research use only

Piperazine Erastin Ferroptosis chemical

Cat.No.E1063

Piperazine Erastin is an analog of Erastin, which can induces ferroptosis in cancer cells, an iron-dependent form of nonapoptotic cell death.
Piperazine Erastin Ferroptosis chemical Chemical Structure

Chemical Structure

Molecular Weight: 645.19

Quality Control

Batch: E106301 DMSO]100 mg/mL]false]Ethanol]100 mg/mL]false]Water]Insoluble]false Purity: 98.83%
98.83

Chemical Information, Storage & Stability

Molecular Weight 645.19 Formula

C35H41ClN6O4

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 1538593-71-3 -- Storage of Stock Solutions

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (154.99 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 100 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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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.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

In vitro

Piperazine Erastin, an analogue of Erastin, induces ferroptosis of cancer cells and upregulates PTGS2 in BJeLR cells that is suppressed when cotreatment of vitamin E.[1]

In vivo

Piperazine Erastin shows efficacy in preventing HT-1080 tumor formation in a mouse xenograft model, through upregulation of Ptgs2, and robust upregulation of the p21 gene, a biomarker for p53 activation induced by doxorubicin-mediated DNA damage.[1]

References

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