The roots of Ononis spinosa subsp. leiosperma (Leguminosae) afforded a
new glycoside, spinonin (1), possessing a novel skeleton, in addition
to the known isoflavonoid glycoside, ononin [7 beta-(glucosyloxy)form
ononetin] (2) and the known pterocarpan, 7-demethoxy-7-D-(glucosyloxy)
-homopterocarpin (3). The structure of the new isolate was elucidated
by spectral methods including H-1 and C-13 NMR, COSY, APT, HETCOR, HMB
C, NOESY, CD, FABMS, HRMS, EIMS, CIMS, and some chemical reactions. Sp
inonin was inactive against a number of human cancer cell Lines and HI
V-1 reverse transcriptase. The compounds 1 and 3 showed weak activity
against Pseudomonas aeruginosa, whereas 2 was active against beta-hemo
lytic Streptococcus.