-
1
-
-
23944515326
-
Intracellular signal transduction pathway proteins as targets for cancer therapy
-
DOI 10.1200/JCO.2005.23.648
-
Adjei, AA; Hidalgo, M. Intracellular signal transduction pathway proteins as targets for cancer therapy. J. Clin. Oncol., 2005, 23, 5386-5403. (Pubitemid 46206992)
-
(2005)
Journal of Clinical Oncology
, vol.23
, Issue.23
, pp. 5386-5403
-
-
Adjei, A.A.1
Hidalgo, M.2
-
2
-
-
64249135764
-
Novel agents on the horizon for cancer therapy
-
Ma, W.W.; Adjei, A.A. Novel agents on the horizon for cancer therapy. CA Cancer J. Clin., 2009, 59, 111-137.
-
(2009)
CA Cancer J. Clin.
, vol.59
, pp. 111-137
-
-
Ma, W.W.1
Adjei, A.A.2
-
3
-
-
0035413610
-
c-Src tyrosine phosphorylation of epidermal growth factor receptor, P190 RhoGAP, and focal adhesion kinase regulates diverse cellular processes
-
Haskell, M.D.; Slack, J.K.; Parsons, J.T.; Parsons, S.J. c-Src tyrosine phosphorylation of epidermal growth factor receptor, P190 RhoGAP, and focal adhesion kinase regulates diverse cellular processes. Chem. Rev., 2001, 101, 2425-2440.
-
(2001)
Chem. Rev.
, vol.101
, pp. 2425-2440
-
-
Haskell, M.D.1
Slack, J.K.2
Parsons, J.T.3
Parsons, S.J.4
-
4
-
-
0037150728
-
Src in cancer: Deregulation and consequences for cell behaviour
-
Frame, M.C. Src in cancer: deregulation and consequences for cell behaviour. Biochim. Biophys. Acta, 2002, 1602, 114-130.
-
(2002)
Biochim. Biophys. Acta
, vol.1602
, pp. 114-130
-
-
Frame, M.C.1
-
5
-
-
0024474916
-
pp60c-Src activation in human colon carcinoma
-
Cartwright, C.A.; Kamps, M.P.; Meisler, A.I.; Pipas, J.M.; Eckhart, W. pp60c-Src activation in human colon carcinoma. J. Clin. Invest., 1989, 83, 2025-2033
-
(1989)
J. Clin. Invest.
, vol.83
, pp. 2025-2033
-
-
Cartwright, C.A.1
Kamps, M.P.2
Meisler, A.I.3
Pipas, J.M.4
Eckhart, W.5
-
6
-
-
0025192786
-
Activation of the pp60(c-src) protein kinase is an early event in colonic carcinogenesis
-
Cartwright, C.A.; Meisler, A.I.; Eckhart, W. Activation of the pp60c-srcprotein kinase is an early event in colonic carcinogenesis. Proc. Natl. Acad. Sci. USA, 1990, 87, 558-562 (Pubitemid 20051409)
-
(1990)
Proceedings of the National Academy of Sciences of the United States of America
, vol.87
, Issue.2
, pp. 558-562
-
-
Cartwright, C.A.1
Meisler, A.I.2
Eckhart, W.3
-
7
-
-
0031979414
-
Characterization of humanepidermal growth factor receptor and c-Src interactions in humanbreast tumor cells
-
Biscardi, J.S.; Belsches, A.P.; Parsons, S.J. Characterization of humanepidermal growth factor receptor and c-Src interactions in humanbreast tumor cells. Mol. Carcinog., 1998, 21, 261-272
-
(1998)
Mol. Carcinog.
, vol.21
, pp. 261-272
-
-
Biscardi, J.S.1
Belsches, A.P.2
Parsons, S.J.3
-
8
-
-
0030474489
-
c-Src protein expression is increased in human breast cancer. An immunohistochemical and biochemical analysis
-
Verbeek, B.S.; Vroom, T.M.; Adriaansen-Slot, S.S.; Ottenhoff-Kalff, A.E.; Geertzema, J.G.; Hennipman, A.; Rijksen G. c-Src protein expression is increased in human breast cancer. An immunohistochemical and biochemical analysis. J. Pathol., 1996, 180, 383-388
-
(1996)
J. Pathol.
, vol.180
, pp. 383-388
-
-
Verbeek, B.S.1
Vroom, T.M.2
Adriaansen-Slot, S.S.3
Ottenhoff-Kalff, A.E.4
Geertzema, J.G.5
Hennipman, A.6
Rijksen, G.7
-
9
-
-
0033521886
-
Activation of Src in human breast tumor cell lines: Elevated levels of phosphotyrosine phosphatase activity that preferentially recognizes the Src carboxy terminal negative regulatory tyrosine530
-
Egan, C.; Pang, A.; Durda, D.; Cheng, H.C.; Wang, J.H.; Fujita, D.J..Activation of Src in human breast tumor cell lines: elevated levels of phosphotyrosine phosphatase activity that preferentially recognizes the Src carboxy terminal negative regulatory tyrosine530. Oncogene, 1999, 18, 1227-1237
-
(1999)
Oncogene
, vol.18
, pp. 1227-1237
-
-
Egan, C.1
Pang, A.2
Durda, D.3
Cheng, H.C.4
Wang, J.H.5
Fujita, D.J.6
-
10
-
-
0345195986
-
Overexpression and activation of the tyrosine kinase Src in human pancreatic carcinoma
-
DOI 10.1006/bbrc.1997.8043
-
Lutz, M.P.; Esser, I.B.; Flossmann-Kast, B.B.; Vogelmann, R.; Luhrs, H.; Friess, H., Buchler, M.W., Adler, G. Overexpression and activation of the tyrosine kinase Src in human pancreatic carcinoma. Biochem. Biophys. Res. Commun., 1998, 243, 503-508 (Pubitemid 28414054)
-
(1998)
Biochemical and Biophysical Research Communications
, vol.243
, Issue.2
, pp. 503-508
-
-
Lutz, M.P.1
Esser, I.B.S.2
Flossmann-Kast, B.B.M.3
Vogelmann, R.4
Luhrs, H.5
Friess, H.6
Buchler, M.W.7
Adler, G.8
-
11
-
-
0026611149
-
Expression of pp60c-src in human small cell and non-small cell lung carcinomas
-
Mazurenko, N.N.; Kogan, E.A.; Zborovskaya, I.B.; Kisseljov, F.L. Expression of pp60c-src in human small cell and non-small cell lung carcinomas. Eur. J. Cancer, 1992, 28, 372-377
-
(1992)
Eur. J. Cancer
, vol.28
, pp. 372-377
-
-
Mazurenko, N.N.1
Kogan, E.A.2
Zborovskaya, I.B.3
Kisseljov, F.L.4
-
12
-
-
0037229627
-
Activated Src protein tyrosine kinase is overexpressed in late-stage human ovarian cancers
-
Wiener, J.R.; Windham, T.C.; Estrella, V.C.; Parikh, N.U.; Thall, P.F.; Deavers, M.T., BastJr, R.C.; Mills, G..; Gallick G.E. Activated Src protein tyrosine kinase is overexpressed in late-stage human ovarian cancers. Gynecol. Oncol., 2003, 88, 73-79
-
(2003)
Gynecol. Oncol.
, vol.88
, pp. 73-79
-
-
Wiener, J.R.1
Windham, T.C.2
Estrella, V.C.3
Parikh, N.U.4
Thall, P.F.5
Deavers, M.T.6
Bast Jr., R.C.7
Mills, G.8
Gallick, G.E.9
-
13
-
-
0031058990
-
Src activation in malignant and premalignant epithelia of Barrett's esophagus
-
Kumble, S.; Omary, M.B.; Cartwright, C.A. Triadafilopoulos G. Src activation in malignant and premalignant epithelia of Barrett's esophagus. Gastroenterology, 1997, 112, 348-356
-
(1997)
Gastroenterology
, vol.112
, pp. 348-356
-
-
Kumble, S.1
Omary, M.B.2
Cartwright, C.A.3
Triadafilopoulos, G.4
-
14
-
-
0026345914
-
Aberrant elevation of tyrosine-specific phosphorylation in human gastric cancer cells
-
Takeshima, E.; Hamaguchi, M.; Watanabe, T.; Akiyama, S.; Kataoka, M.; Ohnishi, Y.; Xiao H.; Nagai Y.; Hiroshi H. Aberrant elevation of tyrosine-specific phosphorylation in human gastric cancer cells. Jpn. J. Cancer Res., 1991, 82, 1428-1435
-
(1991)
Jpn. J. Cancer Res.
, vol.82
, pp. 1428-1435
-
-
Takeshima, E.1
Hamaguchi, M.2
Watanabe, T.3
Akiyama, S.4
Kataoka, M.5
Ohnishi, Y.6
Xiao, H.7
Nagai, Y.8
Hiroshi, H.9
-
15
-
-
18644380911
-
Roles of activated Src and Stat3 signaling in melanoma tumor cell growth
-
DOI 10.1038/sj.onc.1205859
-
Niu, G.; Bowman, T.; Huang, M.; Shivers, S.; Reintgen, D.; Daud, A.; Chang, A.; Kraker, A.; Jove, R.; Yu, H. Roles of activated Src and Stat3 signaling in melanoma tumorcell growth. Oncogene, 2002, 21, 7001-7010 (Pubitemid 35252974)
-
(2002)
Oncogene
, vol.21
, Issue.46
, pp. 7001-7010
-
-
Niu, G.1
Bowman, T.2
Huang, M.3
Shivers, S.4
Reintgen, D.5
Daud, A.6
Chang, A.7
Kraker, A.8
Jove, R.9
Yu, H.10
-
16
-
-
0025012642
-
Early activation of endogenous pp60(src) kinase activity during neuronal differentiation of cultured human neuroblastoma cells
-
Bjelfman, C.; Meyerson, G.; Cartwright, C.A.; Mellstrom, K.; Hammerling, U.; Pahlman, S. Early activation of endogenous pp60 Src kinase activity during neuronal differentiation of cultured human neuroblastoma cells. Mol. Cell Biol., 1990, 10, 361-370 (Pubitemid 20028990)
-
(1990)
Molecular and Cellular Biology
, vol.10
, Issue.1
, pp. 361-370
-
-
Bjelfman, C.1
Meyerson, G.2
Cartwright, C.A.3
Mellstrom, K.4
Hammerling, U.5
Pahlman, S.6
-
17
-
-
0033393771
-
Selective requirement for Src kinases during VEGF-induced angiogenesis and vascular permeability
-
Eliceiri, B.P.; Paul, R.; Schwartzberg, P.L.; Hood, J.D.; Leng, J.; Cheresh, D.A. Selective requirement for Src kinases during VEGF-induced angiogenesis and vascular permeability. Mol. Cell, 1999, 4, 915-924
-
(1999)
Mol. Cell
, vol.4
, pp. 915-924
-
-
Eliceiri, B.P.1
Paul, R.2
Schwartzberg, P.L.3
Hood, J.D.4
Leng, J.5
Cheresh, D.A.6
-
18
-
-
56049110266
-
Recent progress of Src family kinase inhibitors as anti-cancer agents
-
Cao, X.; You, Q.D.; Li, Z.Y.; Wang, X.J.; Lu, X.Y.; Liu, X.R; Xu, D.; Liu, B. Recent progress of Src family kinase inhibitors as anti-cancer agents. Mini Rev. Med. Chem., 2008, 8(10), 1053-1063
-
(2008)
Mini Rev. Med. Chem.
, vol.8
, Issue.10
, pp. 1053-1063
-
-
Cao, X.1
You, Q.D.2
Li, Z.Y.3
Wang, X.J.4
Lu, X.Y.5
Liu, X.R.6
Xu, D.7
Liu, B.8
-
19
-
-
0026484261
-
SH2 and SH3 domains: From structure to function
-
Pawson, T.; Gish, G.D. SH2 and SH3 domains: from structure to function. Cell 1992, 71, 359-362
-
(1992)
Cell
, vol.71
, pp. 359-362
-
-
Pawson, T.1
Gish, G.D.2
-
20
-
-
77956826048
-
SH2 and SH3 domains: Choreographers of multiple signaling pathways
-
Chapter 24
-
Botfield, M.C.; Green, J. Chapter 24. SH2 and SH3 domains: choreographers of multiple signaling pathways. Annu. Rep. Med. Chem., 1995, 30, 227-237
-
(1995)
Annu. Rep. Med. Chem.
, vol.30
, pp. 227-237
-
-
Botfield, M.C.1
Green, J.2
-
21
-
-
0037657546
-
Peptidyl aldehydes as reversible covalent inhibitors of Src homology 2 domains
-
Park, J.;Fu, H.; Pei.D. Peptidyl aldehydes as reversible covalent inhibitors of Src homology 2 domains. Biochemistry, 2003, 42, 5159-5167
-
(2003)
Biochemistry
, vol.42
, pp. 5159-5167
-
-
Park, J.1
Fu, H.2
Pei, D.3
-
22
-
-
0027403027
-
SH2 domains recognize specific phosphopeptide sequences
-
Zhou, S.Y.; Shoelson, S.E.; Chaudhuri, M.; Gish, G.; Pawson, T.; Haser, W.G.; King, F.; Roberts, T.; Ratnofsky, S.; Lechleider, R.J.; Neel, B.G.; Birge, R.B.; Fajardo, J.E.; Chou, M.M.; Hanafusa, H.; Schaffhausen, B.; Cantley, L.C. SH2 domains recognize specific phosphopeptide sequences. Cell, 1993, 72, 767-778
-
(1993)
Cell
, vol.72
, pp. 767-778
-
-
Zhou, S.Y.1
Shoelson, S.E.2
Chaudhuri, M.3
Gish, G.4
Pawson, T.5
Haser, W.G.6
King, F.7
Roberts, T.8
Ratnofsky, S.9
Lechleider, R.J.10
Neel, B.G.11
Birge, R.B.12
Fajardo, J.E.13
Chou, M.M.14
Hanafusa, H.15
Schaffhausen, B.16
Cantley, L.C.17
-
23
-
-
0037116524
-
Calorimetric and structural studies of 1, 2, 3-trisubstituted cyclopropanes as conformationally constrained peptide inhibitors of Src SH2 domain binding
-
Davidson, J.P.; Lubman, O.; Rose, T.; Waksman, G.; Martin, S.F. Calorimetric and structural studies of 1, 2, 3-trisubstituted cyclopropanes as conformationally constrained peptide inhibitors of Src SH2 domain binding. J. Am. Chem. Soc., 2002, 124, 205-215
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 205-215
-
-
Davidson, J.P.1
Lubman, O.2
Rose, T.3
Waksman, G.4
Martin, S.F.5
-
24
-
-
0035833022
-
Selective inhibition of Src SH2 by a novel thiol-targeting tricarbonyl-modified inhibitor and mechanistic analysis by 1H/13C NMR spectroscopy
-
Sundaramoorthi, R.; Siedem, C.; Vu, C.B.; Dalgarno, D.C.; Laird, E.C.; Botfield, M.C.; Combs, A.B.; Adams, S.E.; Yuan, R.W.; Weigele, M.; Narula, S.S. Selective inhibition of Src SH2 by a novel thiol-targeting tricarbonyl-modified inhibitor and mechanistic analysis by 1H/13C NMR spectroscopy. Bioorg. Med. Chem. Lett., 2001, 11, 1665-1669
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1665-1669
-
-
Sundaramoorthi, R.1
Siedem, C.2
Vu, C.B.3
Dalgarno, D.C.4
Laird, E.C.5
Botfield, M.C.6
Combs, A.B.7
Adams, S.E.8
Yuan, R.W.9
Weigele, M.10
Narula, S.S.11
-
25
-
-
0037037399
-
Design and characterization of non-phosphopeptide inhibitors for Src family SH2 domains
-
Park, S.H.; Wona, T.; Leeb, K.H. Design and characterization of non-phosphopeptide inhibitors for Src family SH2 domains. Bioorg. Med. Chem. Lett., 2002, 12, 2711-2714
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 2711-2714
-
-
Park, S.H.1
Wona, T.2
Leeb, K.H.3
-
26
-
-
2542528563
-
Conformationally constrained peptide analogues of pTyr-Glu-Glu-Ile as inhibitors of the Src SH2 domain binding
-
DOI 10.1021/jm040008+
-
Nam, N.H.; Ye, G.F.; Sun, G.H.; Parang, K. Conformationally constrained peptide analogues of pTyr-Glu-Glu-Ile as inhibitors of the Src SH2 domain binding. J. Med. Chem., 2004, 47, 3131-3141 (Pubitemid 38702707)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.12
, pp. 3131-3141
-
-
Nam, N.-H.1
Ye, G.2
Sun, G.3
Parang, K.4
-
27
-
-
0037060906
-
Synthesis and activity of a new methoxytetrahydropyran derivative as dual cyclooxygenase-2,5-lipoxygenase inhibitor
-
Nam, N.H.; Pitts, R.L.; Sun, G.H.; Sardari, S.; Tiemo, A.; Xie, M.X.; Yana, B.F.; Parang, K. Synthesis and activity of a new methoxytetrahydropyran derivative as dual cyclooxygenase-2,5-lipoxygenase inhibitor. Bioorg. Med. Chem. Lett., 2004, 12, 779-782
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 779-782
-
-
Nam, N.H.1
Pitts, R.L.2
Sun, G.H.3
Sardari, S.4
Tiemo, A.5
Xie, M.X.6
Yana, B.F.7
Parang, K.8
-
28
-
-
67649842387
-
Synthesis and evaluation of phosphopeptides containing iminodiacetate groups as binding ligands of the Src SH2 domain
-
Ye, G.F.; Schuler A.D.; Ahmadibeni, Y.; Morgan, J.R.; Faruqui, A.; Huang, K.Z.; Sun, G.Q.; Zebala, J.A.; Parang, K. Synthesis and evaluation of phosphopeptides containing iminodiacetate groups as binding ligands of the Src SH2 domain. Bioorg. Chem., 2009, 37, 133-142
-
(2009)
Bioorg. Chem.
, vol.37
, pp. 133-142
-
-
Ye, G.F.1
Schuler, A.D.2
Ahmadibeni, Y.3
Morgan, J.R.4
Faruqui, A.5
Huang, K.Z.6
Sun, G.Q.7
Zebala, J.A.8
Parang, K.9
-
29
-
-
0033575680
-
Structure-based design and synthesis of a novel class of Src SH2 inhibitors
-
Buchanan, J.L.; Bohacek, R.S.; Luke, G.P.; Hatada, M.; Lu, X.D.; Dalgamo, D.C.; Narua, S.S.; Yuan, R.; Holt, D.A. Structure-based design and synthesis of a novel class of Src SH2 inhibitors. Bioorg. Med. Chem. Lett., 1999, 9, 2353-2358
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 2353-2358
-
-
Buchanan, J.L.1
Bohacek, R.S.2
Luke, G.P.3
Hatada, M.4
Lu, X.D.5
Dalgamo, D.C.6
Narua, S.S.7
Yuan, R.8
Holt, D.A.9
-
30
-
-
17944368273
-
Src SH2 domain
-
Src SH2 domain. Bioorg. Med. Chem. Lett., 2001, 11, 2319-2323
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 2319-2323
-
-
Kawahata, N.1
Yang, M.G.2
Luke, G.P.3
Shakespeare, W.C.4
Sundaramoorthi, R.5
Wang, Y.H.6
Johnson, D.7
Merry, T.8
Violette, S.M.9
Guan, W.10
Bartlett, C.11
Smith, J.12
Hatada, M.13
Lu, X.D.14
Dalgarno, D.C.15
Eyermann, C.J.16
Bohacek, R.S.17
Sawyer, T.K.18
-
31
-
-
0034687218
-
Structure-based design of novel bicyclic nonpeptide inhibitors for the Src SH2 domain
-
Shakespeare, W.C.; Bohacek, R.S.; Azimioara, M.D.; Macek, K.J.; Luke, G.P.; Dalgarno, D.C.; Hatada, M.H.; Lu, X.D.; Violette, S.M.; Bartlett, C.; Sawyer, T.K. Structure-based design of novel bicyclic nonpeptide inhibitors for the Src SH2 domain. J. Med. Chem., 2000, 43, 3815-3819
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3815-3819
-
-
Shakespeare, W.C.1
Bohacek, R.S.2
Azimioara, M.D.3
Macek, K.J.4
Luke, G.P.5
Dalgarno, D.C.6
Hatada, M.H.7
Lu, X.D.8
Violette, S.M.9
Bartlett, C.10
Sawyer, T.K.11
-
32
-
-
0242439332
-
pp60Src Are Identical to Those for High Affinity Binding of Full Length Inhibitors
-
DOI 10.1021/jm020970s
-
Lange, G.; Lesuisse, D.; Deprez, P.; Schoot, B.; Loenze, P.; Bénard, D.; Marquette, J.P.; Broto, P.; Sarubbi, E.; Mandine, E. Requirements for specific binding of low affinity inhibitor fragments to the SH2 domain of pp60Src are identical to those for high affinity binding of full length inhibitors. J. Med. Chem., 2003, 46, 5184-5195 (Pubitemid 37414188)
-
(2003)
Journal of Medicinal Chemistry
, vol.46
, Issue.24
, pp. 5184-5195
-
-
Lange, G.1
Lesuisse, D.2
Deprez, P.3
Schoot, B.4
Loenze, P.5
Benard, D.6
Marquette, J.-P.7
Broto, P.8
Sarubbi, E.9
Mandine, E.10
-
33
-
-
84924253781
-
-
Hur, E. M.; Choi, B.; Park, C.; Lee, J.; Park, D.; Yun, Y.; Lee, K. H.; Oh, J. E.; Ahn, C. S.; Lee, H. S.; Ahn, J. S; Jung, S. I. U.S. Patent 6,140, 363
-
Hur, E. M.; Choi, B.; Park, C.; Lee, J.; Park, D.; Yun, Y.; Lee, K. H.; Oh, J. E.; Ahn, C. S.; Lee, H. S.; Ahn, J. S; Jung, S. I. U.S. Patent 6,140, 363.
-
-
-
-
34
-
-
0038068134
-
Rosmarinic acid inhibits TCR-induced T cell activation and proliferation in an Lck-dependent manner
-
DOI 10.1002/eji.200323010
-
Won, J.; Hur, E. M.; Hur, Y.; Park, S.; Kang, M.; Choi, Y.; Park, C.; Lee, K. H.; Yun, Y. Rosmarinic acid inhibits TCR-induced T cell activation and proliferation in an Lck-dependent manner. Eur. J. Immunol., 2003, 33, 870-879 (Pubitemid 36546674)
-
(2003)
European Journal of Immunology
, vol.33
, Issue.4
, pp. 870-879
-
-
Won, J.1
Hur, Y.-G.2
Hur, E.M.3
Park, S.-H.4
Kang, M.-A.5
Choi, Y.6
Park, C.7
Lee, K.-H.8
Yun, Y.9
-
35
-
-
0141740202
-
Design and synthesis of small chemical inhibitors containing different scaffolds for lck SH2 domain
-
Park, S.H.; Kang, S.H.; Lim, S.H.; Ohb, H.S.; Leeb, K.H. Design and synthesis of small chemical inhibitors containing different scaffolds for lck SH2 domain. Bioorg. Med. Chem. Lett., 2003, 13, 3455-3459
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 3455-3459
-
-
Park, S.H.1
Kang, S.H.2
Lim, S.H.3
Ohb, H.S.4
Leeb, K.H.5
-
36
-
-
65749095573
-
Natural product inhibitors of protein-protein interactions mediated by Src-family SH2 domains
-
Bianca Sperl, Markus H.J.Seifert, Thorsten Berg Natural product inhibitors of protein-protein interactions mediated by Src-family SH2 domains. Bioorg. Med. Chem. Lett., 2009, 19, 3305-3309
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 3305-3309
-
-
Sperl, B.1
Seifert, M.H.J.2
Berg, T.3
-
37
-
-
33846048058
-
Transcription factors control invasion: AP-1 the first among equals
-
Ozanne, B.W.; Spence, H.J.; Mcgarry L.C.; Hennigan R.F. Transcription factors control invasion: AP-1 the first among equals. Oncogene, 2007, 26, 1-10.
-
(2007)
Oncogene
, vol.26
, pp. 1-10
-
-
Ozanne, B.W.1
Spence, H.J.2
Mcgarry, L.C.3
Hennigan, R.F.4
-
38
-
-
0030062879
-
Protein structure-based combinatorial chemistry: Discovery of non-peptide binding elements to Src SH3 domain
-
DOI 10.1021/ja953750v
-
Combs A.P.; Kapoor T.M.; Feng S.B.; Chen J.K.; Daude-Snow L.F., Schreiber S.L. Protein structre-based combinatorial chemistry: discovery of non-peptide binding elements to Src SH3 domain J. Am. Chem. Soc., 1996, 118, 287-288 (Pubitemid 3017427)
-
(1996)
Journal of the American Chemical Society
, vol.118
, Issue.1
, pp. 287-288
-
-
Combs, A.P.1
Kapoor, T.M.2
Feng, S.3
Chen, J.K.4
Daude-Snow, L.F.5
Schreiber, S.L.6
-
39
-
-
0030220960
-
Molecular basis for the binding of SH3 ligands with non-peptide elements identified by combinatorial synthesis
-
Feng S.B.; Kapoor T.M.; Shirai F.; Combs A.P.; Schreiber S.L. Molecular basis for the binding of SH3 ligands with non-peptide elements identified by combinatorial synthesis. Chem. Biol., 1996, 3: 661-670.
-
(1996)
Chem. Biol.
, vol.3
, pp. 661-670
-
-
Feng, S.B.1
Kapoor, T.M.2
Shirai, F.3
Combs, A.P.4
Schreiber, S.L.5
-
40
-
-
0035912062
-
UCS15A, a non-kinase inhibitor of Src signal transduction
-
DOI 10.1038/sj.onc.1204296
-
Sharma, S.V.; Oneyama, C.; Yamashita, Y.; Nakano, H.; Sugawara, K.; Hamada, M.; Kosaka, N; Tamaoki, T. UCS15A, a nonkinase inhibitor of Src signal transduction. Oncogene, 2001, 20, 2068-2079 (Pubitemid 32424001)
-
(2001)
Oncogene
, vol.20
, Issue.17
, pp. 2068-2079
-
-
Sharma, S.V.1
Oneyama, C.2
Yamashita, Y.3
Nakano, H.4
Sugawara, K.5
Hamada, M.6
Kosaka, N.7
Tamaoki, T.8
-
41
-
-
0028220672
-
A target for Src in mitosis
-
Fumagalli, S.; Totty, N.; Hsuan, J.; Courtneidge, S. A target for Src in mitosis. Nature, 1994, 368, 871-875
-
(1994)
Nature
, vol.368
, pp. 871-875
-
-
Fumagalli, S.1
Totty, N.2
Hsuan, J.3
Courtneidge, S.4
-
42
-
-
0037150229
-
UCS15A, a novel small molecule, SH3 domain-mediated protein-protein interaction blocking drug
-
Oneyama, C.; Nakano, H.; Sharma, S.V. UCS15A, a novel small molecule, SH3 domain-mediated protein-protein interaction blocking drug. Oncogene, 2002, 21, 2037-2050
-
(2002)
Oncogene
, vol.21
, pp. 2037-2050
-
-
Oneyama, C.1
Nakano, H.2
Sharma, S.V.3
-
43
-
-
6044275971
-
Identification and specificity studies of small-molecule ligands for SH3 protein domains
-
Inglis, S.R.; Stojkoski, C.; Branson, K.M.; Cawthray, J.F.; Fritz, D.; Wiadrowski, E.; Pyke, S.M.; Booker, G.W. Identification and specificity studies of small-molecule ligands for SH3 protein domains. J. Med. Chem., 2004, 47, 5405-5417
-
(2004)
J. Med. Chem.
, vol.47
, pp. 5405-5417
-
-
Inglis, S.R.1
Stojkoski, C.2
Branson, K.M.3
Cawthray, J.F.4
Fritz, D.5
Wiadrowski, E.6
Pyke, S.M.7
Booker, G.W.8
-
44
-
-
27944493098
-
Synthesis of N-benzylated-2-aminoquinolines as ligands for the Tec SH3 domain
-
Inglis, S.R.; Jones, R.K.; Booker, G.W.; Pyke, S.M. Synthesis of N-benzylated-2-aminoquinolines as ligands for the Tec SH3 domain. Bioorg. Med. Chem. Lett., 2006, 16, 387-390
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 387-390
-
-
Inglis, S.R.1
Jones, R.K.2
Booker, G.W.3
Pyke, S.M.4
-
45
-
-
56449131231
-
Sequential and Selective Buchwald-Hartwig Amination Reactions for the Controlled Functionalization of 6-Bromo-2-chloroquinoline: Synthesis of Ligands for the Tec Src Homology 3 Domain
-
Smith, J. A.; Jones, R. K.; Booker, G. W; and Pyke S. M. Sequential and Selective Buchwald-Hartwig Amination Reactions for the Controlled Functionalization of 6-Bromo-2-chloroquinoline: Synthesis of Ligands for the Tec Src Homology 3 Domain. J. Org. Chem., 2008, 73, 8880-8892.
-
(2008)
J. Org. Chem.
, vol.73
, pp. 8880-8892
-
-
Smith, J.A.1
Jones, R.K.2
Booker, G.W.3
Pyke, S.M.4
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