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The title compound, C 30 H 50 O 5 , was isolated from the bark of  Aglaia smithii . There are two independent mol­ecules in the asymmetric unit that differ in the orientation of the isopropenyl group attached to the cyclo­hexane ring. The cyclo­hexane rings in both mol­ecules adopt chair conformations, whereas the cyclo­pentane and tetra­hydro­furan rings adopt envelope conformations. The independent mol­ecules are linked into a layer parallel to (010) by O—H⋯O hydrogen bonds.

(20S)-24,25-Dihydroxy-20,24-epoxy-3,4-secodammar-4(28)-en-3-oic acid fromAglaia smithii