142 related articles for article (PubMed ID: 33341590)
1. New insight into the role of glutathione reductase in glutathione peroxidase-like activity determination by coupled reductase assay: Molecular Docking Study.
Yu SC; Kim IC; Ri KJ; Ri J; Kühn H
J Inorg Biochem; 2021 Feb; 215():111276. PubMed ID: 33341590
[TBL] [Abstract][Full Text] [Related]
2. Functional mimics of glutathione peroxidase: bioinspired synthetic antioxidants.
Bhabak KP; Mugesh G
Acc Chem Res; 2010 Nov; 43(11):1408-19. PubMed ID: 20690615
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of a new seleninic acid anhydride and mechanistic studies into its glutathione peroxidase activity.
Yu SC; Borchert A; Kuhn H; Ivanov I
Chemistry; 2008; 14(23):7066-71. PubMed ID: 18604859
[TBL] [Abstract][Full Text] [Related]
4. Synthesis, structure, and glutathione peroxidase-like activity of amino acid containing ebselen analogues and diaryl diselenides.
Selvakumar K; Shah P; Singh HB; Butcher RJ
Chemistry; 2011 Nov; 17(45):12741-55. PubMed ID: 21956838
[TBL] [Abstract][Full Text] [Related]
5. Amide-based glutathione peroxidase mimics: effect of secondary and tertiary amide substituents on antioxidant activity.
Bhabak KP; Mugesh G
Chem Asian J; 2009 Jun; 4(6):974-983. PubMed ID: 19378298
[TBL] [Abstract][Full Text] [Related]
6. Reduction of diphenyl diselenide and analogs by mammalian thioredoxin reductase is independent of their gluthathione peroxidase-like activity: a possible novel pathway for their antioxidant activity.
Sausen de Freitas A; de Souza Prestes A; Wagner C; Haigert Sudati J; Alves D; Oliveira Porciúncula L; Kade IJ; Teixeira Rocha JB
Molecules; 2010 Oct; 15(11):7699-714. PubMed ID: 21030914
[TBL] [Abstract][Full Text] [Related]
7. A hydrogen peroxide electrode assay to measure thiol peroxidase activity for organoselenium and organotellurium drugs.
Giles NM; Kumari S; Stamm RA; Patel S; Giles GI
Anal Biochem; 2012 Oct; 429(2):103-7. PubMed ID: 22813709
[TBL] [Abstract][Full Text] [Related]
8. Glutathione peroxidase (GPx)-like antioxidant activity of the organoselenium drug ebselen: unexpected complications with thiol exchange reactions.
Sarma BK; Mugesh G
J Am Chem Soc; 2005 Aug; 127(32):11477-85. PubMed ID: 16089478
[TBL] [Abstract][Full Text] [Related]
9. Diselenoamino acid derivatives as GPx mimics and as substrates of TrxR: in vitro and in silico studies.
Sudati JH; Nogara PA; Saraiva RA; Wagner C; Alberto EE; Braga AL; Fachinetto R; Piquini PC; Rocha JBT
Org Biomol Chem; 2018 May; 16(20):3777-3787. PubMed ID: 29737350
[TBL] [Abstract][Full Text] [Related]
10. Probing the Formation of a Seleninic Acid in Living Cells by the Fluorescence Switching of a Glutathione Peroxidase Mimetic.
Ungati H; Govindaraj V; Narayanan M; Mugesh G
Angew Chem Int Ed Engl; 2019 Jun; 58(24):8156-8160. PubMed ID: 31021048
[TBL] [Abstract][Full Text] [Related]
11. Cyclic Seleninate Esters, Spirodioxyselenuranes and Related Compounds: New Classes of Biological Antioxidants That Emulate Glutathione Peroxidase.
Sands KN; Tuck TA; Back TG
Chemistry; 2018 Jul; 24(39):9714-9728. PubMed ID: 29542192
[TBL] [Abstract][Full Text] [Related]
12. Modeling the Catalytic Cycle of Glutathione Peroxidase by Nuclear Magnetic Resonance Spectroscopic Analysis of Selenocysteine Selenenic Acids.
Masuda R; Kimura R; Karasaki T; Sase S; Goto K
J Am Chem Soc; 2021 May; 143(17):6345-6350. PubMed ID: 33887135
[TBL] [Abstract][Full Text] [Related]
13. Design, synthesis and glutathione peroxidase-like properties of ovothiol-derived diselenides.
Bailly F; Azaroual N; Bernier JL
Bioorg Med Chem; 2003 Oct; 11(21):4623-30. PubMed ID: 14527559
[TBL] [Abstract][Full Text] [Related]
14. Effects of ring size and polar functional groups on the glutathione peroxidase-like antioxidant activity of water-soluble cyclic selenides.
Arai K; Kumakura F; Takahira M; Sekiyama N; Kuroda N; Suzuki T; Iwaoka M
J Org Chem; 2015 Jun; 80(11):5633-42. PubMed ID: 25941977
[TBL] [Abstract][Full Text] [Related]
15. In vitro evaluation of glutathione peroxidase (GPx)-like activity and antioxidant properties of some Ebselen analogues.
Mouithys-Mickalad Mareque A; Faez JM; Chistiaens L; Kohnen S; Deby C; Hoebeke M; Lamy M; Deby-Dupont G
Redox Rep; 2004; 9(2):81-7. PubMed ID: 15231062
[TBL] [Abstract][Full Text] [Related]
16. Chemistry Related to the Catalytic Cycle of the Antioxidant Ebselen.
Sands KN; Burman AL; Ansah-Asamoah E; Back TG
Molecules; 2023 Apr; 28(9):. PubMed ID: 37175141
[TBL] [Abstract][Full Text] [Related]
17. Remarkable activity of a novel cyclic seleninate ester as a glutathione peroxidase mimetic and its facile in situ generation from allyl 3-hydroxypropyl selenide.
Back TG; Moussa Z
J Am Chem Soc; 2002 Oct; 124(41):12104-5. PubMed ID: 12371844
[TBL] [Abstract][Full Text] [Related]
18. Antioxidant activity of the anti-inflammatory compound ebselen: a reversible cyclization pathway via selenenic and seleninic acid intermediates.
Sarma BK; Mugesh G
Chemistry; 2008; 14(34):10603-14. PubMed ID: 18932179
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and biological evaluation of a new series of ebselen derivatives as glutathione peroxidase (GPx) mimics and cholinesterase inhibitors against Alzheimer's disease.
Luo Z; Liang L; Sheng J; Pang Y; Li J; Huang L; Li X
Bioorg Med Chem; 2014 Feb; 22(4):1355-61. PubMed ID: 24461494
[TBL] [Abstract][Full Text] [Related]
20. 2-Phenoxyethanol derived diselenide and related compounds; synthesis of a seven-membered seleninate ester.
Tripathi SK; Sharma S; Singh HB; Butcher RJ
Org Biomol Chem; 2011 Jan; 9(2):581-7. PubMed ID: 21049128
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]