research use only

BTYNB Myc inhibitor

Cat.No.S9871

BTYNB (BTYNB IMP1 Inhibitor, MDK6620) is a potent and selective inhibitor of IMP1 binding to c-Myc mRNA. This compound downregulates β-TrCP1 mRNA and reduces activation of nuclear transcriptional factors-kappa B (NF-κB). It disrupts this enhancer function by impairing IGF2 mRNA-binding protein 1 (IGF2BP1)-RNA association.
BTYNB Myc inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 309.18

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 309.18 Formula

C12H9BrN2OS

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 304456-62-0 -- Storage of Stock Solutions

Synonyms BTYNB IMP1 Inhibitor, MDK6620 Smiles NC(=O)C1=CC=CC=C1N=CC2=CC=C(Br)S2

Solubility

In vitro
Batch:

DMSO : 62 mg/mL ( (200.53 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 4 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
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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
IMP1 [1]
c-Myc [1]
NF-κB [1]
In vitro

In cells, BTYNB downregulates several mRNA transcripts regulated by IMP1. This compound destabilizes c-Myc mRNA, resulting in downregulation of c-Myc mRNA and protein. It downregulates β-TrCP1 mRNA and reduces activation of nuclear transcriptional factors-kappa B (NF-κB). The oncogenic translation regulator, eEF2, emerges as a new IMP1 target mRNA, enabling this chemical to inhibit tumor cell protein synthesis. It potently inhibits proliferation of IMP1-containing ovarian cancer and melanoma cells with no effect in IMP1-negative cells. Overexpression of IMP1 reverses its inhibition of cell proliferation. This compound completely blocks anchorage-independent growth of melanoma and ovarian cancer cells in colony formation assays.[1]

References

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