期刊
JOURNAL OF ANTIBIOTICS
卷 76, 期 2, 页码 83-87出版社
SPRINGERNATURE
DOI: 10.1038/s41429-022-00578-8
关键词
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A new natural product, 1-(6-methylsalicyloyl)glycerol (1), was isolated from the culture extract of the stony coral-derived Micromonospora sp. C029. Its structure and absolute configuration were determined by extensive analysis of NMR spectroscopic data. Compound 1 showed weak antimicrobial activity against Kocuria rizhophila. This study highlights the importance of isolating actinomycetes from less explored environments for the discovery of novel natural products.
A new natural product, 1-(6-methylsalicyloyl)glycerol (1) was isolated from the culture extract of the stony coral-derived Micromonospora sp. C029. The structure of 1 was determined by extensive analysis of 1D and 2D NMR spectroscopic data. The absolute configuration was determined to be S by comparison of specific rotation with synthetic (R)- and (S)-1. Compound 1 showed weak antimicrobial activity against Kocuria rizhophila. Structurally related benzoyl glycerol is not reported from actinomycetes, suggesting that isolation of actinomycetes from little studied environments should be important for the discovery of novel natural products.
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