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Showing papers on "Galangin published in 1995"


Journal ArticleDOI
TL;DR: This study found two compounds which strongly suppressed the mutagenicity of one of the dietary carcinogens, 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2), in oregano (Origanum vulgare).
Abstract: This study found two compounds which strongly suppressed the mutagenicity of one of the dietary carcinogens, 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2), in oregano (Origanum vulgare). The compounds were purified chromatographically monitoring the suppressing activity with Salmonella typhimurium TA98. An instrumental elucidation identified two flavonoids as 3,5,7-trihydroxy-2-phenyl-4H-1-benzopyran-4-one (galangin) and 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one (quercetin). Galangin and quercetin are strong desmutagens that neutralized Trp-P-2 before mutating the bacteria. The amounts of galangin and quercetin required for 50% inhibition against the mutagenicity of 20 ng of Trp-P-2 (IC 50 ) were 0.12 and 0.81 μg, respectively, while the IC 50 of chlorophyll in oregano was 230 μg. Toward the other mutagens, benzo[a]pyrene, 1-nitro-pyrene, 2-(acetylamino)fluorene, and N-methyl-N'-nitro-N-nitrosoguanidine, they were not effective. Galangin and quercetin are the specific desmutagens against the dietary carcinogen Trp-P-2

71 citations