As the result of a structurally guided isolation to identify lead comp
ounds for the treatment of opportunistic infections of AIDS, the dihyd
rochloride salt of a new symmetrical pyrrole dimer debromosceptrin (1)
, and two known pyrrole analogues (2 and 3) were isolated from the Car
ibbean sponge Agelas conifera collected from Belize. The structure of
debromosceptrin was identified by analysis of spectral data. N-15 spec
tral data assignments were made for compounds 1-3. Compounds 2 and 3 s
howed marginal inhibition of Mycobacterium tuberculosis.