ZD6474 inhibits vascular endothelial growth factor signaling, angiogenesis, and tumor growth following oral administration
SR Wedge, DJ Ogilvie, M Dukes, J Kendrew, R Chester… - Cancer research, 2002 - AACR
Abstract ZD6474 [N-(4-bromo-2-fluorophenyl)-6-methoxy-7-[(1-methylpiperidin-4-yl)
methoxy] quinazolin-4-amine] is a potent, po active, low molecular weight inhibitor of kinase …
methoxy] quinazolin-4-amine] is a potent, po active, low molecular weight inhibitor of kinase …
ZD4190: an orally active inhibitor of vascular endothelial growth factor signaling with broad-spectrum antitumor efficacy
SR Wedge, DJ Ogilvie, M Dukes, J Kendrew… - Cancer research, 2000 - AACR
There is evidence that vascular endothelial growth factor (VEGF) contributes to solid tumor
growth through the promotion of both angiogenesis and tumor vascular permeability. To …
growth through the promotion of both angiogenesis and tumor vascular permeability. To …
ZD6474–a novel inhibitor of VEGFR and EGFR tyrosine kinase activity
AJ Ryan, SR Wedge - British journal of cancer, 2005 - nature.com
Angiogenesis is crucial for maintaining the supply of oxygen and nutrients required to
support solid tumour growth. Inhibitors of tumour blood vessel formation are therefore being …
support solid tumour growth. Inhibitors of tumour blood vessel formation are therefore being …
[HTML][HTML] Clinical evaluation of ZD6474, an orally active inhibitor of VEGF and EGF receptor signaling, in patients with solid, malignant tumors
SN Holden, SG Eckhardt, R Basser, R De Boer… - Annals of …, 2005 - Elsevier
Background:: ZD6474 selectively inhibits the tyrosine kinase activity of vascular endothelial
growth factor receptor and epidermal growth factor receptor. The safety, tolerability and …
growth factor receptor and epidermal growth factor receptor. The safety, tolerability and …
AZD2171: a highly potent, orally bioavailable, vascular endothelial growth factor receptor-2 tyrosine kinase inhibitor for the treatment of cancer
SR Wedge, J Kendrew, LF Hennequin, PJ Valentine… - Cancer research, 2005 - AACR
Inhibition of vascular endothelial growth factor-A (VEGF) signaling is a promising therapeutic
approach that aims to stabilize the progression of solid malignancies by abrogating tumor …
approach that aims to stabilize the progression of solid malignancies by abrogating tumor …
Antitumor activity of the novel vascular targeting agent ZD6126 in a panel of tumor models
DC Blakey, FR Westwood, M Walker, GD Hughes… - Clinical Cancer …, 2002 - AACR
Purpose: The purpose of this study was to examine the antitumor effects of the novel
vascular targeting agent ZD6126 and to use histology, CD31 immunohistochemistry, and …
vascular targeting agent ZD6126 and to use histology, CD31 immunohistochemistry, and …
Antitumor effects of ZD6474, a small molecule vascular endothelial growth factor receptor tyrosine kinase inhibitor, with additional activity against epidermal growth …
F Ciardiello, R Caputo, V Damiano, R Caputo… - Clinical Cancer …, 2003 - AACR
Purpose: Vascular endothelial growth factor (VEGF) is a major mitogen for endothelial cells
and enhances vascular permeability. Enhanced VEGF secretion is found in human cancers …
and enhances vascular permeability. Enhanced VEGF secretion is found in human cancers …
Phase I clinical evaluation of weekly administration of the novel vascular-targeting agent, ZD6126, in patients with solid tumors
LV Beerepoot, SA Radema, EO Witteveen… - Journal of clinical …, 2006 - ascopubs.org
Purpose ZD6126 is a novel vascular-targeting agent that induces selective effects on the
morphology of endothelial cells by disrupting the tubulin cytoskeleton. This leads to cell …
morphology of endothelial cells by disrupting the tubulin cytoskeleton. This leads to cell …
PTK787/ZK 222584, a novel and potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, impairs vascular endothelial growth factor-induced …
JM Wood, G Bold, E Buchdunger, R Cozens, S Ferrari… - Cancer research, 2000 - AACR
Abstract PTK787/ZK 222584 (1-[4-chloroanilino]-4-[4-pyridylmethyl] phthalazine succinate)
is a potent inhibitor of vascular endothelial growth factor (VEGF) receptor tyrosine kinases …
is a potent inhibitor of vascular endothelial growth factor (VEGF) receptor tyrosine kinases …
ZD6126: a novel vascular-targeting agent that causes selective destruction of tumor vasculature
PD Davis, GJ Dougherty, DC Blakey, SM Galbraith… - Cancer research, 2002 - AACR
Physiological differences between tumor and normal vasculature provide a target for drug
discovery. In particular, the immature nature of tumor vasculature may render it intrinsically …
discovery. In particular, the immature nature of tumor vasculature may render it intrinsically …