| Literature DB >> 23459021 |
Brunilda Vera1, Abimael D Rodríguez, Edward Avilés, Yasuyuki Ishikawa.
Abstract
The novel bromotriterpene polyethers aplysqualenol A (1) and aplysqualenol B (2) have been isolated from the Caribbean sea slug Aplysia dactylomela collected in Puerto Rico, and their structures and relative configurational assignments established from spectroscopic data aided by quantum mechanical calculations of NMR chemical shifts. Although both these compounds may be conceived as polyoxycyclic derivatives of the C30 squalene skeleton, remarkably 1 and 2 possess an unprecedented C15 to C24 flexible chain of 14S* spatial disposition that contains a unique ether bridge between C16 and C19. Biological activity screening tests revealed that, although aplysqualenol A (1) does not have significant anti-infective properties, it possesses potent antitumoral and antiviral activities.Entities:
Keywords: Antitumor activity; Antiviral activity; Aplysia dactylomela; Polyether; Sea slug
Year: 2009 PMID: 23459021 PMCID: PMC3583239 DOI: 10.1002/ejoc.200900775
Source DB: PubMed Journal: European J Org Chem ISSN: 1099-0690