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ChemicalBook--->CAS DataBase List--->217798-39-5

217798-39-5

217798-39-5 Structure

217798-39-5 Structure
IdentificationBack Directory
[Name]

Ethaselen
[CAS]

217798-39-5
[Synonyms]

BBSKE
Ethaselen
1,2-Benzisoselenazol-3(2H)-one, 2,2'-(1,2-ethanediyl)bis-
[Molecular Formula]

C16H12N2O2Se2
[MOL File]

217798-39-5.mol
[Molecular Weight]

422.2
Chemical PropertiesBack Directory
[Boiling point ]

580.5±60.0 °C(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 12.5 mg/mL (29.61 mM; ultrasonic and warming and heat to 60°C)
[form ]

Solid
[pka]

-1.86±0.20(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

Ethaselen (BBSKE) is an orally active, selective thioredoxin reductase (TrxR) inhibitor with IC50s of 0.5 and 0.35 μM for the wild-type human TrxR1 and rat TrxR1, respectively. Ethaselen specifically binds to the unique selenocysteine-cysteine redox pair in the C-terminal active site of mammalian TrxR1. Ethaselen, an organoselenium compound, is a potent antitumor candidate that exerts potent inhibition on non-small cell lung cancer (NSCLC) by targeting TrxR[1][2].
[in vivo]

Ethaselen?(BBSKE; 36-108 mg/kg/day; PO; for 10 days) shows increased inhibition of tumor growth in a dose-independent manner[2].

Animal Model:Five-week-old female BALB/c nude mice with A549 cell[2]
Dosage:36, 72, 108 mg/kg
Administration:PO; daily; for 10 days
Result:Showed increased inhibition of tumor growth, and the inhibition levels increased with the dose.
The TrxR activity levels of the high dose group (108 mg/kg) decreased more than the middle dose group (72 mg/kg) and low dose group (36 mg/kg).
[References]

[1] Lihui Wang, et al. Ethaselen: a potent mammalian thioredoxin reductase 1 inhibitor and novel organoselenium anticancer agent. Free Radic Biol Med. 2012 Mar 1;52(5):898-908. DOI:10.1016/j.freeradbiomed.2011.11.034
[2] Suo-Fu Ye, et al. Dose-biomarker-response modeling of the anticancer effect of ethaselen in a human non-small cell lung cancer xenograft mouse model. Acta Pharmacol Sin. 2017 Feb;38(2):223-232. DOI:10.1038/aps.2016.114
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