孟松, 张莉亭, 曾建昂, 魏斌, 王鸿, 郭跃伟, 苏明智. 短指软珊瑚Sinularia sp.的化学成分和生物活性研究J. 药学学报, 2026, 61(2): 536-541. DOI: 10.16438/j.0513-4870.2025-1118
引用本文: 孟松, 张莉亭, 曾建昂, 魏斌, 王鸿, 郭跃伟, 苏明智. 短指软珊瑚Sinularia sp.的化学成分和生物活性研究J. 药学学报, 2026, 61(2): 536-541. DOI: 10.16438/j.0513-4870.2025-1118
MENG Song, ZHANG Li-ting, ZENG Jian-ang, WEI Bin, WANG Hong, GUO Yue-wei, SU Ming-zhi. Study on the chemical constituents and biological activity of soft coral Sinularia sp.J. Acta Pharmaceutica Sinica, 2026, 61(2): 536-541. DOI: 10.16438/j.0513-4870.2025-1118
Citation: MENG Song, ZHANG Li-ting, ZENG Jian-ang, WEI Bin, WANG Hong, GUO Yue-wei, SU Ming-zhi. Study on the chemical constituents and biological activity of soft coral Sinularia sp.J. Acta Pharmaceutica Sinica, 2026, 61(2): 536-541. DOI: 10.16438/j.0513-4870.2025-1118

短指软珊瑚Sinularia sp.的化学成分和生物活性研究

Study on the chemical constituents and biological activity of soft coral Sinularia sp.

  • 摘要: 综合运用薄层色谱、硅胶正相柱层析、十八烷基硅烷反相柱层析、凝胶(Sephadex LH-20) 柱层析、高效液相色谱(HPLC) 等多种分离技术对采集自中国南海三亚西瑁岛附近海域的短指软珊瑚Sinularia sp.的化学成分进行分离, 并通过核磁(NMR)、质谱(MS)、红外(IR) 以及量子化学计算等方法确定化合物的平面结构和立体构型。从该短指软珊瑚中分离得到了6个化合物, 分别鉴定为(3R, 6S)-3-((R)-sec-butyl)-6-isopropylmorpholine-2, 5-dione (1)、oculatolide (2)、octahydro-4-hydroxy-3R-methyl-7-methylene-R-(1-methylethyl)-1H-indene-1-methanol (3)、ent-4(15)-eudesmene-1β, 6α-diol (4)、5-epi-eudesm-4(15)-ene-1β, 6β-diol (5)、ergosterol peroxide (6)。其中, 化合物1为新吗啉类化合物, 且化合物3~5为首次从该属软珊瑚中分离得到。在生物活性方面, 对化合物1~6进行了抗菌、抗炎和抗肿瘤活性筛选, 其中化合物2和化合物6具有显著且广谱的抗菌活性, 化合物2有较强的抗炎活性(IC50 = 5 ± 0.03 mmol·L-1) 且对人非小细胞肺癌细胞(A549)、人结直肠腺癌细胞(HT-29) 有较强的抗增殖活性, IC50分别为17.27 ± 2.32和14.14 ± 0.72 mmol·L-1

     

    Abstract: The chemical constituents of the soft coral Sinularia sp. collected off Ximao Island in the South China Sea were isolated by comprehensively utilizing various separation techniques such as thin-layer chromatography, silica gel column chromatography, octadecylsilane reverse phase column chromatography, Sephadex LH-20 column chromatography, and high-performance liquid chromatography (HPLC). The planar structure and stereochemistry of the isolated compounds were determined by nuclear magnetic resonance (NMR), mass spectrometry (MS), infrared spectroscopy (IR), and quantum chemical calculations. Six compounds were isolated from the titled soft coral and identified as (3R, 6S)-3-((R)-sec-butyl)-6-isopropylmorpholine-2, 5-dione (1), oculatolide (2), octahydro-4-hydroxy-3R-methyl-7-methylene-R-(1-methylethyl)-1H-indene-1-methanol (3), ent-4(15)-eudesmene-1β, 6α-diol (4), 5-epi-eudesm-4(15)-ene-1β, 6β-diol (5), and ergosterol peroxide (6), respectively. Among them, compound 1 was characterized as a new morpholine derivative, and compounds 3-5 were isolated for the first time from this genus of soft corals. In terms of biological activity, compounds 1-6 underwent screening for antibacterial, anti-inflammatory, and anti-cancer activities, compounds 2 and 6 exhibited significant and broad-spectrum antimicrobial activity, while compound 2 also showed potent anti-inflammatory (IC50 = 5 ± 0.03 mmol·L-1) and strong anti-proliferative activity against human non-small cell lung cancer cells (A549) and human colorectal adenocarcinoma cells (HT-29) with IC50 values of 17.27 ± 2.32 and 14.14 ± 0.72 mmol·L-1, respectively.

     

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