天然产物研究与开发 ›› 2026, Vol. 38 ›› Issue (9): 1947-1953.doi: 10.16333/j.1001-6880.2026.9.008 cstr: 32307.14.1001-6880.2026.9.008

• 研究简报 • 上一篇    下一篇

爪哇木棉的化学成分及其抗肿瘤活性研究

朱  虹 1,王升志 1,彭佳琪 1,陈旭阳 2,张小坡 1∗,陈德力 1,3∗   

  1. 1海南医科大学& 海南省医学科学院药学院(热带药物创新与转化教育部工程研究中心& 海南省热带药用植物研究开发重点实验室);2 海南医科大学& 海南省医学科学院基础医学与生命科学学院 (热带转化医学教育部重点实验室),海口571199;3 道地药材品质保障与资源持续利用全国重点实验室,北京100700

  • 出版日期:2026-09-24 发布日期:2026-09-22
  • 基金资助:

    国家自然科学基金面上项目(82473803);中央本级重大增减支项目“名贵中药资源可持续利用能力建设项目”(2060302)

Chemical components and anti-tumor activities of Ceiba pentandra L.

ZHU Hong1,WANG Sheng-zhi1, PENG Jia-qi1,CHEN Xu-yang2,ZHANG Xiao-po1,CHEN De-li1,3∗   

  1. 1Engineering Research Center of Tropical Medicine Innovation and Transformation of Ministry of Education & Hainan Provincial Key Laboratory of Research and Development on Tropical Herbs,School of Pharmacy,Hainan Medical University/ Hainan Academy of Medical Sciences;2Key Laboratory of Tropical Translational Medicine of Ministry of Education,School of Basic Medicine and Life Sciences,Hainan Medical University/ Hainan Academy of Medical Sciences, Haikou 571199,China;3State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs,Beijing 100700,China

  • Online:2026-09-24 Published:2026-09-22

摘要:

为阐明爪哇木棉的化学成分和抗肿瘤活性,本研究采用硅胶柱色谱、半制备高效液相色谱技术等对爪哇木棉茎杆乙酸乙酯提取物进行分离纯化,结合NMR、MS 等现代波谱学方法鉴定所得化合物的结构,从中共分离鉴定了 19 个化合物,并采用CCK-8 法,评估了各化合物对BT549 和4T1 肿瘤细胞的体外细胞毒性。鉴定的19 个成分分别为:hibiscusterpene II(1)、hibiscone C(2)、7-hydroxycadalene(3)、7-hydroxycalamenene(4)、(1S)-1-methoxylacinilene C (5)、lacinilene C(6)、(7R,9R,10R)-3,9-di-hidroxicalameneno(7)、mansonone(8)、3ξ-(1ξ-羟基)-7-羟基-1-苯并呋喃酮 (9)、vavain(10)、cleomiscosin B(11)、( + )-medioresinol(12)、邻甲基苯甲醚(13)、对甲酚(14)、丁香醛(15)、(R)- (-)-mellein methyl ether(16)、丹蒽醌(17)、丁香酸乙酯(18)、β-谷甾醇(19)。其中,化合物1、2、4 ~ 9、11 ~ 18 为首次从该属中分离得到。化合物1、2、3、4、6、8、10 对BT549、4T1 细胞增殖有一定的抑制活性,且化合物4 和8 细胞毒活性显著。本研究首次系统阐明了爪哇木棉中的杜松烷型倍半萜类成分为关键的其抗肿瘤活性成分,为该植物在抗肿瘤药物开发中的进一步应用提供了科学依据。

关键词:

"> 爪哇木棉, 化学成分, 细胞毒活性, 杜松烷型倍半萜

Abstract:

To investigate the chemical constituents and anti-tumor activities of the pharmacological effects of Ceiba pentandra L. ,the study was carried out to isolate and purify the chemical components from the ethyl acetate extract of the stem using silica gel and semi-preparative high-performance liquid chromatography and identify the structures of the compounds by modern spectroscopic methods such as NMR,MS,and so on. Meanwhile,the cytotoxic activities of all compounds against BT549 and 4T1 tumor cells were evaluated using the CCK-8 assay. Nineteen compounds were isolated and identified as:hibiscusterpene II (1),hibiscone C (2),7-hydroxycadalene (3),7-hydroxycalamenene (4),(1S)-1-methoxylacinilene C(5),lacinilene C (6),(7R,9R,10R)-3,9-di-hidroxicalameneno (7),mansonone (8),3ξ-(1ξ-hydroxyethyl)-7-hydroxy-1-isobenzofuranone (9),vavain (10),cleomiscosin B(11),( + )-medioresinol (12),1-methoxy-2-methylbenzene (13),p-cresol (14),syringaldehyde (15),(R)-(-)-mellein methyl ether (16),chrysazin (17),ethyl syringate (18) and β-sitosterol (19). Compounds 1,2,4-9,11-18 were isolated for the first time from this genus. The results showed that compounds 1,2,3,4,6,8,and 10 exhibited inhibitory activity against the proliferation of both BT549 and 4T1 cells,among which compounds 4 and 8 demonstrated significant cytotoxicity. This study systematically elucidates for the first time that cadinane-type sesquiterpenoids are the key antitumor constituents in C. pentandra,thereby providing a scientific basis for its further application in anticancer drug development.

Key words:

"> Ceiba pentandra L., chemical constituents, cytotoxic activities, cadinane-type sesquiterpene

中图分类号: 

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