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Bromosporine BET inhibitor

Cat.No.S7233

Bromosporine is a broad spectrum inhibitor for bromodomains with IC50 of 0.41 μM, 0.29 μM, 0.122 μM and 0.017 μM for BRD2, BRD4, BRD9 and CECR2, respectively.
Bromosporine BET inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 404.44

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Quality Control

Batch: Purity: 99.92%
99.92

Solubility

In vitro
Batch:

DMSO : 42 mg/mL (103.84 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
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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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Chemical Information, Storage & Stability

Molecular Weight 404.44 Formula

C17H20N6O4S

Storage (From the date of receipt)
CAS No. 1619994-69-2 Download SDF Storage of Stock Solutions

Synonyms N/A Smiles CCOC(=O)NC1=CC(=NN2C1=NN=C2C)C3=CC(=C(C=C3)C)NS(=O)(=O)C

Mechanism of Action

Targets/IC50/Ki
CECR2
17 nM
BRD9
0.122 μM
BRD4
0.29 μM
BRD2
0.41 μM
In vitro
In cell-based assays, Bromosporine (1 µM) accelerates FRAP recovery of BRD4 and CREBBP, while shows no activities against TIF1α, BAZ2A, and SMARCA2 even at 10 µM. This compound shows moderate cytotoxicity in HeLa cells at 18 µM. It, as a chemical probe for bromodomain functional assays, will be very useful in elucidating further biological roles of reader domains.
References

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