hispidulin and 2-anthramine

hispidulin has been researched along with 2-anthramine* in 1 studies

Other Studies

1 other study(ies) available for hispidulin and 2-anthramine

Article	Year
Mutagenicity and antimutagenicity of hispidulin and hortensin, the flavonoids from Millingtonia hortensis L. Environmental and molecular mutagenesis, 1992, Volume: 20, Issue:4 Studies of the mutagenicity and antimutagenicity of hispidulin and hortensin, the flavonoids from Millingtonia hortensis L. (Bignoniaceae), were performed using the liquid preincubation method of the Salmonella/microsome test. At the highest dose tested, 100 micrograms/plate, both compounds showed no mutagenicity and no cytotoxicity toward S. typhimurium strains TA98 and TA100 either in the presence or absence of S9 mix. However, these substances were antimutagens toward 2-aminoanthracene, aflatoxin B1 (in TA98), and dimethylnitrosamine (in TA100); but neither substance inhibited the direct mutagenic activity of 2-(2-furyl)-3-(5-nitro-2-furyl) acrylamide nor that of sodium azide in strains TA98 and TA100, respectively. Topics: Aflatoxin B1; Anthracenes; Antimutagenic Agents; Azides; Cell Survival; Dimethylnitrosamine; Flavones; Flavonoids; Microsomes, Liver; Mutagenicity Tests; Mutagens; Salmonella typhimurium; Sodium Azide; Suppression, Genetic; Thiophenes	1992

Article

Year

Mutagenicity and antimutagenicity of hispidulin and hortensin, the flavonoids from Millingtonia hortensis L.

Environmental and molecular mutagenesis, 1992, Volume: 20, Issue:4

Studies of the mutagenicity and antimutagenicity of hispidulin and hortensin, the flavonoids from Millingtonia hortensis L. (Bignoniaceae), were performed using the liquid preincubation method of the Salmonella/microsome test. At the highest dose tested, 100 micrograms/plate, both compounds showed no mutagenicity and no cytotoxicity toward S. typhimurium strains TA98 and TA100 either in the presence or absence of S9 mix. However, these substances were antimutagens toward 2-aminoanthracene, aflatoxin B1 (in TA98), and dimethylnitrosamine (in TA100); but neither substance inhibited the direct mutagenic activity of 2-(2-furyl)-3-(5-nitro-2-furyl) acrylamide nor that of sodium azide in strains TA98 and TA100, respectively.

Topics: Aflatoxin B1; Anthracenes; Antimutagenic Agents; Azides; Cell Survival; Dimethylnitrosamine; Flavones; Flavonoids; Microsomes, Liver; Mutagenicity Tests; Mutagens; Salmonella typhimurium; Sodium Azide; Suppression, Genetic; Thiophenes

1992