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玫瑰石斛的化学成分及其生物活性

庄晨曦 王慧敏 陈亚萍 张锐 郑金蓉 李美红 李玉鹏

昆明医科大学学报2023,Vol.44Issue(12):1-5,5.
昆明医科大学学报2023,Vol.44Issue(12):1-5,5.DOI:10.12259/j.issn.2095-610X.S20231231

玫瑰石斛的化学成分及其生物活性

Chemical Compounds Isolated from Dendrobium crepidatum and Their Bioactive Activities

庄晨曦 1王慧敏 2陈亚萍 3张锐 3郑金蓉 3李美红 3李玉鹏3

作者信息

  • 1. 昆明医科大学药学院暨云南省天然药物药理重点实验室,云南 昆明 650500||红河卫生职业学院药学院,云南 红河 661100||昆明医科大学现代生物医药产业学院,云南 昆明 650500
  • 2. 昆明医科大学药学院暨云南省天然药物药理重点实验室,云南 昆明 650500||云南传染病医院药剂科,云南 昆明 650301
  • 3. 昆明医科大学药学院暨云南省天然药物药理重点实验室,云南 昆明 650500||昆明医科大学现代生物医药产业学院,云南 昆明 650500
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摘要

Abstract

Objective To study the chemical constituents from the herbs of Dendrobium crepidatum and identify its antitumor bioactive compounds.Methods The constituents were extracted by methyl alcohol and isolated by CC and Sephadex LH-20.Their structures were identified by spectroscopic analysis(1H NMR,13CNMR and EIMS).The antitumor activity of the constituents was determined by MTT assay in vitro.Results 9 compouds were obtained and identified as p-hydroxybenzaldehyde(1),p-methoxyphenol(2),p-Hydroxybenzyl alcohol(3),hydroquinone(4),(24R)-ethylcholest-5-en-3-ol-7-one(5),sinalexin(6),bis(2-ethylhexyl)benzene-1,2-dicarboxylate(7),pinoresinol(8),Chaenomin B(9).The antitumor activity of compounds 5~9 was tested,and it was found that compound 9 had good inhibitory activity against A549 cell line.Conclusion Compounds 2~5,7~8 were isolated from the herbs for the first time and compounds 6,9 were isolated from this genus for the first time.IC50 of 9 on A549 cell line is 29.35 µM.

关键词

玫瑰石斛/化学成分/生物活性

Key words

Dendrobium crepidatum/Chemical constituents/Bioactive activity

分类

医药卫生

引用本文复制引用

庄晨曦,王慧敏,陈亚萍,张锐,郑金蓉,李美红,李玉鹏..玫瑰石斛的化学成分及其生物活性[J].昆明医科大学学报,2023,44(12):1-5,5.

基金项目

国家自然科学基金资助项目(21202066) (21202066)

云南省科技厅-昆明医科大学联合专项基金资助项目(202301AY070001-212) (202301AY070001-212)

云南省本科教育教学改革研究基金资助项目(JG2023001) (JG2023001)

昆明医科大学教研教改基金资助项目(2022-JY-S-08) (2022-JY-S-08)

云南省创新团队基金资助项目(202005AE160004) (202005AE160004)

云南省天然药物药理重点实验室开放研究基金资助项目(YKLPNP-G2407) (YKLPNP-G2407)

昆明医科大学学报

OACSTPCD

1003-4706

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