Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Chemical Compound Review:

PubChem9842 2-(3,4- dihydroxyphenyl)chromen-4-one

Synonyms: CHEMBL222556, SureCN345706, AG-D-95197, ACMC-20anf0, CHEBI:473563, ...

Schlupper, D. et al., Perry, J.D. et al.

Perry, Morris, James, Oliver, Gould,

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Disease relevance of ZINC00057659

Conclusions: Alizarin-beta-d-glucoside is a highly sensitive substrate for detection of bacterial beta-glucosidase and compares favourably with existing substrates. beta-glucosides of 3',4'-dihydroxyflavone and 3-hydroxyflavone are effective substrates for the detection of beta-glucosidase in enterococci and Listeria spp [1].

High impact information on ZINC00057659

Influence of biotransformation of luteolin, luteolin 7-O-glucoside, 3',4'-dihydroxyflavone and apigenin by cultured rat hepatocytes on antioxidative capacity and inhibition of EGF receptor tyrosine kinase activity [2].
Herein we investigated the biotransformation of four different flavonoids, 3',4'-dihydroxyflavone, apigenin, luteolin and luteolin 7-O-glucoside, by cultured rat hepatocytes using a combination of enzymatic deconjugation, HPLC separation and high-resolution mass spectrometry [2].

References

Evaluation of novel chromogenic substrates for the detection of bacterial beta-glucosidase. Perry, J.D., Morris, K.A., James, A.L., Oliver, M., Gould, F.K. J. Appl. Microbiol. (2007) [Pubmed]
Influence of biotransformation of luteolin, luteolin 7-O-glucoside, 3',4'-dihydroxyflavone and apigenin by cultured rat hepatocytes on antioxidative capacity and inhibition of EGF receptor tyrosine kinase activity. Schlupper, D., Giesa, S., Gebhardt, R. Planta Med. (2006) [Pubmed]

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