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Volumn 41, Issue 22, 1998, Pages 4365-4377

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

Author keywords

[No Author keywords available]

Indexed keywords

2 [4 (2 DIETHYLAMINOETHOXY)PHENYLAMINO] 8 ETHYL 6 PHENYL 8H PYRIDO[2,3 D]PYRIMIDIN 7 ONE; 2 AMINO 6 (2,6 DICHLOROPHENYL) 8 METHYL 8H PYRIDO[2,3 D]PYRIMIDIN 7 ONE; 2 AMINO 8H PYRIDO[2,3 D]PYRIMIDINE DERIVATIVE; FIBROBLAST GROWTH FACTOR RECEPTOR; ONCOPROTEIN; PLATELET DERIVED GROWTH FACTOR RECEPTOR; PROTEIN TYROSINE KINASE INHIBITOR; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 15644374929     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm980398y     Document Type: Article
Times cited : (96)

References (57)
  • 1
    • 0028968949 scopus 로고
    • Tyrosine Kinase Inhibition: An Approach to Drug Development
    • Levitzki, A.; Gazit, A. 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
  • 2
    • 0030992914 scopus 로고    scopus 로고
    • Protein Tyrosine Kinase Inhibitors in Cancer Treatment
    • Traxler, P. M. Protein Tyrosine Kinase Inhibitors in Cancer Treatment. Exp. Opin. Ther. Patents 1997, 7, 571-588.
    • (1997) Exp. Opin. Ther. Patents , vol.7 , pp. 571-588
    • Traxler, P.M.1
  • 4
    • 0028929803 scopus 로고
    • Angiogenesis in Cancer, Vascular, Rheumatoid and other Disease
    • Folkman, J. Angiogenesis in Cancer, Vascular, Rheumatoid and other Disease. Nature Medicine 1995, 1, 27-31.
    • (1995) Nature Medicine , vol.1 , pp. 27-31
    • Folkman, J.1
  • 5
    • 0029166153 scopus 로고
    • Current Concepts in Restenosis Following Balloon Angioplasty
    • Mattsson, E.; Clowes, A. W. Current Concepts in Restenosis Following Balloon Angioplasty. Trends Cardiovas. Med. 1995, 5, 200-204.
    • (1995) Trends Cardiovas. Med. , vol.5 , pp. 200-204
    • Mattsson, E.1    Clowes, A.W.2
  • 6
    • 0028863534 scopus 로고
    • Pharmacological Inhibition of Restenosis: Learning from Experience
    • Shaw, L. A.; Rudin, M.; Cook, N. S. Pharmacological Inhibition of Restenosis: Learning from Experience. Trends Pharm. Sci. 1995, 16, 401-404.
    • (1995) Trends Pharm. Sci. , vol.16 , pp. 401-404
    • Shaw, L.A.1    Rudin, M.2    Cook, N.S.3
  • 7
    • 0030131145 scopus 로고    scopus 로고
    • Multiple Growth Factors are Associated with Lesions of Atherosclerosis: Specificity or Redunancy?
    • Raines, E. W.; Ross, R. Multiple Growth Factors are Associated with Lesions of Atherosclerosis: Specificity or Redunancy? BioEssays 1996, 18, 271-282.
    • (1996) BioEssays , vol.18 , pp. 271-282
    • Raines, E.W.1    Ross, R.2
  • 8
    • 0030009071 scopus 로고    scopus 로고
    • The Epidermal Growth Factor Receptor Family of Tyrosine Kinases and Cancer: Can an Atypical Exemplar be a Sound Therapeutic Target?
    • Bridges, A. J. The Epidermal Growth Factor Receptor Family of Tyrosine Kinases and Cancer: Can an Atypical Exemplar be a Sound Therapeutic Target? Curr. Med. Chem. 1996, 3, 167-194.
    • (1996) Curr. Med. Chem. , vol.3 , pp. 167-194
    • Bridges, A.J.1
  • 9
    • 0023885305 scopus 로고
    • The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic Domains
    • Hanks, S. K.; Quinn, A. M.; Hunter, T. The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic Domains. Science 1988, 242, 42-52.
    • (1988) Science , vol.242 , pp. 42-52
    • Hanks, S.K.1    Quinn, A.M.2    Hunter, T.3
  • 10
    • 0028243048 scopus 로고
    • A New Series of PDGF Receptor Tyrosine Kinase Inhibitors: 3-Substituted Quinoline Derivatives
    • Maguire, M. P.; Sheets, K. R.; McVety, K.; Spada, A. P.; Zilberstein, A. A New Series of PDGF Receptor Tyrosine Kinase Inhibitors: 3-Substituted Quinoline Derivatives. J. Med. Chem. 1994, 37, 2129-2137.
    • (1994) J. Med. Chem. , vol.37 , pp. 2129-2137
    • Maguire, M.P.1    Sheets, K.R.2    McVety, K.3    Spada, A.P.4    Zilberstein, A.5
  • 12
    • 0028968622 scopus 로고
    • Selective Inhibition of the Platelet-Derived Growth Factor Signal Transduction Pathway by a Protein-Tyrosine Kinase Inhibitor of the 2-Phenylaminopyrimidine Class
    • Buchdunger, E.; Zimmerman, J.; Mett, H.; Meyer, T.; Muller, M.; Regenass, U.; Lydon, N. B. Selective Inhibition of the Platelet-Derived Growth Factor Signal Transduction Pathway by a Protein-Tyrosine Kinase Inhibitor of the 2-Phenylaminopyrimidine Class. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 2558-2562.
    • (1995) Proc. Natl. Acad. Sci. U.S.A. , vol.92 , pp. 2558-2562
    • Buchdunger, E.1    Zimmerman, J.2    Mett, H.3    Meyer, T.4    Muller, M.5    Regenass, U.6    Lydon, N.B.7
  • 13
    • 0029951570 scopus 로고    scopus 로고
    • Phenylamino-pyrimidine (PAP)-Derivatives: A New Class of Potent and Highly Selective PDGF-Receptor Autophosphorylation Inhibitors
    • Zimmerman, J.; Buchdunger, E.; Mett, H.; Meyer, T.; Lydon, N. B.; Traxler, P. Phenylamino-pyrimidine (PAP)-Derivatives: A New Class of Potent and Highly Selective PDGF-Receptor Autophosphorylation Inhibitors. Bioorg. Med. Chem. Lett. 1996, 6, 1221-1226.
    • (1996) Bioorg. Med. Chem. Lett. , vol.6 , pp. 1221-1226
    • Zimmerman, J.1    Buchdunger, E.2    Mett, H.3    Meyer, T.4    Lydon, N.B.5    Traxler, P.6
  • 14
    • 0029899585 scopus 로고    scopus 로고
    • Tyrphostins. 5. Potent Inhibitors of Platelet-Derived Growth Factor Receptor Tyrosine Kinaee: Structure- Activity Relationships in Quinoxalines, Quinolines, and Indole Tyrphostins
    • Gazit, A.; App, H.; McMahon, G.; Chen, J.; Levitzki, A.; Bohmer, F. D. Tyrphostins. 5. Potent Inhibitors of Platelet-Derived Growth Factor Receptor Tyrosine Kinaee: Structure- Activity Relationships in Quinoxalines, Quinolines, and Indole Tyrphostins. J. Med. Chem. 1996, 39, 2170-2177.
    • (1996) J. Med. Chem. , vol.39 , pp. 2170-2177
    • Gazit, A.1    App, H.2    McMahon, G.3    Chen, J.4    Levitzki, A.5    Bohmer, F.D.6
  • 18
    • 0030945871 scopus 로고    scopus 로고
    • Structures of the Tyrosine Kinase Domain of Fibroblast Growth Factor Receptor in Complex with Inhibitors
    • Mohammadi, M.; McMahon, G.; Sun, L.; Tang, C.; Hirth, P.; Yeh, B. K.; Hubbard, S. R.; Schlessinger, J. Structures of the Tyrosine Kinase Domain of Fibroblast Growth Factor Receptor in Complex with Inhibitors. Science 1997, 276, 955-960.
    • (1997) Science , vol.276 , pp. 955-960
    • Mohammadi, M.1    McMahon, G.2    Sun, L.3    Tang, C.4    Hirth, P.5    Yeh, B.K.6    Hubbard, S.R.7    Schlessinger, J.8
  • 19
    • 0030220783 scopus 로고    scopus 로고
    • Tyrphostins IV-Highly Potent Inhibitors of EGF Receptor Kinase. Structure-Activity Relationship Study of 4-Anilidoquinazolines
    • Gazit, A.; Chan, J.; App, H.; McMahon, G.; Hirth, P.; Chen, I.; Levitzki, A. Tyrphostins IV-Highly Potent Inhibitors of EGF Receptor Kinase. Structure-Activity Relationship Study of 4-Anilidoquinazolines. Bioorg. Med. Chem. 1996, 4, 1203-1207.
    • (1996) Bioorg. Med. Chem. , vol.4 , pp. 1203-1207
    • Gazit, A.1    Chan, J.2    App, H.3    McMahon, G.4    Hirth, P.5    Chen, I.6    Levitzki, A.7
  • 20
    • 0030008414 scopus 로고    scopus 로고
    • 4-(Phenylamino)pyrrolopyrimidines: Potent and Selective, ATP Site Directed Inhibitors of the EGF-Receptor Protein Tyrosine Kinase
    • Traxler, P. M.; Furet, P.; Mett, H.; Buchdunger, E.; Meyer, T.; Lydon, N. 4-(Phenylamino)pyrrolopyrimidines: Potent and Selective, ATP Site Directed Inhibitors of the EGF-Receptor Protein Tyrosine Kinase. J. Med. Chem. 1996, 39, 2285-2292.
    • (1996) J. Med. Chem. , vol.39 , pp. 2285-2292
    • Traxler, P.M.1    Furet, P.2    Mett, H.3    Buchdunger, E.4    Meyer, T.5    Lydon, N.6
  • 21
    • 9844235351 scopus 로고    scopus 로고
    • Use of a Pharmacophore Model for the Design of EGF-R Tyrosine Kinase Inhibitors: 4-(Phenylamino)pyrazolo[3,4-d]pyrimidines
    • Traxler, P.; Bold, G.; Frei, J.; Lang, M.; Lydon, N.; Mett, H.; Buchdunger, E.; Meyer, T.; Mueller, M.; Furet, P. 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, 3601-3616.
    • (1997) J. Med. Chem. , vol.40 , pp. 3601-3616
    • Traxler, P.1    Bold, G.2    Frei, J.3    Lang, M.4    Lydon, N.5    Mett, H.6    Buchdunger, E.7    Meyer, T.8    Mueller, M.9    Furet, P.10
  • 24
    • 0031026055 scopus 로고    scopus 로고
    • Potent and Selective Inhibitors of the abl-Kinase: Phenylaminopyrimidine (PAP) Derivatives
    • Zimmerman, J.; Buchdunger, E.; Mett, H.; Meyer, T.; Lydon, N. B. Potent and Selective Inhibitors of the abl-Kinase: Phenylaminopyrimidine (PAP) Derivatives. Bioorg. Med. Chem. Lett. 1997, 7, 187-192.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 187-192
    • Zimmerman, J.1    Buchdunger, E.2    Mett, H.3    Meyer, T.4    Lydon, N.B.5
  • 27
    • 0029130763 scopus 로고
    • Tyrosine Kinase Inhibitors: 5. Synthesis and Structure-Activity Relationships for 4-[(Phenyl-methyl)amino]- and 4-(Phenylamino)quinazolines as Potent Adenosine 5′-Triphosphate Binding Site Inhibitors of the Tyrosine Kinase Domain of the Epidermal Growth Factor Receptor
    • Rewcastle, G. W.; Denny, W. A.; Bridges, A. J.; Zhou, H.; Cody, D. R.; McMichael, A.; Fry, D. W. Tyrosine Kinase Inhibitors: 5. Synthesis and Structure-Activity Relationships for 4-[(Phenyl-methyl)amino]- and 4-(Phenylamino)quinazolines as Potent Adenosine 5′-Triphosphate Binding Site Inhibitors of the Tyrosine Kinase Domain of the Epidermal Growth Factor Receptor. J. Med. Chem. 1995, 35, 3482-3487.
    • (1995) J. Med. Chem. , vol.35 , pp. 3482-3487
    • Rewcastle, G.W.1    Denny, W.A.2    Bridges, A.J.3    Zhou, H.4    Cody, D.R.5    McMichael, A.6    Fry, D.W.7
  • 28
    • 0029123125 scopus 로고
    • Tyrosine Kinase Inhibitors: 7. 7-Amino-4-(phenylamino)-and 7-Amino-4-[(phenylmethyl)amino]pyrido[4,3-d]pyrimidines: A New Class of Inhibitors of Tyrosine Kinase Activity of the Epidermal Growth Factor Receptor
    • Thompson, A. M.; Bridges, A. J.; Fry, D. W.; Kraker, A. J.; Denny, W. A. Tyrosine Kinase Inhibitors: 7. 7-Amino-4-(phenylamino)-and 7-Amino-4-[(phenylmethyl)amino]pyrido[4,3-d]pyrimidines: A New Class of Inhibitors of Tyrosine Kinase Activity of the Epidermal Growth Factor Receptor. J. Med. Chem. 1995, 38, 3780-3788.
    • (1995) J. Med. Chem. , vol.38 , pp. 3780-3788
    • Thompson, A.M.1    Bridges, A.J.2    Fry, D.W.3    Kraker, A.J.4    Denny, W.A.5
  • 29
    • 0030039555 scopus 로고    scopus 로고
    • Tyrosine Kinase Inhibitors: 8. An Unusually Steep Structure-Activity Relationship for Analogues of 4-(3-Bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a Potent Inhibitor of the Epidermal Growth Factor Receptor
    • Bridges, A. J.; Zhou, H.; Cody, D. R.; Rewcastle, G. W.; Mc-Michael, A.; Showalter, H. D. H.; Fry, D. W.; Kraker, A. J.; Denny, W. A. Tyrosine Kinase Inhibitors: 8. An Unusually Steep Structure-Activity Relationship for Analogues of 4-(3-Bromoanilino)-6,7-dimethoxyquinazoline (PD 153035), a Potent Inhibitor of the Epidermal Growth Factor Receptor. J. Med. Chem. 1996, 39, 267-276.
    • (1996) J. Med. Chem. , vol.39 , pp. 267-276
    • Bridges, A.J.1    Zhou, H.2    Cody, D.R.3    Rewcastle, G.W.4    Mc-Michael, A.5    Showalter, H.D.H.6    Fry, D.W.7    Kraker, A.J.8    Denny, W.A.9
  • 30
    • 13344262678 scopus 로고    scopus 로고
    • Tyrosine Kinase Inhibitors: 9. Synthesis and Evaluation of Fused Tricyclic Quinazoline Analogues as ATP Site Inhibitors of the Tyrosine Kinase Activity of the Epidermal Growth Factor Receptor
    • Rewcastle, G. W.; Palmer, B. D.; Bridges, A. J.; Showalter, H. D. H.; Sun, L.; Nelson, J.; McMichael, A.; Kraker, A. J.; Fry, D. W.; Denny, W. A. Tyrosine Kinase Inhibitors: 9. Synthesis and Evaluation of Fused Tricyclic Quinazoline Analogues as ATP Site Inhibitors of the Tyrosine Kinase Activity of the Epidermal Growth Factor Receptor. J. Med. Chem. 1996, 39, 918-928.
    • (1996) J. Med. Chem. , vol.39 , pp. 918-928
    • Rewcastle, G.W.1    Palmer, B.D.2    Bridges, A.J.3    Showalter, H.D.H.4    Sun, L.5    Nelson, J.6    McMichael, A.7    Kraker, A.J.8    Fry, D.W.9    Denny, W.A.10
  • 31
    • 0029975029 scopus 로고    scopus 로고
    • Tyrosine Kinase Inhibitors: 10. Isomeric 4-[(3-Bromophenyl)amino]pyrido[d]pyrimides are Potent ATP Binding Site Inhibitors of the Tyrosine Kinase Function of the Epidermal Growth Factor Receptor
    • Rewcastle, G. W.; Palmer, B. D.; Thompson, A. M.; Bridges, A. J.; Cody, D. R.; Zhong, H.; Fry, D. W.; McMichael, A.; Denny, W. A. Tyrosine Kinase Inhibitors: 10. Isomeric 4-[(3-Bromophenyl)amino]pyrido[d]pyrimides are Potent ATP Binding Site Inhibitors of the Tyrosine Kinase Function of the Epidermal Growth Factor Receptor. J. Med. Chem. 1996, 39, 1823-1835.
    • (1996) J. Med. Chem. , vol.39 , pp. 1823-1835
    • Rewcastle, G.W.1    Palmer, B.D.2    Thompson, A.M.3    Bridges, A.J.4    Cody, D.R.5    Zhong, H.6    Fry, D.W.7    McMichael, A.8    Denny, W.A.9
  • 32
    • 0030907052 scopus 로고    scopus 로고
    • 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, B. D.; Trumpp-Kallmeyer, S.; Fry, D. W.; Nelson, J. M.; Showalter, H. D. H.; Denny, W. A. 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, 1519-1529.
    • (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
  • 33
    • 0030968950 scopus 로고    scopus 로고
    • Tyrosine Kinase Inhibitors: 12. Synthesis and Structure-Activity Relationships for 6-Substituted 4-(Phenylamino)pyrimido[5,4-d]pyrimidines Designed as Inhibitors of the Epidermal Growth Factor Receptor
    • Rewcastle, G. W.; Bridges, A. J.; Fry, D. W.; Rubin, R.; Denny, W. A. Tyrosine Kinase Inhibitors: 12. Synthesis and Structure-Activity Relationships for 6-Substituted 4-(Phenylamino)pyrimido[5,4-d]pyrimidines Designed as Inhibitors of the Epidermal Growth Factor Receptor. J. Med. Chem. 1997, 40, 1820-1826.
    • (1997) J. Med. Chem. , vol.40 , pp. 1820-1826
    • Rewcastle, G.W.1    Bridges, A.J.2    Fry, D.W.3    Rubin, R.4    Denny, W.A.5
  • 34
    • 0030773557 scopus 로고    scopus 로고
    • Tyrosine Kinase Inhibitors: 13. Structure-Activity Relationships for Soluble 7-Substituted 4-[(3-Bromophenyl)amino]pyrido-[4,3-d]pyrimidines as Inhibitors of the Tyrosine Kinase Activity of the Epidermal Growth Factor Receptor
    • Thompson, A. M.; Murray, D. K.; Fry, D. W.; Nelson, J. M.; Showalter, H. D. H.; Roberts, B. J.; Vincent, P. W.; Denny, W. A. Tyrosine Kinase Inhibitors: 13. Structure-Activity Relationships for Soluble 7-Substituted 4-[(3-Bromophenyl)amino]pyrido-[4,3-d]pyrimidines as Inhibitors of the Tyrosine Kinase Activity of the Epidermal Growth Factor Receptor. J. Med. Chem. 1997, 40, 3915-1925.
    • (1997) J. Med. Chem. , vol.40 , pp. 3915-11925
    • Thompson, A.M.1    Murray, D.K.2    Fry, D.W.3    Nelson, J.M.4    Showalter, H.D.H.5    Roberts, B.J.6    Vincent, P.W.7    Denny, W.A.8
  • 35
    • 15444361739 scopus 로고    scopus 로고
    • Tyrosine Kinase Inhibitors: 14. Structure-Activity Relationships for Methylamino-Substituted Derivatives of 4-[(3-Bromopheny)-amino]-6-(methylamino)-pyrido[4,3-d]pyrimidine (PD 158780), a Potent and Specific Inhibitor of the Tyrosine Kinase Activity of Receptors of the EGF Family of Growth Factors
    • Rewcastle, G. W.; Murray, D. K.; Elliot, W. L.; Fry, D. W.; Howard, C. T.; Nelson, J. M.; Roberts, B. J.; Vincent, P. W.; Showalter, H. D. H.; Winters, R. T.; Denny, W. A. Tyrosine Kinase Inhibitors: 14. Structure-Activity Relationships for Methylamino-Substituted Derivatives of 4-[(3-Bromopheny)-amino]-6-(methylamino)-pyrido[4,3-d]pyrimidine (PD 158780), a Potent and Specific Inhibitor of the Tyrosine Kinase Activity of Receptors of the EGF Family of Growth Factors. J. Med. Chem. 1998, 47, 742-751.
    • (1998) J. Med. Chem. , vol.47 , pp. 742-751
    • Rewcastle, G.W.1    Murray, D.K.2    Elliot, W.L.3    Fry, D.W.4    Howard, C.T.5    Nelson, J.M.6    Roberts, B.J.7    Vincent, P.W.8    Showalter, H.D.H.9    Winters, R.T.10    Denny, W.A.11
  • 38
    • 0030665627 scopus 로고    scopus 로고
    • 1-Oxo-3-aryl-1H-indene-2-carboxylic Acid Derivatives as Selective Inhibitors of Fibroblast Growth Factor Receptor-1 Tyrosine Kinase
    • Barvian, M. R.; Panek, R. L.; Lu, G. H.; Kraker, A. J.; Amar, A.; Hartl, B.; Hamby, J. M.; Showalter, H. D. H. 1-Oxo-3-aryl-1H-indene-2-carboxylic Acid Derivatives as Selective Inhibitors of Fibroblast Growth Factor Receptor-1 Tyrosine Kinase. Bioorg. Med. Chem. Lett. 1997, 7, 2903-2908.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 2903-2908
    • Barvian, M.R.1    Panek, R.L.2    Lu, G.H.3    Kraker, A.J.4    Amar, A.5    Hartl, B.6    Hamby, J.M.7    Showalter, H.D.H.8
  • 40
    • 0020533055 scopus 로고
    • Simian Sarcoma Virus one Gene, v-sis, is Derived from the Gene (or genes) Encoding Platelet-derived Growth Factor
    • Doolittle, R. F.; Hunkapiller, M. W.; Hood, L. E.; Devare, S. G.; Robbins, K. C.; Aaronson, S. A.; Antoniades, H. N. Simian Sarcoma Virus one Gene, v-sis, is Derived from the Gene (or genes) Encoding Platelet-derived Growth Factor. Science 1983, 221, 275-277.
    • (1983) Science , vol.221 , pp. 275-277
    • Doolittle, R.F.1    Hunkapiller, M.W.2    Hood, L.E.3    Devare, S.G.4    Robbins, K.C.5    Aaronson, S.A.6    Antoniades, H.N.7
  • 41
    • 0023747564 scopus 로고
    • Expression of Messenger RNAs for Platelet-derived Growth Factor and Transforming Growth Factor-α and Their Receptors in Human Maligant Glioma Cell Lines
    • Nister, M.; Libermann, T. A.; Betsholtz, C.; Pettersson, M.; Claesson-Welsh, L.; Heldin, C.-H.; Schlessinger, J.; Westermark, B. Expression of Messenger RNAs for Platelet-derived Growth Factor and Transforming Growth Factor-α and Their Receptors in Human Maligant Glioma Cell Lines. Cancer Res. 1988, 48, 3910-3918.
    • (1988) Cancer Res. , vol.48 , pp. 3910-3918
    • Nister, M.1    Libermann, T.A.2    Betsholtz, C.3    Pettersson, M.4    Claesson-Welsh, L.5    Heldin, C.-H.6    Schlessinger, J.7    Westermark, B.8
  • 42
    • 15644377522 scopus 로고
    • Differential Expression of Platelet-derived Growth Factor Responses in Human Malignant Glioma Cell Lines
    • Nister, M.; Claesson-Welsh, L.; Eriksson, A.; Heldin, C.-H.; Westermark, B. Differential Expression of Platelet-derived Growth Factor Responses in Human Malignant Glioma Cell Lines. Cancer Res. 1991, 51, 16755-16763.
    • (1991) Cancer Res. , vol.51 , pp. 16755-16763
    • Nister, M.1    Claesson-Welsh, L.2    Eriksson, A.3    Heldin, C.-H.4    Westermark, B.5
  • 43
    • 0026772431 scopus 로고
    • Platelet-derived Growth Factor and Its Receptors in Human Glioma Tissue: Expression of Messenger RNA and Protein Suggests the Presence of Autocrine and Paracrine Loops
    • Hermanson, M.; Funa, K.; Hartman, M.; Claesson-Welsh, L.; Heldin, C.-H.; Westermark, B.; Nister, M. Platelet-derived Growth Factor and Its Receptors in Human Glioma Tissue: Expression of Messenger RNA and Protein Suggests the Presence of Autocrine and Paracrine Loops. Cancer Res. 1992, 52, 3213-3219.
    • (1992) Cancer Res. , vol.52 , pp. 3213-3219
    • Hermanson, M.1    Funa, K.2    Hartman, M.3    Claesson-Welsh, L.4    Heldin, C.-H.5    Westermark, B.6    Nister, M.7
  • 44
    • 0026649809 scopus 로고
    • Demonstration of an Activated Platelet-derived Growth Factor Autocrine Pathway and its Role in Human Tumor Cell Proliferation in Vitro
    • Fleming, T. P.; Matsui, T.; Heidaran, M. A.; Molloy, C. J.; Artrip, J.; Aaronson, S. A. Demonstration of an Activated Platelet-derived Growth Factor Autocrine Pathway and its Role in Human Tumor Cell Proliferation in Vitro. Oncogene 1992, 7, 1355-1359.
    • (1992) Oncogene , vol.7 , pp. 1355-1359
    • Fleming, T.P.1    Matsui, T.2    Heidaran, M.A.3    Molloy, C.J.4    Artrip, J.5    Aaronson, S.A.6
  • 48
    • 0030921482 scopus 로고    scopus 로고
    • Inhibition of Growth Factor-mediated Tyrosine Phosphorylation in Vascular Smooth Muscle by PD 089828, a New Synthetic Protein Tyrosine Kinase Inhibitor
    • Dahring, T. K.; Lu, G. H.; Hamby, J. M.; Batley, B. L.; Kraker, A. J.; Panek, R. L. Inhibition of Growth Factor-mediated Tyrosine Phosphorylation in Vascular Smooth Muscle by PD 089828, a New Synthetic Protein Tyrosine Kinase Inhibitor. J. Pharmacol. Exp. Ther. 1997, 281, 1446-1456.
    • (1997) J. Pharmacol. Exp. Ther. , vol.281 , pp. 1446-1456
    • Dahring, T.K.1    Lu, G.H.2    Hamby, J.M.3    Batley, B.L.4    Kraker, A.J.5    Panek, R.L.6
  • 49
    • 0032554818 scopus 로고    scopus 로고
    • Development of a Binding Model to Protein Tyrosine Kinases for Substituted Pyrido[2,3-d]pyrimidine Inhibitors
    • Trumpp-Kallmeyer, S.; Rubin, J. R.; Humblet, C.; Hamby, J. M.; Showalter, H. D. H. Development of a Binding Model to Protein Tyrosine Kinases for Substituted Pyrido[2,3-d]pyrimidine Inhibitors. J. Med. Chem. 1998, 41, 1752-1763.
    • (1998) J. Med. Chem. , vol.41 , pp. 1752-1763
    • Trumpp-Kallmeyer, S.1    Rubin, J.R.2    Humblet, C.3    Hamby, J.M.4    Showalter, H.D.H.5
  • 51
  • 52
    • 84980249929 scopus 로고
    • Thieno[2,3-d]pyrimidines. I. A New Method for the Preparation of Esters and Amides of Thieno[2,3-d]pyrimidine-6-carboxylic Acids
    • Santilli, A. A.; Kim, D. H.; Wanser, S. V. Thieno[2,3-d]pyrimidines. I. A New Method for the Preparation of Esters and Amides of Thieno[2,3-d]pyrimidine-6-carboxylic Acids. J. Heterocycl. Chem. 1971, 8, 445-453.
    • (1971) J. Heterocycl. Chem. , vol.8 , pp. 445-453
    • Santilli, A.A.1    Kim, D.H.2    Wanser, S.V.3
  • 53
    • 0000129855 scopus 로고
    • (±) trans-2-(Phenylsulfonyl)-3-phenyloxaziridine
    • Vishwakarama, L. C.; Stringer, O. D.; Davis, F. A. (±) trans-2-(Phenylsulfonyl)-3-phenyloxaziridine. Org. Synth. 1987, 66, 203-210.
    • (1987) Org. Synth. , vol.66 , pp. 203-210
    • Vishwakarama, L.C.1    Stringer, O.D.2    Davis, F.A.3
  • 54
    • 15644366696 scopus 로고    scopus 로고
    • For assay protocols, see refs 36, 37, 47, and 48
    • For assay protocols, see refs 36, 37, 47, and 48.
  • 56
    • 0024415638 scopus 로고
    • Sequence and Schedule-dependent Synergy of Trimetrexate in Combination with 5-Fluorouracil in Vitro and in Mice
    • Elliott, W. L.; Howard, C. T.; Dykes, D. J.; Leopold, W. R. Sequence and Schedule-dependent Synergy of Trimetrexate in Combination with 5-Fluorouracil in Vitro and in Mice. Cancer Res. 1989, 49, 5586-5590.
    • (1989) Cancer Res. , vol.49 , pp. 5586-5590
    • Elliott, W.L.1    Howard, C.T.2    Dykes, D.J.3    Leopold, W.R.4
  • 57
    • 0028048474 scopus 로고
    • Chemotherapy with CI-973 ([SP-4-3-(R)]-[1,1-cyclobutanedicarboxylato (2-)]2-methyl-1,4-butanediamine-N,N')platinum, NK121 in Combination with Standard Agents against Murine Tumors in Vivo
    • Elliott, W. L.; Roberts, B. J.; Howard, C. T.; Leopold, W. R., III. Chemotherapy with CI-973 ([SP-4-3-(R)]-[1,1-cyclobutanedicarboxylato (2-)]2-methyl-1,4-butanediamine-N,N')platinum, NK121) in Combination with Standard Agents against Murine Tumors in Vivo. Cancer Res. 1994, 54, 4412-4418.
    • (1994) Cancer Res. , vol.54 , pp. 4412-4418
    • Elliott, W.L.1    Roberts, B.J.2    Howard, C.T.3    Leopold Jr., W.R.4


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