Anithiactins A-C, modified 2-phenylthiazoles from a mudflat-derived Streptomyces sp.

J Nat Prod

Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Sciences, and ∥Research Institute of Oceanography, Seoul National University, NS-80, 151-747, Seoul, Republic of Korea.

Published: December 2014


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Article Abstract

Intensive investigation of the chemical components of a Streptomyces sp. isolated from mudflat sediments collected on the southern coast of the Korean peninsula led to the isolation of three new compounds, anithiactins A-C (1-3). The chemical structures of anithiactins A and C were determined by interpretation of NMR data analyses, while the chemical structure of anithiactin B was established from a combination of NMR spectroscopic and crystallographic data analyses. The structure of anithiactin A was also confirmed by total synthesis. These three anithiactins displayed moderate acetylcholinesterase inhibitory activity with no significant cytotoxicity.

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http://dx.doi.org/10.1021/np500558bDOI Listing

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Anithiactins A-C, modified 2-phenylthiazoles from a mudflat-derived Streptomyces sp.

J Nat Prod

December 2014

Center for Marine Natural Products and Drug Discovery, School of Earth and Environmental Sciences, and ∥Research Institute of Oceanography, Seoul National University, NS-80, 151-747, Seoul, Republic of Korea.

Intensive investigation of the chemical components of a Streptomyces sp. isolated from mudflat sediments collected on the southern coast of the Korean peninsula led to the isolation of three new compounds, anithiactins A-C (1-3). The chemical structures of anithiactins A and C were determined by interpretation of NMR data analyses, while the chemical structure of anithiactin B was established from a combination of NMR spectroscopic and crystallographic data analyses.

View Article and Find Full Text PDF