| Literature DB >> 27440074 |
Shengtian Chen1,2, Junfeng Wang1, Xiuping Lin1, Bingxin Zhao2, Xiaoyi Wei3, Guangqiang Li2, Kumaravel Kaliaperumal1, Shengrong Liao1, Bin Yang1, Xuefeng Zhou1, Juan Liu1, Shihai Xu2, Yonghong Liu1.
Abstract
Three dimeric nitrophenyl trans-epoxyamides, chrysamides A-C (1-3), were obtained from the deep-sea-derived fungus Penicillium chrysogenum SCSIO41001. Their structures were characterized by spectroscopic analysis, electronic circular dichroism computations, and X-ray single-crystal diffraction analysis. Notably, compound 1 possesses a novel centrosymmetric dimer skeleton featuring an unprecedented 7-oxa-2,5-diazabicyclo[2.2.1]heptane ring system, which represents the first example of dimeric nitrophenyl trans-epoxyamide in nature. Compound 3 suppresses the production of proinflammatory cytokine interleukin-17. A possible biosynthetic pathway of 1-3 was proposed.Entities:
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Year: 2016 PMID: 27440074 DOI: 10.1021/acs.orglett.6b01699
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005