Marine Drugs · 2018 · 32 citations · 15 references
Natural SciencesMedicinal ChemistryPharmacologyBiochemical PharmacologyDrug DiscoveryStructure-activity RelationshipsMarine Bioactive CompoundsMarine Natural ProductsMarine PharmacologyAntimalarial AgentsBioactive Compounds From Marine SpongesBioactive Marine MetabolitesMarine AlkaloidsMarine Compound Structure ElucidationMarine Sponge MetabolitesPlant AlkaloidsSponges-derived Metabolites
Two new bromotyrosine alkaloids, ceratinadins E (1) and F (2), were isolated from an Okinawan marine sponge Pseudoceratina sp. as well as a known bromotyrosine alkaloid, psammaplysin F (3). The gross structures of 1 and 2 were elucidated on the basis of spectroscopic data. The absolute configurations of 1 and 2 were assigned by comparison of the NMR and ECD data with those of a known related bromotyrosine alkaloid, psammaplysin A (4). Ceratinadins E (1) and F (2) are new bromotyrosine alkaloids possessing an 8,10-dibromo-9-methoxy-1,6-dioxa-2-azaspiro[4.6]undeca-2,7,9-trien-4-ol unit with two or three 11-N-methylmoloka’iamine units connected by carbonyl groups, respectively. Ceratinadin E (1) exhibited antimalarial activities against a drug-resistant and a drug-sensitive strains of Plasmodium falciparum (K1 and FCR3 strains, respectively).
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Potent Antimalarial Activities of Polyether Antibiotic, X-206.
Kazuhiko Otoguro, Akiko Kohana, Chizu Manabe et al. · The Journal of Antibiotics · 2001 · 107 citations · Full text
Structure of the psammaplysins
Deborah M. Roll, Clifford W. J. Chang, Paul J. Scheuer et al. · Journal of the American Chemical Society · 1985 · 72 citations