4.7 Article

Myritonines A-C, Alkaloids from Myrioneuron tonkinensis Based on a Novel Hexacyclic Skeleton

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 79, Issue 4, Pages 1203-1207

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.5b01130

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Funding

  1. National Natural Science Foundation of China [21372228]
  2. Yunnan Applied Basic Research Projects [2014FB166]
  3. Youth Innovation Promotion Association of CAS [2015323]

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Myritonines A-C (1-3), three new alkaloids bearing an unprecedented heterohexacyclic skeleton, were isolated from Myrioneuron tonkinensis. Their structures were determined by a combination of spectroscopic data and single crystal X-ray diffraction analysis. Compound 3 represents the first Myrioneuron alkaloid featuring a unique trans-decahydroquinoline motif and was also found to possess a rare cyano functionality. Compounds 1 and 2 showed inhibition against the hepatitis C virus in vitro.

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