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

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Chemical Compound Review:

AC1O5248 (4E)-4-[(3,4-dihydroxyphenyl) methylidene]...

Synonyms:

Hwang, E.I. et al., Hwang, E.I. et al.

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High impact information on AIDS-096759

In addition, phellinsin A inhibited xanthine oxidase activity with an IC50 value of 31.0 microM, whereas allopurinol, a xanthine oxidase inhibitor, showed an IC50 value of 40.7 microM [1].
Phellinsin A selectively inhibited chitin synthase I and II of Saccharomyces cerevisiae with an IC50 value of 76 and 28 microg/ml, respectively, in our cell free assay system [2].

Analytical, diagnostic and therapeutic context of AIDS-096759

Phellinsin A was purified by solvent partition, silica gel, ODS column chromatographies, and preparative HPLC, consecutively [2].

References

Phellinsin A from Phellinus sp. PL3 exhibits antioxidant activities. Hwang, E.I., Kim, J.R., Jeong, T.S., Lee, S., Rho, M.C., Kim, S.U. Planta Med. (2006) [Pubmed]
Phellinsin A, a novel chitin synthases inhibitor produced by Phellinus sp. PL3. Hwang, E.I., Yun, B.S., Kim, Y.K., Kwon, B.M., Kim, H.G., Lee, H.B., Jeong, W.J., Kim, S.U. J. Antibiot. (2000) [Pubmed]

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