Lyngbyastatins 5-7, potent elastase inhibitors from Floridian marine cyanobacteria, Lyngbya spp.

J Nat Prod

Department of Medicinal Chemistry, University of Florida, 1600 SW Archer Road, Gainesville, Florida 32610, USA.

Published: October 2007

AI Article Synopsis

  • Three new variants of dolastatin 13, named lyngbyastatins 5-7, were isolated from marine cyanobacteria in South Florida.
  • Their structures were determined using NMR techniques and their absolute configurations were analyzed using a modified Marfey's method.
  • These compounds, along with somamide B, demonstrated strong selective inhibition of elastase, showing IC50 values between 3 and 10 nM.

Article 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.

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http://dx.doi.org/10.1021/np0702436DOI Listing

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Article Synopsis
  • Three new variants of dolastatin 13, named lyngbyastatins 5-7, were isolated from marine cyanobacteria in South Florida.
  • Their structures were determined using NMR techniques and their absolute configurations were analyzed using a modified Marfey's method.
  • These compounds, along with somamide B, demonstrated strong selective inhibition of elastase, showing IC50 values between 3 and 10 nM.
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