P-3 Diversity of Chemical Constituents and Base Sequences of Ligularia kanaitzensis, Ligularia vellerea, Ligularia subspicata, and Ligularia lamarum (Compositae) collected in China
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- Okamoto Yasuko
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Watanabe Aki
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Mihara Kanako
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Matsuo Sachie
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Tachikawa Kana
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Nakamizo Hiromi
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Nakashima Katsuyuki
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Saito Yoshinori
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Sono Masakazu
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
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- Hanai Ryo
- Department of Life Science
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- Kuroda Chiaki
- Department of Chemistry, Rikkyo University
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- Gong Xun
- Kunming Institute of Botany
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- Shen Yuemao
- Kunming Institute of Botany
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- Tori Motoo
- Faculty of Pharmaceutical Sciences, Tokushima Bunri University
Bibliographic Information
- Other Title
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- P-3 中国産キク科Ligularia kanaitzensis,Ligularia vellerea,Ligularia subspicataおよびLigularia lamarumの化学成分と遺伝子の多様性(ポスター発表の部)
Description
Four Ligularia species, L. kanaitzensis, L. vellerea, L. subspicata, and L. lamarum collected in Yunnan province of China were examined and 64 compounds were isolated. Compounds 1-15 were new. The samples of L. kanaitzensis could be divided into two groups, based on chemical composition of the root extract. Furanoeremophilane-6β,10β-diol and its derivatives were isolated from one group, while eremophilan-8-one derivatives were isolated from the other group. In contrast, intra-specific diversity was found to be small in the atpB-rbcL intergenic sequence. The samples of L. vellerea could be divided into three groups. The major components isolated from types A, B, and C were 6,15-dioxygenated furanoeremophilanes, 1,6-dioxygenated furanoeremophilanes, and 6,15-dioxygenated eremophilanolides. The difference in chemical composition is consistent with geographic distribution. Intra-specific diversity in the atpB-rbcL sequence was small. The samples of L. subspicata were grouped into two, that is, a group A producing 1-angeloyloxy derivatives and a group B producing ligularol (35) and its derivatives. Diversity was found to be present in the nucleotide sequences as well. 1,10-Dioxygenated derivatives from L. lamarum were isolated. The chemical composition was diverse. However, the DNA sequence of atpB-rbcL is currently under investigation.
Journal
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- Symposium on the Chemistry of Natural Products, symposium papers
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Symposium on the Chemistry of Natural Products, symposium papers 49 (0), 247-252, 2007
Symposium on the Chemistry of Natural Products Steering Committee
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Details 詳細情報について
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- CRID
- 1390001206077785600
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- NII Article ID
- 110006682772
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- ISSN
- 24331856
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- Text Lang
- ja
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- Data Source
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- JaLC
- CiNii Articles
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- Abstract License Flag
- Disallowed