Lyngbyastatins 5–7, Potent Elastase Inhibitors from Floridian Marine Cyanobacteria, <i>Lyngbya</i> spp.

Kanchan Taori(University of Florida), Susan Matthew(University of Florida), James R. Rocca(University of Florida), Valerie J. Paul(University of Florida), Hendrik Luesch(Smithsonian Marine Station)
Journal of Natural Products
October 1, 2007
Cited by 127

Abstract

Three new analogues of dolastatin 13, termed lyngbyastatins 5-7 ( 1- 3), were isolated from two different collections of marine cyanobacteria, Lyngbya spp., from South Florida. Their planar structures were deduced by a combination of NMR techniques, and the absolute configurations were established by modified Marfey's analysis of the acid hydrolyzates. The related cyclodepsipeptide somamide B ( 4), previously reported from a Fijian cyanobacterium, has also been found in one of the extracts, and its absolute stereochemistry was unambiguously assigned for the first time. Compounds 1- 4 were found to selectively inhibit elastase over several other serine proteases, with IC50 values for porcine pancreatic elastase ranging from 3 to 10 nM.


Related Papers

No related papers found

Powered by citation graph analysis