159 related articles for article (PubMed ID: 12067256)
21. Rates of reaction of indoleacetic acids with horseradish peroxidase compound I and their dependence on the redox potentials.
Candeias LP; Folkes LK; Porssa M; Parrick J; Wardman P
Biochemistry; 1996 Jan; 35(1):102-8. PubMed ID: 8555162
[TBL] [Abstract][Full Text] [Related]
22. Induction of oxidative stress in Prototheca zopfii by indole-3-acetic acid/HRP or 2,4-pentanedione/HRP systems and their oxidation products.
Cunha LT; Pugine SM; Lins PG; Brunetti IL; De Melo MP
Mycopathologia; 2015 Feb; 179(1-2):73-9. PubMed ID: 25173924
[TBL] [Abstract][Full Text] [Related]
23. Horseradish peroxidase-catalyzed aerobic oxidation and peroxidation of indole-3-acetic acid. I. Optical spectra.
Metodiewa D; de Melo MP; Escobar JA; Cilento G; Dunford HB
Arch Biochem Biophys; 1992 Jul; 296(1):27-33. PubMed ID: 1605635
[TBL] [Abstract][Full Text] [Related]
24. Recombinant horseradish peroxidase variants for targeted cancer treatment.
Bonifert G; Folkes L; Gmeiner C; Dachs G; Spadiut O
Cancer Med; 2016 Jun; 5(6):1194-203. PubMed ID: 26990592
[TBL] [Abstract][Full Text] [Related]
25. An electron spin resonance study of free radical intermediates in the oxidation of indole acetic acid by horseradish peroxidase.
Mottley C; Mason RP
J Biol Chem; 1986 Dec; 261(36):16860-4. PubMed ID: 3023369
[TBL] [Abstract][Full Text] [Related]
26. Potential of unglycosylated horseradish peroxidase variants for enzyme prodrug cancer therapy.
Humer D; Furlanetto V; Schruef AK; Wlodarczyk A; Kuttke M; Divne C; Spadiut O
Biomed Pharmacother; 2021 Oct; 142():112037. PubMed ID: 34392084
[TBL] [Abstract][Full Text] [Related]
27. Enhancing the efficacy of photodynamic cancer therapy by radicals from plant auxin (indole-3-acetic acid).
Folkes LK; Wardman P
Cancer Res; 2003 Feb; 63(4):776-9. PubMed ID: 12591725
[TBL] [Abstract][Full Text] [Related]
28. Horseradish peroxidase-encapsulated chitosan nanoparticles for enzyme-prodrug cancer therapy.
Cao X; Chen C; Yu H; Wang P
Biotechnol Lett; 2015 Jan; 37(1):81-8. PubMed ID: 25257586
[TBL] [Abstract][Full Text] [Related]
29. Efficient enzyme-activated therapy based on the different locations of protein and prodrug in nanoMOFs.
Wang F; Yang J; Li Y; Zhuang Q; Gu J
J Mater Chem B; 2020 Jul; 8(28):6139-6147. PubMed ID: 32568339
[TBL] [Abstract][Full Text] [Related]
30. Development of a novel enzyme/prodrug combination for gene therapy of cancer: horseradish peroxidase/indole-3-acetic acid.
Greco O; Folkes LK; Wardman P; Tozer GM; Dachs GU
Cancer Gene Ther; 2000 Nov; 7(11):1414-20. PubMed ID: 11129283
[TBL] [Abstract][Full Text] [Related]
31. Kinetics and mechanism for reduction of the anticancer prodrug trans,trans,trans-[PtCl2(OH)2(c-C6H11NH2)(NH3)] (JM335) by thiols.
Lemma K; Shi T; Elding LI
Inorg Chem; 2000 Apr; 39(8):1728-34. PubMed ID: 12526561
[TBL] [Abstract][Full Text] [Related]
32. Nitro-fatty acid reaction with glutathione and cysteine. Kinetic analysis of thiol alkylation by a Michael addition reaction.
Baker LM; Baker PR; Golin-Bisello F; Schopfer FJ; Fink M; Woodcock SR; Branchaud BP; Radi R; Freeman BA
J Biol Chem; 2007 Oct; 282(42):31085-93. PubMed ID: 17720974
[TBL] [Abstract][Full Text] [Related]
33. The conversion of horseradish peroxidase C to a verdohemoprotein by a hydroperoxide derived enzymatically from indole-3-acetic acid and by m-nitroperoxybenzoic acid.
Nakajima R; Yamazaki I
J Biol Chem; 1980 Mar; 255(5):2067-71. PubMed ID: 7354079
[TBL] [Abstract][Full Text] [Related]
34. Kinetics of oxidation of aliphatic and aromatic thiols by myeloperoxidase compounds I and II.
Burner U; Jantschko W; Obinger C
FEBS Lett; 1999 Jan; 443(3):290-6. PubMed ID: 10025950
[TBL] [Abstract][Full Text] [Related]
35. Oxidation of indole-3-acetic acid by horseradish peroxidase induces apoptosis in G361 human melanoma cells.
Kim DS; Jeon SE; Park KC
Cell Signal; 2004 Jan; 16(1):81-8. PubMed ID: 14607278
[TBL] [Abstract][Full Text] [Related]
36. Peroxidase-catalyzed co-oxidation of indole-3-acetic acid and xanthene dyes in the absence of hydrogen peroxide.
Krylov SN; Chebotareva AB
FEBS Lett; 1993 Jun; 324(1):6-8. PubMed ID: 8504861
[TBL] [Abstract][Full Text] [Related]
37. Thiols as peroxidase substrates.
Svensson BE; Gräslund A; Ström G; Moldeus P
Free Radic Biol Med; 1993 Feb; 14(2):167-75. PubMed ID: 8381104
[TBL] [Abstract][Full Text] [Related]
38. The binding of the peroxidase oxidation products of indole-3-acetic acid to histone.
Demorest DM; Stahmann MA
Biochem Biophys Res Commun; 1972 Apr; 47(1):227-33. PubMed ID: 5063634
[No Abstract] [Full Text] [Related]
39. Horseradish peroxidase: a modern view of a classic enzyme.
Veitch NC
Phytochemistry; 2004 Feb; 65(3):249-59. PubMed ID: 14751298
[TBL] [Abstract][Full Text] [Related]
40. pH-sensitive pHluorins as a molecular sensor for in situ monitoring of enzyme-catalyzed prodrug activation.
Liu H; Cao X; Wang P; Ma X
Biotechnol Appl Biochem; 2017 Jul; 64(4):482-489. PubMed ID: 27222443
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
