Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5230154 | Tetrahedron | 2007 | 10 Pages |
Abstract
Five new polycyclic guanidine alkaloids, 16β-hydroxycrambescidin 359 (1), batzelladines K, L, M, and N (2-5), along with the previously reported ptilomycalin A (6), crambescidine 800 (7), batzelladine C (8), and dehydrobatzelladine C (9), were isolated from the Jamaican sponge Monanchora unguifera. Their structures were assigned on the basis of detailed analysis of 1D and 2D NMR, and mass spectral data. Their activities against cancer cell lines, protozoa, HIV-1 and AIDS opportunistic infectious pathogens (AIDS-OIs) including Mtb were evaluated.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hui-Ming Hua, Jiangnan Peng, D. Chuck Dunbar, Raymond F. Schinazi, Arcadio G. de Castro Andrews, Carmen Cuevas, Luis F. Garcia-Fernandez, Michelle Kelly, Mark T. Hamann,