-
1
-
-
34147137124
-
Discovery of N-(4-(3-amino-1H-indazol-4-yl)phenyl)-N'-(2-fluoro-5- Methylphenyl)urea (ABT-869), a 3-aminoindazole-based orally active multitargeted receptor tyrosine kinase inhibitor
-
DOI 10.1021/jm061280h
-
Dai Y, Hartandi K, Ji Z, et al. Discovery of N-(4-(3-amino-1H-indazol-4- yl) phenyl)-N'-(2-fluoro-5-methylphenyl)urea (ABT-869), a 3-aminoindazolebased orally active multitargeted receptor tyrosine kinase inhibitor. J Med Chem. 2007;50:1584-1597. (Pubitemid 46564379)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.7
, pp. 1584-1597
-
-
Dai, Y.1
Hartandi, K.2
Ji, Z.3
Ahmed, A.A.4
Albert, D.H.5
Bauch, J.L.6
Bouska, J.J.7
Bousquet, P.F.8
Cunha, G.A.9
Glaser, K.B.10
Harris, C.M.11
Hickman, D.12
Guo, J.13
Li, J.14
Marcotte, P.A.15
Marsh, K.C.16
Moskey, M.D.17
Martin, R.L.18
Olson, A.M.19
Osterling, D.J.20
Pease, L.J.21
Soni, N.B.22
Stewart, K.D.23
Stoll, V.S.24
Tapang, P.25
Reuter, D.R.26
Davidsen, S.K.27
Michaelides, M.R.28
more..
-
2
-
-
0034907881
-
The angiotensin-I-converting enzyme inhibitor perindopril suppresses tumor growth and angiogenesis: Possible role of the vascular endothelial growth factor
-
Yoshiji H, Kuriyama S, Kawata M, et al. The angiotensin-I-converting enzyme inhibitor perindopril suppresses tumor growth and angiogenesis: possible role of the vascular endothelial growth factor. Clin Cancer Res. 2001;7:1073-1078. (Pubitemid 32708747)
-
(2001)
Clinical Cancer Research
, vol.7
, Issue.4
, pp. 1073-1078
-
-
Yoshiji, H.1
Kuriyama, S.2
Kawata, M.3
Yoshii, J.4
Ikenaka, Y.5
Noguchi, R.6
Nakatani, T.7
Tsujinoue, H.8
Fukui, H.9
-
3
-
-
34547681379
-
Phase I clinical study of AZD2171, an oral vascular endothelial growth factor signaling inhibitor, in patients with advanced solid tumors
-
DOI 10.1200/JCO.2006.07.2066
-
Drevs J, Siegert P, Medinger M, et al. Phase I clinical study of AZD2171, an oral vascular endothelial growth factor signaling inhibitor, in patients with advanced solid tumors. J Clin Oncol. 2007;25:3045-3054. (Pubitemid 47218051)
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.21
, pp. 3045-3054
-
-
Drevs, J.1
Siegert, P.2
Medinger, M.3
Mross, K.4
Strecker, R.5
Zirrgiebel, U.6
Harder, J.7
Blum, H.8
Robertson, J.9
Jurgensmeier, J.M.10
Puchalski, T.A.11
Young, H.12
Saunders, O.13
Unger, C.14
-
4
-
-
20144370978
-
AZD2171: A highly potent, orally bioavailable, vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for the treatment of cancer
-
DOI 10.1158/0008-5472.CAN-04-4409
-
Wedge SR, Kendrew J, Hennequin LF, et al. AZD2171: a highly potent, orally bioavailable, vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for the treatment of cancer. Cancer Res. 2005;65: 4389-4400. (Pubitemid 40775678)
-
(2005)
Cancer Research
, vol.65
, Issue.10
, pp. 4389-4400
-
-
Wedge, S.R.1
Kendrew, J.2
Hennequin, L.F.3
Valentine, P.J.4
Barry, S.T.5
Brave, S.R.6
Smith, N.R.7
James, N.H.8
Dukes, M.9
Curwen, J.O.10
Chester, R.11
Jackson, J.A.12
Boffey, S.J.13
Kilburn, L.L.14
Barnett, S.15
Richmond, G.H.P.16
Wadsworth, P.F.17
Walker, M.18
Bigley, A.L.19
Taylor, S.T.20
Cooper, L.21
Beck, S.22
Jurgensmeier, J.M.23
Ogilvie, D.J.24
more..
-
5
-
-
0028930121
-
Differential requirement of a motif within the carboxyl-terminal domain of alpha-platelet-derived growth factor (alpha PDGF) receptor for PDGF focus forming activity chemotaxis, or growth
-
Yu JC, Li W, Wang LM, et al. Differential requirement of a motif within the carboxyl-terminal domain of alpha-platelet-derived growth factor (alpha PDGF) receptor for PDGF focus forming activity chemotaxis, or growth. J Biol Chem. 1995;270:7033-7036.
-
(1995)
J Biol Chem
, vol.270
, pp. 7033-7036
-
-
Yu, J.C.1
Li, W.2
Wang, L.M.3
-
6
-
-
34447635695
-
Angiogenesis Inhibitor Therapies: Focus on Kidney Toxicity and Hypertension
-
DOI 10.1053/j.ajkd.2007.04.025, PII S0272638607008359
-
Izzedine H, Rixe O, Billemont B, et al. Angiogenesis inhibitor therapies: focus on kidney toxicity and hypertension. Am J Kidney Dis. 2007;50: 203-218. (Pubitemid 47095077)
-
(2007)
American Journal of Kidney Diseases
, vol.50
, Issue.2
, pp. 203-218
-
-
Izzedine, H.1
Rixe, O.2
Billemont, B.3
Baumelou, A.4
Deray, G.5
-
7
-
-
33845656482
-
Angiotensin-converting enzyme inhibitors for bevacizumab-induced hypertension [3]
-
DOI 10.1345/aph.1H244
-
Dincer M, Altundag K. Angiotensin-converting enzyme inhibitors for bevacizumab-induced hypertension. Ann Pharmacother. 2006;40: 2278-2279. (Pubitemid 44954457)
-
(2006)
Annals of Pharmacotherapy
, vol.40
, Issue.12
, pp. 2278-2279
-
-
Dincer, M.1
Altundag, K.2
-
8
-
-
34547683305
-
Hypertension, proteinuria, and antagonism of vascular endothelial growth factor signaling: Clinical toxicity, therapeutic target, or novel biomarker?
-
DOI 10.1200/JCO.2007.11.5113
-
van Heeckeren WJ, Ortiz J, Cooney MM, et al. Hypertension, proteinuria, and antagonism of vascular endothelial growth factor signaling: clinical toxicity, therapeutic target, or novel biomarker? J Clin Oncol. 2007;25: 2993-2995. (Pubitemid 47218042)
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.21
, pp. 2993-2995
-
-
Van Heeckeren, W.J.1
Ortiz, J.2
Cooney, M.M.3
Remick, S.C.4
-
9
-
-
33646586669
-
Preclinical activity of ABT-869, a multitargeted receptor tyrosine kinase inhibitor
-
DOI 10.1158/1535-7163.MCT-05-0410
-
Albert DH, Tapang P, Magoc TJ, et al. Preclinical activity of ABT-869, a multitargeted receptor tyrosine kinase inhibitor. Mol Cancer Ther. 2006; 5:995-1006. (Pubitemid 43724600)
-
(2006)
Molecular Cancer Therapeutics
, vol.5
, Issue.4
, pp. 995-1006
-
-
Albert, D.H.1
Tapang, P.2
Magoc, T.J.3
Pease, L.J.4
Reuter, D.R.5
Wei, R.-Q.6
Li, J.7
Guo, J.8
Bousquet, P.F.9
Ghoreishi-Haack, N.S.10
Wang, B.11
Bukofzer, G.T.12
Wang, Y.-C.13
Stavropoulos, J.A.14
Hartandi, K.15
Niquette, A.L.16
Soni, N.17
Johnson, E.F.18
McCall, J.O.19
Bouska, J.J.20
Luo, Y.21
Donawho, C.K.22
Dai, Y.23
Marcotte, P.A.24
Glaser, K.B.25
Michaelides, M.R.26
Davidsen, S.K.27
more..
-
10
-
-
67650877206
-
Phase 1 study of AVT869, a multiple receptor tyrosine kinase inhibitor, in patents with refractory solid malignancies
-
Goh BC, Thng CH, Sukri N, et al. Phase 1 study of AVT869, a multiple receptor tyrosine kinase inhibitor, in patents with refractory solid malignancies. Eur J Cancer Suppl. 2006;4:108.
-
(2006)
Eur J Cancer Suppl
, vol.4
, pp. 108
-
-
Goh, B.C.1
Thng, C.H.2
Sukri, N.3
-
11
-
-
67650916263
-
Modification of sunitinib malate (SU1248) blood pressure changes in rats
-
Paper Presented at
-
Blasi E, Steidl J, Patyna S, et al. Modification of sunitinib malate (SU1248) blood pressure changes in rats. Paper Presented at: Annual Meeting of the American Association for Cancer Research; April 14-18, 2007; Los Angeles, CA.
-
Annual Meeting of the American Association for Cancer Research; April 14-18, 2007; Los Angeles, CA
-
-
Blasi, E.1
Steidl, J.2
Patyna, S.3
-
12
-
-
49649091098
-
Inhibition of vascular endothelial growth factor-A signaling induces hypertension: Examining the effect of cediranib (recentin; AZD2171) treatment on blood pressure in rat and the use of concomitant antihypertensive therapy
-
Curwen JO, Musgrove HL, Kendrew J, et al. Inhibition of vascular endothelial growth factor-A signaling induces hypertension: examining the effect of cediranib (recentin; AZD2171) treatment on blood pressure in rat and the use of concomitant antihypertensive therapy. Clin Cancer Res. 2008;14:3124-3131.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 3124-3131
-
-
Curwen, J.O.1
Musgrove, H.L.2
Kendrew, J.3
-
13
-
-
33744918043
-
Blood pressure regulation by ETA and ETB receptors in conscious, telemetry-instrumented mice and role of ETA in hypertension produced by selective ETB blockade
-
Fryer RM, Rakestraw PA, Banfor PN, et al. Blood pressure regulation by ETA and ETB receptors in conscious, telemetry-instrumented mice and role of ETA in hypertension produced by selective ETB blockade. Am J Physiol Heart Circ Physiol. 2006;290:H2554-H2559.
-
(2006)
Am J Physiol Heart Circ Physiol
, vol.290
-
-
Fryer, R.M.1
Rakestraw, P.A.2
Banfor, P.N.3
-
14
-
-
0029945669
-
2,4-Diarylpyrrolidine-3-carboxylic acids-potent ET(A) selective endothelin receptor antagonists. 1. Discovery of A-127722
-
DOI 10.1021/jm9505369
-
Winn M, von Geldern TW, Opgenorth TJ, et al. 2,4-Diarylpyrrolidine- 3-carboxylic acids-potent ETA selective endothelin receptor antagonists. 1. Discovery of A-127722. J Med Chem. 1996;39:1039-1048. (Pubitemid 26082937)
-
(1996)
Journal of Medicinal Chemistry
, vol.39
, Issue.5
, pp. 1039-1048
-
-
Winn, M.1
Von Geldern, T.W.2
Opgenorth, T.J.3
Jae, H.-S.4
Tasker, A.S.5
Boyd, S.A.6
Kester, J.A.7
Mantei, R.A.8
Bal, R.9
Sorensen, B.K.10
Wu-Wong, J.R.11
Chiou, W.J.12
Dixon, D.B.13
Novosad, E.I.14
Hernandez, L.15
Marsh, K.C.16
-
15
-
-
0033673350
-
Endothelin and ET(A) receptors in long-term arterial pressure homeostasis in conscious nonhuman primates
-
Reinhart GA, Preusser LC, Opgenorth TJ, et al. Endothelin and ET(A) receptors in long-term arterial pressure homeostasis in conscious nonhuman primates. Am J Physiol Regul Integr Comp Physiol. 2000; 279:R1701-R1706.
-
(2000)
Am J Physiol Regul Integr Comp Physiol
, vol.279
-
-
Reinhart, G.A.1
Preusser, L.C.2
Opgenorth, T.J.3
-
16
-
-
34247102347
-
VEGF and VEGFR-2 (KDR) internalization is required for endothelial recovery during wound healing
-
DOI 10.1016/j.yexcr.2007.02.020, PII S0014482707000560
-
Santos SC, Miguel C, Domingues I, et al. VEGF and VEGFR-2 (KDR) internalization is required for endothelial recovery during wound healing. Exp Cell Res. 2007;313:1561-1574. (Pubitemid 46589434)
-
(2007)
Experimental Cell Research
, vol.313
, Issue.8
, pp. 1561-1574
-
-
Constantino Rosa Santos, S.1
Miguel, C.2
Domingues, I.3
Calado, A.4
Zhu, Z.5
Wu, Y.6
Dias, S.7
-
17
-
-
0037441843
-
Effect of endothelin-A receptor blockade with atrasentan on tumor progression in men with hormone-refractory prostate cancer: A randomized, phase II, placebo-controlled trial
-
DOI 10.1200/JCO.2003.04.176
-
Carducci MA, Padley RJ, Breul J, et al. Effect of endothelin-A receptor blockade with atrasentan on tumor progression in men with hormonerefractory prostate cancer: a randomized, phase II, placebo-controlled trial. J Clin Oncol. 2003;21:679-689. (Pubitemid 46621903)
-
(2003)
Journal of Clinical Oncology
, vol.21
, Issue.4
, pp. 679-689
-
-
Carducci, M.A.1
Padley, R.J.2
Breul, J.3
Vogelzang, N.J.4
Zonnenberg, B.A.5
Daliani, D.D.6
Schulman, C.C.7
Nabulsi, A.A.8
Humerickhouse, R.A.9
Weinberg, M.A.10
Schmitt, J.L.11
Nelson, J.B.12
-
18
-
-
40949108811
-
Phase I/II study of atrasentan, an endothelin a receptor antagonist, in combination with paclitaxel and carboplatin as first-line therapy in advanced non-small cell lung cancer
-
Chiappori AA, Haura E, Rodriguez FA, et al. Phase I/II study of atrasentan, an endothelin A receptor antagonist, in combination with paclitaxel and carboplatin as first-line therapy in advanced non-small cell lung cancer. Clin Cancer Res. 2008;14:1464-1469.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 1464-1469
-
-
Chiappori, A.A.1
Haura, E.2
Rodriguez, F.A.3
-
19
-
-
0037303203
-
Role of endothelin-1 in osteoblastic bone metastases
-
Guise TA, Yin JJ, Mohammad KS. Role of endothelin-1 in osteoblastic bone metastases. Cancer. 2003;97:779-784. (Pubitemid 36131076)
-
(2003)
Cancer
, vol.97
, Issue.3 SUPPL.
, pp. 779-784
-
-
Guise, T.A.1
Yin, J.J.2
Mohammad, K.S.3
-
20
-
-
0037112435
-
Growth inhibition of cervix carcinoma cells in vivo by endothelin a receptor blockade
-
Bagnato A, Cirilli A, Salani D, et al. Growth inhibition of cervix carcinoma cells in vivo by endothelin A receptor blockade. Cancer Res. 2002;62:6381-6384. (Pubitemid 35364090)
-
(2002)
Cancer Research
, vol.62
, Issue.22
, pp. 6381-6384
-
-
Bagnato, A.1
Cirilli, A.2
Salani, D.3
Simeone, P.4
Muller, A.5
Nicotra, M.R.6
Natali, P.G.7
Venuti, A.8
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