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The title compound, enmenol, C 20 H 30 O 6 , a natural  ent -kaurane diterpenoid, comprises five fused rings, four of which are six-membered. Cyclo­hexane ring  A  adopts a chair conformation, rings  B  and  C  adopt boat conformations, while ring  D  has an envelope conformation, and two intramolecular O—H⋯O interactions occur. In the crystal, inter­molecular O—H⋯O hydrogen bonds generate a two dimensional network.

1α,6β,7β,14β,15β-Pentahydroxy-7α,20-epoxy-ent-kaur-16-ene