Abstract
A collection of the marine cyanobacterium Moorea bouillonii from Apra Harbor in Guam afforded apratyramide, a linear depsipeptide consisting of four amino acid residues and one hydroxy acid moiety. The structure was elucidated by a combination 1D/2D NMR spectroscopic and mass spectrometric analysis. The absolute configuration of the stereocenters was determined by LC-MS analysis of the acid hydrolyzate. Apratyramide was then synthesized and tested for bioactivity. Apratyramide induced the transcription and secretion of vascular endothelial growth factor A (VEGF-A) in multiple cell types. This activity is being explored for various applications where VEGF-A upregulation would be beneficial.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.