Summary. Eucosterol and 16,!-hydroxy-cucosterol which have been isolated from several Euconzis species have been shown to be (23 S)-1.7,23-cpoxy-3P, 31-dihydroxy-27-nor-5cr-lanost-8-ene-l5,24-dione (1) and (23 S)-17,23-cpoxy-3P, 16/3,31-trihydroxy-27-nor-5a-lanost-8-ene-l5,24-dionc (2) by chemical transformations and spectral data. The spiro-fused furanoic ether linkage of both metabolites represents a novel structural element for natural nortritcrpenes. The structure of another metabolite (16), 3~-hydroxy-4,!-hydroxymethyl-4,14a-dimethyl-15-oxo-24-nor-5~-chola-8,16-diene-23-ok acid, from Eucornis autumnalzs (Mill.) Chitt. was elucidated by chemical correlation of its methyl ester 17 with a degradation product of eucosterol (1).