Published February 28, 2023 | Version v1
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Anti-inflammatory diterpenoid alkaloids from Aconitum tanguticum (Maxim.) Stapf

  • 1. * & ** & Institute of Chinese Materia Medica, National Engineering Laboratory for Quality Control Technology of Chinese Herbal Medicines, China Academy of Chinese Medical

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Ye, Xiao, Wang, Yue, Chen, Qianwen, Feng, Qingmei, Liu, Ting, Feng, Weihong, Liang, Yaohua, Liu, Xiaoqian, Li, Chun, Wang, Zhimin (2023): Anti-inflammatory diterpenoid alkaloids from Aconitum tanguticum (Maxim.) Stapf. Phytochemistry (113524) 206: 1-16, DOI: 10.1016/j.phytochem.2022.113524, URL: http://dx.doi.org/10.1016/j.phytochem.2022.113524

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urn:lsid:plazi.org:pub:72766D5EFFCB7E5CD472FFDC2435FF83

References

  • Aneja, R., Pelletier, S.W., 1965. The diterpene alkaloids: the pyrolysis and absolute configuration of heteratisine. Tetrahedron Lett. 42, 215-223. https://doi.org/ 10.1016/S0040-4039(01)99596-6.
  • Bessonova, I.A., Saidkhodzhaeva, Sh A., 2000. Hetisane-type diterpenoid alkaloids.
  • Brouet, I., Ohshima, H., 1995. Curcumin, an anti-tumour promoter and anti-inflammatory agent, inhibits induction of nitric oxide synthase in activated macrophages. Biochem. Biophys. Res. Commun. 206, 533-540. https://doi.org/ 10.1006/bbrc.1995.1076.
  • Cao, J.X., Li, L.B., Ren, J., Jiang, S.P., Tian, R.R., Chen, X.L., Peng, S.L., Zhang, J., Zhu, H. J., 2008. Two new C20-diterpenoid alkaloids from the Tibetan medicinal plant Aconitum naviculare Stapf. Helv. Chim. Acta 91, 1954-1960. https://doi.org/ 10.1002/hlca.200890209.
  • Desai, H.K., Pelletier, S.W., 1993. C-NMR assignments for lactone-type norditerpenoid alkaloids. J. Nat. Prod. 56 (12), 2193-2197. https://doi.org/10.1021/np50102a027.
  • Fan, X.R., Yang, L.H., Lin, L.M., Li, C., Guo, S.S., Wang, Z.M., Wang, Z.J., Sui, F., 2019. Diterpenoid alkaloids from the whole plant of Aconitum tanguticum (Maxim.). Stapf. Phytochemistry 160, 71-77. https://doi.org/10.1016/j.phytochem.2018.11.008.
  • Joshi, B.S., Bai, Y.L., Chen, D.H., Pelletier, S.W., 1993. Tangirine, a novel dimeric alkaloid from Aconitum tanguticum (Maxim.) stapf, W. T. Wang. Tetrahedron Lett. 34 (47), 7252-7528. https://doi.org/10.1016/S0040-4039(00)60390-8.
  • Joshi, B.S., Chen, D.H., Zhang, X.L., Snyder, J.K., Pelletier, S.W., 1991. Tangutisine, a new diterpenoid alkaloid from Aconitum tanguticum (Maxim.) Stapf, W. T. Wang.
  • Heterocycles. 32 (9), 1793-1804. https://doi.org/10.3987/COM-91-5809.
  • Li, H.Y., Yan, B.C., Wei, L.X., Sun, H.D., Puno, P.T., 2021. Tangutidines A-C, three amphoteric diterpene alkaloids from Aconitum tanguticum. Natur Prod. & Biopro. 11, 459-464. https://doi.org/10.1007/s13659-021-00310-3.
  • Lin, L., Chen, D.L., Liu, X.Y., Chen, Q.H., Wang, F.P., Yang, C.Y., 2009. Bis-diterpenoid alkaloids from Aconitum Tanguticum var. trichocarpum. Nat. Prod. Commun. 4 (7), 897-901. https://doi.org/10.1177/1934578X0900400703.
  • Lin, L., Chen, D.L., Liu, X.Y., Chen, Q.H., Wang, F.P., 2010. Trichocarpinine, a novel hetidine-hetisine type bisditerpenoid alkaloid from Aconitum tanguticum var.
  • Li, L., Zhao, J.F., Wang, Y.B., Zhang, H.B., 2004. A novel 19, 21-secohetisan diterpenoid alkaloid from Aconitum tanguticum. Helv. Chim. Acta 87, 866-868. https://doi.org/ 10.1002/hlca.200490084.
  • Qu, S.J., Tan, C.H., Liu, Z.L., Jiang, S.H., Yu, L., Zhu, D.Y., 2011. Diterpenoid alkaloids from Aconitum tanguticum. Phytochem Lett 4, 144-146. https://doi.org/10.1016/j. phytol.2011.02.003.
  • Reinecke, M.G., Watson, W.H., Chang, C.D., Mei, Y.W., 1986. A 2-D NMR structure determination of guan-fu base Z, a new diterpene alkaloid from the Chinese herb guan-Bai-Fu-Tzu (Aconitum koreanum). Heterocycles 24, 49-61. https://doi.org/ 10.3987/R-1986-01-0049.
  • Shan, L.H., 2017. Studies on Dierpernoid Alkaloids Constituents of Four Herb Aconitum. Thesis. Southwest Jiaotong University, 203.
  • Shen, Y., Liang, W., Shi, Y., Kennelly, E.J., Zhao, D., 2020. Structural diversity, bioactivities, and biosynthesis of natural diterpenoid alkaloids. Nat. Prod. Rep. 37, 764-796. https://doi.org/10.1039/D0NP00002G.
  • Shin, E.M., Zhou, H.Y., Guo, L.Y., Kim, J.A., Lee, S.H., Merfort, I., Kang, S.S., Kim, H.S., Kim, S., Kim, Y.S., 2008. Anti-inflammatory effects of glycyrol isolated from Glycyrrhiza uralensis in LPS-stimulated RAW264.7 macrophages. Int.
  • Immunopharm. 8, 1524-1532. https://doi.org/10.1016/j.intimp.2008.06.008.
  • Thawabteh, A.M., Thawabteh, A., Lelario, F., Bufo, S.A., Scrano, L., 2021. Classification, toxicity and bioactivity of natural diterpenoid alkaloids. Molecules 26, 4103-4131. https://doi.org/10.3390/molecules26134103.
  • Wang, Y.B., Huang, R., Zhang, H.B., Li, L., 2005. Diterpenoid alkaloids from Aconitum tanguticum. Helv. Chim. Acta 88, 1081-1084. https://doi.org/10.1016/j.
  • Wu, G.T., Du, L.D., Zhao, L., Shang, R.F., Liu, D.L., Jing, Q., Liang, J.P., Ren, Y., 2014. The total alkaloids of Aconitum tanguticum protect against lipopolysaccharide-induced acute lung injury in rats. J. Ethnopharmacol. 155, 1483-1491. https://doi. org/10.1016/j.jep.2014.07.041.
  • Yang, L.H., Lin, L.M., Wang, Z.M., Li, C., Li, Z., 2016. Research progress on Aconitum tanguticum. Chin J Exp Tradit Med Form 22 (10), 43-49. https://doi.org/10.13422/j. cnki.syfjx.2016100043.
  • Yang, L.H., Wang, Y., Liu, X.Q., Liang, Y.H., Li, C., Wang, Z.M., 2021. A novel dimeric diterpenoid alkaloid from the Tibetan medicinal plant Aconitum tanguticum (Maxim.) Stapf. Acta Pharm. Sin. 56 (5), 1429-1433. https://doi.org/10.16438/j.0513- 4870.2020-1912.