Abstract
Bioassay-guided fractionation of the EtOAc-soluble extract of Pueraria lobata based on the inhibition of Aβ-induced toxicity in PC12 cells resulted in the isolation of four known active compounds, genistein (8), biochanin A (9), sissotrin (10), and puerol B (11). Of these, genistein (8) and biochanin A (9) exhibited potent neuroprotective effects with ED50 values of 33.7 and 27.8 μM, respectively. In addition, a new coumestan, 2-(α,α-dimethylallyl)coumestrol (1) was isolated and characterized, but proved to be inactive, as were additional seven known compounds. The structure of new compound 1 was determined using spectroscopic techniques.
Original language | English |
---|---|
Pages (from-to) | 1651-1654 |
Number of pages | 4 |
Journal | Archives of pharmacal research |
Volume | 33 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2010 Oct |
Keywords
- 2-(α,α-dimethylallyl)coumestrol
- Beta-amyloid
- Fabaceae
- Isoflavone
- Pueraria lobata
ASJC Scopus subject areas
- Molecular Medicine
- Drug Discovery
- Organic Chemistry