Abstract
Chemical investigation of the ethyl acetate extract of the sponge Acanthostrongylophora ingens afford one new pyrimidine-ß-carboline alkaloid named acanthomine A (2), together with two known compounds annomontine (1) and 1,2,3,4-tetrahydronorharman-1-one (3). Their structures were unambiguously established on the basis of NMR spectroscopy (H, C, H-H COSY, HMQC and HMBC) and mass spectrometry. The isolated compounds were tested for cytotoxic activity using brine shrimp bioassay and different cancer cell lines.
Original language | English |
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Pages (from-to) | 175-178 |
Number of pages | 4 |
Journal | Natural Product Communications |
Volume | 3 |
Issue number | 2 |
Publication status | Published - 2008 |
Keywords
- Acanthomine A
- Acanthostrongylophora ingens
- alkaloids
- cytotoxic activity
- Pyrimidine-ß-carboline