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从海绵中发现艾氏胺D-G以及艾氏胺D的全合成。

Discovery of ianthelliformisamines D-G from the sponge and the total synthesis of ianthelliformisamine D.

作者信息

Hayes Sasha, Lu Yaoying, Rehm Bernd H A, Davis Rohan A

机构信息

Institute for Biomedicine and Glycomics, Griffith University, Don Young Road, Brisbane, 4111, Australia.

NatureBank, Griffith University, Don Young Road, Brisbane, 4111, Australia.

出版信息

Beilstein J Org Chem. 2024 Dec 9;20:3205-3214. doi: 10.3762/bjoc.20.266. eCollection 2024.

Abstract

The marine sponge was investigated for new chemistry after the recent discovery that polyamines ianthelliformisamines A-C (-) - originally sourced from this Australian sponge - act as biofilm inhibitors and antibiotic enhancers. Large-scale extraction and isolation studies resulted in the discovery of four new and minor natural products, ianthelliformisamines D-G (-) and the known steroid, aplysterol (). Compounds - were fully characterised following 1D/2D NMR, MS and UV data analyses. All compounds were assessed for their inhibition on planktonic growth of PAO1 in addition to their ability to inhibit the formation of biofilms. None of the tested natural products inhibited planktonic growth or biofilm formation of PAO1 when screened at 50 µM. Ianthelliformisamine D () contains a rare -(3-aminopropyl)-2-pyrrolidone moiety only found in <30 natural products. Owing to the novelty of compound , we undertook the first total synthesis of this natural product, which was achieved in three steps.

摘要

最近发现源自澳大利亚海绵的聚胺海绵胺A-C(-)可作为生物膜抑制剂和抗生素增强剂后,对该海洋海绵进行了新化学物质的研究。大规模提取和分离研究发现了四种新的微量天然产物,海绵胺D-G(-)以及已知的甾体化合物阿普利甾醇()。通过一维/二维核磁共振、质谱和紫外数据分析对化合物-进行了全面表征。除了评估所有化合物抑制PAO1生物膜形成的能力外,还评估了它们对PAO1浮游生长的抑制作用。在50μM浓度下筛选时,所测试的天然产物均未抑制PAO1的浮游生长或生物膜形成。海绵胺D()含有一种罕见的-(3-氨丙基)-2-吡咯烷酮部分,仅在不到30种天然产物中发现。由于化合物的新颖性,我们首次对这种天然产物进行了全合成,该合成通过三步完成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1615/11650616/29569c571ccb/Beilstein_J_Org_Chem-20-3205-g002.jpg

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