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具有抗高血脂活性的深海放线菌 SCSIO15079 产生的芳香酸和亮氨酸衍生物。

Aromatic Acids and Leucine Derivatives Produced from the Deep-Sea Actinomycetes SCSIO15079 with Antihyperlipidemic Activities.

机构信息

Guangdong Provincial Key Laboratory of Chinese Medicine Pharmaceutics, School of Traditional Chinese Medicine, Southern Medical University, Guangzhou 510515, China.

CAS Key Laboratory of Tropical Marine Bio-Resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou 510301, China.

出版信息

Mar Drugs. 2022 Apr 7;20(4):259. doi: 10.3390/md20040259.

DOI:10.3390/md20040259
PMID:35447932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9026450/
Abstract

Six new aromatic acids (-) and three new leucine derivatives containing an unusual oxime moiety (-) were isolated and identified from the deep-sea-derived actinomycetes strain SCSIO15079, together with two known compounds (-). The structures of - including absolute configurations were determined by detailed NMR, MS, and experimental and calculated electronic circular dichroism spectroscopic analyses. Compounds - were evaluated for their antimicrobial and cytotoxicity activities, as well as their effects on intracellular lipid accumulation in HepG2 cells. Compounds and , with the most potent inhibitory activity on intracellular lipid accumulation at 10 μM, were revealed with potential antihyperlipidemic effects, although the mechanism needs to be further studied.

摘要

从深海来源的放线菌菌株 SCSIO15079 中分离并鉴定了六个新的芳香酸(-)和三个含有不寻常肟部分的新亮氨酸衍生物(-),以及两个已知化合物(-)。通过详细的 NMR、MS 以及实验和计算的电子圆二色谱光谱分析确定了-的结构,包括绝对构型。评估了化合物-的抗菌和细胞毒性活性,以及它们对 HepG2 细胞内脂质积累的影响。化合物-和-具有最强的抑制细胞内脂质积累的活性,在 10 μM 时效果最佳,具有潜在的抗高血脂作用,尽管其机制仍需进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/02ccd1d6f1a6/marinedrugs-20-00259-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/5df8b872d8e8/marinedrugs-20-00259-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/164c7a5bb923/marinedrugs-20-00259-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/bb0571a52580/marinedrugs-20-00259-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/02ccd1d6f1a6/marinedrugs-20-00259-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/5df8b872d8e8/marinedrugs-20-00259-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/164c7a5bb923/marinedrugs-20-00259-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/bb0571a52580/marinedrugs-20-00259-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd15/9026450/02ccd1d6f1a6/marinedrugs-20-00259-g004.jpg

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