79703-25-6Relevant articles and documents
Total synthesis of dimeric pyrrole-imidazole alkaloids: Sceptrin, ageliferin, nagelamide E, oxysceptrin, nakamuric acid, and the axinellamine carbon skeleton
O'Malley, Daniel P.,Li, Ke,Maue, Michael,Zografos, Alexandros L.,Baran, Phil S.
, p. 4762 - 4775 (2007/10/03)
The dimeric pyrrole imidazole natural products are a growing class of alkaloids with exotic connectivity, unique topologies, high nitrogen content, and exciting bioactivities. This full account traces the evolution of a strategy that culminated in the fir
Bioactive Bromopyrrole Metabolites from the Caribbean Sponge Agelas conifera
Keifer, Paul A.,Schwartz, Robert E.,Koker, Moustapha E. S.,Hughes, Robert G.,Rittschof, Dan,Rinehart, Kenneth L.
, p. 2965 - 2975 (2007/10/02)
Biologically active extracts of the Carribean sponge Agelas conifera have yielded, in exhaustive studies, the diacetate salts of seven new bromopyrroles (1, 3-8), as well as that of the known debromooroidin dimer sceptrin (2).These compounds were found to be antiviral and antibacterial and were active in barnacle settlement and biochemical prophage induction assays.The structures assigned were based on spectroscopic comparison to sceptrin and two-dimensional NMR data.Synthetic bromopyrroles were used to verify bromine substitution patterns.The oxysceptrins (4, 5) are characterized by their aminoimidazolinone group, the ageliferins (6-8) by a unique cyclohexene-based skeleton.
