Issue 38, 2015

Saccharothriolides A–C, novel phenyl-substituted 10-membered macrolides isolated from a rare actinomycete Saccharothrix sp.

Abstract

Three new 10-membered macrolides, saccharothriolides A–C (1–3), were discovered from a rare actinomycete Saccharothrix sp. A1506. All of the sp3 carbons in the 10-membered ring had chirality, which was determined by extensive spectroscopic analysis and TDDFT-calculation of ECD spectra. Saccharothriolide B (2) exhibited cytotoxicity against human tumor cell lines HeLa and HT1080.

Graphical abstract: Saccharothriolides A–C, novel phenyl-substituted 10-membered macrolides isolated from a rare actinomycete Saccharothrix sp.

Supplementary files

Article information

Article type
Communication
Submitted
08 Mar 2015
Accepted
31 Mar 2015
First published
01 Apr 2015
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2015,51, 8074-8077

Saccharothriolides A–C, novel phenyl-substituted 10-membered macrolides isolated from a rare actinomycete Saccharothrix sp.

S. Lu, S. Nishimura, G. Hirai, M. Ito, T. Kawahara, M. Izumikawa, M. Sodeoka, K. Shin-ya, T. Tsuchida and H. Kakeya, Chem. Commun., 2015, 51, 8074 DOI: 10.1039/C5CC01953B

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