Antitumor-promoting effects and cytotoxic activities of dammar resin triterpenoids and their derivatives.

Nineteen known triterpenoids, 1-19. and one known sesquiterpenoid, 20. were isolated from dammar resin obtained from Shorea javanica K & V (Dipterocarpaceae) One of the acidic triterpenoids, dammarenolic acid (I), was converted to fourteen derivatives, namely. an alcohol, 21, an aldehyde. 22. and twelve L-amino acid conjugates, 23-34 Compounds 1-34 were examined for their inhibitory effects on the induction of Epstein Barr virus early antigen (EBV-EA) by 12-O-tetradecanoylphorbol 13-acetate (TPA) in Raji cells, a known primary screening test for antitumor promoters. All of the compounds tested. except for compounds 4, 5, 12-14, 16, and 17, showed inhibitory effects against EBV-EA activation with potencies either comparable with or stronger than that of beta-carotene, a known natural antitumor promoter In addition, (20S)-20-hydroxy-3,4-secodammara-4(28),24-dien-3-al (22) exhibited inhibitory effects on skin tumor promotion in an in vivo two-stage mouse skin carcinogenesis test based on 7,12-dimethylbenz[a]anthracene (DMBA) as initiator, and with TPA as promoter Furthermore, evaluation of the cytotoxic activities of compounds 1-34 against human cancer cell lines showed that reduction (i a 21 and 22) or conjugation with L-amino acids (i e 23-34) of compound I enhanced the cytotoxicity against human melanoma cell line CRL1579