research use only

FDI-6 FOXM1 inhibitor

Cat.No.S9689

FDI-6 (NCGC00099374) is an inhibitor of the Forkhead box protein M1 transcription factor (FOXM1) with IC50 of 22.5 μM.
FDI-6 FOXM1 inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 437.43

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 437.43 Formula

C19H11F4N3OS2

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 313380-27-7 -- Storage of Stock Solutions

Synonyms NCGC00099374 Smiles NC1=C(SC2=NC(=CC(=C12)C(F)(F)F)C3=CC=CS3)C(=O)NC4=CC=C(F)C=C4

Solubility

In vitro
Batch:

DMSO : 87 mg/mL (198.88 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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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.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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Mechanism of Action

Targets/IC50/Ki
FOXM1 [1]
(Cell-free assay)
22.5 μM
In vitro

FDI-6 (NCGC00099374) is characterized in depth and is shown to bind directly to FOXM1 protein, to displace this compound from genomic targets in MCF-7 breast cancer cells, and induces concomitant transcriptional down-regulation. Global transcript profiling of MCF-7 cells by RNA-seq shows that this chemical specifically down-regulates FOXM1-activated genes with FOXM1 occupancy confirmed by ChIP-seq.[1]

In vivo

Inhibiting FOXM1 with FDI-6 inhibits liver cancer cell growth in vivo.[2]

References

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