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New secondary metabolite with cytotoxicity from spawning soft coral Asterospicularia laurae in Taiwan.
Su, Jui-Hsin; Liu, Chih-I; Lu, Mei-Chin; Chang, Chi-I; Hsieh, Min-Ying; Lin, Yu-Chi; Dai, Chang-Feng; Zhang, Ya-Han; Lin, Zheng-Yu; Lin, Yun-Sheng.
Afiliação
  • Su JH; National Museum of Marine Biology & Aquarium, Pingtung, Taiwan.
  • Liu CI; Department of Nursing, Meiho University, Pingtung, Taiwan.
  • Lu MC; Graduate Institute of Marine Biology, National Dong Hwa University, Pingtung, Taiwan.
  • Chang CI; Department of Biological Science and Technology, National Pingtung University of Science and Technology, Pingtung, Taiwan.
  • Hsieh MY; Graduate Institute of Marine Biology, National Dong Hwa University, Pingtung, Taiwan.
  • Lin YC; National Research Institute of Chinese Medicine, Taipei, Taiwan.
  • Dai CF; Institute of Oceanography, National Taiwan University, Taipei, Taiwan.
  • Zhang YH; Department of Biological Science and Technology, National Pingtung University of Science and Technology, Pingtung, Taiwan.
  • Lin ZY; Department of Biological Science and Technology, Meiho University, Pingtung, Taiwan.
  • Lin YS; Department of Biological Science and Technology, Meiho University, Pingtung, Taiwan.
Nat Prod Res ; 35(6): 967-975, 2021 Mar.
Article em En | MEDLINE | ID: mdl-31364881
ABSTRACT
We have conducted a long-term research on the Taiwanese soft coral Asterospicularia laurae, which resulted in many xenicane-type diterpenoids such as asterolaurins A-M from A. laurae coral tissues during the non-spawning period were isolated. Here, we report a new xenicane diterpenoid, asterolaurin N (1), along with three known xenicane-type monocarbocyclic diterpenes [13-epi-9-desacetylxenicin (2), xeniolide-B 9-acetate (3) and asterolaurin I (4)] from A. laurae during the spawning period. The structures of the new secondary metabolite were established with an extensive spectroscopic analysis. The 1D and 2D nuclear magnetic resonance (NMR) data of the compounds were discussed. We discovered that the C-15 of 1 contains two methyl groups on a carbon bearing an acetyl group, which has not been reported previously. In addition, Compounds 1, 3, and 4 showed selective cytotoxic activity against Molt 4, while 2 exhibited significant cytotoxicity against Molt 4, K562, Sup-T1 and U937 cell lines.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antozoários / Metabolismo Secundário Limite: Animals / Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antozoários / Metabolismo Secundário Limite: Animals / Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2021 Tipo de documento: Article