Anlotinib Hydrochloride (CAS: 1360460-82-7)
Catalog #:EBC52231
Biological Activity
Synonyms AL3818 dihydrochloride; AL-3818; Anlotinib HCl; AL3818; Anlotinib dihydrochloride; Anlotinib HCl; Anlotinib; Catequentinib
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%
Molecular Weight 480.36
Molecular Formula C23H22FN3O3·2HCl
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
Preparing Stock Solutions Molecular Structure
ConcentrationSolventMass 1 mg 5 mg 10 mg
1 mM 2.0818 ml 10.4089 ml 20.8177 ml
5 mM 0.4164 ml 2.0818 ml 4.1635 ml
10 mM 0.2082 ml 1.0409 ml 2.0818 ml
50 mM 0.0416 ml 0.2082 ml 0.4164 ml
Solubility
DMSO: ≥50mg/ml
Product Description

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. 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.

For Research Use Only, Not For Diagnostic Or Therapeutic Procedures.
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