-
1
-
-
84859789219
-
Potent preclinical anti-tumor activity of MGCD265, an oral Met/VEGFR kinase inhibitor in Phase II clinical development, in combination with taxanes or erlotinib
-
Besterman JM, Fournel M, Dupont I, Bonfils C, Dubay M, Ste-Croix H and Maroun CR. Potent preclinical anti-tumor activity of MGCD265, an oral Met/VEGFR kinase inhibitor in Phase II clinical development, in combination with taxanes or erlotinib. Journal of Clinical Oncology (Meeting Abstracts). 2010; 28(15 suppl.): e13595.
-
(2010)
Journal of Clinical Oncology
, vol.28
, Issue.15 SUPPL
, pp. e13595
-
-
Besterman, J.M.1
Fournel, M.2
Dupont, I.3
Bonfils, C.4
Dubay, M.5
Ste-Croix, H.6
Maroun, C.R.7
-
2
-
-
44149124282
-
Discovery of orally active pyrrolopyridine- and aminopyridine-based Met kinase inhibitors
-
Cai ZW, Wei D, Schroeder GM, Cornelius LA, Kim K, Chen XT and Borzilleri RM. Discovery of orally active pyrrolopyridine- and aminopyridine-based Met kinase inhibitors. Bioorganic and Medicinal Chemistry Letters 2008; 18: 3224-3229.
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, pp. 3224-3229
-
-
Cai, Z.W.1
Wei, D.2
Schroeder, G.M.3
Cornelius, L.A.4
Kim, K.5
Chen, X.T.6
Borzilleri, R.M.7
-
3
-
-
19544389146
-
c-Met as a target for human cancer and characterization of inhibitors for therapeutic intervention
-
Christensen JG, Burrows J and Salgia R. c-Met as a target for human cancer and characterization of inhibitors for therapeutic intervention. Cancer Letters 2005; 225(1): 1-26.
-
(2005)
Cancer Letters
, vol.225
, Issue.1
, pp. 1-26
-
-
Christensen, J.G.1
Burrows, J.2
Salgia, R.3
-
4
-
-
85165471956
-
A phase I dose-escalation study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and early antitumor activity of foretinib
-
Eder JP, Shapiro GI, Appleman L, Zhu AX, Miles D, Keer H, Cancilla B, Chu F, Hitchcock-Bryan S, Sherman L, McCallum S, Heath EI, Boerner SA and LoRusso PM. A phase I dose-escalation study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and early antitumor activity of foretinib. Clinical Cancer Research 2010; 16(13): 3297.
-
(2010)
Clinical Cancer Research
, vol.16
, Issue.13
, pp. 3297
-
-
Eder, J.P.1
Shapiro, G.I.2
Appleman, L.3
Zhu, A.X.4
Miles, D.5
Keer, H.6
Cancilla, B.7
Chu, F.8
Hitchcock-Bryan, S.9
Sherman, L.10
McCallum, S.11
Heath, E.I.12
Boerner, S.A.13
LoRusso, P.M.14
-
5
-
-
85165460336
-
Abstract C272: Antitumor activity of the dual AXL/c-Met inhibitor CEP-40783 in champions primary TumorGraft™ models of human non-small cell lung cancer (NSCLC)
-
Friedman JA, Donaldson R, Miknyoczki S, Cheng MG, Hudkins R, Dorsey B, Ator M, Angeles T, Ruggeri B and Bruckheimer E. Abstract C272: Antitumor activity of the dual AXL/c-Met inhibitor CEP-40783 in champions primary TumorGraft™ models of human non-small cell lung cancer (NSCLC). Molecular Cancer Therapeutics 2013; 12 (11 Supplement): C272-C272.
-
(2013)
Molecular Cancer Therapeutics
, vol.12
, Issue.11 SUPPLEMENT
, pp. C272-C272
-
-
Friedman, J.A.1
Donaldson, R.2
Miknyoczki, S.3
Cheng, M.G.4
Hudkins, R.5
Dorsey, B.6
Ator, M.7
Angeles, T.8
Ruggeri, B.9
Bruckheimer, E.10
-
6
-
-
85165487838
-
-
(2-phenoxy) quinoline derivatives and their use. CN Patent ZL201310045375.5
-
Gong P, Liu YJ, Zhao YF, Zhai X and Li S. (2-phenoxy) quinoline derivatives and their use. CN Patent ZL201310045375.5, 2013.
-
(2013)
-
-
Gong, P.1
Liu, Y.J.2
Zhao, Y.F.3
Zhai, X.4
Li, S.5
-
7
-
-
0035937595
-
Nanoparticulate systems for brain delivery of drugs
-
Kreuter J. Nanoparticulate systems for brain delivery of drugs. Advanced Drug Delivery Reviews 2001; 47: 65-81.
-
(2001)
Advanced Drug Delivery Reviews
, vol.47
, pp. 65-81
-
-
Kreuter, J.1
-
8
-
-
34248631794
-
A phase I dose-escalation study of the safety and pharmacokinetics of a XL184, a VEGFR and Met kinase inhibitor, administered orally to subjects with advanced malignancies
-
Kurzrock R, Camacho L, Hong D, Ng C, Janisch L, Ratain MJ, Salgia R and Anderson MD. A phase I dose-escalation study of the safety and pharmacokinetics of a XL184, a VEGFR and Met kinase inhibitor, administered orally to subjects with advanced malignancies. European Journal of Cancer Supplements 2006; 4(12): 124-125.
-
(2006)
European Journal of Cancer Supplements
, vol.4
, Issue.12
, pp. 124-125
-
-
Kurzrock, R.1
Camacho, L.2
Hong, D.3
Ng, C.4
Janisch, L.5
Ratain, M.J.6
Salgia, R.7
Anderson, M.D.8
-
9
-
-
84877823163
-
Discovery of novel 4-(2-fluorophenoxy) quinoline derivatives bearing 4-oxo-1, 4-dihydrocinnoline-3-carboxamide moiety as c-Met kinase inhibitors
-
Li S, Zhao YF, Wang KW, Gao YL, Han JM, Cui BB and Gong P. Discovery of novel 4-(2-fluorophenoxy) quinoline derivatives bearing 4-oxo-1, 4-dihydrocinnoline-3-carboxamide moiety as c-Met kinase inhibitors. Bioorganic& Medicinal Chemistry Letters 2013; 21: 2843-2855.
-
(2013)
Bioorganic& Medicinal Chemistry Letters
, vol.21
, pp. 2843-2855
-
-
Li, S.1
Zhao, Y.F.2
Wang, K.W.3
Gao, Y.L.4
Han, J.M.5
Cui, B.B.6
Gong, P.7
-
10
-
-
70349331541
-
A phase I study of a novel spectrum-selective kinase inhibitor(SSKI), XL880, administered orally in patients with advanced solid malignancies(ASM)
-
LoRusso P, Appleman L, Heath E, Malburg L, Zhu AX, Carey M, Shapiro GI and Eder JP. A phase I study of a novel spectrum-selective kinase inhibitor(SSKI), XL880, administered orally in patients with advanced solid malignancies(ASM). Journal of Clinical Oncology 2006; 24(18): 131S-131S.
-
(2006)
Journal of Clinical Oncology
, vol.24
, Issue.18
, pp. 131S-131S
-
-
LoRusso, P.1
Appleman, L.2
Heath, E.3
Malburg, L.4
Zhu, A.X.5
Carey, M.6
Shapiro, G.I.7
Eder, J.P.8
-
11
-
-
71749102468
-
N-(4-(6,7-disubstituted-quinolin-4-yloxy)-3-fluorophenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors
-
Mannion M, Raeppel S, Claridge S, Zhou N, Saavedra O, Isakovic L and Vaisburg A. N-(4-(6, 7-disubstituted-quinolin-4-yloxy)-3-fluorophenyl)-2-oxo-3-phenylimidazolidine-1-carboxamides: a novel series of dual c-Met/VEGFR2 receptor tyrosine kinase inhibitors. Bioorganic and Medicinal Chemistry Letters 2009; 19: 6552-6556.
-
(2009)
Bioorganic and Medicinal Chemistry Letters
, vol.19
, pp. 6552-6556
-
-
Mannion, M.1
Raeppel, S.2
Claridge, S.3
Zhou, N.4
Saavedra, O.5
Isakovic, L.6
Vaisburg, A.7
-
12
-
-
84856540747
-
A comparison of the pharmacokinetics of the anticancer MET inhibitor foretinib free base tablet formulation to bisphosphate salt capsule formulation in patients with solid tumors
-
Naing A, Kurzrock R, Adams LM, Kleha JF, Laubscher KH, Bonate PL, Weller S, Fitzgerald C, Xu YM and LoRusso PM. A comparison of the pharmacokinetics of the anticancer MET inhibitor foretinib free base tablet formulation to bisphosphate salt capsule formulation in patients with solid tumors. Investigational New Drugs 2012; 30(1): 327-334.
-
(2012)
Investigational New Drugs
, vol.30
, Issue.1
, pp. 327-334
-
-
Naing, A.1
Kurzrock, R.2
Adams, L.M.3
Kleha, J.F.4
Laubscher, K.H.5
Bonate, P.L.6
Weller, S.7
Fitzgerald, C.8
Xu, Y.M.9
LoRusso, P.M.10
-
13
-
-
76149091189
-
Small molecule c-Met kinase inhibitors: a review of recent patents
-
Porter J. Small molecule c-Met kinase inhibitors: a review of recent patents. Expert Opinion on Therapeutic Patents 2010; 20: 159-177.
-
(2010)
Expert Opinion on Therapeutic Patents
, vol.20
, pp. 159-177
-
-
Porter, J.1
-
14
-
-
70350230210
-
Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases
-
Qian F, Engst S, Yamaguchi K, Yu PW, Won K, Mock L, Lou T, Tan J, Li C, Tam D, Lougheed JL, Yakes FM, Bentzien F, Xu W, Zaks T, Wooster R, Greshock J and Joly AH. Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases. Cancer Research 2009; 69(20): 8009-8016.
-
(2009)
Cancer Research
, vol.69
, Issue.20
, pp. 8009-8016
-
-
Qian, F.1
Engst, S.2
Yamaguchi, K.3
Yu, P.W.4
Won, K.5
Mock, L.6
Lou, T.7
Tan, J.8
Li, C.9
Tam, D.10
Lougheed, J.L.11
Yakes, F.M.12
Bentzien, F.13
Xu, W.14
Zaks, T.15
Wooster, R.16
Greshock, J.17
Joly, A.H.18
-
15
-
-
66149135285
-
The MET receptor tyrosine kinase is a potential novel therapeutic target for head and neck squamous cell carcinoma
-
Seiwert TY, Jagadeeswaran R, Faoro L, Janamanchi V, Nallasura V, Dinali M, Yala S, Kanteti R, Cohen EEW, Lingen MW, Martin L, Krishnaswamy S, Klein-Szanto A, Christensen JG, Vokes EE and Salgia R. The MET receptor tyrosine kinase is a potential novel therapeutic target for head and neck squamous cell carcinoma. Cancer Research 2013; 69: 3021-3031.
-
(2013)
Cancer Research
, vol.69
, pp. 3021-3031
-
-
Seiwert, T.Y.1
Jagadeeswaran, R.2
Faoro, L.3
Janamanchi, V.4
Nallasura, V.5
Dinali, M.6
Yala, S.7
Kanteti, R.8
Cohen, E.E.W.9
Lingen, M.W.10
Martin, L.11
Krishnaswamy, S.12
Klein-Szanto, A.13
Christensen, J.G.14
Vokes, E.E.15
Salgia, R.16
-
16
-
-
84879110331
-
A Phase 1 dose-escalation study of the safety and pharmacokinetics of once-daily oral foretinib, a multi-kinase inhibitor, in patients with solid tumors
-
Shapiro GI, McCallum S, Adams LM, Sherman L, Weller S, Swann S, Keer H, Miles D, Müller T and Lorusso P. A Phase 1 dose-escalation study of the safety and pharmacokinetics of once-daily oral foretinib, a multi-kinase inhibitor, in patients with solid tumors. Investigational New Drugs 2013; 31(3):742-750.
-
(2013)
Investigational New Drugs
, vol.31
, Issue.3
, pp. 742-750
-
-
Shapiro, G.I.1
McCallum, S.2
Adams, L.M.3
Sherman, L.4
Weller, S.5
Swann, S.6
Keer, H.7
Miles, D.8
Müller, T.9
Lorusso, P.10
-
17
-
-
67349189814
-
MET receptor tyrosine kinase as a therapeutic anticancer target
-
Stellrecht CM and Gandhi V. MET receptor tyrosine kinase as a therapeutic anticancer target. Cancer Letters 2009; 280(1): 1-14.
-
(2009)
Cancer Letters
, vol.280
, Issue.1
, pp. 1-14
-
-
Stellrecht, C.M.1
Gandhi, V.2
-
18
-
-
84874937924
-
Inhibitors of the TAM subfamily of tyrosine kinases: synthesis and biological evaluation
-
Suárez RM, Chevot F, Cavagnino A, Saettel N, Radvanyi F, Piguel S, Bernard-Pierrot I, Stoven V and Legraverend M. Inhibitors of the TAM subfamily of tyrosine kinases: synthesis and biological evaluation. European Journal of Medicinal Chemistry 2013; 61: 2-25.
-
(2013)
European Journal of Medicinal Chemistry
, vol.61
, pp. 2-25
-
-
Suárez, R.M.1
Chevot, F.2
Cavagnino, A.3
Saettel, N.4
Radvanyi, F.5
Piguel, S.6
Bernard-Pierrot, I.7
Stoven, V.8
Legraverend, M.9
-
19
-
-
78651375983
-
An adjacent arginine, and the phosphorylated tyrosine in the c-Met receptor target sequence, dictates the orientation of c-Cbl binding
-
Sun Q, Ng C, Guy GR and Sivaraman J. An adjacent arginine, and the phosphorylated tyrosine in the c-Met receptor target sequence, dictates the orientation of c-Cbl binding. FEBS Letters 2011; 585: 281-285.
-
(2011)
FEBS Letters
, vol.585
, pp. 281-285
-
-
Sun, Q.1
Ng, C.2
Guy, G.R.3
Sivaraman, J.4
-
20
-
-
84883262213
-
Design, synthesis, and structure-activity relationships of novel 6,7-disubstituted-4-phenoxyquinoline derivatives as potential antitumor agents
-
Tang QD, Zhao YF, Du XM, Chong LE, Gong P and Guo C. Design, synthesis, and structure-activity relationships of novel 6, 7-disubstituted-4-phenoxyquinoline derivatives as potential antitumor agents. European Journal of Medicinal Chemistry 2013; 69: 77-89.
-
(2013)
European Journal of Medicinal Chemistry
, vol.69
, pp. 77-89
-
-
Tang, Q.D.1
Zhao, Y.F.2
Du, X.M.3
Chong, L.E.4
Gong, P.5
Guo, C.6
-
22
-
-
85165435569
-
-
FDA Guidance for Industry: Bioanalytical Method Validation. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research: Rockville, MD
-
US Food and Drug Administration. FDA Guidance for Industry: Bioanalytical Method Validation. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research: Rockville, MD, 2001.
-
(2001)
-
-
-
23
-
-
77955984715
-
Down-regulation of c-Met expression inhibits human HCC cells growth and invasion by RNA interference
-
Xie B, Xing R, Chen P, Gou YB, Li S, Xiao J and Dong JH. Down-regulation of c-Met expression inhibits human HCC cells growth and invasion by RNA interference. Journal of Surgical Research 2010; 162(2): 231-238.
-
(2010)
Journal of Surgical Research
, vol.162
, Issue.2
, pp. 231-238
-
-
Xie, B.1
Xing, R.2
Chen, P.3
Gou, Y.B.4
Li, S.5
Xiao, J.6
Dong, J.H.7
-
24
-
-
79959215032
-
Foretinib (GSK1363089), an orally available multikinase inhibitor of c-Met and VEGFR-2, blocks proliferation, induces anoikis, and impairs ovarian cancer metastasis
-
Zillhardt M, Park SM, Romero IL, Sawada K, Montag A, Krausz T, Yamada S, Peter ME and Lengyel E. Foretinib (GSK1363089), an orally available multikinase inhibitor of c-Met and VEGFR-2, blocks proliferation, induces anoikis, and impairs ovarian cancer metastasis. Clinical Cancer Research 2011; 17(12): 4042-4051.
-
(2011)
Clinical Cancer Research
, vol.17
, Issue.12
, pp. 4042-4051
-
-
Zillhardt, M.1
Park, S.M.2
Romero, I.L.3
Sawada, K.4
Montag, A.5
Krausz, T.6
Yamada, S.7
Peter, M.E.8
Lengyel, E.9
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