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BRD-6929 HDAC inhibitor

Cat.No.E0391

BRD-6929 is an inhibitor of histone deacetylase 1 (HDAC1) and HDAC2 with an IC50s of 0.04 µM and 0.1 µM, respectively. It exhibits antiproliferative activities against a human cancer cell line (HCT116) and in human mammary epithelial cells (HMEC).
BRD-6929 HDAC inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 351.42

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Quality Control

Batch: E039101 DMSO]17 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 98.15%
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98.15

Solubility

In vitro
Batch:

DMSO : 17 mg/mL (48.37 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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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.

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Chemical Information, Storage & Stability

Molecular Weight 351.42 Formula

C₁₉H₁₇N₃O₂S

Storage (From the date of receipt)
CAS No. 849234-64-6 Download SDF Storage of Stock Solutions

Mechanism of Action

Targets/IC50/Ki
HDAC1
0.04 μM
HDAC2
0.1 μM
References

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