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Sephin1

Cat. No. M8509

All AbMole products are for research use only, cannot be used for human consumption.

Sephin1 Structure

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Quality Control & Documentation
Biological Activity

Sephin1 (selective inhibitor of a holophosphatase) is a guanabez derivative that binds to and inhibits a regulatory subunit of the stress-induced protein phosphatase 1 (PPP1R15A), but not the constitutive PPP1R15B, and lacks ?2-adrenergic activity. Phosphorylation of eIF2α, α subunit of eukaryotic translation initiation factor 2, reduces protein synthesis and prevents the accumulation of misfolded protein in the endoplasmic reticulum (ER). PPP1R15A recruits the serine/threonine-protein phosphatase PP1 to dephosphorylate eIF2α, so inihbiting PPP1R15A activity prolongs the phosphorylation of eIF2α and aids in its prevention of the accumulation of misfolded protein. In vitro Sephin1 protected cells from lethal protein misfolding and cytotoxic ER stress. In vivo Sephin1 prevented two unrelated protein misfolding diseases in mice (Charchot-Marie-Tooth 1B and ALS).

Chemical Information
Molecular Weight 196.64
Formula C8H9ClN4
CAS Number 951441-04-6
Solubility (25°C) DMSO: 20 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Asier Ruiz, et al. Sephin1 Protects Neurons against Excitotoxicity Independently of the Integrated Stress Response

[2] Simrika Thapa, et al. Sephin1 Reduces Prion Infection in Prion-Infected Cells and Animal Model

[3] Yanan Chen, et al. Sephin1, which prolongs the integrated stress response, is a promising therapeutic for multiple sclerosis

[4] Ana Crespillo-Casado, et al. A Sephin1-insensitive tripartite holophosphatase dephosphorylates translation initiation factor 2α

[5] Indrajit Das, et al. Preventing proteostasis diseases by selective inhibition of a phosphatase regulatory subunit

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Keywords: Sephin1 supplier, inhibitors, activators

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