4.7 Article

Mappianines A-E, structurally diverse monoterpenoid indole alkaloids from &ITMappianthus iodoides&IT

Journal

PHYTOCHEMISTRY
Volume 145, Issue -, Pages 68-76

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2017.10.009

Keywords

Mappianthus iodoides Hand-Mazz; Icacinaceae; Monoterpenoid indole alkaloids; Cytotoxic activities

Funding

  1. National Natural Science Foundation of China [81402817, 21431001, 81760626]
  2. Innovation Fund of the Ministry of Education [IRT_16R15]
  3. Natural Science Foundation of Guangxi [2016GXNSFGA380005, 2014GXNSFBA118189]
  4. project of the State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources [CMEMR2016-A02]

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Five previously undescribed monoterpenoid indole alkaloids, mappianines A-E, along with twelve known analogues, were isolated from the stems of Mappianthus iodoides Hand.-Mazz. Their structures and absolute configurations were determined by spectroscopic analysis, single-crystal X-ray diffraction, and ECD calculations. The plausible biogenetic pathway of mappianine A was proposed. All the isolated compounds were evaluated for their cytotoxic effects on MGC-803, Bel-7404, A549, NCI-H460, and HepG2 cancer cell lines. Mappianine B, tetrahydroalstonine, beta-carbolin-1-one, and 1,2,3,4-tetrahydronorharman-1-one displayed moderate cytotoxicity against all cell lines tested, with IC50 values ranging from 5.19 to 42.86 mu M. (C) 2017 Elsevier Ltd. All rights reserved.

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