(+)-Medicarpin

CAS: 33983-40-3

Ref. 3D-FM138692

Produktinformation

• Name: (+)-Medicarpin
• Synonyme: (±)-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
• CAS: 33983-40-3

Beschreibung

(+)-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

• Marke: Biosynth

Chemische Eigenschaften

• Reinheit: Min. 95%