-
1
-
-
0036174736
-
Inhibition of LFA-1/ICAM-1 and VLA-4/VCAM-1 as a therapeutic approach to inflammation and autoimmune diseases
-
Yusuf-Makagiansar, H.; Anderson, M. E.; Yakovleva, T. V.; Murray, J. S.; Siahaan, T. J. Inhibition of LFA-1/ICAM-1 and VLA-4/VCAM-1 as a therapeutic approach to inflammation and autoimmune diseases. Med. Res. Rev. 2002, 22, 146-167.
-
(2002)
Med. Res. Rev.
, vol.22
, pp. 146-167
-
-
Yusuf-Makagiansar, H.1
Anderson, M.E.2
Yakovleva, T.V.3
Murray, J.S.4
Siahaan, T.J.5
-
3
-
-
0037413467
-
A controlled trial of natalizumab for relapsing multiple sclerosis
-
Miller, D. H.; Khan, O. A.; Sheremata, W. A.; Blumhardt, L. D.; Rice, G. P. A.; Libonati, M. A.; Willmer-Hulme, A. J.; Dalton, C. M.; Miszkiel, K. A.; O'Connor, P. W. A controlled trial of natalizumab for relapsing multiple sclerosis. N. Engl. J. Med. 2003, 348, 15-23.
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 15-23
-
-
Miller, D.H.1
Khan, O.A.2
Sheremata, W.A.3
Blumhardt, L.D.4
Rice, G.P.A.5
Libonati, M.A.6
Willmer-Hulme, A.J.7
Dalton, C.M.8
Miszkiel, K.A.9
O'Connor, P.W.10
-
4
-
-
33744780931
-
-
FDA press release P04-107, November 23
-
FDA press release P04-107, November 23, 2004. http://www.fda.gov/bbs/ topics/news/2004/NEW01141.html (accessed January 2006).
-
(2004)
-
-
-
5
-
-
33744802550
-
-
Biogen Idec and Elan Corporation press release, February 28
-
(a) Biogen Idec and Elan Corporation press release, February 28, 2005. http://www.elan.com/News/full.asp?ID=679361 (accessed January 2006).
-
(2005)
-
-
-
6
-
-
27644561433
-
Selective adhesion-molecule therapy and inflammatory bowel disease - A tale of Janus?
-
(b) Podolsky, D. K. Selective adhesion-molecule therapy and inflammatory bowel disease - a tale of Janus? N. Engl. J. Med. 2005, 353, 1965-1967.
-
(2005)
N. Engl. J. Med.
, vol.353
, pp. 1965-1967
-
-
Podolsky, D.K.1
-
7
-
-
33744799080
-
-
note
-
Following completion of a safety evaluation, Biogen Idec and Elan submitted to the FDA in September 2005 a supplemental Biologics License Application supporting market re-entry of Tysabri; an FDA advisory committee voted unanimously in March 2006 to recommend its reintroduction.
-
-
-
-
8
-
-
0037413468
-
Natalizumab for active Crohn's disease
-
(a) Ghosh, S.; Goldin, E.; Gordon, F. H.; Malchow, H. A.; Rask-Madsen, J.; Rutgeerts, P.; Vyhnálek, P.; Zádorová, Z.; Palmer, T.; Donoghue, S. Natalizumab for active Crohn's disease. N. Engl. J. Med. 2003, 348, 24-32.
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 24-32
-
-
Ghosh, S.1
Goldin, E.2
Gordon, F.H.3
Malchow, H.A.4
Rask-Madsen, J.5
Rutgeerts, P.6
Vyhnálek, P.7
Zádorová, Z.8
Palmer, T.9
Donoghue, S.10
-
9
-
-
27644441529
-
Natalizumab induction and maintenance therapy for Crohn's disease
-
(b) Sandborn, W. J.; Colombel, J. F.; Enns, R.; Feagan, B. G.; Hanauer, S. B.; Lawrance, I. C.; Panaccione, R.; Sanders, M.; Schreiber, S.; Targan, S.; van Deventer, S.; Goldblum, R.; Despain, D.; Hogge, G. S.; Rutgeerts, P. Natalizumab induction and maintenance therapy for Crohn's disease. N. Engl. J. Med. 2005, 353, 1912-1925.
-
(2005)
N. Engl. J. Med.
, vol.353
, pp. 1912-1925
-
-
Sandborn, W.J.1
Colombel, J.F.2
Enns, R.3
Feagan, B.G.4
Hanauer, S.B.5
Lawrance, I.C.6
Panaccione, R.7
Sanders, M.8
Schreiber, S.9
Targan, S.10
Van Deventer, S.11
Goldblum, R.12
Despain, D.13
Hogge, G.S.14
Rutgeerts, P.15
-
10
-
-
20444469332
-
7 integrin
-
7 integrin. N. Engl. J. Med. 2005, 352, 2499-2507.
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 2499-2507
-
-
Feagan, B.G.1
Greenberg, G.R.2
Wild, G.3
Fedorak, R.N.4
Paré, P.5
McDonald, J.W.D.6
Dubé, R.7
Cohen, A.8
Steinhart, A.H.9
Landau, S.10
Aguzzi, R.A.11
Fox, I.H.12
Vandervoort, M.K.13
-
11
-
-
0035655590
-
VLA-4 antagonists
-
Reviews: (a) Tilley, J. W.; Sidduri, A. VLA-4 antagonists. Drugs Future 2001, 26, 985-998.
-
(2001)
Drugs Future
, vol.26
, pp. 985-998
-
-
Tilley, J.W.1
Sidduri, A.2
-
12
-
-
0037405890
-
VLA-4 antagonists: Potent inhibitors of lymphocyte migration
-
(b) Yang, G. X.; Hagmann, W. K. VLA-4 antagonists: potent inhibitors of lymphocyte migration. Med. Res. Rev. 2003, 23, 369-392.
-
(2003)
Med. Res. Rev.
, vol.23
, pp. 369-392
-
-
Yang, G.X.1
Hagmann, W.K.2
-
13
-
-
0036259277
-
Alpha 4 integrin antagonists
-
(c) Jackson, D. Y. Alpha 4 integrin antagonists. Curr. Pharm. Des. 2002, 8, 1229-1253.
-
(2002)
Curr. Pharm. Des.
, vol.8
, pp. 1229-1253
-
-
Jackson, D.Y.1
-
14
-
-
0036667327
-
7 integrin antagonists and their potential as anti-inflammatory agents
-
7 integrin antagonists and their potential as anti-inflammatory agents. J. Med. Chem. 2002, 45, 3451-3457.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 3451-3457
-
-
Dubree, N.J.P.1
Artis, D.R.2
Castanedo, G.3
Marsters, J.4
Sutherlin, D.5
Caris, L.6
Clark, K.7
Keating, S.M.8
Beresini, M.H.9
Chiu, H.10
Fong, S.11
Lowman, H.B.12
Skelton, N.J.13
Jackson, D.Y.14
-
15
-
-
0036009903
-
1 integrin antagonist
-
1 integrin antagonist. Bioorg. Med. Chem. 2002, 10, 2051-2066.
-
(2002)
Bioorg. Med. Chem.
, vol.10
, pp. 2051-2066
-
-
Sircar, I.1
Gudmundsson, K.S.2
Martin, R.3
Liang, J.4
Nomura, S.5
Jayakumar, H.6
Teegarden, B.R.7
Nowlin, D.M.8
Cardarelli, P.M.9
Mah, J.R.10
Connell, S.11
Griffith, R.C.12
Lazarides, E.13
-
16
-
-
0035935194
-
The discovery of sulfonylated dipeptides as potent VLA-4 antagonists
-
4 integrin antagonists: (a) Hagmann, W. K.; Durette, P. L.; Lanza, T.; Kevin, N. J.; de Laszlo, S. E.; Kopka, I. E.; Young, D.; Magriotis, P. A.; Li, B.; Lin, L. S.; Yang, G.: Kamenecka, T.; Chang, L. L.; Wilson, J.; MacCoss, M.; Mills, S. G.; Van Riper, G.; McCauley, E.; Egger, L. A.; Kidambi, U.; Lyons, K.; Vincent, S.; Stearns, R.; Colletti, A.; Teffera, J.; Tong, S.; Fenyk-Melody, J.; Owens, K.; Levorse, D.; Kim, P.; Schmidt, J. A.; Mumford, R. A. The discovery of sulfonylated dipeptides as potent VLA-4 antagonists. Bioorg. Med. Chem. Lett. 2001, 11, 2709-2713.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2709-2713
-
-
Hagmann, W.K.1
Durette, P.L.2
Lanza, T.3
Kevin, N.J.4
De Laszlo, S.E.5
Kopka, I.E.6
Young, D.7
Magriotis, P.A.8
Li, B.9
Lin, L.S.10
Yang, G.11
Kamenecka, T.12
Chang, L.L.13
Wilson, J.14
MacCoss, M.15
Mills, S.G.16
Van Riper, G.17
McCauley, E.18
Egger, L.A.19
Kidambi, U.20
Lyons, K.21
Vincent, S.22
Stearns, R.23
Colletti, A.24
Teffera, J.25
Tong, S.26
Fenyk-Melody, J.27
Owens, K.28
Levorse, D.29
Kim, P.30
Schmidt, J.A.31
Mumford, R.A.32
more..
-
17
-
-
0037013432
-
N-Tetrahydrofuroyl-(L)-phenylalanines as potent VLA-4 antagonists
-
(b) Yang, G. X.; Chang, L. L.; Truong, Q.; Doherty, G. A.; Magriotis, P. A.; de Laszlo, S. E.; Li, B.; MacCoss, M.; Kidambi, U.; Egger, L. A.; McCauley, E.; Van Riper, G.; Mumford, R. A.; Schmidt, J. A.; Hagmann, W. K. N-Tetrahydrofuroyl-(L)-phenylalanines as potent VLA-4 antagonists. Bioorg. Med. Chem. Lett. 2002, 12, 1497-1500.
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 1497-1500
-
-
Yang, G.X.1
Chang, L.L.2
Truong, Q.3
Doherty, G.A.4
Magriotis, P.A.5
De Laszlo, S.E.6
Li, B.7
MacCoss, M.8
Kidambi, U.9
Egger, L.A.10
McCauley, E.11
Van Riper, G.12
Mumford, R.A.13
Schmidt, J.A.14
Hagmann, W.K.15
-
18
-
-
0041570557
-
Direct synthesis of unprotected 4-aryl phenylalanines via the Suzuki reaction under microwave irradiation
-
Gong, Y.; He, W. Direct synthesis of unprotected 4-aryl phenylalanines via the Suzuki reaction under microwave irradiation. Org. Lett. 2002, 4, 3803-3805.
-
(2002)
Org. Lett.
, vol.4
, pp. 3803-3805
-
-
Gong, Y.1
He, W.2
-
19
-
-
0035843377
-
Suzuki reactions on chloropyridazinones: An easy approach towards arylated 3(2H)-pyridazinones
-
Maes, B. U. W.; R'kyek, O.; Kosmrlj, J.; Lemiere, G. L. F.; Esmans, E.; Rozenski, J.; Dommisse, R. A.; Haemers, A. Suzuki reactions on chloropyridazinones: an easy approach towards arylated 3(2H)-pyridazinones. Tetrahedron 2001, 57, 1323-1330.
-
(2001)
Tetrahedron
, vol.57
, pp. 1323-1330
-
-
Maes, B.U.W.1
R'kyek, O.2
Kosmrlj, J.3
Lemiere, G.L.F.4
Esmans, E.5
Rozenski, J.6
Dommisse, R.A.7
Haemers, A.8
-
20
-
-
0001539697
-
Dehalogenation of 1-methyl-5-halo-4-substituted-pyridazin-6-ones
-
Nucleophilic substitution of 5-alkoxypyridazinones (as byproduct): Kweon, D.-H.; Kang, Y.-J.; Chung, H.-A.; Yoon, Y.-J. Dehalogenation of 1-methyl-5-halo-4-substituted-pyridazin-6-ones. J. Heterocycl. Chem. 1998, 35, 819-826.
-
(1998)
J. Heterocycl. Chem.
, vol.35
, pp. 819-826
-
-
Kweon, D.-H.1
Kang, Y.-J.2
Chung, H.-A.3
Yoon, Y.-J.4
-
21
-
-
0033169045
-
4 integrins mediate initial attachment, and E-selectin mediates rolling
-
4 integrins mediate initial attachment, and E-selectin mediates rolling. J. Immunol. 1999, 163, 343-350.
-
(1999)
J. Immunol.
, vol.163
, pp. 343-350
-
-
Ulfman, L.H.1
Kuijper, P.H.M.2
Van Der Linden, J.A.M.3
Lammers, J.-W.J.4
Zwaginga, J.J.5
Koenderman, L.6
-
23
-
-
33744788810
-
-
note
-
Cell-cell adhesion assays were conducted by Cerep, Poitiers, France.
-
-
-
-
24
-
-
0027462141
-
Rapid analysis of leukocyte-endothelial adhesion
-
(a) Vaporciyan, A. A.; Jones, M. L.; Ward, P. A. Rapid analysis of leukocyte-endothelial adhesion. J. Immunol. Methods. 1993, 159, 93-100.
-
(1993)
J. Immunol. Methods.
, vol.159
, pp. 93-100
-
-
Vaporciyan, A.A.1
Jones, M.L.2
Ward, P.A.3
-
25
-
-
0027963348
-
Modulation of pyrogen-induced upregulation of endothelial cell adhesion molecules (CAMs) by interleukin-4: Transcriptional mechanisms and CAM-shedding
-
(b) Kapiotis, S.; Quehenberger, P.; Sengoelge, G.; Pärtan, C.; Eher, R.; Strobl, H.; Bevec, D.; Zapolska, D.; Schwarzinger, I.; Speiser, W. Modulation of pyrogen-induced upregulation of endothelial cell adhesion molecules (CAMs) by interleukin-4: Transcriptional mechanisms and CAM-shedding. Circ. Shock 1994, 43, 18-25.
-
(1994)
Circ. Shock
, vol.43
, pp. 18-25
-
-
Kapiotis, S.1
Quehenberger, P.2
Sengoelge, G.3
Pärtan, C.4
Eher, R.5
Strobl, H.6
Bevec, D.7
Zapolska, D.8
Schwarzinger, I.9
Speiser, W.10
-
26
-
-
0024592732
-
Functional cloning of ICAM-2, a cell adhesion ligand for LFA-1 homologous to ICAM-1
-
(c) Staunton, D. E.; Dustin, M. L.; Springer, T. A. Functional cloning of ICAM-2, a cell adhesion ligand for LFA-1 homologous to ICAM-1. Nature 1989, 339, 61-64.
-
(1989)
Nature
, vol.339
, pp. 61-64
-
-
Staunton, D.E.1
Dustin, M.L.2
Springer, T.A.3
-
27
-
-
33744788284
-
-
note
-
The absence of observable plasma concentrations of ester prodrugs is consistent with rapid hydrolysis, which may have occurred in blood or other compartments. However, the possibility of incomplete hydrolysis at the time of withdrawal of blood samples and continued hydrolysis during storage at -70 °C and/or extraction of plasma samples cannot be excluded; therefore, observed concentrations of carboxylic acid drugs following prodrug administration are best interpreted as an upper limit of the actual concentration in blood at the time of collection.
-
-
-
-
28
-
-
12144288312
-
Synthesis, characterization and evaluation of pro-drugs of VLA-4 antagonists
-
Huryn, D. M.; Ashwell, S.; Baudy, R.; Dressen, D. B.; Gallaway, W.; Grant, F. S.; Konradi, A.; Ley, R. W.; Petusky, S.; Pleiss, M. A.; Sarantakis, D.; Semko, C. M.; Sherman, M. M.; Tio, C.; Zhang, L. Synthesis, characterization and evaluation of pro-drugs of VLA-4 antagonists. Bioorg. Med. Chem. Lett. 2004, 14, 1651-1654.
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 1651-1654
-
-
Huryn, D.M.1
Ashwell, S.2
Baudy, R.3
Dressen, D.B.4
Gallaway, W.5
Grant, F.S.6
Konradi, A.7
Ley, R.W.8
Petusky, S.9
Pleiss, M.A.10
Sarantakis, D.11
Semko, C.M.12
Sherman, M.M.13
Tio, C.14
Zhang, L.15
-
29
-
-
1642296611
-
Prodrugs as therapeutics
-
Stella, V. J. Prodrugs as therapeutics. Expert Opin. Ther. Pat. 2004, 14, 277-280.
-
(2004)
Expert Opin. Ther. Pat.
, vol.14
, pp. 277-280
-
-
Stella, V.J.1
-
30
-
-
0038137501
-
1 inhibitors, the monoclonal antibody TA-2 and the small molecule BIO5192, in rat experimental autoimmune encephalomyelitis
-
1 inhibitors, the monoclonal antibody TA-2 and the small molecule BIO5192, in rat experimental autoimmune encephalomyelitis. J. Pharmacol. Exp. Ther. 2003, 305, 1150-1162.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.305
, pp. 1150-1162
-
-
Leone, D.R.1
Giza, K.2
Gill, A.3
Dolinski, B.M.4
Yang, W.5
Perper, S.6
Scott, D.M.7
Lee, W.-C.8
Cornebise, M.9
Wortham, K.10
Nickerson-Nutter, C.11
Chen, L.L.12
Lepage, D.13
Spell, J.C.14
Whalley, E.T.15
Petter, R.C.16
Adams, S.P.17
Lobb, R.R.18
Pepinsky, R.B.19
-
31
-
-
0000806063
-
Concurrent alkylation-methoxylation of 4,5-dihalopyridazin-6-ones and synthesis of 5-halo-4-hydroxypyridazin-6-ones
-
Cho, S.-D.; Choi, W.-Y.; Yoon, Y.-J. Concurrent alkylation-methoxylation of 4,5-dihalopyridazin-6-ones and synthesis of 5-halo-4-hydroxypyridazin-6-ones. J. Heterocycl. Chem. 1996, 33, 1579-1582.
-
(1996)
J. Heterocycl. Chem.
, vol.33
, pp. 1579-1582
-
-
Cho, S.-D.1
Choi, W.-Y.2
Yoon, Y.-J.3
-
32
-
-
84987343073
-
4(and 5)-Cyclopropylamino-5(and 4)-halo-3(2H) pyridazinones. Formation and characterization of isomers
-
Pilgram, K. H.; Pollard, G. E. 4(and 5)-Cyclopropylamino-5(and 4)-halo-3(2H) pyridazinones. Formation and characterization of isomers. J. Heterocycl. Chem. 1977, 14, 1039-1043.
-
(1977)
J. Heterocycl. Chem.
, vol.14
, pp. 1039-1043
-
-
Pilgram, K.H.1
Pollard, G.E.2
-
33
-
-
11144255122
-
Vanilloid receptor 1 antagonists attenuate disease severity in dextran sulfate sodium induced colitis in mice
-
Kimball, E. S.; Wallace, N. H.; Schneider, C. R.; D'Andrea, M. R.; Hornby, P. J. Vanilloid receptor 1 antagonists attenuate disease severity in dextran sulfate sodium induced colitis in mice. Neurogastroenterol. Motility 2004, 16, 811-818.
-
(2004)
Neurogastroenterol. Motility
, vol.16
, pp. 811-818
-
-
Kimball, E.S.1
Wallace, N.H.2
Schneider, C.R.3
D'Andrea, M.R.4
Hornby, P.J.5
|