-
1
-
-
0034093737
-
Signal transduction by the TCR for antigen
-
Kane LP, Lin J, Weiss A. Signal transduction by the TCR for antigen. Curr Opin Immunol 2000;12:242-9
-
(2000)
Curr Opin Immunol
, vol.12
, pp. 242-9
-
-
Kane, L.P.1
Lin, J.2
Weiss, A.3
-
2
-
-
0030891168
-
Leukocyte protein tyrosine kinases: Potential targets for drug discovery
-
Bolen JB, Brugge JS. Leukocyte protein tyrosine kinases: potential targets for drug discovery. Annu Rev Immunol 1997;15:371-404
-
(1997)
Annu Rev Immunol
, vol.15
, pp. 371-404
-
-
Bolen, J.B.1
Brugge, J.S.2
-
3
-
-
0029786988
-
Knockouts of Src-family kinases: Stiff bones, wimpy T cells, and bad memories
-
Lowell CA, Soriano P. Knockouts of Src-family kinases: stiff bones, wimpy T cells, and bad memories. Genes Dev 1996;10:1845-57
-
(1996)
Genes Dev
, vol.10
, pp. 1845-57
-
-
Lowell, C.A.1
Soriano, P.2
-
4
-
-
0024590237
-
Lymphocyte activation provokes modification of a lymphocyte specific protein tyrosine kinase (p56lck)
-
Marth JD, Lewis DB, Cooke MP, et al. Lymphocyte activation provokes modification of a lymphocyte specific protein tyrosine kinase (p56lck). J Immunol 1989;142:2430-7
-
(1989)
J Immunol
, vol.142
, pp. 2430-7
-
-
Marth, J.D.1
Lewis, D.B.2
Cooke, M.P.3
-
5
-
-
0030294283
-
Fyn can partially substitute for Lck in T lymphocyte development
-
Groves T, Smiley P, Cooke MP, et al. Fyn can partially substitute for Lck in T lymphocyte development. Immunity 1996;5:417-28
-
(1996)
Immunity
, vol.5
, pp. 417-28
-
-
Groves, T.1
Smiley, P.2
Cooke, M.P.3
-
6
-
-
7944231534
-
Function of the Src-family kinases, Lck and Fyn, in T-cell development and activation
-
Palacios EH, Weiss A. Function of the Src-family kinases, Lck and Fyn, in T-cell development and activation. Oncogene 2004;23:7990-8000
-
(2004)
Oncogene
, vol.23
, pp. 7990-8000
-
-
Palacios, E.H.1
Weiss, A.2
-
7
-
-
61849128182
-
T-cell receptor proximal signaling via the Src-family kinases, Lck and Fyn, influences T-cell activation, differentiation, and tolerance
-
Salmond RJ, Filby A, Qureshi I, et al. T-cell receptor proximal signaling via the Src-family kinases, Lck and Fyn, influences T-cell activation, differentiation, and tolerance. Immunol Rev 2009;228:9-22
-
(2009)
Immunol Rev
, vol.228
, pp. 9-22
-
-
Salmond, R.J.1
Filby, A.2
Qureshi, I.3
-
8
-
-
0026522204
-
Profound block in thymocyte development in mice lacking p56lck
-
Molina TJ, Kishihara K, Siderovskid DP, et al. Profound block in thymocyte development in mice lacking p56lck. Nature 1992;357:161-4
-
(1992)
Nature
, vol.357
, pp. 161-4
-
-
Molina, T.J.1
Kishihara, K.2
Siderovskid, D.P.3
-
9
-
-
0027467796
-
A dominant-negative transgene defines a role for p56lck in thymopoiesis
-
Levin SD, Anderson SJ, Forbush KA, Perlmutter RM. A dominant-negative transgene defines a role for p56lck in thymopoiesis. EMBO J 1993;12:1671-80
-
(1993)
EMBO J
, vol.12
, pp. 1671-80
-
-
Levin, S.D.1
Anderson, S.J.2
Forbush, K.A.3
Perlmutter, R.M.4
-
10
-
-
0037105615
-
TCR signals mediated by Src family kinases are essential for the survival of naive T cells
-
Seddon B, Zamoyska R. TCR signals mediated by Src family kinases are essential for the survival of naive T cells. J Immunol 2002;169:2997-3005
-
(2002)
J Immunol
, vol.169
, pp. 2997-3005
-
-
Seddon, B.1
Zamoyska, R.2
-
11
-
-
0026705903
-
Genetic evidence for the involvement of the lck tyrosine kinase in signal transduction through the T cell antigen receptor
-
Straus DB, Weiss A. Genetic evidence for the involvement of the lck tyrosine kinase in signal transduction through the T cell antigen receptor. Cell 1992;70:585-93
-
(1992)
Cell
, vol.70
, pp. 585-93
-
-
Straus, D.B.1
Weiss, A.2
-
12
-
-
0032527136
-
Defective expression of p56lck in an infant with severe combined immunodeficiency
-
Goldman FD, Ballas ZK, Schutte BC, et al. Defective expression of p56lck in an infant with severe combined immunodeficiency. J Clin Invest 1998;102:421-9
-
(1998)
J Clin Invest
, vol.102
, pp. 421-9
-
-
Goldman, F.D.1
Ballas, Z.K.2
Schutte, B.C.3
-
13
-
-
0033624875
-
Defective p56lck activity in T cells from an adult patient with idiopathic CD4+ lymphocytopenia
-
Hubert P, Bergeron F, Ferreirea V, et al. Defective p56lck activity in T cells from an adult patient with idiopathic CD4+ lymphocytopenia. Int Immunol 2000;12:449-57
-
(2000)
Int Immunol
, vol.12
, pp. 449-57
-
-
Hubert, P.1
Bergeron, F.2
Ferreirea, V.3
-
14
-
-
49649092618
-
Small molecule inhibitors of Lck: The search for specificity within a kinase family
-
Meyn MA III, Smithgall TE. Small molecule inhibitors of Lck: the search for specificity within a kinase family. Mini Rev Med Chem 2008;8:628-37
-
(2008)
Mini Rev Med Chem
, vol.8
, pp. 628-37
-
-
Meyn Iii, M.A.1
Smithgall, T.E.2
-
15
-
-
60449117455
-
Kinase inhibitors for the treatment of inflammatory and autoimmune disorders
-
Bhagwat S. Kinase inhibitors for the treatment of inflammatory and autoimmune disorders. Purinergic Signal 2009;5:107-15
-
(2009)
Purinergic Signal
, vol.5
, pp. 107-15
-
-
Bhagwat, S.1
-
16
-
-
0035151006
-
Inhibitors of p56lck: Assessing their potential as tools for manipulating T-lymphocyte activation
-
Dowden J, Ward SG. Inhibitors of p56lck: assessing their potential as tools for manipulating T-lymphocyte activation. Expert Opin Ther Patents 2001;11:295-306
-
(2001)
Expert Opin Ther Patents
, vol.11
, pp. 295-306
-
-
Dowden, J.1
Ward, S.G.2
-
17
-
-
25444479747
-
Recent advances in the discovery of Src kinase inhibitors
-
Parang K, Sun G. Recent advances in the discovery of Src kinase inhibitors. Expert Opin Ther Patents 2005;15:1183-207
-
(2005)
Expert Opin Ther Patents
, vol.15
, pp. 1183-207
-
-
Parang, K.1
Sun, G.2
-
18
-
-
0033152210
-
Structural analysis of the lymphocyte-specific kinase Lck in complex with non-selective and Src family selective kinase inhibitors
-
Zhu X, Kim JL, Newcomb JR, et al. Structural analysis of the lymphocyte-specific kinase Lck in complex with non-selective and Src family selective kinase inhibitors. Structure 1999;7:651-61
-
(1999)
Structure
, vol.7
, pp. 651-61
-
-
Zhu, X.1
Kim, J.L.2
Newcomb, J.R.3
-
19
-
-
16144364951
-
Structural basis for activation of human lymphocyte kinase Lck upon tyrosine phosphorylation
-
Yamaguchi H, Hendrickson WA. Structural basis for activation of human lymphocyte kinase Lck upon tyrosine phosphorylation. Nature 1996;388:484-9
-
(1996)
Nature
, vol.388
, pp. 484-9
-
-
Yamaguchi, H.1
Hendrickson, W.A.2
-
20
-
-
0031025991
-
Three-dimensional structure of the tyrosine kinase c-Src
-
Xu W, Harrison SC, Eck MJ. Three-dimensional structure of the tyrosine kinase c-Src. Nature 1997;385:595-602
-
(1997)
Nature
, vol.385
, pp. 595-602
-
-
Xu, W.1
Harrison, S.C.2
Eck, M.J.3
-
21
-
-
0031034930
-
Crystal structure of the Src family tyrosine kinase Hck
-
Sicheri F, Moarefi I, Kuriyan J. Crystal structure of the Src family tyrosine kinase Hck. Nature 1997;385:602-9
-
(1997)
Nature
, vol.385
, pp. 602-9
-
-
Sicheri, F.1
Moarefi, I.2
Kuriyan, J.3
-
22
-
-
1642323740
-
Protein kinase inhibitors: Insights into drug design from structure
-
Noble MEM, Endicott JA, Johnson LN. Protein kinase inhibitors: insights into drug design from structure. Science 2004;303:1800-5
-
(2004)
Science
, vol.303
, pp. 1800-5
-
-
Mem, N.1
Endicott, J.A.2
Johnson, L.N.3
-
23
-
-
33745298429
-
Rational design of inhibitors that bind to inactive kinase conformations
-
Liu Y, Gray NS. Rational design of inhibitors that bind to inactive kinase conformations. Nat Chem Biol 2006;2:358-64
-
(2006)
Nat Chem Biol
, vol.2
, pp. 358-64
-
-
Liu, Y.1
Gray, N.S.2
-
24
-
-
33748851665
-
Discovery of aminoquinazolines as potent, orally bioavailable inhibitors of Lck: Synthesis, SAR, and in vivo anti-inflammatory activity
-
DiMauro EF, Newcomb J, Nunes JJ, et al. Discovery of aminoquinazolines as potent, orally bioavailable inhibitors of Lck: synthesis, SAR, and in vivo anti-inflammatory activity. J Med Chem 2006;49:5671-86
-
(2006)
J Med Chem
, vol.49
, pp. 5671-86
-
-
Dimauro, E.F.1
Newcomb, J.2
Nunes, J.J.3
-
25
-
-
77950573400
-
"Gatekeeper Door": Exploiting the active kinase conformation
-
Zuccotto F, Ardini E, Casale E, Angiolini M. Through the "Gatekeeper Door": exploiting the active kinase conformation. J Med Chem 2010;53:2681-94
-
(2010)
J Med Chem
, vol.53
, pp. 2681-94
-
-
Zuccotto, F.1
Ardini, E.2
Casale, E.3
The Through, A.M.4
-
26
-
-
77649204688
-
Selectively nonselective kinase inhibition: Strking the right balance
-
Morphy R. Selectively nonselective kinase inhibition: strking the right balance. J Med Chem 2010;53:1413-37
-
(2010)
J Med Chem
, vol.53
, pp. 1413-37
-
-
Morphy, R.1
-
27
-
-
0037255931
-
Inhibitors of p38 mitogen-activated protein kinase: Potential as anti-inflammatory agents in asthma?
-
Newton R, Holden N. Inhibitors of p38 mitogen-activated protein kinase: potential as anti-inflammatory agents in asthma? BioDrugs 2003;17:113-29
-
(2003)
BioDrugs
, vol.17
, pp. 113-29
-
-
Newton, R.1
Holden, N.2
-
28
-
-
0037699954
-
The biology of VEGF and its receptor
-
Ferrara N, Gerber H, LeCouter J. The biology of VEGF and its receptor. Nat Med 2003;9:669-76
-
(2003)
Nat Med
, vol.9
, pp. 669-76
-
-
Ferrara, N.1
Gerber, H.2
Lecouter, J.3
-
29
-
-
11144343254
-
Janus kinase 3: A novel target for selective transplant immunosuppression
-
Podder H, Kahan BD. Janus kinase 3: a novel target for selective transplant immunosuppression. Expert Opin Ther Targets 2004;8:613-29
-
(2004)
Expert Opin Ther Targets
, vol.8
, pp. 613-29
-
-
Podder, H.1
Kahan, B.D.2
-
30
-
-
0242405592
-
Role of angiopoietins and Tie receptor tyrosine kinases in angiogenesis and lymphangiogenesis
-
Thurston G. Role of angiopoietins and Tie receptor tyrosine kinases in angiogenesis and lymphangiogenesis. Cell Tissue Res 2003;34:61-8
-
(2003)
Cell Tissue Res
, vol.34
, pp. 61-8
-
-
Thurston, G.1
-
32
-
-
0030029143
-
Discovery of a novel, potent, and Src family-selective tyrosine kinase inhibitor. Study of Lck-and FynT-dependent T cell activation
-
Hanke JH, Gardner JP, Dow RL, et al. Discovery of a novel, potent, and Src family-selective tyrosine kinase inhibitor. Study of Lck-and FynT-dependent T cell activation. J Biol Chem 1996;271(2):695-701
-
(1996)
J Biol Chem
, vol.271
, Issue.2
, pp. 695-701
-
-
Hanke, J.H.1
Gardner, J.P.2
Dow, R.L.3
-
33
-
-
0034597072
-
Pyrrolo[2,3-d] pyrimidines containing an extended 5-substituent as potent and selective inhibitors of Lck i
-
Arnold LD, Calderwood DJ, Dixon RW, et al. Pyrrolo[2,3-d] pyrimidines containing an extended 5-substituent as potent and selective inhibitors of Lck I. Bioorg Med Chem Lett 2000;10:2167-70
-
(2000)
Bioorg Med Chem Lett
, vol.10
, pp. 2167-70
-
-
Arnold, L.D.1
Calderwood, D.J.2
Dixon, R.W.3
-
34
-
-
0034597116
-
Pyrrolo[2,3-d]pyrimidines containing an extended 5-substituent as potent and selective inhibitors of Lck II
-
Burchat AF, Calderwood DJ, Hirst GC, et al. Pyrrolo[2,3-d]pyrimidines containing an extended 5-substituent as potent and selective inhibitors of Lck II. Bioorg Med Chem Lett 2000;10:2171-4
-
(2000)
Bioorg Med Chem Lett
, vol.10
, pp. 2171-4
-
-
Burchat, A.F.1
Calderwood, D.J.2
Hirst, G.C.3
-
35
-
-
0037124205
-
Pyrrolo[2,3-d] pyrimidines containing diverse N-7 substituents as potent inhibitors of Lck
-
Calderwood DJ, Johnston DN, Munschauer R, et al. Pyrrolo[2,3-d] pyrimidines containing diverse N-7 substituents as potent inhibitors of Lck. Bioorg Med Chem Lett 2002;12:1683-6
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 1683-6
-
-
Calderwood, D.J.1
Johnston, D.N.2
Munschauer, R.3
-
36
-
-
0037124207
-
Pyrazolo[3,4-d] pyrimidines containing an extended 3-substituent as potent inhibitors of Lck - A selectivity insight
-
Burchat AF, Calderwood DJ, Friedman MM, et al. Pyrazolo[3,4-d] pyrimidines containing an extended 3-substituent as potent inhibitors of Lck-a selectivity insight. Bioorg Med Chem Lett 2002;12:1687-90
-
(2002)
Bioorg Med Chem Lett
, vol.12
, pp. 1687-90
-
-
Burchat, A.F.1
Calderwood, D.J.2
Friedman, M.M.3
-
38
-
-
11144354668
-
A-420983: A potent, orally active inhibitor of Lck with efficacy in a model of transplant rejection
-
Borhani DW, Calderwood DJ, Friedman MM, et al. A-420983: a potent, orally active inhibitor of Lck with efficacy in a model of transplant rejection. Bioorg Med Chem Lett 2004;14:2613-16
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 2613-16
-
-
Borhani, D.W.1
Calderwood, D.J.2
Friedman, M.M.3
-
39
-
-
27744600732
-
Discovery of A-770041, a Src-family selective orally active Lck inhibitor that prevents organ allograft rejection
-
Burchat A, Borhani DW, Calderwood DJ, et al. Discovery of A-770041, a Src-family selective orally active Lck inhibitor that prevents organ allograft rejection. Bioorg Med Chem Lett 2006;16:118-22
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 118-22
-
-
Burchat, A.1
Borhani, D.W.2
Calderwood, D.J.3
-
40
-
-
25644432071
-
A-770041, a novel and selective small-molecule inhibitor of Lck, prevents heart allograft rejection
-
Stachlewitz RF, Hart MA, Bettencourt B, et al. A-770041, a novel and selective small-molecule inhibitor of Lck, prevents heart allograft rejection. J Pharm Exp Ther 2005;315:36-41
-
(2005)
J Pharm Exp Ther
, vol.315
, pp. 36-41
-
-
Stachlewitz, R.F.1
Hart, M.A.2
Bettencourt, B.3
-
41
-
-
33846927050
-
Discovery of thienopyridines as Src-family selective Lck inhibitors
-
Abbott L, Betschmann P, Burchat A, et al. Discovery of thienopyridines as Src-family selective Lck inhibitors. Bioorg Med Chem Lett 2007;17:1167-71
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 1167-71
-
-
Abbott, L.1
Betschmann, P.2
Burchat, A.3
-
42
-
-
77958472248
-
-
Abbott Laboratories US20050020619
-
Abbott Laboratories. Thienopyridine kinase inibitors. US20050020619; 2005
-
(2005)
Thienopyridine Kinase Inibitors
-
-
-
49
-
-
24944543833
-
Thienopyrimidine ureas as novel and potent multitargeted receptor tyrosine kinase inhibitors
-
Dai Y, Guo Y, Frey RR, et al. Thienopyrimidine ureas as novel and potent multitargeted receptor tyrosine kinase inhibitors. J Med Chem 2005;48:6066-83
-
(2005)
J Med Chem
, vol.48
, pp. 6066-83
-
-
Dai, Y.1
Guo, Y.2
Frey, R.R.3
-
53
-
-
77958482069
-
-
Amgen Inc WO06004658
-
Amgen, Inc. Furanopyrimidines. WO06004658; 2006
-
(2006)
Furanopyrimidines
-
-
-
54
-
-
33947573110
-
Discovery of 4-amino-5-6-biaryl-furo[2,3-d] pyrimidines as inhibitors of Lck: Development of an expedient and divergent synthetic route and preliminary
-
DiMauro EF, Newcomb J, Nunes JJ, et al. Discovery of 4-amino-5,6-biaryl- furo[2,3-d] pyrimidines as inhibitors of Lck: development of an expedient and divergent synthetic route and preliminary SAR Bioorg Med Chem Lett 2007;17:2305-9
-
(2007)
SAR Bioorg Med Chem Lett
, vol.17
, pp. 2305-9
-
-
Dimauro, E.F.1
Newcomb, J.2
Nunes, J.J.3
-
55
-
-
0027235324
-
A non-receptor tyrosine kinase that inhibits the GTPase activity of p21cdc42
-
Manser E, Leung T, Salihuddin H, et al. A non-receptor tyrosine kinase that inhibits the GTPase activity of p21cdc42. Nature 1993;363:364-7
-
(1993)
Nature
, vol.363
, pp. 364-7
-
-
Manser, E.1
Leung, T.2
Salihuddin, H.3
-
56
-
-
34347328253
-
An ultrasensitive high-throughput electrochemiluminescence immunoassay for the Cdc42-associated protein tyrosine kinase ACK1
-
Xiao S-H, Farrelly E, Anzola J, et al. An ultrasensitive high-throughput electrochemiluminescence immunoassay for the Cdc42-associated protein tyrosine kinase ACK1. Anal Biochem 2007;367:179-89
-
(2007)
Anal Biochem
, vol.367
, pp. 179-89
-
-
Xiao, S.-H.1
Farrelly, E.2
Anzola, J.3
-
59
-
-
33947575136
-
Discovery of novel 2 3-diarylfuro [2,3-b]pyridin-4-amines as potent and selective inhibitors of Lck: Synthesis, SAR, and pharmacokinetic properties
-
Martin MW, Newcomb J, Nunes JJ, et al. Discovery of novel 2,3-diarylfuro [2,3-b]pyridin-4-amines as potent and selective inhibitors of Lck: synthesis, SAR, and pharmacokinetic properties. Bioorg Med Chem Lett 2007;17:2299-304
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 2299-304
-
-
Martin, M.W.1
Newcomb, J.2
Nunes, J.J.3
-
65
-
-
0034308176
-
Biochemical and cellular effects of c-Src kinase-selective pyrido[2,3-d]pyrimidine tyrosine kinase inhibitors
-
Kraker AJ, Hartl BG, Amam AM, et al. Biochemical and cellular effects of c-Src kinase-selective pyrido[2,3-d]pyrimidine tyrosine kinase inhibitors. Biochem Pharmacol 2000;60:885-98
-
(2000)
Biochem Pharmacol
, vol.60
, pp. 885-98
-
-
Kraker, A.J.1
Hartl, B.G.2
Amam, A.M.3
-
72
-
-
41149118544
-
Structure-based design of novel 2-Amino-6-phenylpyrimido[5',4':5 6] pyrimido[1,2-a]benzimidazol-5(6H)-ones as potent and orally active inhibitors of lymphocyte specific kinase (Lck): Synthesis, SAR, and in vivo anti-inflammatory activity
-
Martin MW, Newcomb J, Nunes JJ, et al. Structure-based design of novel 2-Amino-6-phenylpyrimido[5',4':5,6] pyrimido[1,2-a]benzimidazol-5(6H)-ones as potent and orally active inhibitors of lymphocyte specific kinase (Lck): synthesis, SAR, and in vivo anti-inflammatory activity. J Med Chem 2008;51:1637-48
-
(2008)
J Med Chem
, vol.51
, pp. 1637-48
-
-
Martin, M.W.1
Newcomb, J.2
Nunes, J.J.3
-
75
-
-
33746930843
-
Novel 2-aminopyrimidine carbamates as potent and orally active inhibitors of Lck: Synthesis, SAR, and in vivo antiinflammatory activity
-
Martin MW, Newcomb J, Nunes JJ, et al. Novel 2-aminopyrimidine carbamates as potent and orally active inhibitors of Lck: synthesis, SAR, and in vivo antiinflammatory activity. J Med Chem 2006;49:4981-91
-
(2006)
J Med Chem
, vol.49
, pp. 4981-91
-
-
Martin, M.W.1
Newcomb, J.2
Nunes, J.J.3
-
81
-
-
53449083913
-
Discovery of pyrimidine benzimidazoles as Lck inhibitors: Part i
-
Zhang G, Ren, P, Gray NS, et al. Discovery of pyrimidine benzimidazoles as Lck inhibitors: part I. Bioorg Med Chem Lett 2008;18:5618-21
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 5618-21
-
-
Zhang, G.1
Ren, P.2
Gray, N.S.3
-
82
-
-
71749086550
-
Discovery of pyrimidine benzimidazoles as Src-family selective Lck inhibitors: Part II
-
Zhang G, Ren, P, Gray NS, et al. Discovery of pyrimidine benzimidazoles as Src-family selective Lck inhibitors: part II. Bioorg Med Chem Lett 2009;19:6691-5
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 6691-5
-
-
Zhang, G.1
Ren, P.2
Gray, N.S.3
-
89
-
-
84961978146
-
Discovery of 2-phenylamino-imidazo[4,5-h]isoquinolin-9-ones: A new class of inhibitors of Lck kinase
-
Snow RJ, Cardozo MG, Morwick TM, et al. Discovery of 2-phenylamino- imidazo[4,5-h]isoquinolin-9-ones: a new class of inhibitors of Lck kinase. J Med Chem 2002;45:3394-405
-
(2002)
J Med Chem
, Issue.45
, pp. 3394-405
-
-
Snow, R.J.1
Cardozo, M.G.2
Morwick, T.M.3
-
90
-
-
0037431414
-
Optimization of 2-phenylaminoimidazo[4,5-h] isoquinolin-9-ones: Orally active inhibitors of Lck kinase
-
Goldberg DR, Butz T, Cardozo MG, et al. Optimization of 2-phenylaminoimidazo[4,5-h] isoquinolin-9-ones: orally active inhibitors of Lck kinase. J Med Chem 2003;46:1337-49
-
(2003)
J Med Chem
, Issue.46
, pp. 1337-49
-
-
Goldberg, D.R.1
Butz, T.2
Cardozo, M.G.3
-
97
-
-
8844271817
-
Discovery of novel 2-(heteroaryl)-thiazole-5-carboxamides as potent and orally active Src-family kinsae p56-Lck inhibitors
-
Chen P, Norris D, Das J, et al. Discovery of novel 2-(heteroaryl)- thiazole-5-carboxamides as potent and orally active Src-family kinsae p56-Lck inhibitors. Bioorg Med Chem Lett 2004;14:6061-6
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 6061-6
-
-
Chen, P.1
Norris, D.2
Das, J.3
-
98
-
-
33750989362
-
2-Aminothiazole as a novel kinase inhibitor template. Structure-activity studies toward the discovery of N-(2-Chloro-6-methylphenyl)-2-[[6-[4-(2- hydroxyethyl)-1-piperazinyl]]-2-methyl-4-pyrimidinyl] amino)]-1,3-thiazole-5- carboxamide (Dasatinib, BMS-354825) as a potent pan-Src Kinase Inhibitor
-
Das J, Chen P, Norris D, et al. 2-Aminothiazole as a novel kinase inhibitor template. Structure-activity studies toward the discovery of N-(2-Chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]] -2-methyl-4-pyrimidinyl] amino)]-1,3-thiazole-5-carboxamide (Dasatinib, BMS-354825) as a potent pan-Src Kinase Inhibitor. J Med Chem 2006;49:6819-32
-
(2006)
J Med Chem
, vol.49
, pp. 6819-32
-
-
Das, J.1
Chen, P.2
Norris, D.3
-
100
-
-
41149161326
-
Discovery of 2-amino-6-carboxamidobenzothiazoles as potent Lck inhinitors
-
Huang S, Liu Z, Tian SS, et al. Discovery of 2-amino-6- carboxamidobenzothiazoles as potent Lck inhinitors. Bioorg Med Chem Lett 2008;18:2324-8
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 2324-8
-
-
Huang, S.1
Liu, Z.2
Tian, S.S.3
-
101
-
-
10744226526
-
Discovery of 2-amino-heteroaryl-benzothiazole-6-anilides as potent p56-Lck inhibitors
-
Das J, Moquin R, Lin J, et al. Discovery of 2-amino-heteroaryl- benzothiazole-6-anilides as potent p56-Lck inhibitors. Bioorg Med Chem Lett 2003;13:2587-90
-
(2003)
Bioorg Med Chem Lett
, vol.13
, pp. 2587-90
-
-
Das, J.1
Moquin, R.2
Lin, J.3
-
102
-
-
77958473258
-
-
Taisho Pharmaceutical Co. Ltd. WO05123671
-
Taisho Pharmaceutical Co. Ltd. Pyrrole derivative. WO05123671; 2005
-
(2005)
Pyrrole Derivative
-
-
-
103
-
-
72049107793
-
Pyrrole derivatives as potent inhibitors of lymphocyte-specific kinase: Structure synthesis and SAR
-
Takayama T, Umemiya H, Amada H, et al. Pyrrole derivatives as potent inhibitors of lymphocyte-specific kinase: Structure, synthesis, and SAR. Bioorg Med Chem Lett 2010;20:108-11
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 108-11
-
-
Takayama, T.1
Umemiya, H.2
Amada, H.3
-
104
-
-
77958454807
-
-
Taisho Pharmaceutical Co Ltd WO07026720;
-
Taisho Pharmaceutical Co. Ltd. Ring-fused pyrrole derivative. WO07026720; 2007
-
(2007)
Ring-fused Pyrrole Derivative
-
-
-
105
-
-
72049098176
-
Ring-fused pyrazole derivatives as potent inhibitors of lymphocyte-specific kinase (Lck): Structure synthesis and SAR
-
Takayama T, Umemiya H, Amada H, et al. Ring-fused pyrazole derivatives as potent inhibitors of lymphocyte-specific kinase (Lck): structure, synthesis, and SAR. Bioorg Med Chem Lett 2010;20:112-16
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 112-16
-
-
Takayama, T.1
Umemiya, H.2
Amada, H.3
-
110
-
-
77958502791
-
-
Novartis Institutes for Biomedical Research, Inc US20100029636
-
Novartis Institutes for Biomedical Research, Inc. Lck Inhibitors. US20100029636, 2010
-
(2010)
Lck Inhibitors
-
-
-
113
-
-
41149146105
-
Structure-guided design of aminopyrimidine amides as potent, selective inhibitors of Lck: Syn thesis, SAR, and inhibition of in vivo T-cell activation
-
DiMauro EF, Newcomb J, Nunes JJ, et al. Structure-guided design of aminopyrimidine amides as potent, selective inhibitors of Lck: synthesis, SAR, and inhibition of in vivo T-cell activation. J Med Chem 2008;51:1681-94
-
(2008)
J Med Chem
, vol.51
, pp. 1681-94
-
-
Dimauro, E.F.1
Newcomb, J.2
Nunes, J.J.3
-
114
-
-
38749084544
-
N-(3-(Phenylcarbamoyl)arylpyrimidine)-5-carboxamides as potent and selective inhibitors of Lck: Structure, synthesis and SAR
-
Deak HL, Newcomb JR, Nunes JJ, et al. N-(3-(Phenylcarbamoyl) arylpyrimidine)-5-carboxamides as potent and selective inhibitors of Lck: structure, synthesis and SAR. Bioorg Med Chem Lett 2008;18:1172-6
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 1172-6
-
-
Deak, H.L.1
Newcomb, J.R.2
Nunes, J.J.3
-
116
-
-
33847413104
-
Alkynylpyrimidine Amide derivatives as potent, selective, and orally active inhibitors of Tie-2 kinase
-
Cee VJ, Albrecht BK, Geuns-Meyer S, et al. Alkynylpyrimidine Amide derivatives as potent, selective, and orally active inhibitors of Tie-2 kinase. J Med Chem 2007;50:627-40
-
(2007)
J Med Chem
, vol.50
, pp. 627-40
-
-
Cee, V.J.1
Albrecht, B.K.2
Geuns-Meyer, S.3
-
119
-
-
41149086287
-
Naphthamides as novel and potent vascular endothelial growth factor receptor tyrosine kinase inhibitors: Design, synthesis, and evaluation
-
Harmange JC, Weiss MM, Germain J, et al. Naphthamides as novel and potent vascular endothelial growth factor receptor tyrosine kinase inhibitors: design, synthesis, and evaluation. J Med Chem 2008;51:1649-67
-
(2008)
J Med Chem
, vol.51
, pp. 1649-67
-
-
Harmange, J.C.1
Weiss, M.M.2
Germain, J.3
-
120
-
-
41149143717
-
Evaluation of a series of naphthamides as potent, orally active vascular endothelial growth factor receptor-2 tyrosine kinase inhibitors
-
Weiss MM, Harmange JC, Polverino AJ, et al. Evaluation of a series of naphthamides as potent, orally active vascular endothelial growth factor receptor-2 tyrosine kinase inhibitors. J Med Chem 2008;51:1668-80
-
(2008)
J Med Chem
, vol.51
, pp. 1668-80
-
-
Weiss, M.M.1
Harmange, J.C.2
Polverino, A.J.3
-
121
-
-
35748952165
-
MAP kinase inhibitors in inflammation and autoimmune disorders
-
Bhagwat SS. MAP kinase inhibitors in inflammation and autoimmune disorders. Ann Rep Med Chem 2007;42:265-78
-
(2007)
Ann Rep Med Chem
, vol.42
, pp. 265-78
-
-
Bhagwat, S.S.1
-
123
-
-
59649127763
-
Inhibition ofp38: Has the fat lady sung?
-
Genovese MC. Inhibition ofp38: has the fat lady sung? Arthritis Rheum 2009;60:37-320
-
(2009)
Arthritis Rheum
, vol.60
, pp. 37-320
-
-
Genovese, M.C.1
|