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中国南海鳞指形软珊瑚的化学成分和生物活性研究
引用本文:卜庆,杨敏,张玲,严献云,葛增跃,姚励功,梁林富,郭跃伟. 中国南海鳞指形软珊瑚的化学成分和生物活性研究[J]. 中国海洋药物, 2024, 43(1): 39-46
作者姓名:卜庆  杨敏  张玲  严献云  葛增跃  姚励功  梁林富  郭跃伟
作者单位:中南林业科技大学,中国科学院上海药物研究所 新药研究国家重点实验室,中南林业科技大学 材料科学与工程学院,中南林业科技大学 材料科学与工程学院,中南林业科技大学 材料科学与工程学院,中国科学院上海药物研究所 新药研究国家重点实验室,中南林业科技大学,中国科学院上海药物研究所 新药研究国家重点实验室
基金项目:国家自然科学基金资助项目(41876194)
摘    要:目的 对采自中国南海的鳞指形软珊瑚化学成分和生物活性进行研究。方法 综合利用薄层色谱、硅胶柱色谱、凝胶柱层析、半制备高效液相色谱(HPLC)等分离手段进行纯化,结合核磁共振(NMR)和质谱(MS)等波谱数据分析及比对文献数据,开展化合物的结构鉴定。结果 从鳞指形软珊瑚中共分离鉴定了18个化合物,包括2个倍半萜:(E)-β-金合欢烯(1)和β-榄香烯(2);6个二萜:xiguscabrate A(3)、19-hydroxylcembrene-C(4)、xiguscabrate B(5)、(11S,12S)-11,12-epoxycembrene-C(6)、sinulariol C(7)和isosarcophytoxide(8);9个降二萜:10-epi-gyrosanolide E(9)、scabrolide D(10)、scabrolide G(11)、5-epi-sinuleptolide(12)、sinuleptolide(13)、gyrosanolide F(14)、ineleganolide(15)、scabrolide A(16)和scabrolide B(17);1个甾醇:crassarosterol A(18)。结论 化合物1为首次从软珊瑚科软珊瑚中分离得到,2、9、12、13、15和18为首次从该种软珊瑚中分离得到。抗炎活性测试时,化合物8对脂多糖(LPS)诱导的B淋巴细胞的增殖具有显著的抑制作用(IC50 = 4.4 μmol/L)。

关 键 词:短指软珊瑚属  鳞指形软珊瑚    甾醇  抗炎活性
收稿时间:2022-05-09
修稿时间:2022-06-12

Study on the chemical constituents from South China Sea soft coral Sinularia scabra and their bioactivities
BU Qing,YANG Min,ZHANG Ling,YAN Xian-yun,GE Zeng-yue,YAO Li-gong,LIANG Lin-fu and GUO Yue-wei. Study on the chemical constituents from South China Sea soft coral Sinularia scabra and their bioactivities[J]. Chinese Journal of Marine Drugs, 2024, 43(1): 39-46
Authors:BU Qing  YANG Min  ZHANG Ling  YAN Xian-yun  GE Zeng-yue  YAO Li-gong  LIANG Lin-fu  GUO Yue-wei
Affiliation:College of Material Science and Engineering, Central South University of Forestry and Technology,State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences,State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica,Chinese Academy of Sciences,State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica,Chinese Academy of Sciences,State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica,Chinese Academy of Sciences,State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences,College of Material Science and Engineering, Central South University of Forestry and Technology,State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences
Abstract:Objective To investigate the chemical constituents and bioactivities of soft coral Sinularia scabra collected from South China Sea. Methods The isolation and purification of these compounds were performed by thin layer chromatography (TLC), silica gel, Sephadex LH-20 column chromatography and semi-preparative high performance liquid chromatography (HPLC). Their structures were characterized by analysis of NMR and MS data and comparison with the data reported in literature. Results Eighteen known compounds with diverse skeletons were isolated from the soft coral Sinularia scabra, including two sesquiterpenes: (E)-β-farnesene (1), β-elemene (2); six diterpenes: xiguscabrate A (3), 19-hydroxylcembrene-C (4), xiguscabrate B (5), (11S,12S)-11,12-epoxycembrene-C (6), sinulariol C (7), isosarcophytoxide (8), nine norditerpenes: 10-epi-gyrosanolide E (9), scabrolide D (10), scabrolide G (11), 5-epi-sinuleptolide (12), sinuleptolide (13), gyrosanolide F (14), ineleganolide (15), scabrolide A (16), scabrolide B (17); one sterol: crassarosterol A (18). Conclusion Eighteen known compounds with diverse structural features were obtained from the title specimen. Compound 1 was isolated from the family Alcyoniidae for the first time, while compounds 2, 9, 12, 13, 15 and 18 were isolated from this species for the first time. In the anti-inflammatory bioassay, compound 8 exhibited significant inhibitory against the proliferation of LPS-induced B cell (IC50 = 4.4 μmol/L).
Keywords:Sinularia   Sinularia scabra   terpenes   sterol   anti-inflammatory activity
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