CAS 212141-54-3 appears in our catalog under these names: Vatalanib, 95%, Vatalanib, Vatalanib free base/ 99.27% (existing batch purity), Vatalanib HCl, Vatalanib, 98%. Offered by: Combi-blocks, GLPBio, TargetMol, Biosynth, Thermo Scientific (Acros). Available pack sizes: 100mg, 10mg, 10mM (in 1ml dmso), 50mg, 5mg, 25mg, 500mg, 1g.
Vatalanib is a member of the class of phthalazines that is phthalazine in which the hydrogens at positions 1 and 4have been replaced by a p-chlorophenylamino group and a pyridin-4-ylmethyl group, respectively. It is a multi-targeted tyrosine kinase inhibitor for all isoforms of VEGFR, PDGFR and c-Kit. It has a role as an antineoplastic agent, an angiogenesis inhibitor, an EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor and a vascular endothelial growth factor receptor antagonist. It is a member of pyridines, a member of phthalazines, a secondary amino compound and a member of monochlorobenzenes.
Source: ChEBI
| Molecular formula | C20H15ClN4 |
|---|---|
| Molecular weight | 346.8 g/mol |
| IUPAC name | N-(4-chlorophenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine |
| InChIKey | YCOYDOIWSSHVCK-UHFFFAOYSA-N |
| SMILES | C1=CC=C2C(=C1)C(=NN=C2NC3=CC=C(C=C3)Cl)CC4=CC=NC=C4 |
Computed by PubChem (NCBI)