Two polycyclic thioalkaloides dassonmycins A () and B () were isolated from SCSIO 40065 associated with marine sponge sp. Structures of and were elucidated by comprehensive spectroscopic analysis and confirmed by single-crystal X-ray diffraction experiments, to have a 6/6/6/6-fused tetracyclic ring featuring a naphthoquinone[2,3-]piperazine[1,2-]thiomorpholine scaffold. Compound formed a caged core through an additional ether bridge. Both compounds exhibited moderate antibacterial and cytotoxic activities.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.1c00328 | DOI Listing |
Org Lett
April 2021
Key Laboratory of Tropical Marine Bioresources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.
Two polycyclic thioalkaloides dassonmycins A () and B () were isolated from SCSIO 40065 associated with marine sponge sp. Structures of and were elucidated by comprehensive spectroscopic analysis and confirmed by single-crystal X-ray diffraction experiments, to have a 6/6/6/6-fused tetracyclic ring featuring a naphthoquinone[2,3-]piperazine[1,2-]thiomorpholine scaffold. Compound formed a caged core through an additional ether bridge.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!