Ebselen
Chemical Name: 2-Phenyl-1,2-benzisoselenazol-3(2H)-one
Purity: ≥98%
Biological Activity
Ebselen is a glutathione peroxidase mimic; peroxynitrite scavenger. Inhibits ferroptosis. Also inhibits lipoxygenase, cyclooxygenase, nitric oxide synthase, protein kinase C and H+/K+-ATPase activity. Inhibits the hepatic carcinogenic effects of aflatoxin B1. Antioxidant and anti-inflammatory. Selectively inhibits Gq protein signaling and enhances differentiation of brown adipocytes. Inhibits SARS-CoV-2 Mpro in vitro (IC50 = 0.67 μM in FRET assay)Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Molecular actions of ebselen--an antiinflammatory antioxidant.
Schewe
Gen.Pharmacol., 1995;26:1153 -
Inhibition of ebselen on aflatoxin B(1)-induced hepatocarcinogenesis in Fischer 344 rats.
Yang et al.
Carcinogenesis, 2000;21:2237 -
Kinetic studies of the radical-scavenging activity of ebselen, a seleno-organic compound.
Fujisawa and Kadoma
Anticancer Res., 2005;25:3989 -
Ferroptosis: process and function.
Xie et al.
Cell.Death.Differ, 2016;23:369 -
Cell-permeable high-affinity tracers for Gq proteins provide structural insights, reveal distinct binding kinetics, and identify small molecule inhibitors.
Kuschak et al.
Br.J.Pharmacol., 2019; -
Structure of Mpro from SARS-CoV-2 and discovery of its inhibitors.
Jin et al.
Nature., 2020;582:289
Product Datasheets
Citations for Ebselen
The citations listed below are publications that use Tocris products. Selected citations for Ebselen include:
2 Citations: Showing 1 - 2
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β2-adrenergic receptor regulates ER-mitochondria contacts.
Authors: Ginam Et al.
Sci Rep 2021;11:21477
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Cell-permeable high-affinity tracers for Gq proteins provide structural insights, reveal distinct binding kinetics, and identify small molecule inhibitors.
Authors: Kuschak Et al.
Br.J.Pharmacol. 2019;177:1898
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