Publication | Open Access
Manzamine B and E and Ircinal A Related Alkaloids from an Indonesian <i>Acanthostrongylophora</i> Sponge and Their Activity against Infectious, Tropical Parasitic, and Alzheimer's Diseases
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Citations
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References
2006
Year
BiologyManzamine BBiochemistryAntiparasitic AgentNatural SciencesMedicineHerbal MedicineTropical ParasiticSecondary MetaboliteOrganic ChemistryCarbons 12-28PhytopharmacologyTheir ActivityCarbons 11PharmacologyNew Manzamine-type AlkaloidsDrug DiscoveryNatural Product Synthesis
Four new manzamine-type alkaloids, 12,28-oxamanzamine E (2), 12,34-oxa-6-hydroxymanzamine E (3), 8-hydroxymanzamine B (5), and 12,28-oxaircinal A (11), were isolated from three collections of an Indonesian sponge of the genus Acanthostrongylophora together with 13 known manzamine alkaloids, ircinal A, ircinol A, xestomanzamine A, manzamines A, E, F, J, and Y, manadomanzamines A and B, neo-kauluamine, 8-hydroxymanzamine A, and manzamine A N-oxide. The structures of the new compounds were elucidated by means of 1D and 2D NMR spectroscopic methods. Three of these compounds (2, 3, and 11) possess a unique manzamine-type aminal ring system generated through an ether linkage between carbons 12-28 or between carbons 12-34. In the case of manzamine B and related metabolites, carbons 11 and 12 of the typical manzamine structure have an epoxide group and add to our growing understanding of manzamine structure-activity relationships (SAR) and metabolism. The bioactivity and SAR for a number of previously reported manzamine-related metabolites against malaria, leishmania, tuberculosis, and HIV-1 are also presented. Manzamine Y (9) showed significant inhibitory activity of GSK3, an enzyme implicated in Alzheimer's disease pathology. The toxicity of manzamine A and neo-kauluamine was evaluated against both medaka fry and eggs.
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