-
1
-
-
0032706396
-
Novel Anti-Cancer Agents in Development: Exciting Prospects and New Challenges
-
Seymore, L. Novel Anti-Cancer Agents in Development: Exciting Prospects and New Challenges. Cancer Treat. Revs. 1999, 25, 301-312.
-
(1999)
Cancer Treat. Revs.
, vol.25
, pp. 301-312
-
-
Seymore, L.1
-
2
-
-
0006996918
-
Novel Molecular Targets for Cancer Drug Discovery
-
Coleman, W. B.; Tsongalis, G. J., Eds.; Humana Press: Totowa, NJ
-
Buolamwini, J. K. Novel Molecular Targets for Cancer Drug Discovery In The Molecular Basis of Human Cancer; Coleman, W. B.; Tsongalis, G. J., Eds.; Humana Press: Totowa, NJ, 2002; pp 521-540.
-
(2002)
The Molecular Basis of Human Cancer
, pp. 521-540
-
-
Buolamwini, J.K.1
-
3
-
-
0035908493
-
Blocking Oncogenic Ras Signaling for Cancer Therapy
-
Adjei, A. A. Blocking Oncogenic Ras Signaling for Cancer Therapy. J. Natl. Cancer Inst. 2001, 93, 1062-1074.
-
(2001)
J. Natl. Cancer Inst.
, vol.93
, pp. 1062-1074
-
-
Adjei, A.A.1
-
4
-
-
0036216405
-
STI571 (Gleevec) as a Paradigm for Cancer Therapy
-
Druker, B. J. STI571 (Gleevec) as a Paradigm for Cancer Therapy. Trends Mol. Med. 2002, 8, S14-S18.
-
(2002)
Trends Mol. Med.
, vol.8
-
-
Druker, B.J.1
-
5
-
-
0027245034
-
Signaling by Receptor Tyrosine Kinases
-
Fantl, W. J.; Johnson, D. E.; Williams, L. T. Signaling by Receptor Tyrosine Kinases. Annu. Rev. Biochem. 1993, 62, 453-481.
-
(1993)
Annu. Rev. Biochem.
, vol.62
, pp. 453-481
-
-
Fantl, W.J.1
Johnson, D.E.2
Williams, L.T.3
-
6
-
-
0025343230
-
Signal Transduction by Receptors with Tyrosine Kinase Activity
-
Ullrich, A. and Schlessinger, J. Signal Transduction by Receptors with Tyrosine Kinase Activity. Cell 1991, 61, 203-212.
-
(1991)
Cell
, vol.61
, pp. 203-212
-
-
Ullrich, A.1
Schlessinger, J.2
-
8
-
-
0026316096
-
Growth Factors and Cancer
-
Aaronson, S. A. Growth Factors and Cancer. Science 1991, 254, 1146-1152.
-
(1991)
Science
, vol.254
, pp. 1146-1152
-
-
Aaronson, S.A.1
-
9
-
-
0036214044
-
The ErbB Receptor Family: A Therapeutic Target for Cancer
-
de Bono, J. S.; Rowinsky, E. K. The ErbB Receptor Family: A Therapeutic Target for Cancer. Trends Mol. Med. 2002, 8, S19-S26.
-
(2002)
Trends Mol. Med.
, vol.8
-
-
De Bono, J.S.1
Rowinsky, E.K.2
-
10
-
-
0142050676
-
The Potential for Molecular Oncology to Define New Drug Targets
-
Kerr, D. J.; Workman, P., Eds., CRC Press: Boca Raton, FL
-
Workman, P. The Potential for Molecular Oncology to Define New Drug Targets In New Molecular Targets for Cancer Chemotherapy; Kerr, D. J.; Workman, P., Eds., CRC Press: Boca Raton, FL, 1994; pp 1-44.
-
(1994)
New Molecular Targets for Cancer Chemotherapy
, pp. 1-44
-
-
Workman, P.1
-
11
-
-
0142050910
-
Growth Factors and Growth Factor Inhibitors
-
Teicher, B., Eds., Humana Press: Totowa, NJ
-
Sauseville, E. A.; Longo, D. L. Growth Factors and Growth Factor Inhibitors In Cancer Therapeutics: Experimental and Clinical Agents; Teicher, B., Eds., Humana Press: Totowa, NJ, 1994; pp 337-370.
-
(1994)
Cancer Therapeutics: Experimental and Clinical Agents
, pp. 337-370
-
-
Sauseville, E.A.1
Longo, D.L.2
-
12
-
-
0035869407
-
Use of Chemotherapy Plus a Monoclonal Antibody against HER-2 for Metastatic Breast Cancer that Overexpresses HER-2
-
Slamon, D. J.; Leyland-Jones, B.; Shak, S.; Fuchs, H.; Paton, V.; Bajamonde, A.; Fleming, T.; Eiermann, W.; Wolter, J.; Pegram, M.; Baselga, J.; Norton, L. Use of Chemotherapy Plus a Monoclonal Antibody against HER-2 for Metastatic Breast Cancer that Overexpresses HER-2. N. Engl. J. Med. 2001, 344, 783-792.
-
(2001)
N. Engl. J. Med.
, vol.344
, pp. 783-792
-
-
Slamon, D.J.1
Leyland-Jones, B.2
Shak, S.3
Fuchs, H.4
Paton, V.5
Bajamonde, A.6
Fleming, T.7
Eiermann, W.8
Wolter, J.9
Pegram, M.10
Baselga, J.11
Norton, L.12
-
14
-
-
0035385131
-
3D QSAR Analyses of Novel Tyrosine Kinase Inhibitors Based on Pharmacophore Alignment
-
Zhu, L. L.; Hou, T. J.; Chen, L. R.; Xu, X. J. 3D QSAR Analyses of Novel Tyrosine Kinase Inhibitors Based on Pharmacophore Alignment. J. Chem. Inf. Comput. Sci. 2001, 41, 1032-1040.
-
(2001)
J. Chem. Inf. Comput. Sci.
, vol.41
, pp. 1032-1040
-
-
Zhu, L.L.1
Hou, T.J.2
Chen, L.R.3
Xu, X.J.4
-
15
-
-
0023751431
-
Comparative Molecular Field Analysis (CoMFA). 1. Effect of Shape on Binding of Steroids to Carrier Proteins
-
Cramer, III, R. D.; Patterson, D. E.; Bunce, J. D. Comparative Molecular Field Analysis (CoMFA). 1. Effect of Shape on Binding of Steroids to Carrier Proteins. J. Am. Chem. Soc. 1988, 110, 5959-5967.
-
(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 5959-5967
-
-
Cramer R.D. III1
Patterson, D.E.2
Bunce, J.D.3
-
16
-
-
0027944195
-
Molecular Similarity Indices in a Comparative Analysis (CoMSIA) of Drug Molecules to Correlate and Predict their Biological Activity
-
Klebe, G.; Abraham, U.; Mietzner, T. Molecular Similarity Indices in a Comparative Analysis (CoMSIA) of Drug Molecules to Correlate and Predict their Biological Activity. J. Med. Chem. 1994, 37, 4130-4146.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 4130-4146
-
-
Klebe, G.1
Abraham, U.2
Mietzner, T.3
-
17
-
-
0024434810
-
Tyrphostins 1: Synthesis and Biological Activity of Protein Tyrosine Kinase Inhibitors J
-
Gazit, A.; Yaish, P.; Gilon, C.; Levitzki, A. Tyrphostins 1: Synthesis and Biological Activity of Protein Tyrosine Kinase Inhibitors J. Med. Chem. 1989, 32, 2344-2352.
-
(1989)
Med. Chem.
, vol.32
, pp. 2344-2352
-
-
Gazit, A.1
Yaish, P.2
Gilon, C.3
Levitzki, A.4
-
18
-
-
0025833550
-
Tyrphostins 2: Heterocyclic and α-Substituted Benzomalonitrile Tyrphostins as Potent Inhibitors of EGF Receptor and HER-2/neu Tyrosine Kinases
-
Gazit, A.; Osherov, N.; Posner, I.; Yaish, P.; Poradosu, E.; Gilon, C.; Levitzki, A. Tyrphostins 2: Heterocyclic and α-Substituted Benzomalonitrile Tyrphostins as Potent Inhibitors of EGF Receptor and HER-2/neu Tyrosine Kinases. J. Med. Chem. 1991, 34, 1896-1907.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 1896-1907
-
-
Gazit, A.1
Osherov, N.2
Posner, I.3
Yaish, P.4
Poradosu, E.5
Gilon, C.6
Levitzki, A.7
-
19
-
-
0027131289
-
Tyrphostins 3: Structure-Activity Relationship Studies of α-Substituted Benzylidene Malonitrile 5-S-Aryltyrphostins
-
Gazit, A.; Osherov, N.; Posner, I.; Bar-Sinai, Gilon, C.; Levitzki, A. Tyrphostins 3: Structure-Activity Relationship Studies of α-Substituted Benzylidene Malonitrile 5-S-Aryltyrphostins. J. Med. Chem. 1993, 36, 3556-3564.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3556-3564
-
-
Gazit, A.1
Osherov, N.2
Posner, I.3
Bar-Sinai4
Gilon, C.5
Levitzki, A.6
-
20
-
-
0028968949
-
Tyrosine Kinase Inhibition: An Approach to Drug Development
-
Levitzki, A.; Gazit Aviv. Tyrosine Kinase Inhibition: An Approach to Drug Development. Science 1995, 267, 1782-1788.
-
(1995)
Science
, vol.267
, pp. 1782-1788
-
-
Levitzki, A.1
Gazit, A.2
-
21
-
-
0027198702
-
Selective Inhibition of Epidermal Growth Factor and HER-2/Neu Receptors by Tyrphostins
-
Osherov, N., Gazit, A., Gilon, C. and Levistzki, A. Selective Inhibition of Epidermal Growth Factor and HER-2/Neu Receptors by Tyrphostins. J. Biol. Chem. 1993, 268, 11134-11142.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 11134-11142
-
-
Osherov, N.1
Gazit, A.2
Gilon, C.3
Levistzki, A.4
-
22
-
-
0031552362
-
Development and Validation of a Genetic Algorithm for Flexible Docking
-
Jones, G.; Willet, P.; Glen, R. C.; Leach, A. R.; Taylor, R. Development and Validation of a Genetic Algorithm for Flexible Docking. J. Mol. Biol. 1997, 267, 727-748.
-
(1997)
J. Mol. Biol.
, vol.267
, pp. 727-748
-
-
Jones, G.1
Willet, P.2
Glen, R.C.3
Leach, A.R.4
Taylor, R.5
-
23
-
-
0024716284
-
Atomic and Physichochemical Parameters for Three-Dimensional Structure-Directed Quantitative Structure-Activity Relationships. 4. Additional Parameters for Hydrophobic and Dispersive Interactions and their Application for an Automated Superposition of Certain Naturally Occurring Antibiotics
-
Viswanadhan, V. N.; Ghose, A. K.; Revenkar, G. R.; Robins, R. Atomic and Physichochemical Parameters for Three-Dimensional Structure-Directed Quantitative Structure-Activity Relationships. 4. Additional Parameters for Hydrophobic and Dispersive Interactions and their Application for an Automated Superposition of Certain Naturally Occurring Antibiotics. J. Chem. Inf. Comput. Sci. 1989, 29, 163-172.
-
(1989)
J. Chem. Inf. Comput. Sci.
, vol.29
, pp. 163-172
-
-
Viswanadhan, V.N.1
Ghose, A.K.2
Revenkar, G.R.3
Robins, R.4
-
24
-
-
0033602541
-
Use of a Pharmacophore Model for the Design of EGFR Tyrosine Kinase Inhibitors: Isoflavones and 3-Phenyl-4(1H)-quinolones
-
Taxler, P., Green, J., Mett, H., Sequin, U., Furet P. Use of a Pharmacophore Model for the Design of EGFR Tyrosine Kinase Inhibitors: Isoflavones and 3-Phenyl-4(1H)-quinolones. J. Med. Chem. 1999, 42, 1018-1026.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 1018-1026
-
-
Taxler, P.1
Green, J.2
Mett, H.3
Sequin, U.4
Furet, P.5
-
25
-
-
0036893503
-
Kinase Inhibitors and the Case for CH ⋯ O Hydrogen Bonds in Protein-ligand Binding
-
Pierce, A. C., Sandretto, K. L., Bemis G. W. Kinase Inhibitors and the Case for CH ⋯ O Hydrogen Bonds in Protein-ligand Binding. Proteins: Struct. Funct. Genet. 2001, 49, 567-576.
-
(2001)
Proteins: Struct. Funct. Genet.
, vol.49
, pp. 567-576
-
-
Pierce, A.C.1
Sandretto, K.L.2
Bemis, G.W.3
-
26
-
-
0037674323
-
Mutation of Threonine 766 in the Epidermal Growth Factor Receptor Reveals a Hotspot for Resistance Formation against Selective Tyrosine Kinase Inhibitors
-
Blencke, S., Ullrich, A., Daub, H. Mutation of Threonine 766 in the Epidermal Growth Factor Receptor Reveals a Hotspot for Resistance Formation against Selective Tyrosine Kinase Inhibitors J. Biol. Chem. 2003, 278, 15435-15440.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 15435-15440
-
-
Blencke, S.1
Ullrich, A.2
Daub, H.3
|