4.7 Article

Anti-inflammation furanoditerpenoids from Caesalpinia minax Hance

Journal

PHYTOCHEMISTRY
Volume 117, Issue -, Pages 325-331

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2015.06.025

Keywords

Caesalpinia minax Hance; Caesalpinia; A-seco-rearranged cassane; Anti-inflammation activity; Circular dichroism; Conformation analysis

Funding

  1. National Natural Science Foundation Project of China [81274189, 81374066]
  2. National Program for College Students Innovation and Entrepreneurship Training in University [201310163021]
  3. Project of Key Laboratory of Structure-Based Drug Design AMP
  4. Discovery of Ministry of Education of Shenyang Pharmaceutical University

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Cassane skeletons are rare in nature, but often possess valuable medicinal properties. A furanoditerpenoid with an unusual A-seco-rearranged cassane skeleton, neocaesalminin A, and five furanoditerpenoids were isolated from seeds of Caesalpinia minax Hance, along with six known cassane derivatives, 7-O-acetyl-bonducellpin C, caesalmin F, caesalmin C, zeta-caesalmin E1 and caesalpinin K. Compound structures were determined by spectroscopy (HR-ESI-MS, UV, IR, 1D NMR, 2D NMR), X-ray crystallography and quantum chemical computation of electronic circular dichroism). Three of the previously known compounds exhibited significant inhibition of nitric oxide production of RAW264.7 macrophages stimulated by lipopolysaccharide (LPS). (C) 2015 Elsevier Ltd. All rights reserved.

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