-
1
-
-
0025343230
-
Signal transduction by receptors with tyrosine kinase activity
-
Ullrich A, Schlessinger J. Signal transduction by receptors with tyrosine kinase activity. Cell 1990; 61: 203-12.
-
(1990)
Cell
, vol.61
, pp. 203-212
-
-
Ullrich, A.1
Schlessinger, J.2
-
2
-
-
0026316096
-
Growth factors and cancer
-
Aaronson SA. Growth factors and cancer. Science 1991; 254: 1146-53.
-
(1991)
Science
, vol.254
, pp. 1146-1153
-
-
Aaronson, S.A.1
-
3
-
-
15644374929
-
Synthesis and tyrosine kinase inhibitory activity of a series of 2-amino-8H-pyrido[2,3-d]pyrimidines: Identification of potent, selective platelet-derived growth factor receptor tyrosine kinase inhibitors
-
Boschelli DH, Wu Z, Klutchko SR, Showalter HDH, Hamby JM, Lu GH, et al. Synthesis and tyrosine kinase inhibitory activity of a series of 2-amino-8H-pyrido[2,3-d]pyrimidines: identification of potent, selective platelet-derived growth factor receptor tyrosine kinase inhibitors. J Med Chem 1998; 41: 4365-77.
-
(1998)
J Med Chem
, vol.41
, pp. 4365-4377
-
-
Boschelli, D.H.1
Wu, Z.2
Klutchko, S.R.3
Showalter, H.D.H.4
Hamby, J.M.5
Lu, G.H.6
-
4
-
-
0035413617
-
Chemical inhibitors of protein kinases
-
Alexander JB. Chemical inhibitors of protein kinases. Chem Rev 2001; 101: 2541-72.
-
(2001)
Chem Rev
, vol.101
, pp. 2541-2572
-
-
Alexander, J.B.1
-
5
-
-
0033026444
-
Strategies toward the design of novel and selective protein tyrosine kinase inhibitors
-
Traxler P, Furet P. Strategies toward the design of novel and selective protein tyrosine kinase inhibitors. Pharmacol Ther 1999; 82: 195-206.
-
(1999)
Pharmacol Ther
, vol.82
, pp. 195-206
-
-
Traxler, P.1
Furet, P.2
-
6
-
-
0029003828
-
Protein kinase in human breast cancer
-
Cance WG, Liu ET. Protein kinase in human breast cancer. Breast Cancer Res Treat 1995; 35: 105-14.
-
(1995)
Breast Cancer Res Treat
, vol.35
, pp. 105-114
-
-
Cance, W.G.1
Liu, E.T.2
-
7
-
-
0028266876
-
Egf receptor expression, regulation, and function in breast cancer
-
Chrysogelos SA, Dickson RB. Egf receptor expression, regulation, and function in breast cancer. Breast Cancer Res Treat 1994; 29: 29-40.
-
(1994)
Breast Cancer Res Treat
, vol.29
, pp. 29-40
-
-
Chrysogelos, S.A.1
Dickson, R.B.2
-
8
-
-
0031471224
-
Expression and functions of growth-factors and growth-factor receptors in liver-cancer
-
Yang EB, Wang DF, Cheng Y, Mack P. Expression and functions of growth-factors and growth-factor receptors in liver-cancer. Cancer J 1997; 10: 319-24.
-
(1997)
Cancer J
, vol.10
, pp. 319-324
-
-
Yang, E.B.1
Wang, D.F.2
Cheng, Y.3
Mack, P.4
-
9
-
-
0035905545
-
Inhibition of epidermal growth factor receptor tyrosine kinase by chalcome derivatives
-
Yang EB, Guo YJ, Zhang K, Chen YZ, Mack P. Inhibition of epidermal growth factor receptor tyrosine kinase by chalcome derivatives. Biochim Biophys Acta 2001; 1550: 144-50.
-
(2001)
Biochim Biophys Acta
, vol.1550
, pp. 144-150
-
-
Yang, E.B.1
Guo, Y.J.2
Zhang, K.3
Chen, Y.Z.4
Mack, P.5
-
10
-
-
0034788453
-
Tyrosine kinase inhibitors: From rational design to clinical trials
-
Traxler P, Bold G, Buchdunger E, Caravatti G, Furet P, Manley P, et al. Tyrosine kinase inhibitors: from rational design to clinical trials. J Med Res Rev 2001; 21: 499-512.
-
(2001)
J Med Res Rev
, vol.21
, pp. 499-512
-
-
Traxler, P.1
Bold, G.2
Buchdunger, E.3
Caravatti, G.4
Furet, P.5
Manley, P.6
-
11
-
-
0035413615
-
Comparative QSAR study of tyrosine kinase inhibitors
-
Kurup A, Garg R, Hansch C. Comparative QSAR study of tyrosine kinase inhibitors. Chem Rev 2001; 101: 2573-600.
-
(2001)
Chem Rev
, vol.101
, pp. 2573-2600
-
-
Kurup, A.1
Garg, R.2
Hansch, C.3
-
13
-
-
0028142387
-
A specific inhibitor of the epidermal growth factor receptor tyrosine kinase
-
Fry DW, Kraker AJ, McMichael A, Ambroso LA, Nelson JM, Leopold WR, et al. A specific inhibitor of the epidermal growth factor receptor tyrosine kinase. Science 1994; 265: 1093-5.
-
(1994)
Science
, vol.265
, pp. 1093-1095
-
-
Fry, D.W.1
Kraker, A.J.2
McMichael, A.3
Ambroso, L.A.4
Nelson, J.M.5
Leopold, W.R.6
-
14
-
-
0034611617
-
Tyrosine kinase inhibitors. 17. Irreversible inhibitors of the epidermal growth factor receptor: 4-(phenylamino) quinazoline- and 4-(phenylamino) pyrido[3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions
-
Smaill JB, Rewcastle GW, Loo JA, Greis KD, Chan OH, Reyner, EL, et al. Tyrosine kinase inhibitors. 17. Irreversible inhibitors of the epidermal growth factor receptor: 4-(phenylamino) quinazoline- and 4-(phenylamino) pyrido[3,2-d]pyrimidine-6-acrylamides bearing additional solubilizing functions. J Med Chem 2000; 43: 1380-97.
-
(2000)
J Med Chem
, vol.43
, pp. 1380-1397
-
-
Smaill, J.B.1
Rewcastle, G.W.2
Loo, J.A.3
Greis, K.D.4
Chan, O.H.5
Reyner, E.L.6
-
15
-
-
9844235351
-
Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(phenylamino)pyrazolo[3,4-d]pyrimidines
-
Traxeler P, Bold G, Frei J, Lang M, Lydon N, Mett H, et al. Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(phenylamino)pyrazolo[3,4-d]pyrimidines. J Med Chem 1997; 40: 3601-16.
-
(1997)
J Med Chem
, vol.40
, pp. 3601-3616
-
-
Traxeler, P.1
Bold, G.2
Frei, J.3
Lang, M.4
Lydon, N.5
Mett, H.6
-
16
-
-
0037413550
-
Synthesis and structure-activity relationships of 6,7-disubstituted 4-anilinoquinoline-3- carbonitriles. The design of an orally active, irreversible inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR) and the human epidermal growth factor receptor-2 (HER-2)
-
Wissner A, Overbeek E, Reich MF, Floyd MB, Johnson BD, Mamuya N, et al. Synthesis and structure-activity relationships of 6,7-disubstituted 4-anilinoquinoline-3- carbonitriles. The design of an orally active, irreversible inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR) and the human epidermal growth factor receptor-2 (HER-2). J Med Chem 2003; 46: 49-63.
-
(2003)
J Med Chem
, vol.46
, pp. 49-63
-
-
Wissner, A.1
Overbeek, E.2
Reich, M.F.3
Floyd, M.B.4
Johnson, B.D.5
Mamuya, N.6
-
17
-
-
0030907052
-
Tyrosine kinase inhibitors. 11. Soluble analogues of pyrrolo- and pyrazoloquinazolines as epidermal growth factor receptor inhibitors: Synthesis, biological evaluation, and modeling of the mode of binding
-
Palmer BD, Trumpp-Kallmeyer S, Fry DW, Nelson JM, Showalter HDH, Denny WA. Tyrosine kinase inhibitors. 11. Soluble analogues of pyrrolo- and pyrazoloquinazolines as epidermal growth factor receptor inhibitors: synthesis, biological evaluation, and modeling of the mode of binding. J Med Chem 1997; 40: 1519-29.
-
(1997)
J Med Chem
, vol.40
, pp. 1519-1529
-
-
Palmer, B.D.1
Trumpp-Kallmeyer, S.2
Fry, D.W.3
Nelson, J.M.4
Showalter, H.D.H.5
Denny, W.A.6
-
18
-
-
19244370071
-
Design, synthesis, and evaluations of substituted 3-[(3-or4-carboxyethyl-pyrrol-2-yl) methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinases
-
Sun L, Tran N, Liang C, Tang F, Rice A, Schreck R, et al. Design, synthesis, and evaluations of substituted 3-[(3-or4-carboxyethyl-pyrrol-2-yl) methylidenyl]indolin-2-ones as inhibitors of VEGF, FGF, and PDGF receptor tyrosine kinases. J Med Chem 1999; 42: 5120-30.
-
(1999)
J Med Chem
, vol.42
, pp. 5120-5130
-
-
Sun, L.1
Tran, N.2
Liang, C.3
Tang, F.4
Rice, A.5
Schreck, R.6
-
19
-
-
0032474915
-
Synthesis and biological evaluations of 3-substituted indolin-2-ones: A novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases
-
Sun L, Tran N, Tang F, App H, McMahon G, Tang C. Synthesis and biological evaluations of 3-substituted indolin-2-ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases. J Med Chem 1998; 41: 2588-603.
-
(1998)
J Med Chem
, vol.41
, pp. 2588-2603
-
-
Sun, L.1
Tran, N.2
Tang, F.3
App, H.4
McMahon, G.5
Tang, C.6
-
20
-
-
0030945871
-
Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors
-
Mohammadi M, McMahon G. Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors. Science 1997; 276: 955-60.
-
(1997)
Science
, vol.276
, pp. 955-960
-
-
Mohammadi, M.1
McMahon, G.2
-
21
-
-
0016915828
-
-
Battersby AR, Hunt E, McDonald E, Paine III JB, Saunders J. Biosynthesis of porphrins and related macrocycles. Part VIII. Enzymic decarboxylation of uroporphyrinogen-III: structure of an intermediate, phyriaporphyrinogen-III, and synthesis of the corresponding porphyrin and of two isomeric porphrins. J Chem Soc Perk I 1976; 1008-21.
-
Battersby AR, Hunt E, McDonald E, Paine III JB, Saunders J. Biosynthesis of porphrins and related macrocycles. Part VIII. Enzymic decarboxylation of uroporphyrinogen-III: structure of an intermediate, phyriaporphyrinogen-III, and synthesis of the corresponding porphyrin and of two isomeric porphrins. J Chem Soc Perk I 1976; 1008-21.
-
-
-
-
22
-
-
3242798249
-
Evaluation of active recombinant catalytic domain of human ErbB-2 tyrosine kinase, and suppression of activity by a naturally derived inhibitor, ZH-4B
-
Guo XN, Zhong L, Zhang XH, Zhao WM, Zhang XW, Lin LP, et al. Evaluation of active recombinant catalytic domain of human ErbB-2 tyrosine kinase, and suppression of activity by a naturally derived inhibitor, ZH-4B. Biochim Biophys Acta 2004; 1673: 186-93.
-
(2004)
Biochim Biophys Acta
, vol.1673
, pp. 186-193
-
-
Guo, X.N.1
Zhong, L.2
Zhang, X.H.3
Zhao, W.M.4
Zhang, X.W.5
Lin, L.P.6
-
23
-
-
33846017392
-
Erbb-2 selective small molecule kinase inhibitors
-
US patent 2004023957-A1. 2004
-
Wang S, Yang D, Enyedy I. Erbb-2 selective small molecule kinase inhibitors. US patent 2004023957-A1. 2004.
-
-
-
Wang, S.1
Yang, D.2
Enyedy, I.3
-
24
-
-
33645887630
-
in vitro murine model of a penicillin specific IgE anamnestic response
-
Mosmann T. An in vitro murine model of a penicillin specific IgE anamnestic response. J Immunol Methods 1983; 139: 55-60.
-
(1983)
J Immunol Methods
, vol.139
, pp. 55-60
-
-
Mosmann, T.A.1
-
25
-
-
33845997838
-
-
Origin. Version 7.0. Northampton, MA: Microcal Software Inc, 2002, cited 2005 Jul 20, Available from
-
Origin. Version 7.0. Northampton, MA: Microcal Software Inc, 2002. [cited 2005 Jul 20]. Available from: www.microcal.com.
-
-
-
-
26
-
-
0033954256
-
The protein data bank
-
Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, et al. The protein data bank. Nucleic Acids Res 2000; 28: 235-42.
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 235-242
-
-
Berman, H.M.1
Westbrook, J.2
Feng, Z.3
Gilliland, G.4
Bhat, T.N.5
Weissig, H.6
-
27
-
-
33846007419
-
-
Sybyl molecular modeling package Computer program, Version 6.8. St Louis, MO: Tripos Associates, 2000
-
Sybyl molecular modeling package (Computer program). Version 6.8. St Louis, MO: Tripos Associates, 2000.
-
-
-
-
28
-
-
0021757436
-
A new force field for molecular mechanical simulation of nucleic acids and proteins
-
Weiner SJ, Kollman PA, Case DA, Singh UC, Ghio C, Alagona G, et al. A new force field for molecular mechanical simulation of nucleic acids and proteins. J Am Chem Soc 1984; 106: 765-84.
-
(1984)
J Am Chem Soc
, vol.106
, pp. 765-784
-
-
Weiner, S.J.1
Kollman, P.A.2
Case, D.A.3
Singh, U.C.4
Ghio, C.5
Alagona, G.6
-
29
-
-
49149147973
-
Iterative partial equalization of orbital electronegativity - a rapid access to atomic charges
-
Gasteiger J, Marsili M. Iterative partial equalization of orbital electronegativity - a rapid access to atomic charges. Tetrahedron 1980; 36: 3219-88.
-
(1980)
Tetrahedron
, vol.36
, pp. 3219-3288
-
-
Gasteiger, J.1
Marsili, M.2
-
30
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function
-
Morris GM, Goodsell DS, Halliday RS, Huey R, Hart WE, Belew RK, et al. Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function. J Comput Chem 1998; 19: 1639-62.
-
(1998)
J Comput Chem
, vol.19
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Hart, W.E.5
Belew, R.K.6
-
31
-
-
33846014001
-
-
Morris GM, Goodsell DS, Halliday RS, Huey R, Hart WE, Belew RK, et al. Autodock Version 3.0.3, Molecular Graphics Laboratory, Department of Molecular Biology, The Scripps Research Institute, La Jolla, CA, USA. 1999
-
Morris GM, Goodsell DS, Halliday RS, Huey R, Hart WE, Belew RK, et al. Autodock (Version 3.0.3), Molecular Graphics Laboratory, Department of Molecular Biology, The Scripps Research Institute, La Jolla, CA, USA. 1999.
-
-
-
-
32
-
-
33846020626
-
-
Case DA, Pearlman DA, Caldwell JW, Cheatham TE III, Ross WS, Simmerling CL, et al. AMBER 5.1, 5th ed, San Francisco, CA: University of California; 1997.
-
Case DA, Pearlman DA, Caldwell JW, Cheatham TE III, Ross WS, Simmerling CL, et al. AMBER 5.1, 5th ed, San Francisco, CA: University of California; 1997.
-
-
-
-
33
-
-
0345099649
-
Structure-based discovery of potassium channel blockers from natural products: Virtual screening and electrophysiological assay testing
-
Liu H, Li Y, Song M, Tan X, Cheng F, Zheng S, et al. Structure-based discovery of potassium channel blockers from natural products: virtual screening and electrophysiological assay testing. Chem Biol 2003; 10: 1103-13.
-
(2003)
Chem Biol
, vol.10
, pp. 1103-1113
-
-
Liu, H.1
Li, Y.2
Song, M.3
Tan, X.4
Cheng, F.5
Zheng, S.6
-
34
-
-
33846009870
-
-
POV-ray. Version 3. POV-ray-Team, 1999, cited 2005 Jul 20, Available from
-
POV-ray. Version 3. POV-ray-Team, 1999. [cited 2005 Jul 20]. Available from: www.povray.org.
-
-
-
-
35
-
-
5144226672
-
13C NMR approach to categorizing potential limitations of a, b-unsaturated carbonyl systems in drug-like molecules
-
13C NMR approach to categorizing potential limitations of a, b-unsaturated carbonyl systems in drug-like molecules. Bioorg Med Chem Lett 2004; 14: 5503-7
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 5503-5507
-
-
Usack, K.P.1
Arnold, L.D.2
Barberis, C.E.3
Chen, H.P.4
Ericsson, A.M.5
Gaza-Bulseco, G.S.6
-
36
-
-
0001329837
-
Pyrrole chemistry. An improved synthesis of ethyl pyrrole-2-carboxylate esters from diethyl aminomalonate
-
John B, Dolphin D. Pyrrole chemistry. An improved synthesis of ethyl pyrrole-2-carboxylate esters from diethyl aminomalonate. J Org Chem 1985; 50: 5598-604.
-
(1985)
J Org Chem
, vol.50
, pp. 5598-5604
-
-
John, B.1
Dolphin, D.2
-
38
-
-
0003708387
-
The DIRIDIF-94 program system
-
The Netherlands: University of Nijmegen
-
Beurskens PT, Admiraal B, Beurskens G, Bosman WP, Garcia-Granda S, Gould RO, et al. The DIRIDIF-94 program system. Technical report of the crystallography laboratory. The Netherlands: University of Nijmegen, 1994.
-
(1994)
Technical report of the crystallography laboratory
-
-
Beurskens, P.T.1
Admiraal, B.2
Beurskens, G.3
Bosman, W.P.4
Garcia-Granda, S.5
Gould, R.O.6
-
40
-
-
0000940732
-
Dispersion corrections and crystal structure refinements
-
Ibers JA, Hamilton WC. Dispersion corrections and crystal structure refinements. Acta Cryst 1964; 17: 781-2.
-
(1964)
Acta Cryst
, vol.17
, pp. 781-782
-
-
Ibers, J.A.1
Hamilton, W.C.2
|