The aerial part of Werneria ciliolata afforded a series of new diterpe
nes: two ent-kaurane derivatives, a nor-kaurane, an ent-manoyloxide de
rivative, a dimeric diterpene, as well as a rare diterpene. Their stru
ctures were elucidated by spectroscopic methods, including the concert
ed application of 1D NMR techniques (DEFT and NOEDS) and 2D NMR techni
ques (H-1-H-1 COSY and HETCOR). In addition, four known kauranes, four
coumarins and 6-hydroxytremetone were isolated. All isolated compound
s from W. ciliolata and W. dactylophylla were tested in vitro for anti
-viral activity against HIV-1, but only 6-hydroxytremetone showed a si
gnificant anti-HIV-1 activity.