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Lenvatinib Mesylate

Name: Lenvatinib Mesylate
Brand: Selleck Chemicals
SKU: S5240
Rating: 5 (31 reviews)

Synonyms: E7080 mesylate

Catalog No.S5240 Purity: 99.96%

Lenvatinib Mesylate is a synthetic, orally available tyrosine kinase inhibitor that inhibits vascular endothelial growth factor receptor (VEGFR1-3), fibroblast growth factor receptor (FGFR1-4), platelet-derived growth factor receptor α (PDGFRα), stem cell factor receptor (Kit (c-Kit)), and rearranged during transfection (RET (c-RET)). Lenvatinib Mesylate has potential antineoplastic activity.

Lenvatinib Mesylate Chemical Structure

CAS: 857890-39-2

Selleck's Lenvatinib Mesylate has been cited by 31 publications

Purity & Quality Control

Batch: Purity: 99.96%

99.96

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Cell Data

Cell Lines	Assay Type	Activity Description	PMID
DAOY	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells	29435139
SJ-GBM2	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells	29435139
A673	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells	29435139
SK-N-MC	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells	29435139
BT-37	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells	29435139
NB-EBc1	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells	29435139
SK-N-SH	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells	29435139
NB1643	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells	29435139
LAN-5	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells	29435139
BT-12	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells	29435139
Rh18	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh18 cells	29435139
RD	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for RD cells	29435139
Rh41	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 cells	29435139
SK-N-MC	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-MC cells	29435139
TC32	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for TC32 cells	29435139
Rh41	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh41 cells	29435139
Rh18	qHTS assay	qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh18 cells	29435139
Click to View More Cell Line Experimental Data

Biological Activity

Description

Targets

c-RET ^[2]	VEGFR2 ^[1] (Cell-free assay)	VEGFR3 ^[1] (Cell-free assay)	VEGFR1 ^[1] (Cell-free assay)	PDGFRβ ^[1] (Cell-free assay)	Click to View More Targets
	4.0 nM	5.2 nM	22 nM	39 nM	Click to View More Targets

In vitro
In vitro	E7080 is an orally active inhibitor of multiple receptor tyrosine kinases including VEGF, FGF and SCF receptors.
Experimental Result Images	Methods	Biomarkers	Images	PMID
	Western blot	phospho-FGFR1 / FGFR1 /phospho-FRS2 / FRS2 / phospho-MEK / phospho-ERK phospho-RET / phospho-ERK Ki-67 / Cyclin D1 / CDK4 / p21 / p53 / Apaf-1 / p-NFκB / Bcl-2 / Cleaved-caspase 3 Vimentin / E-cadherin / Snail / Zeb1		25295214
	Growth inhibition assay	Cell viability		25425971
	Immunofluorescence	β-catenin		30286728

NCT Number	Recruitment	Conditions	Sponsor/Collaborators	Start Date	Phases
Clinical Trial Information (data from https://clinicaltrials.gov, updated on 2024-01-11)
NCT05846724	Not yet recruiting	Kaposi Sarcoma\|Classic Kaposi Sarcoma\|Refractory Kaposi Sarcoma	Fondazione IRCCS Ca'' Granda Ospedale Maggiore Policlinico	February 1 2024	Phase 2
NCT05903833	Not yet recruiting	Recurrent Vulvar Cancer\|Persistent Vulvar Cancer\|Metastatic Vulva Cancer\|Locally Advanced Vulvar Cancer	AGO Research GmbH	January 1 2024	Phase 2
NCT06161558	Not yet recruiting	Neoplasms	National Cancer Institute (NCI)\|National Institutes of Health Clinical Center (CC)	January 12 2024	Phase 1
NCT05901194	Not yet recruiting	Hepatocellular Carcinoma Non-resectable	Assistance Publique - Hôpitaux de Paris\|Laboratoire EISAI	June 2023	Phase 1\|Phase 2
NCT05733715	Recruiting	Renal Cell Carcinoma	Abramson Cancer Center at Penn Medicine\|Merck Sharp & Dohme LLC	May 3 2023	Early Phase 1
NCT05433116	Recruiting	Head and Neck Squamous Cell Carcinoma	Universität des Saarlandes	May 25 2023	Phase 2

References

Chemical lnformation & Solubility

Molecular Weight	522.96	Formula	C₂₁H₁₉ClN₄O₄.CH₄O₃S
CAS No.	857890-39-2	SDF	--
Smiles	COC1=CC2=NC=CC(=C2C=C1C(=O)N)OC3=CC(=C(C=C3)NC(=O)NC4CC4)Cl.CS(=O)(=O)O
Storage (From the date of receipt)	3 years -20°C powder	Storage of Stock Solutions Aliquot the stock solutions to avoid repeated freeze-thaw cycles	1 year-80°Cin solvent
Storage (From the date of receipt)	3 years -20°C powder		1 month-20°Cin solvent

In vitro
Batch:

DMSO : 39 mg/mL ( (74.57 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Molecular Weight Calculator

In vivo
Batch:

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In vivo Formulation Calculator

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH₂O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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