全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

白蓝翠雀花化学成分的提取及抑菌活性研究
Extraction and Antibacterial Activity of Chemical Components from Delphinium albocoeruleum Maxim.

DOI: 10.12677/jocr.2025.132013, PP. 126-132

Keywords: 天然产物,白蓝翠雀花,抑菌活性
Natural Products
, Delphinium albocoeruleum Maxim., Antibacterial Activity

Full-Text   Cite this paper   Add to My Lib

Abstract:

我国中医药文化历史悠久,白蓝翠雀花作为一味重要药材,主产于甘肃、青海、四川、西藏等高海拔地区,一般使用全草入药,具有清热燥湿功效,传统中医常将其用于痢疾、肠炎等临床治疗。通过文献可知,翠雀属植物中的主要成分为二萜生物碱和黄酮,但目前国内外缺乏对白蓝翠雀花化学成分的研究,故而本研究针对该物种分别使用薄层色谱法、硅胶柱层析法、高效液相色谱法等方法相互结合,分离并鉴定其中所含主要的化学成分。本研究共得到8个单体化合物,通过鉴定可知其分别为3个生物碱和5个黄酮类化合物,并使用滤纸片法检验其抑菌活性。发现这些化合物均对大肠杆菌有明显的抑制作用,但对枯草芽孢杆菌和其他真菌的抑制效果不好。
China has a long history of traditional Chinese medicine culture. Delphinium albocoeruleum Maxim., an important medicinal herb, is mainly produced in high-altitude regions such as Gansu, Qinghai, Sichuan, and Xizang. The whole herb is commonly used as a medicine, possessing the efficacy of clearing heat and drying dampness. Traditional Chinese medicine practitioners often apply it in clinical treatments for diseases such as dysentery and enteritis. Literature review indicates that the primary components of plants in the Delphinium genus are diterpenoid alkaloids and flavonoids. However, there is currently a lack of research on the chemical components of D. albocoeruleum both domestically and internationally. Therefore, this study employed a combination of methods including thin-layer chromatography (TLC), silica gel column chromatography, and high-performance liquid chromatography (HPLC) to isolate and identify the main chemical components. A total of 8 monomeric compounds were obtained in this study. Through identification, they were confirmed as 3 alkaloids and 5 flavonoid compounds. The antibacterial activity of these compounds was tested using the filter paper disc method. The results showed that all these compounds exhibited significant inhibitory effects against Escherichia coli, but had poor inhibitory effects on Bacillus subtilis and other fungi.

References

[1]  Liu, Y., Zhao, Y.D., Zhong, H.Y., et al. (2024) Diterpenoid Alkaloids from Delphinium liangshanense. Chemistry & Biodiversity, 21, e202301923.
[2]  Huang, S., Wang, J., Pu, Y., Liu, Y., Chen, Y., Chen, L., et al. (2024) Diterpenoid Alkaloids from Delphinium trichophorum. Phytochemistry, 225, Article ID: 114186.
https://doi.org/10.1016/j.phytochem.2024.114186
[3]  Nan, Z., Shang, Y., Deng, C., Zhu, Y., Jiang, G., Wang, Z., et al. (2024) Two New Cytotoxic Diterpenoid Alkaloids from Delphinium grandiflorum. Phytochemistry Letters, 61, 11-15.
https://doi.org/10.1016/j.phytol.2024.03.003
[4]  Li, X.Y., Chen, R.S., Li, G.C., et al. (2024) Four New Lycoctonine-Type C19-Diterpenoid Alkaloids from the Whole Plants of Delphinium kamaonense. Journal of Asian Natural Products Research, 27, 658-668.
[5]  Li, Q., Wang, Z., Wang, M., Yu, H., Chen, L., Cai, Z., et al. (2024) Brunonianines A-C, C20-Diterpenoid Alkaloids with Cyano Group from Delphinium brunonianum Royle. Phytochemistry, 219, Article ID: 113987.
https://doi.org/10.1016/j.phytochem.2024.113987
[6]  Li, Q., Gu, M., Wu, H., Xu, C., Yu, H., Zhang, Y., et al. (2024) Brunonianines D-F, Three New C19-Diterpenoid Alkaloids from the Delphinium brunonianum, with Therapeutic Effect on Ovarian Cancer in Vitro and in Vivo. Bioorganic Chemistry, 148, Article ID: 107478.
https://doi.org/10.1016/j.bioorg.2024.107478
[7]  Kurbanov, U.K., Levkovich, M.G. and Mukarramov, N.I. (2024) New Diterpene Alkaloid from Delphinium paradoxum. Chemistry of Natural Compounds, 60, 115-118.
https://doi.org/10.1007/s10600-024-04271-0
[8]  Wu, J., Li, G., Ruan, H., Lu, R., Huang, S., Chen, L., et al. (2025) Five New C19-Diterpenoid Alkaloids from Delphinium pachycentrum Hemsl. and Delphinium majus Ulbr. as Potential Acetylcholinesterase Inhibitors. Fitoterapia, 182, Article ID: 106431.
https://doi.org/10.1016/j.fitote.2025.106431
[9]  Wang, X., Xu, Y., Zhang, Z., Li, H. and Chen, L. (2025) C19-Diterpenoid Alkaloids Isolated from Delphinium forrestii var. viride. Phytochemistry, 233, Article ID: 114405.
https://doi.org/10.1016/j.phytochem.2025.114405
[10]  Sun, G., Fu, C., Yang, Y., Li, X., Ma, J., Huang, S., et al. (2024) Diterpenoid Alkaloids from Delphinium sherriffii. Journal of Asian Natural Products Research, 27, 143-152.
https://doi.org/10.1080/10286020.2024.2376244
[11]  刘世军, 廖志新, 唐志书, 等. 蓝翠雀花的化学成分研究[J]. 中药材, 2016(2): 318-321.
[12]  何隽, 邵倩, 付茂洁, 等. 大花还亮草中的黄酮类化合物[J]. 中南民族大学学报(自然科学版), 2018, 37(2): 60-62+73.
[13]  Alhilal, M., Sulaiman, Y., Alhilal, S., Gomha, S. and Ouf, S. (2021) Antifungal Activity of New Diterpenoid Alkaloids Isolated by Different Chromatographic Methods from Delphinium peregrinum L. var. eriocarpum Boiss. Molecules, 26, Article No. 1375.
https://doi.org/10.3390/molecules26051375
[14]  Jennings, K.R., Brown, D.G. and Wright, D.P. (1986) Methyllycaconitine, a Naturally Occurring Insecticide with a High Affinity for the Insect Cholinergic Receptor. Experientia, 42, 611-613.
https://doi.org/10.1007/bf01955557
[15]  Ahmad, S., Ahmad, H., Khan, H.U., Shahzad, A., Khan, E., Ali Shah, S.A., et al. (2016) Crystal Structure, Phytochemical Study and Enzyme Inhibition Activity of Ajaconine and Delectinine. Journal of Molecular Structure, 1123, 441-448.
https://doi.org/10.1016/j.molstruc.2016.06.051
[16]  郑思建, 徐婵, 杨洁, 等. 藏药抗肝癌活性研究[J]. 华中师范大学学报(自然科学版), 2017, 51(3): 328-334.
[17]  Meriçli, A.H., Pırıldar, S., Süzgeç, S., Bitiş, L., Meriçli, F., Özçelik, H., et al. (2006) Norditerpenoid Alkaloids from the Aerial Parts of Aconitum cochleare Woroschin. Helvetica Chimica Acta, 89, 210-217.
https://doi.org/10.1002/hlca.200690023
[18]  Usmanova, S.K., Tel’nov, V.A., Yunusov, M.S., Abdullaev, N.D., Shreter, A.I. and Filippova, G.B. (1987) Sepaconitine—A New Alkaloid from Aconitum septentrionale. Chemistry of Natural Compounds, 23, 734-737.
https://doi.org/10.1007/bf00596656
[19]  Park, H., Baek, M.Y., Cho, J.G., et al. (2011) Insecticidal Alkaloids on Aphids from Corydalis turtschaninovii Tubers. Journal of the Korean Society for Applied Biological Chemistry, 54, 345-352.
https://doi.org/10.3839/jksabc.2011.055
[20]  Lou, H., Li, G. and Wang, F. (2002) A Cytotoxic Diterpenoid and Antifungal Phenolic Compounds from Frullania muscicola Steph. Journal of Asian Natural Products Research, 4, 87-94.
https://doi.org/10.1080/10286020290027353
[21]  Aldana-Mejía, J.A., Ribeiro, V.P., Katragunta, K., Avula, B., Tatapudi, K.K., Bastos, J.K., et al. (2024) Chemical Characterization and Antimicrobial Activity of Green Propolis from the Brazilian Caatinga Biome. Plants, 13, Article No. 3576.
https://doi.org/10.3390/plants13243576
[22]  杨云裳, 何荔, 杨爱梅, 等. 藏药短穗兔耳草化学成分研究[J]. 中国中药杂志, 2005(2): 74-75.
[23]  周威, 程清洲, 陈新, 等. 浙江桐庐产蜂胶中黄酮类化合物研究[J]. 中华中医药杂志, 2013, 28(2): 394-397.
[24]  田菁, 赵毅民, 栾新慧. 马鞭草化学成分的研究[J]. 中国中药杂志, 2005(4): 29-30.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133