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Vatalanib
Products Details
Product Description
– Vatalanib (PTK787; ZK-222584; CGP-79787) is an inhibitor of VEGFR2/KDR with IC50 of 37 nM.
Web ID
– HY-10203
Shipping
– Room temperature
Applications
– Cancer-Kinase/protease
Molecular Formula
– C20H15ClN4
Citations
– Drug Metab Pharmacokinet. 2017 Jun;32(3):179-188. |J Microbiol Biotechnol. 2015 Aug;25(8):1227-33. |J Pharm Anal. 2023 Sep 11.|Patent. US20170349880A1.|Bioact Mater. 2 January 2022.|Br J Pharmacol. 2019 Sep;176(17):3143-3160. |Evid-Based Compl Alt. 2021 Apr 27.|Kitazato Graduate School of Pharmaceutical Sciences. Kitasato University. 2017.|Oncol Rep. 2016 Mar;35(3):1297-308.|Oxid Med Cell Longev. 18 Jul 2022.|Sci Transl Med. 2018 Jul 18;10(450):eaaq1093.|Ulm University. 2023 Mar 21.
References
– [1]Wood JM, et al. PTK787/ZK 222584, a novel and potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, impairs vascular endothelial growth factor-induced responses and tumor growth after oral administration. Cancer Res. 2000, 60(8|[2]Murakami M, et al. Tyrosine kinase inhibitor PTK/ZK enhances the antitumor effects of interferon-α/5-fluorouracil therapy for hepatocellular carcinoma cells. Ann Surg Oncol. 2011, 18(2), 589-596.|[3]Wan J, et al. Local recurrence of small cell lung cancer following radiofrequency ablation is induced by HIF-1α expression in the transition zone. Oncol Rep. 2016 Mar;35(3):1297-308.
CAS Number
– 212141-54-3
Molecular Weight
– 346.81
SMILES
– ClC1=CC=C(C=C1)NC2=NN=C(CC3=CC=NC=C3)C4=C2C=CC=C4
Clinical Information
– Phase 3
Research Area
– Cancer
Solubility
– DMSO : 125 mg/mL (ultrasonic;warming)
Target
– VEGFR
Isoform
– VEGFR2/KDR/Flk-1
Pathway
– Protein Tyrosine Kinase/RTK
Product type
– Reference compound
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