research use only
Cat.No.S9871
| Related Targets | CDK HSP PD-1/PD-L1 ROCK Wee1 DNA/RNA Synthesis Microtubule Associated Ras KRas Aurora Kinase |
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| Other Myc Inhibitors | MYCi975 10058-F4 10074-G5 MYCi361 EN4 APTO-253 Mycro 3 Cpd. 37 ML327 MYCMI-6 |
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In vitro |
DMSO
: 62 mg/mL
(200.53 mM)
Ethanol : 4 mg/mL Water : Insoluble |
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In vivo |
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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 | 309.18 | Formula | C12H9BrN2OS |
Storage (From the date of receipt) | 3 years -20°C powder |
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| CAS No. | 304456-62-0 | -- | Storage of Stock Solutions |
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| Synonyms | BTYNB IMP1 Inhibitor, MDK6620 | Smiles | NC(=O)C1=CC=CC=C1N=CC2=CC=C(Br)S2 | ||
| Targets/IC50/Ki |
IMP1
c-Myc
NF-κB
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| 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. |
References |
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