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Lenvatinib mesylate
Cat. No.:
0225LY-0772
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
Add to basket
Product Overview
Description:
Lenvatinib mesylate is an orally administered, multi-targeted inhibitor that displays strong antitumor activity by targeting KIT, RET, PDGFR, FGFR1-4, and VEGFR1-3.
Synonym:
857890-39-2; Lenvima; Lenvatinib methanesulfonate; N-(4-((6-Carbamoyl-7-methoxyquinolin-4-yl)oxy)-2-chlorophenyl)-N'-cyclopropylurea monomethanesulfonate; 4-[3-chloro-4-(cyclopropylcarbamoylamino)phenoxy]-7-methoxyquinoline-6-carboxamide; 6-carbamoyl-4-(3-chloro-4-((cyclopropylcarbamoyl)amino)phenoxy)-7-methoxyquinolin-1-ium methanesulfonate; 4-[3-Chloro-4-[[(cyclopropylamino)carbonyl]amino]phenoxy]-7-methoxy-6-quinolinecarboxamide monomethanesulfonate
CAS No.:
857890-39-2
Compound CID:
11237762
Formula:
C22H23ClN4O7S
Formula Weight:
522.96
Specification
Targets&IC50:
FGFR1: 46 nM; PDGFRβ: 39 nM; PDGFRα: 51 nM; c-Kit: 100 nM; VEGFR1: 22 nM; VEGFR2: 4 nM; VEGFR3: 5.2 nM
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Lenvatinib mesylate can be used in thyroid cancer and hepatology research to study the multi-target inhibition of VEGFR, FGFR, and PDGFR.
Library Information
Target:
PDGFR; c-Kit; FGFR; VEGFR; c-RET
Receptor:
c-Kit; FGFR1; PDGFRα; PDGFRβ; RET; VEGFR1; VEGFR3
Pathways:
Tyrosine kinase/adaptors; Angiogenesis; Apoptosis
Plate Number:
AOCL-10
Plate Location:
h11
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
32.67 mg/mL; 62.47 mM
ALogP:
2.418
HBA_Count:
5
HBD_Count:
3
Rotatable Bond:
6





