Lc. Chang et al., ACTIVITY-GUIDED ISOLATION OF STEROIDAL ALKALOID ANTIESTROGEN-BINDING SITE INHIBITORS FROM PACHYSANDRA-PROCUMBENS, Journal of natural products, 61(10), 1998, pp. 1257-1262
Four novel steroidal alkaloids, 0-(dimethylamino)-3-(3'alpha-isopropop
yl)-lactam-5 alpha-pregn-2-en-4-one (1), (+)-(20S)-20-(dimethylamino)-
16 alpha-hydroxy-3-(3'alpha-isopropyl)-lactam-5 alpha-preg-2-en-4-one
(2), (+)-(20S)-3-(benzoylamino)-20-(dimethylamino)-5 alpha-pregn-2-en-
4 beta-yl acetate (3), and (+)-(20S)-2 alpha-hydroxy-20-(dimethylamino
)-3 beta-phthalimido-5 alpha-pregnan-4 beta-yl acetate (4), as well as
five known compounds, (-)-pachyaximine A (5), (+)-spiropachysine (6),
(+)-axillaridine A (7), (+)-epipachysamine D (8), and (+)-pachysamine
B (9), were isolated from Pachysandra procumbens, using a bioassay-gu
ided fractionation based on inhibition of H-3-tamoxifen binding at the
antiestrogen binding site (AEBS). Compounds 1-7 and 9 demonstrated si
gnificant activity as AEBS-inhibitory agents, and compounds 3, 5 and 9
were found to potentiate significantly the antiestrogenic effect medi
ated by tamoxifen in cultured Ishikawa cells. The structure elucidatio
n of compounds 1-4 was carried out by spectral data interpretation.