Determination of the absolute configuration of the novel anti-trypanosomal iridoid molucidin isolated from Morinda lucida by X-ray analysis

Satoru Karasawa, Kenji Yoza, Nguyen Huu Tung, Takuhiro Uto, Osamu Morinaga, Mitsuko Suzuki, Kofi D. Kwofie, Michael Amoa-Bosompem, Daniel A. Boakye, Irene Ayi, Richard Adegle, Maxwell Sakyiamah, Frederick Ayertey, Frederic Aboagye, Alfred A. Appiah, Kofi B.A. Owusu, Isaac Tuffour, Philip Atchoglo, Kwadwo K. Frempong, William K. AnyanRegina Appiah-Opong, Alexander K. Nyarko, Taizo Yamashita, Yasuchika Yamaguchi, Dominic Edoh, Kwadwo Koram, Shoji Yamaoka, Nobuo Ohta, Yukihiro Shoyama

研究成果: Contribution to journalArticle査読

4 被引用数 (Scopus)

抄録

The strong anti-trypanosomal active compound, molucidin, contains a spirolactone tetracyclic iridoid skeleton and is isolated from Morinda lucida as an enantiomer of oruwacin, which is isolated from the same plant. To confirm the absolute configuration of molucidin, we prepared single crystals of molucidin for X-ray analysis. The absolute configuration of the afforded single crystal was determined by X-ray crystallography using a Cu radiation source. X-ray diffraction data were collected at 93 K in the 2θ range 7.468-134.99° and analyzed using the SHELXL-2014 program. The corresponding chiral quaternary carbon atoms in molucidin were unambiguously determined as 1R, 5S, 8S, 9S, and 10S. Notably, both enantiomers of a single molecule, molucidin and oruwacin, with a rigid structure have been isolated from the same plant species. The biosynthetic pathway for the formation of molucidin is also discussed on the basis of the absolute configuration. Our results for the first time support for structural elucidation of tetracyclic iridoids using X-ray analysis.

本文言語英語
ページ(範囲)7158-7160
ページ数3
ジャーナルTetrahedron Letters
56
52
DOI
出版ステータス出版済み - 12 30 2015
外部発表はい

All Science Journal Classification (ASJC) codes

  • 生化学
  • 創薬
  • 有機化学

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