Anti-tumor promoting diterpenes from the stem bark of Thuja standishii (Cupressaceae)

Three new labdane-type diterpenoids, labda-8(17),13-dien-15,12R-olid-19-oic acid (1), 12S-hydroxylabda-8(17),13(16), 14-trien-19-oic acid (2) and 13-e thoxylabda-8(17),11,14-trien-19-oic acid (3), along with known dilerpenoids . trans-communic acid (4), totarol (5), 12-methoxyabieta-8,11,13-trien-11-o l (6), and 7 alpha ,8 alpha -epoxy-6 alpha -hydroxyabieta-9(11),13-dien-12- one(7) were isolated from the stem bark of Thuja standishii. The structures of 13 were established by spectroscopic methods and chemical conversion. T hese compounds together with standishinal (8), 12-hydroxy-6,7-seco-abieta-8 ,11,13-trien-6,7-dial (9) and 6 alpha -hydroxysugiol (10) were tested for t heir inhibitory effects on Epstein-Barr virus early antigen (EBV-EA) activa tion induced by 12-O-tetradecanoylphorbol-13-acetate (TPA), as a test for p otential cancer chemopreventive agents. Compound 10 showed strong inhibitor y effect on EBV-EA induction (100% inhibition at 1000 mol ratio;TPA). and c ompounds 2 and 6 showed moderate inhibitory effects on EBV-EA induction. In addition, 15-oxolabda-8(17),11Z,13E-trien-19-oic acid (11) was found to ex hibit the antitumor promoting activity in two-stage mouse skin carcinogenes is test using 7,12-dimethylbenz[a]anthracene and TPA. (C) 2001 Elsevier Sci ence Ltd. All rights reserved.