Product Information
- (±)-3-Demethylhomopterocarpin
- (±)-3-Hydroxy-9-methoxypterocarpan
- (±)-Demethylhomopterocarpin
- 6H-Benzofuro[3,2-c][1]benzopyran-3-ol, 6a,11a-dihydro-9-methoxy-
- 6H-Benzofuro[3,2-c][1]benzopyran-3-ol, 6a,11a-dihydro-9-methoxy-, (6aR,11aR)-rel-
- 6H-Benzofuro[3,2-c][1]benzopyran-3-ol, 6a,11a-dihydro-9-methoxy-, cis-
- 6H-Benzofuro[3,2-c][1]benzopyran-3-ol, 6aβ,11aβ-dihydro-9-methoxy-, (±)-
- Medicarpin
- rel-(6aR,11aR)-6a,11a-Dihydro-9-methoxy-6H-benzofuro[3,2-c][1]benzopyran-3-ol
(+)-Medicarpin is a naturally occurring isoflavonoid that possesses anti-inflammatory and anticancer activities. It has been shown to inhibit the production of pro-inflammatory cytokines such as IL-10, IL-6, and TNF-α. (+)-Medicarpin also inhibits the production of xanthine oxidase and lipoxygenase, which are enzymes involved in the inflammatory process. In addition, (+)-medicarpin has been shown to have a high resistance against c. glabrata, which may be due to its structural analysis and enzyme activity properties. Medicarpin (a precursor of (+)-medicarpin) can be synthesized from p-hydroxybenzoic acid by chemical oxidation with hydrogen peroxide or sodium hypochlorite under acidic conditions. The synthetic pathway for medicarpin was elucidated through x-ray crystal structures of medicarpin synthase from Streptomyces sp. The wild type strain was
Chemical properties
Technical inquiry about: 3D-FM138692 (+)-Medicarpin
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