Tc. Mckee et al., THE LOBATAMIDES, NOVEL CYTOTOXIC MACROLIDES FROM SOUTHWESTERN PACIFICTUNICATES, Journal of organic chemistry, 63(22), 1998, pp. 7805-7810
Novel macrolides, lobatamides A-F (1-6), have been isolated from shall
ow water Australian collections of Aplidium lobatum, from a deep water
collection of Aplidium sp., and from an unidentified Philippine ascid
ian. Full details of the isolation and structure elucidation of 1-6 ar
e provided herein, along with results and analyses of the testing of l
obatamides A-D (1-4) in the NCI human tumor 60 cell-line screen. The l
obatamides share a common core structure with the recently described s
alicylihalamides, which were isolated from a Haliclona sp. sponge. COM
PARE analyses of the mean-graph differential cytotoxicity profiles of
the lobatamides and the salicylihalamides showed high correlations wit
h each other but not with members of the NCI's standard agents databas
e. These compounds, therefore, appear to comprise a new mechanistic cl
ass, meriting further antitumor investigations.