Abstract
Polycavernoside E (1), a new polycavernoside analog, was isolated from a marine Okeania sp. cyanobacterium. The relative configuration was elucidated primarily by analyzing the two dimensional nuclear magnetism resonance (2D NMR) data. The absolute configuration was clarified by comparing the electronic circular dichroism (ECD) data of 1 with those of known analogs. Polycavernoside E (1) exhibited moderate antitrypanosomal activity against Trypanosoma brucei rhodesiense. Furthermore, the isolation of polycavernoside E (1) from marine cyanobacteria provides additional evidence that marine cyanobacteria, and not red algae, are responsible for the biosynthesis of polycavernosides.
| Original language | English |
|---|---|
| Pages (from-to) | 645-652 |
| Number of pages | 8 |
| Journal | Beilstein Journal of Organic Chemistry |
| Volume | 20 |
| DOIs | |
| Publication status | Published - 2024 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 14 Life Below Water
Keywords
- macrolide glycoside
- marine cyanobacterium
- marine natural products
- polycavernosides
- terminal alkyne
ASJC Scopus subject areas
- Organic Chemistry
Fingerprint
Dive into the research topics of 'Isolation and structure determination of a new analog of polycavernosides from marine Okeania sp. cyanobacterium'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS