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Four new bi-2-(2-phenylethyl)chromone derivatives of agarwood from Aquilaria crassna.
Yang, Yang; Mei, Wen-Li; Kong, Fan-Dong; Chen, Hui-Qin; Li, Wei; Chen, Zhi-Bao; Dai, Hao-Fu.
Afiliação
  • Yang Y; College of Life Science and Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
  • Mei WL; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China.
  • Kong FD; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China.
  • Chen HQ; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China.
  • Li W; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China.
  • Chen ZB; College of Life Science and Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China. Electronic address: chenzhibao_2000@sina.com.
  • Dai HF; Key Laboratory of Biology and Genetic Resources of Tropical Crops, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou 571101, China. Electronic address: daihaofu@itbb.org.cn.
Fitoterapia ; 119: 20-25, 2017 Jun.
Article em En | MEDLINE | ID: mdl-28300702
Four new bi-2-(2-phenylethyl)chromone derivatives, crassins A-D (1-4), were isolated from the EtOAc extract of agarwood originating from Aquilaria crassna. The structures including the absolute configurations of compounds were unambiguously elucidated by extensive spectroscopic methods (1D and 2D NMR, UV, ECD, IR, MS), and by comparison with the literature. The isolated compounds were tested for their acetylcholinesterase (AChE) and α-glucosidase inhibitory activities, as well as cytotoxic activities. All the compounds showed weak inhibitory activity against AChE, while compounds 3 and 4 also displayed weak cytotoxicity against human myeloid leukemia cell line (K562).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Madeira / Flavonoides / Thymelaeaceae Limite: Humans Idioma: En Revista: Fitoterapia Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Madeira / Flavonoides / Thymelaeaceae Limite: Humans Idioma: En Revista: Fitoterapia Ano de publicação: 2017 Tipo de documento: Article País de afiliação: China País de publicação: Holanda