Page last updated: 2024-08-25

hypobromous acid and bromouracil

hypobromous acid has been researched along with bromouracil in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Byun, J; Heinecke, JW; Henderson, JP; Mueller, DM	1
Hu, X; Li, H; Liang, W	1

Other Studies

2 other study(ies) available for hypobromous acid and bromouracil

Article	Year
The eosinophil peroxidase-hydrogen peroxide-bromide system of human eosinophils generates 5-bromouracil, a mutagenic thymine analogue. Biochemistry, 2001, Feb-20, Volume: 40, Issue:7 Topics: Bromates; Bromides; Bromine; Bromodeoxyuridine; Bromouracil; Catalase; Enzyme Activation; Enzyme Inhibitors; Eosinophil Peroxidase; Eosinophils; Humans; Hydrogen Peroxide; Hydrogen-Ion Concentration; Mutagens; Peroxidases; Pyrimidines; Sodium Compounds; Thymidine Phosphorylase; Uracil	2001
Reaction mechanism of uracil bromination by HBrO: a new way to generate the enol-keto form of 5-bromouracil. The journal of physical chemistry. A, 2006, Sep-28, Volume: 110, Issue:38 Topics: Bromates; Bromine; Bromouracil; Carbon; Hydroxylation; Isomerism; Ketones; Models, Molecular; Molecular Structure	2006

Article

Year

The eosinophil peroxidase-hydrogen peroxide-bromide system of human eosinophils generates 5-bromouracil, a mutagenic thymine analogue.

Biochemistry, 2001, Feb-20, Volume: 40, Issue:7

Topics: Bromates; Bromides; Bromine; Bromodeoxyuridine; Bromouracil; Catalase; Enzyme Activation; Enzyme Inhibitors; Eosinophil Peroxidase; Eosinophils; Humans; Hydrogen Peroxide; Hydrogen-Ion Concentration; Mutagens; Peroxidases; Pyrimidines; Sodium Compounds; Thymidine Phosphorylase; Uracil

2001

Reaction mechanism of uracil bromination by HBrO: a new way to generate the enol-keto form of 5-bromouracil.

The journal of physical chemistry. A, 2006, Sep-28, Volume: 110, Issue:38

Topics: Bromates; Bromine; Bromouracil; Carbon; Hydroxylation; Isomerism; Ketones; Models, Molecular; Molecular Structure

2006