Phytochemical examination of a Papua New Guinea collection of Lyngbya majuscula resulted in the discovery of wewakazole (1), a novel cyclic dodecapeptide containing an unprecedented six five-membered heterocycles. Multiple NMR experiments and MS/MS data were required to assemble its planar structure because of its extensively signal-overlapped NMR spectra. In particular, a 1D HMBC was utilized to orient a three amino acid fragment that could not be placed by standard spectroscopic methods. [structure--see text]
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/ol026811k | DOI Listing |
Org Biomol Chem
October 2016
The Fourth People's Hospital of Shenzhen, Shenzhen 518033, China. and Shenzhen Institute of Geriatrics, Shenzhen 518020, China and The Second People's Hospital of Shenzhen, Shenzhen 518035, China.
Wewakazole B is a novel cyclodecapeptide with highly potent cytotoxic activity isolated from a sample of M. producens collected from the Red Sea. It contains nine common and three modified amino acid residues.
View Article and Find Full Text PDFOrg Lett
January 2003
College of Pharmacy, Oregon State University, Corvallis, OR 97331, USA.
Phytochemical examination of a Papua New Guinea collection of Lyngbya majuscula resulted in the discovery of wewakazole (1), a novel cyclic dodecapeptide containing an unprecedented six five-membered heterocycles. Multiple NMR experiments and MS/MS data were required to assemble its planar structure because of its extensively signal-overlapped NMR spectra. In particular, a 1D HMBC was utilized to orient a three amino acid fragment that could not be placed by standard spectroscopic methods.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!