Comparison

Vatalanib (dihydrochloride) European Partner

Item no. HY-12018-100mg
Manufacturer MedChem Express
CASRN 212141-51-0
Amount 100 mg
Quantity options 100 mg 10 mM/1 mL 10 mg 25 mg 50 mg 5 mg
Category
Type Inhibitors
Specific against other
Purity 99.68
Citations [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.
Bioact Mater. 2 January 2022.|Br J Pharmacol. 2019 Sep;176(17):3143-3160. |Evid-Based Compl Alt. 2021 Apr 27.|JCI Insight. 2024 May 22;9(10):e166402.|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.|Drug Metab Pharmacokinet. 2017 Jun;32(3):179-188. |Int J Mol Sci. 2024 Nov 15;25(22):12277.|J Microbiol Biotechnol. 2015 Aug;25(8):1227-33. |J Pharm Anal. 2023 Sep 11.|Patent. US20170349880A1.
Smiles ClC1=CC=C(C=C1)NC2=NN=C(C3=C2C=CC=C3)CC4=CC=NC=C4.[H]Cl.[H]Cl
ECLASS 10.1 32160490
ECLASS 11.0 32160490
UNSPSC 12000000
Alias PTK787 (dihydrochloride),ZK-222584 (dihydrochloride),CGP-797870 (dihydrochloride)
Shipping Condition Room temperature
Available
Manufacturer - Type
Reference compound
Manufacturer - Applications
Cancer-Kinase/protease
Manufacturer - Targets
Apoptosis; VEGFR
Shipping Temperature
Room Temperature
Storage Conditions
4°C (Powder, sealed storage, away from moisture)
Molecular Weight
419.73
Product Description
Vatalanib dihydrochloride (PTK787 dihydrochloride) is an inhibitor of VEGFR2/KDR with IC50 of 37 nM.
Manufacturer - Research Area
Cancer
Solubility
DMSO: 50 mg/mL (ultrasonic; warming; heat to 80°C)|H2O: 50 mg/mL (ultrasonic)
Manufacturer - Pathway
Apoptosis; Protein Tyrosine Kinase/RTK
Isoform
VEGFR2/KDR/Flk-1
Clinical information
Phase 3

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 mg
Available: In stock
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