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vatalanib

Known as: 1-(4-chloroanilino)-4-(pyridylmethyl)phthalazine, N-(4-Chlorophenyl)-4-(4-pyridinylmethyl)-1-phthalazinamine, PTK/ZK 
An orally bioavailable anilinophthalazine with potential antineoplastic activity. Vatalanib binds to and inhibits the protein kinase domain of… 
National Institutes of Health

Related topics

Related topics

14 relations

Narrower (4)

CGP79787DPTK 787PTK787/ZK 222584ZK 222584
FLT1 protein, humanNCIt Antineoplastic Agent TerminologyReceptor Tyrosine Kinase InhibitionVascular Endothelial Growth Factor Receptor 2, human

Broader (3)

PhthalazinesProtein Kinase InhibitorsPyridines

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Vatalanib in advanced colorectal cancer: two studies with identical results.
Because of biologic variability, limited impact of treatment, chance, and sometimes bias, the results of clinical trials in… 
2010
2010
Phase 1 study of combination treatment with PTK 787/ZK 222584 and cetuximab for patients with advanced solid tumors: safety, pharmacokinetics, pharmacodynamics analysis.
INTRODUCTION PTK/ZK is a small-molecule inhibitor of all three vascular endothelial growth factor (VEGF) receptors, platelet… 
2008
2008
Open-label, non-randomized, multicenter phase II study evaluating the angiogenesis inhibitor PTK787/ ZK222584 (PTK/ZK) in patients with advanced neuroendocrine carcinomas (NEC)
2007
2007
PTK787/ZK 222584, a small molecule tyrosine kinase receptor inhibitor of vascular endothelial growth factor (VEGF), has modest activity in myelofibrosis with myeloid metaplasia.
Highly Cited
2005
Highly Cited
2005
PTK787/ZK222584, a tyrosine kinase inhibitor of vascular endothelial growth factor receptor, reduces uptake of the contrast agent GdDOTA by murine orthotopic B16/BL6 melanoma tumours and inhibits…
Assessment of tumour vascularity may characterize malignancy as well as predict responsiveness to anti‐angiogenic therapy. Non… 
2005
2005
A phase IB, open label, safety and pharmacokinetic (PK) study of escalating doses of PTK787/ZK 222584 (PTK/ZK) in combination with paclitaxel and carboplatin in patients (Pts) with stage IC to IV…
5075 Background: Vascular endothelial growth factors (VEGFs) and VEGF receptors (VEGFRs) are important mediators of tumor growth… 
Review
2004
Review
2004
A phase I/II trial of single-agent PTK 787/ZK 222584 (PTK/ZK), a novel, oral angiogenesis inhibitor, in patients with recurrent glioblastoma multiforme (GBM).
1512 Background: VEGF-mediated signaling pathways may be critical to GBM neovascularization, and inhibition of VEGF pathways may… 
Highly Cited
2004
Highly Cited
2004
A phase I/II trial of PTK787/ZK 222584 (PTK/ZK), a novel, oral angiogenesis inhibitor, in combination with either temozolomide or lomustine for patients with recurrent glioblastoma multiforme (GBM).
1513 Background: VEGF-mediated signaling through VEGF receptors is integral to GBM neovascularization and therefore an attractive… 
Highly Cited
2004
Highly Cited
2004
Phase I/II study of PTK787/ZK 222584 (PTK/ZK), a novel, oral angiogenesis inhibitor in combination with FOLFIRI as first-line treatment for patients with metastatic colorectal cancer.
3558 Background: Increased angiogenesis is correlated with poor prognosis in patients with advanced metastatic colorectal cancer… 
Review
2003
Review
2003
Soluble markers for the detection of hypoxia under antiangiogenic treatment.
Antiangiogenic therapy is a promising new strategy to inhibit tumor growth and formation of metastases. VEGF (vascular… 
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