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.2014 Jan 17;16(2):456-9.
doi: 10.1021/ol4033418. Epub 2013 Dec 16.

Ruthmycin, a new tetracyclic polyketide from Streptomyces sp. RM-4-15

Affiliations

Ruthmycin, a new tetracyclic polyketide from Streptomyces sp. RM-4-15

Xiachang Wang et al. Org Lett..

Abstract

The isolation and structural elucidation of a new tetracyclic polyketide (ruthmycin) from Streptomyces sp. RM-4-15, a bacteria isolated near thermal vents from the Ruth Mullins underground coal mine fire in eastern Kentucky, is reported. In comparison to the well-established frenolicin core scaffold, ruthmycin possesses an unprecedented signature C3 bridge and a corresponding fused six member ring. Preliminary in vitro antibacterial, anticancer, and antifungal assays revealed ruthmycin to display moderate antifungal activity.

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Conflict of interest statement

The authors declare the following competing financial interest: J.S.T. is a co-founder of Centrose (Madison, WI, USA).

Figures

Figure 1
Figure 1
Ruthmycin (1) and representative naturally-occurring frenolicin analogs.
Figure 2
Figure 2
COSY, key HMBC and ROESY correlations of ruthmycin (1).
Figure 3
Figure 3
Experimental and theoretical ECD spectra of ruthmycin (1).
Figure 4
Figure 4
The structure of hebarone, a metabolite of the sea hare-associated fungusTorula herbarum.
See this image and copyright information in PMC

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