spiroiminodihydantoin and hypobromous-acid

spiroiminodihydantoin has been researched along with hypobromous-acid* in 1 studies

Other Studies

1 other study(ies) available for spiroiminodihydantoin and hypobromous-acid

ArticleYear
Reaction of 3',5'-di-O-acetyl-2'-deoxyguansoine with hypobromous acid.
    Bioorganic & medicinal chemistry, 2013, Jul-01, Volume: 21, Issue:13

    Hypobromous acid (HOBr) is formed by eosinophil peroxidase and myeloperoxidase in the presence of H2O2, Cl(-), and Br(-) in the host defense system of humans, protecting against invading bacteria. However, the formed HOBr may cause damage to DNA and its components in the host. When a guanine nucleoside (3',5'-di-O-acetyl-2'-deoxyguansoine) was treated with HOBr at pH 7.4, spiroiminodihydantoin, guanidinohydantoin/iminoallantoin, dehydro-iminoallantoin, diimino-imidazole, amino-imidazolone, and diamino-oxazolone nucleosides were generated in addition to an 8-bromoguanine nucleoside. The major products were spiroiminodihydantoin under neutral conditions and guanidinohydantoin/iminoallantoin under mildly acidic conditions. All the products were formed in the reaction with HOCl in the presence of Br(-). These products were also produced by eosinophil peroxidase or myeloperoxidase in the presence of H2O2, Cl(-), and Br(-). The results suggest that the products other than 8-bromoguanine may also have importance for mutagenesis by the reaction of HOBr with guanine residues in nucleotides and DNA.

    Topics: Acetylation; Allantoin; Bromates; Deoxyguanosine; Eosinophil Peroxidase; Guanosine; Humans; Hydrogen Peroxide; Peroxidase; Spiro Compounds

2013