-
1
-
-
2342591455
-
The discovery of receptor tyrosine kinases: targets for cancer therapy
-
Gschwind A., Fischer O.M., Ullrich A. (2004) The discovery of receptor tyrosine kinases: targets for cancer therapy. Nat Rev Cancer;4:361-370.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 361-370
-
-
Gschwind, A.1
Fischer, O.M.2
Ullrich, A.3
-
2
-
-
0036139884
-
Receptor tyrosine kinases as targets for anticancer drugs
-
Zwick E., Bange J., Ullrich A. (2002) Receptor tyrosine kinases as targets for anticancer drugs. Trends Mol Med;8:17-23.
-
(2002)
Trends Mol Med
, vol.8
, pp. 17-23
-
-
Zwick, E.1
Bange, J.2
Ullrich, A.3
-
4
-
-
0043210670
-
FDA drug approval summary: gefitinib (ZD1839) (Iressa) tablets
-
Cohen M.H., Williams G.A., Sridhara R., Chen G., Pazdur R. (2003) FDA drug approval summary: gefitinib (ZD1839) (Iressa) tablets. Oncologist;8:303-306.
-
(2003)
Oncologist
, vol.8
, pp. 303-306
-
-
Cohen, M.H.1
Williams, G.A.2
Sridhara, R.3
Chen, G.4
Pazdur, R.5
-
5
-
-
24644458654
-
FDA drug approval summary: erlotinib (Tarceva) tablets
-
Cohen M.H., Johnson J.R., Chen Y.F., Sridhara R., Pazdur R. (2005) FDA drug approval summary: erlotinib (Tarceva) tablets. Oncologist;10:461-466.
-
(2005)
Oncologist
, vol.10
, pp. 461-466
-
-
Cohen, M.H.1
Johnson, J.R.2
Chen, Y.F.3
Sridhara, R.4
Pazdur, R.5
-
6
-
-
84901290217
-
FDA drug approval summary: lapatinib in combination with capecitabine for previously treated metastatic breast cancer that overexpresses HER-2
-
Ryan Q., Ibrahim A., Cohen M.H., Johnson J., Ko C.W., Sridhara R., Justice R., Pazdur R. (2008) FDA drug approval summary: lapatinib in combination with capecitabine for previously treated metastatic breast cancer that overexpresses HER-2. Oncologist;13:1114-1119.
-
(2008)
Oncologist
, vol.13
, pp. 1114-1119
-
-
Ryan, Q.1
Ibrahim, A.2
Cohen, M.H.3
Johnson, J.4
Ko, C.W.5
Sridhara, R.6
Justice, R.7
Pazdur, R.8
-
7
-
-
77953325590
-
Design and synthesis of novel Gefitinib analogues with improved anti-tumor activity
-
3812
-
Wu X., Li M., Qu Y., Tang W., Zheng Y., Lian J., Ji M., Xu L. (2010) Design and synthesis of novel Gefitinib analogues with improved anti-tumor activity. Bioorg Med Chem;18:3812-3822.
-
(2010)
Bioorg Med Chem
, vol.18
, pp. 3822
-
-
Wu, X.1
Li, M.2
Qu, Y.3
Tang, W.4
Zheng, Y.5
Lian, J.6
Ji, M.7
Xu, L.8
-
8
-
-
0029130763
-
Tyrosine kinase inhibitors. 5. Synthesis and structure-activity-relationships for 4-[(Phenylmethyl)Amino]-quinazolines 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.R., Cody D.R., Mcmichael A., Fry D.W. (1995) Tyrosine kinase inhibitors. 5. Synthesis and structure-activity-relationships for 4-[(Phenylmethyl)Amino]-quinazolines 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;38:3482-3487.
-
(1995)
J Med Chem
, vol.38
, pp. 3482-3487
-
-
Rewcastle, G.W.1
Denny, W.A.2
Bridges, A.J.3
Zhou, H.R.4
Cody, D.R.5
Mcmichael, A.6
Fry, D.W.7
-
9
-
-
0030039555
-
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., McMichael A., Showalter H.D.H., Fry D.W., Kraker A.J., Denny W.A. (1996) 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;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
McMichael, A.5
Showalter, H.D.H.6
Fry, D.W.7
Kraker, A.J.8
Denny, W.A.9
-
10
-
-
0033587022
-
Tyrosine kinase inhibitors. 15. 4-(phenylamino)quinazoline and 4-(phenylamino)pyrido[d] pyrimidine acrylamides as irreversible inhibitors of the ATP binding site of the epidermal growth factor receptor
-
Smaill J.B., Palmer B.D., Rewcastle G.W., Denny W.A., McNamara D.J., Dobrusin E.M., Bridges A.J., et al. (1999) Tyrosine kinase inhibitors. 15. 4-(phenylamino)quinazoline and 4-(phenylamino)pyrido[d] pyrimidine acrylamides as irreversible inhibitors of the ATP binding site of the epidermal growth factor receptor. J Med Chem;42:1803-1815.
-
(1999)
J Med Chem
, vol.42
, pp. 1803-1815
-
-
Smaill, J.B.1
Palmer, B.D.2
Rewcastle, G.W.3
Denny, W.A.4
McNamara, D.J.5
Dobrusin, E.M.6
Bridges, A.J.7
-
11
-
-
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 (vol 43, pg 1380, 2000)
-
Smaill J.B., Rewcastle G.W., Loo J.A., Greis K.D., Chan O.H., Reyner E.L., Lipka E., Showalter H.D., Vincent P.W., Elliott W.L., Denny W.A. (2000) 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 (vol 43, pg 1380, 2000). J Med Chem;43:3180-1397.
-
(2000)
J Med Chem
, vol.43
, pp. 3180-1397
-
-
Smaill, J.B.1
Rewcastle, G.W.2
Loo, J.A.3
Greis, K.D.4
Chan, O.H.5
Reyner, E.L.6
Lipka, E.7
Showalter, H.D.8
Vincent, P.W.9
Elliott, W.L.10
Denny, W.A.11
-
12
-
-
0034710707
-
4-Anilino-6,7-dialkoxyquinoline-3-carbonitrile inhibitors of epidermal growth factor receptor kinase and their bioisosteric relationship to the 4-anilino-6,7-dialkoxyquinazoline inhibitors
-
Wissner A., Berger D.M., Boschelli D.H., Floyd M.B. Jr, Greenberger L.M., Gruber B.C., Johnson B.D., et al. (2000) 4-Anilino-6, 7-dialkoxyquinoline-3-carbonitrile inhibitors of epidermal growth factor receptor kinase and their bioisosteric relationship to the 4-anilino-6, 7-dialkoxyquinazoline inhibitors. J Med Chem;43:3244-3256.
-
(2000)
J Med Chem
, vol.43
, pp. 3244-3256
-
-
Wissner, A.1
Berger, D.M.2
Boschelli, D.H.3
Floyd Jr., M.B.4
Greenberger, L.M.5
Gruber, B.C.6
Johnson, B.D.7
-
13
-
-
0346264753
-
3D-QSAR and docking studies on 4-anilinoquinazoline and 4-anilinoquinoline epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors
-
Assefa H., Kamath S., Buolamwini J.K. (2003) 3D-QSAR and docking studies on 4-anilinoquinazoline and 4-anilinoquinoline epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors. J Comput Aided Mol Des;17:475-493.
-
(2003)
J Comput Aided Mol Des
, vol.17
, pp. 475-493
-
-
Assefa, H.1
Kamath, S.2
Buolamwini, J.K.3
-
14
-
-
0347517814
-
Synthesis and SAR of potent EGFR/erbB2 dual inhibitors
-
Zhang Y.M., Cockerill S., Guntrip S.B., Rusnak D., Smith K., Vanderwall D., Wood E., Lackey K. (2004) Synthesis and SAR of potent EGFR/erbB2 dual inhibitors. Bioorg Med Chem Lett;14:111-114.
-
(2004)
Bioorg Med Chem Lett
, vol.14
, pp. 111-114
-
-
Zhang, Y.M.1
Cockerill, S.2
Guntrip, S.B.3
Rusnak, D.4
Smith, K.5
Vanderwall, D.6
Wood, E.7
Lackey, K.8
-
15
-
-
33746196584
-
Optimization and SAR for dual ErbB-1/ErbB-2 tyrosine kinase inhibition in the 6-furanylquinazoline series
-
Petrov K.G., Zhang Y.M., Carter M., Cockerill G.S., Dickerson S., Gauthier C.A., Guo Y., Mook R.A. Jr, Rusnak D.W., Walker A.L., Wood E.R., Lackey K.E. (2006) Optimization and SAR for dual ErbB-1/ErbB-2 tyrosine kinase inhibition in the 6-furanylquinazoline series. Bioorg Med Chem Lett;16:4686-4691.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 4686-4691
-
-
Petrov, K.G.1
Zhang, Y.M.2
Carter, M.3
Cockerill, G.S.4
Dickerson, S.5
Gauthier, C.A.6
Guo, Y.7
Mook Jr., R.A.8
Rusnak, D.W.9
Walker, A.L.10
Wood, E.R.11
Lackey, K.E.12
-
16
-
-
33747035894
-
Inhibitors of epidermal growth factor receptor tyrosine kinase: optimisation of potency and in vivo pharmacokinetics
-
Ballard P., Bradbury R.H., Harris C.S., Hennequin L.F., Hickinson M., Kettle J.G., Kendrew J., Klinowska T., Ogilvie D.J., Pearson S.E., Williams E.J., Wilson I. (2006) Inhibitors of epidermal growth factor receptor tyrosine kinase: optimisation of potency and in vivo pharmacokinetics. Bioorg Med Chem Lett;16:4908-4912.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 4908-4912
-
-
Ballard, P.1
Bradbury, R.H.2
Harris, C.S.3
Hennequin, L.F.4
Hickinson, M.5
Kettle, J.G.6
Kendrew, J.7
Klinowska, T.8
Ogilvie, D.J.9
Pearson, S.E.10
Williams, E.J.11
Wilson, I.12
-
17
-
-
69449101642
-
Design, synthesis, crystal structure and antitumor activity of a new ethyl 3-(quinazolin-4-ylamino)-1H-pyrrole-2-carboxylate derivative
-
Zheng Y.G., Wu X.Q., Sun M., Feng L.H., Li M.D., Ji M. (2009) Design, synthesis, crystal structure and antitumor activity of a new ethyl 3-(quinazolin-4-ylamino)-1H-pyrrole-2-carboxylate derivative. Lett Drug Des Discov;6:538-541.
-
(2009)
Lett Drug Des Discov
, vol.6
, pp. 538-541
-
-
Zheng, Y.G.1
Wu, X.Q.2
Sun, M.3
Feng, L.H.4
Li, M.D.5
Ji, M.6
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