19--, 20--, and -Halimane-Type Furanoditerpenoids from .

The phytochemical investigation of the roots of led to the isolation of 16 new halimane furanoditerpenoids, crohalifuranes A-P (-), along with 15 known analogues, -. The new structures including their absolute configurations were elucidated by NMR and MS data analysis, comparison of experimental and calculated electronic circular dichroism data, single-crystal X-ray diffraction data, and chemical methods. Crohalifuranes A () and B () are - and 19--halimane diterpenoids featuring a rare decahydroacenaphthene core, respectively, which might be derived from the accompanying crassifoliusin A by loss of the furan ring or the C-19 substituent. Crohalifurane C () represents the first example of a 20--halimane diterpenoid, and crohalifurane D () is characterized by an unusual 6,20-δ-lactone moiety. All compounds were examined for their inhibitory effects on nitric oxide (NO) production induced by lipopolysaccharide in RAW264.7 cells, and and exhibited moderate inhibition on NO production with IC values of 17.2 ± 1.3 and 23.7 ± 1.4 μM, respectively.