| Name | Ningetinib |
| Description | Ningetinib (CT-053) (CT053PTSA) is an orally bioavailable tyrosine kinase inhibitor with IC50s of <1.0, 1.9 and 6.7 nM for Axl, VEGFR2, and c-Met, respectively. |
| In vitro | In cell-based functional assays, Ningetinib inhibits VEGF and HGF-stimulated HUVEC proliferation and microvascular angiogenesis in rat aortic rings with IC50 values of 6.3 and 8.6 nM, respectively. |
| In vivo | In the orthotopic U87MG human glioblastoma xenograft model, Ningetinib prolongs the median survival time and yields a significant increase in life-span value (ILS=32%) at an oral dose of 20 mg/kg/day (dosed 21 days) versus the vehicle-treated group. When single dosed orally (3 mg/kg) to U87MG tumor-bearing nude mice, Ningetinib potently inhibits the phosphorylation of c-Met and its downstream signaling kinases AKT and ERK1/2 for up to 6 hours in tumor tissues. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO : 15 mg/mL (26.95 mM), Sonication is recommended.
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| Keywords | VEGFR2 | VEGFR | Vascular endothelial growth factor receptor | Tyro3 | TAMReceptor | TAM Receptor | Ningetinib | Mer | Inhibitor | inhibit | HGFR | CT053 | CT 053 | c-Met/HGFR | cMet/HGFR | c-Met | cMet | Axl |
| Inhibitors Related | Ribociclib | Bemcentinib | Gilteritinib | Decanoic Acid | Sorafenib | glycine | Nintedanib esylate | Afatinib | Chloramphenicol | Bacitracin Zinc | Lenvatinib | Pazopanib |
| Related Compound Libraries | Reprogramming Compound Library | Failed Clinical Trials Compound Library | Bioactive Compound Library | Membrane Protein-targeted Compound Library | Kinase Inhibitor Library | Tyrosine Kinase Inhibitor Library | Anti-Cancer Clinical Compound Library | Drug Repurposing Compound Library | Inhibitor Library | Bioactive Compounds Library Max | Anti-Cancer Drug Library | Anti-Cancer Active Compound Library |