Abstract

Two pyridoacridines, N-hydroxymethylisocystodamine (1) and neolabuanine A (2), together with the known ecionine A (3), ecionine B (4), isocystodamine (5), N-methylisocystodamine (6), 9-hydroxyisoascididemin (7), and biemnadin (8), were isolated from a marine sponge Biemna sp. Several of these compounds were shown to induce cell differentiation of K562 leukemia cells into erythrocytes. Following inspection of the NMR data, and comparison of these data with literature values, we demonstrated that neolabuanine A (2) had the structure previously reported as labuanine A (2), and that the compound initially reported under the name of labuanine A possessed the structure assigned to ecionine A (3). We found that both neolabuanine A (2) and ecionine A (3) were gradually converted to 9-hydroxyisoascididemin (7), indicating that 2 and 3 can be considered both as precursors of 7.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.