Three naphthomycin type polyketide compounds isolated from strain Streptomyces sp. HKIB0008

Three new naphthomycin derivatives were isolated and identified from Streptomyces sp. HKIB0008, and were designated as naphthomycin R (1), naphthomycin S (2), and naphthomycin T (3). Their structures were elucidated using a combination of spectroscopic techniques, including high-resolution mass spectrometry, and NMR. The naphthoquinone core of 1 underwent carbon-carbon bond cleavage, resulting in a novel structural feature, and a corresponding Baeyer-Villiger oxidation mechanism was proposed. Compounds 2 and 3 possess a complex side chain when compared to known cystine modification on the naphthalenoid core as in the case of naphthomycins I and J. In addition, the minimum inhibitory concentration (MIC) assays for these compounds were conducted.

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Publication Details

Journal
Natural Products and Bioprospecting
Published
2026-03-03
DOI
https://doi.org/10.1007/s13659-026-00591-6
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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Three naphthomycin type polyketide compounds isolated from strain Streptomyces sp. HKIB0008

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Three naphthomycin type polyketide compounds isolated from strain Streptomyces sp. HKIB0008

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article en

Abstract

Three new naphthomycin derivatives were isolated and identified from Streptomyces sp. HKIB0008, and were designated as naphthomycin R (1), naphthomycin S (2), and naphthomycin T (3). Their structures were elucidated using a combination of spectroscopic techniques, including high-resolution mass spectrometry, and NMR. The naphthoquinone core of 1 underwent carbon-carbon bond cleavage, resulting in a novel structural feature, and a corresponding Baeyer-Villiger oxidation mechanism was proposed. Compounds 2 and 3 possess a complex side chain when compared to known cystine modification on the naphthalenoid core as in the case of naphthomycins I and J. In addition, the minimum inhibitory concentration (MIC) assays for these compounds were conducted.

Natural Products and BioprospectingVol. 16(1)
Kunming Institute of Botany (CN), University of Chinese Academy of Sciences (CN)
National Science Foundation, National Natural Science Foundation of China, Youth Innovation Promotion Association of the Chinese Academy of Sciences, Yunnan Provincial Science and Technology Department, Youth Innovation Promotion Association
Openalex Percentile: Top 37%
Microbial Natural Products and Biosynthesis
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