research use only

RK-701 G9a/GLP inhibitor

Cat.No.E1607

RK-701 is a highly selective, potent, and low-toxicity inhibitor of histone methyltransferases G9a and GLP1 with IC50 values of 23-27 nM and 53 nM. This compound treatment induces fetal globin expression in human erythroid cells and in mice and plays an essential role in γ-globin induction. It is used in the research of sickle cell disease.
RK-701 G9a/GLP inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 446.54

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Quality Control

Batch: E160701 DMSO]89 mg/mL]false]Ethanol]89 mg/mL]false]Water]Insoluble]false Purity: 99.03%
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99.03

Solubility

In vitro
Batch:

DMSO : 89 mg/mL (199.31 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 89 mg/mL

Water : Insoluble

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In vivo
Batch:

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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.

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Chemical Information, Storage & Stability

Molecular Weight 446.54 Formula

C26H30N4O3

Storage (From the date of receipt)
CAS No. 2648855-18-7 Download SDF Storage of Stock Solutions

Mechanism of Action

Targets/IC50/Ki
G9a
23-27 nM
GLP1
53 nM
References

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