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research use only
Cat.No.S9689
| Related Targets | CDK HSP K-Ras PD-1/PD-L1 ROCK Wee1 DNA/RNA Synthesis Microtubule Associated Ras Aurora Kinase |
|---|---|
| Other FOXM1 Products | RCM-1 FoxM1 Antibody [K19K15] |
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In vitro |
DMSO
: 87 mg/mL
(198.88 mM)
Water : Insoluble Ethanol : Insoluble |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
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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| 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 |
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| Synonyms | NCGC00099374 | Smiles | NC1=C(SC2=NC(=CC(=C12)C(F)(F)F)C3=CC=CS3)C(=O)NC4=CC=C(F)C=C4 | ||
| Targets/IC50/Ki |
FOXM1
(Cell-free assay) 22.5 μM
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|---|---|
| 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. |
| In vivo |
Inhibiting FOXM1 with FDI-6 inhibits liver cancer cell growth in vivo. |
References |
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