| Name | thioredoxin reductase |
|---|---|
| Synonyms | ACR 1; PLP; ACR1; AOEB166; Alu corepressor 1; Antioxidant enzyme B166; B166; Liver tissue 2D page spot 71B… |
| Name | cycloheximide |
|---|---|
| CAS |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 20005201 | Sengupta R, Billiar TR, Kagan VE, Stoyanovsky DA: and thioredoxin type 1 modulate the activity of caspase 8 in HepG2 cells. Biochem Biophys Res Commun. 2010 Jan 1;391(1):1127-30. Epub 2009 Dec 11. Herein, we report that (NO) and the thioredoxin/thioredoxin reductase system affect the activity of caspase 8 in HepG2 cells. |
2(0,0,0,2) | Details |
| 17110078 | El-Sayed WM, Aboul-Fadl T, Roberts JC, Lamb JG, Franklin MR: Murine hepatoma (Hepa1c1c7) cells: a responsive in vitro system for chemoprotective enzyme induction by organoselenium compounds. Toxicol In Vitro. 2007 Feb;21(1):157-64. Epub 2006 Oct 7. All four selenazolidine 4-carboxylic acid (SCA) derivatives examined elevated thioredoxin reductase (Txnrd1), alpha-class glutathione transferases (Gsta), and UDP-glucuronosyltransferase (Ugt) 1a6 mRNAs. Induction responses to the selenazolidines were also eliminated (most) or reduced (Txnrd1 by 2-methylSCA) by cycloheximide, with the exception of Ugt1a6. |
1(0,0,0,1) | Details |
| 16405428 | Midwinter RG, Cheah FC, Moskovitz J, Vissers MC, Winterbourn CC: IkappaB is a sensitive target for oxidation by cell-permeable chloramines: inhibition of NF-kappaB activity by chloramine through oxidation. Biochem J. 2006 May 15;396(1):71-8. Reversion occurred in the presence of cycloheximide, but was prevented if thioredoxin reductase was inhibited, suggesting that it was due to endogenous sulphoxide reductase activity. |
31(0,1,1,1) | Details |
| 15652504 | Park YS, Misonou Y, Fujiwara N, Takahashi M, Miyamoto Y, Koh YH, Suzuki K, Taniguchi N: Induction of thioredoxin reductase as an adaptive response to acrolein in human umbilical vein endothelial cells. Biochem Biophys Res Commun. 2005 Feb 25;327(4):1058-65. |
2(0,0,0,2) | Details |