bennion, C.; Bent, J.; Boden, K.; Brough, S.; Cooper, A.; Kinchin, E.; Kindon, N.; McInally, T.; Mortimore, M.; Roberts, B.; Unitt, J. Hit-to-lead studies: The discovery of potent, orally bioavailable triazolethiol CXCR2 receptor antagonists. Bioorg. Med. Chem., 2003, 13(16), 2625-2628.
-
(2003)
Bioorg. Med. Chem
, vol.13
, Issue.16
, pp. 2625-2628
-
-
Baxter, A.1
Bennion, C.2
Bent, J.3
Boden, K.4
Brough, S.5
Cooper, A.6
Kinchin, E.7
Kindon, N.8
McInally, T.9
Mortimore, M.10
Roberts, B.11
Unitt, J.12
-
126
-
-
40749109329
-
Carboxylic acid bioisosteres acylsulfonamides, acylsulfamides, and sulfonylureas as novel antagonists of the CXCR2 receptor
-
Winters, M. P.; Crysler, C.; Subasinghe, N.; Ryan, D.; Leong, L.; Zhao, S.; Donatelli, R.; Yurkow, E.; Mazzulla, M.; Boczon, L.; Manthey, C. L.; Molloy, C.; Raymond, H.; Murray, L.; McAlonan, L.; Tomczuk, B. Carboxylic acid bioisosteres acylsulfonamides, acylsulfamides, and sulfonylureas as novel antagonists of the CXCR2 receptor. Bioorg. Med. Chem. Lett., 2008, 18(6), 1926-1930.
-
(2008)
Bioorg. Med. Chem. Lett
, vol.18
, Issue.6
, pp. 1926-1930
-
-
Winters, M.P.1
Crysler, C.2
Subasinghe, N.3
Ryan, D.4
Leong, L.5
Zhao, S.6
Donatelli, R.7
Yurkow, E.8
Mazzulla, M.9
Boczon, L.10
Manthey, C.L.11
Molloy, C.12
Raymond, H.13
Murray, L.14
McAlonan, L.15
Tomczuk, B.16
-
127
-
-
3142717401
-
Synthesis and structure-activity relationships of 3, 5-diarylisoxazoles and 3, 5-diaryl-1, 2, 4-oxadiazoles, novel classes of small molecule interleukin-8 (IL-8) receptor antagonists
-
Weidner-Wells, M. A.; Henninger, T. C.; Fraga-Spano, S. A.; Boggs, C. M.; Matheis, M.; Ritchie, D. M.; Argentieri, D. C.; Wachter, M. P.; Hlasta, D. J. Synthesis and structure-activity relationships of 3, 5-diarylisoxazoles and 3, 5-diaryl-1, 2, 4-oxadiazoles, novel classes of small molecule interleukin-8 (IL-8) receptor antagonists. Bioorg. Med. Chem. Lett., 2004, 14(16), 4307-4311.
-
(2004)
Bioorg. Med. Chem. Lett
, vol.14
, Issue.16
, pp. 4307-4311
-
-
Weidner-Wells, M.A.1
Henninger, T.C.2
Fraga-Spano, S.A.3
Boggs, C.M.4
Matheis, M.5
Ritchie, D.M.6
Argentieri, D.C.7
Wachter, M.P.8
Hlasta, D.J.9
-
128
-
-
0033913570
-
IL-8-expression in malignant melanoma: Implications in growth and metastasis
-
Singh, R. K.; Varney, M. L. IL-8-expression in malignant melanoma: implications in growth and metastasis. Histol. Histopathol., 2000, 15(3), 843-849.
-
(2000)
Histol. Histopathol
, vol.15
, Issue.3
, pp. 843-849
-
-
Singh, R.K.1
Varney, M.L.2
-
129
-
-
84877855446
-
CXCR2: A target for pancreatic cancer treatment?
-
Hertzer, K. M.; Donald, G. W.; Hines, O. J. CXCR2: a target for pancreatic cancer treatment? Expert Opin. Ther. Targets, 2013, 17(6), 667-680.
-
(2013)
Expert Opin. Ther. Targets
, vol.17
, Issue.6
, pp. 667-680
-
-
Hertzer, K.M.1
Donald, G.W.2
Hines, O.J.3
|