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Published September 30, 2020 | Version v1
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Ten undescribed cembrane-type diterpenoids from the gum resin of Boswellia sacra and their biological activities

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Wang, Jia-Jia, Sun, Hao-Ran, Suo, Xin-Yue, Wang, Xue, Sun, Hua, Wang, Xiao-Liang, Jiang, Jian-Dong, Ji, Teng-Fei (2020): Ten undescribed cembrane-type diterpenoids from the gum resin of Boswellia sacra and their biological activities. Phytochemistry (112425) 177: 1-10, DOI: 10.1016/j.phytochem.2020.112425, URL: http://dx.doi.org/10.1016/j.phytochem.2020.112425

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urn:lsid:plazi.org:pub:BB24FFE8FFA8FFB8FF90FFF3FF86FF93

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Figure: 10.5281/zenodo.8295796 (DOI)
Figure: 10.5281/zenodo.8295798 (DOI)
Figure: 10.5281/zenodo.8295800 (DOI)
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Figure: 10.5281/zenodo.8295810 (DOI)

References

  • Al-Harrasi, A., Csuk, R., Khan, A., Hussain, J., 2019. Distribution of the anti-inflammatory and anti-depressant compounds: incensole and incensole acetate in genus Boswellia. Phytochemistry 161, 28-40.
  • Breitmaier, E., 2006. Terpenes: Flavors, Fragrances, Pharmaca, Pheromones. John Wiley & Sons.
  • Chen, W.T., Li, Y., Guo, Y.W., 2012. Terpenoids of Sinularia soft corals: chemistry and bioactivity. Acta Pharm. Sin. B 2 (3), 227-237.
  • Cheng, S.Y., Wen, Z.H., Chiou, S.F., Hsu, C.H., Wang, S.K., Dai, C.F., Chiang, M.Y., Duh, C.Y., 2008. Durumolides A-E, anti-inflammatory and antibacterial cembranolides from the soft coral Lobophytum durum. Tetrahedron 64 (41), 9698-9704.
  • Corsano, S., Nicoletti, R., 1967. The structure of incensole. Tetrahedron 23 (4), 1977-1984.
  • CotC, Pharmacopia, 2015. The Chinese Pharmacopeia, 1 China. Medical Science Press, Beijing, pp. 223.
  • Frelek, J., Szczepek, W., 1999. [Rh2 (OCOCF3)] as an auxiliary chromophore in chiroptical studies on steroidal alcohols. Tetrahedron: Asymmetry 10 (8), 1507-1520.
  • Gerards, M., Snatzke, G., 1990. Circular dichroism, XCIII determination of the absolute configuration of alcohols, olefins, epoxides, and ethers from the CD of their "in situ" complexes with [Rh2 (O2CCF3) 4]. Tetrahedron: Asymmetry 1 (4), 221-236.
  • Greve, H.L., Kaiser, M., Brun, R., Schmidt, T., 2017. Terpenoids from the oleo-gum-resin of Boswellia serrata and their antiplasmodial effects in vitro. Planta Med. 83 (14/15), 1214-1226.
  • Heemann, V., Bylov, A.M., Brummer, U., Hass, W., Seehofer, F., 1983. 3, 7, 11, 15- Cembratetraen-6-ol, a new cembranoid from tobacco, III. Z. Naturforsch. C Biosci. 38 (7-8), 517-518.
  • Jiangsu New Medical College, 1977. Dictionary of Chinese Materia Medicia. Shanghai People's Publisher, Shanghai, pp. 1379-1380.
  • Li, F., Xu, K., Yuan, S., Yan, D., Liu, R., Tan, J., Zeng, G., Zhou, Y., Tan, G., 2010. Macrocyclic diterpenes from Boswellia carterii Birdwood (frankincense). Chin. J. Org. Chem. 30, 107-111.
  • Li, C., Li, C.J., Ma, J., Chen, F.Y., Li, L., Wang, X.L., Zhang, D.M., 2018. Magterpenoids A-C, three polycyclic meroterpenoids with PTP1B inhibitory activity from the bark of magnolia officinalis var. biloba. Org. Lett. 20 (12), 3682-3686.
  • Lin, W.Y., Su, J.H., Lu, Y., Wen, Z.H., Dai, C.F., Kuo, Y.H., Sheu, J.H., 2010. Cytotoxic and anti-inflammatory cembranoids from the Dongsha Atoll soft coral Sarcophyton crassocaule. Bioorg. Med. Chem. 18 (5), 1936-1941.
  • Liu, Y.M., 1999. Pharmacography of Uighur, Part One. Xinjiang Science Technology and Hygiene Publishing House, Urumqi, pp. 222.
  • Matsuzawa, A., Shiraiwa, J., Kasamatsu, A., Sugita, K., 2018. Enantioselective, protectinggroup-free total synthesis of boscartin. F. Org. Lett. 20 (4), 1031-1033.
  • Maya, S., Prakash, T., Madhu, K., 2018. Assessment of neuroprotective effects of Gallic acid against glutamate-induced neurotoxicity in primary rat cortex neuronal culture. Neurochem. Int. 121, 50-58.
  • Morikawa, T., Matsuda, H., Yoshikawa, M., 2017. A review of anti-inflammatory terpenoids from the incense gum resins frankincense and myrrh. J. Oleo Sci., ess16149.
  • Nicoletti, R., Forcellese, M., 1968. The structure of incensole-oxide. Tetrahedron 24 (22), 6519-6525.
  • Ren, J., Wang, Y.G., Wang, A.G., Wu, L.Q., Zhang, H.J., Wang, W.J., Su, Y.L., Qin, H.L., 2015. Cembranoids from the gum resin of Boswellia carterii as potential antiulcerative colitis agents. J. Nat. Prod. 78 (10), 2322-2331.
  • Sun, X.W., Geng, Y.L., Wang, X., Qin, D.W., Yu, J.Q., 2020. Cembrane-type diterpenoids from the gum resin of Boswellia carterii and their biological activities. RSC Adv. 10 (2), 746-755.
  • Wang, Y.G., Ren, J., Wang, A.G., Yang, J.B., Ji, T.F., Ma, Q.G., Tian, J., Su, Y.l., 2013. Hepatoprotective prenylaromadendrane-type diterpenes from the gum resin of Boswellia carterii. J. Nat. Prod. 76 (11), 2074-2079.
  • Wang, Y.G., Ren, J., Ma, J., Yang, J.B., Ji, T.F., Wang, A.G., 2019a. Bioactive cembrane-type diterpenoids from the gum-resin of Boswellia carterii. Fitoterapia 137, 104263.
  • Wang, J.J., Zhen, B., Hu, J.W., Shi, M.J., Wei, C.J., Wang, X., Sun, H., Ji, T.F., 2019b. Boscartins L-O: cembrane-type diterpenoids from the gum resin of Boswellia sacra Flueck. Phytochemistry 163, 126-131.
  • Xiao, P.G., Li, D.P., Yang, S.L., 2002. Modern Chinese Materia Medica Three. Chemical Industry Press, Beijing, pp. 856-859.
  • Yang, B., Zhou, X.F., Lin, X.P., Liu, J., Peng, Y., Yang, X.W., Liu, Y., 2012. Cembrane diterpenes chemistry and biological properties. Curr. Org. Chem. 16 (12), 1512.
  • Yu, J.Q., Geng, Y.L., Zhao, H., Wang, X., 2018. Diterpenoids from the gum resin of Boswellia carterii and their biological activities. Tetrahedron 74 (40), 5858-5866.
  • Zhao, M., Yin, J., Jiang, W., Ma, M., Lei, X., Xiang, Z., Dong, J., Huang, K., Yan, P., 2013. Cytotoxic and antibacterial cembranoids from a South China Sea soft coral. Lobophytum sp. Mar. Drugs 11 (4), 1162-1172.
  • Zhou, J., Cui, R., 2002. Chemical components of Boswellia carterii. Acta Pharm. Sin. 37 (8), 633-635.