Two new <i>α</i> -pyrone derivatives from the marine-derived <i>Streptomyces</i> sp. SYPHU 0003

Four <i>α</i>-pyrone derivatives (<b>1-4</b>) were isolated from marine-derived <i>Streptomyces</i> sp. SYPHU 0003, among which two new compounds (<b>1</b> and <b>2</b>). The structures and absolute configurations of compounds <b>1-4</b> were established by comprehensive spectroscopic analyses (MS and NMR), combined with ECD calculations and modified Mosher's method. Antibacterial activity revealed that compounds <b>1-4</b> exhibited identical activity against <i>Acinetobacter baumannii</i> with the MIC values of 64 μg mL<sup>-1</sup>.

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Publication Details

Journal
Natural Product Research
Published
2025-12-14
DOI
https://doi.org/10.1080/14786419.2025.2602039
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
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article

Two new α -pyrone derivatives from the marine-derived Streptomyces sp. SYPHU 0003

Huanzhang Xia, Pengyun Mou, Tingting Tian, Yuan Peng et al.
Natural Product Research
Microbial Natural Products and Biosynthesis
article

Two new α -pyrone derivatives from the marine-derived Streptomyces sp. SYPHU 0003

Huanzhang Xia, Pengyun Mou, Tingting Tian, Yuan Peng, Xianpu Ni
article en

Abstract

Four <i>α</i>-pyrone derivatives (<b>1-4</b>) were isolated from marine-derived <i>Streptomyces</i> sp. SYPHU 0003, among which two new compounds (<b>1</b> and <b>2</b>). The structures and absolute configurations of compounds <b>1-4</b> were established by comprehensive spectroscopic analyses (MS and NMR), combined with ECD calculations and modified Mosher's method. Antibacterial activity revealed that compounds <b>1-4</b> exhibited identical activity against <i>Acinetobacter baumannii</i> with the MIC values of 64 μg mL<sup>-1</sup>.

Natural Product Research
Shenyang Pharmaceutical University (CN), Guangxi University (CN), Guangxi Veterinary Research Institute (CN)
Openalex Percentile: Top 57%
Microbial Natural Products and Biosynthesis
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