

| Biological Activity | |||||||||||||||||||||||||
| Synonyms | AL3818 dihydrochloride; AL-3818 dihydrochloride; AL 3818 dihydrochloride; Anlotinib HCl; AL3818; Anlotinib Dihydrochloride | ||||||||||||||||||||||||
| Chemical Name | 1-[[4-[(4-fluoro-2-methyl-1H-indol-5-yl)oxy]-6-methoxyquinolin-7-yl]oxymethyl]cyclopropan-1-amine;dihydrochloride | ||||||||||||||||||||||||
| Application | Anlotinib Dihydrochloride (formerlyknown as AL3818 Dihydrochloride) is a novel and potent multi-kinase inhibitor that inhibits VEGFR2/3,FGFR1-4,PDGFRα/β,c-Kit, and Ret. | ||||||||||||||||||||||||
| CAS Number | 1360460-82-7 | ||||||||||||||||||||||||
| Purity | ≥98.0% | ||||||||||||||||||||||||
| Molecular Weight | 480.36 | ||||||||||||||||||||||||
| Molecular Formula | C23H24CL2FN3O3 | ||||||||||||||||||||||||
| SMILES | CC1=CC2=C(N1)C=CC(=C2F)OC3=C4C=C(C(=CC4=NC=C3)OCC5(CC5)N)OC.Cl.Cl | ||||||||||||||||||||||||
| Target & IC50 | VEGFR2: IC50 = 0.2 nM VEGFR3: IC50 = 0.7 nM c-Kit: IC50 = 14.8 nM |
||||||||||||||||||||||||
| Shipping | Gel Pack | ||||||||||||||||||||||||
| Storage | Store at -20°C | ||||||||||||||||||||||||
|
|||||||||||||||||||||||||
| Solubility | |
| DMSO: ≥ 60 mg/mL |
| Product Description | |
Anlotinib is a potential antineoplastic and anti-angiogenic receptor tyrosine kinase (RTK) inhibitor. Anlotinib dramatically lowers the number of AN3CA cells in vitro, which are identified by high levels of mutated FGFR2 protein expression. After a 29-day treatment cycle, daily oral administration of anlotinib (5 mg/kg) resulted in a complete response in 55% of treated animals and in a reduced tumor volume and tumor weights of AN3CA tumors by 94% and 96%, respectively. While paclitaxel and carboplatin were unable to stop the growth of the tumor, their combination with anlotinib did not appear to have a better result than Anlotinib treatment alone. |