Published January 31, 2022
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Lanostane triterpenoids from the fruiting bodies of Fomitopsis pinicola and their anti-inflammatory activities
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- 1. * & The Laboratory of Effective Substances of Jiangxi Genuine Medicinal Materials, College of Life Sciences, Jiangxi Normal University, Nanchang, 330022, China & * & Key Laboratory of Plant Resources and Chemistry of Arid Zone, State Key Laboratory of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical & State Key Laboratory of Natural Medicines and Jiangsu Key Laboratory of Bioactive Natural Product Research, School of Traditional Chinese Pharmacy, China
Description
Liu, Yushuang, Liu, Wei, Li, Miaomiao, Yuan, Tao (2022): Lanostane triterpenoids from the fruiting bodies of Fomitopsis pinicola and their anti-inflammatory activities. Phytochemistry (112985) 193: 1-9, DOI: 10.1016/j.phytochem.2021.112985, URL: http://dx.doi.org/10.1016/j.phytochem.2021.112985
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- urn:lsid:plazi.org:pub:FF9AFF87853BFF80FF82FFE52D7DFF97
References
- Ahamd, S., Hussain, G., Razaq, S., 1976. Triterpenoids of Phellinus gilvus. Phytochemistry 15. https://doi.org/10.1016/S0031-9422(00)88876-7, 2000.
- Akihisa, T., Mizushina, Y., Ukiya, M., oshikubo, M., kondo, S., kimura, Y., Tai, T., 2004. Dehydrotrametenonic acid and dehydroeburiconic acid from Poria cocos and their inhibitory effects on eukaryotic DNA polymerase α and β. Biosci. Biotechnol. Biochem. 68, 448-450. https://doi.org/10.1271/bbb.68.448.
- Chen, Y., Gao, J., Chen, Q., Liu, W., Qi, Y., Aisa, H.A., Yuan, T., 2020. Applanaic acids A-C, three new highly oxygenated lanostane triterpenoids from the fruiting bodies of Ganoderma applanatum. Nat. Prod. Res. 1-7 https://doi.org/10.1080/ 14786419.2020.1749612.
- de Silva, E.D., van der Sar, S.A., Santha, R.L., Wijesundera, R.L., Cole, A.L., Blunt, J.W., Munro, M.H., 2006. Lanostane triterpenoids from the Sri Lankan basidiomycete Ganoderma applanatum. J. Nat. Prod. 69, 1245-1248. https://doi.org/10.1021/ np0602214.
- Grienke, U., Z¨oll, M., Peintner, U., Rollinger, J.M., 2014. European medicinal polypores-A modern view on traditional uses. J. Ethnopharmacol. 154, 564-583. https://doi.org/10.1016/j.jep.2014.04.030.
- Haight, J.-E., Laursen, G.A., Glaeser, J.A., Taylor, D.L., 2016. Phylogeny of Fomitopsis pinicola: a species complex. Mycologia 108, 925-938. https://doi.org/10.3852/14- 225R1.
- Han, J., Li, L., Zhong, J., Tohtaton, Z., Ren, Q., Han, L., Yuan, T., 2016. Officimalonic acids A H, lanostane triterpenes from the fruiting bodies of Fomes officinalis. Phytochemistry 130, 193-200. https://doi.org/10.1016/j.phytochem.2016.05.004.
- Keller, A.C., Maillard, M.P., Hostettmann, K., 1996. Antimicrobial steroids from the fungus Fomitopsis pinicola. Phytochemistry 41, 1041-1046. https://doi.org/10.1016/ 0031-9422(95)00762-8.
- Khalilov, Q., Li, L., Liu, Y., Liu, W., Numonov, S., Aisa, H.A., Yuan, T., 2019. Brassinosteroid analogues from the fruiting bodies of Laetiporus sulphureus and their anti-inflammatory activity. Steroids 151, 108468. https://doi.org/10.1016/j. steroids.2019.108468.
- Kuo, P.C., Tai, S.H., Hung, C.C., Hwang, T.L., Kuo, L.M., Lam, S.H., Wu, T.S., 2020. Anti-inflammatory triterpenoids from the fruiting bodies of Fomitopsis pinicola. Bioorg. Chem. 104562. https://doi.org/10.1016/j.bioorg.2020.104562.
- Lee, S., Lee, D., Lee, S.O., Ryu, J.Y., Choi, S.Z., Kang, K.S., Kim, K.H., 2017. Anti-inflammatory activity of the sclerotia of edible fungus, Poria cocos Wolf and their active lanostane triterpenoids. J. Funct. Foods 32, 27-36. https://doi.org/10.1016/j. jff.2017.02.012.
- Liu, W., Gao, J., Li, M., Aisa, H.A., Yuan, T., 2021. Tirucallane triterpenoids from the mastic (Pistacia lentiscus) and their anti-inflammatory and cytotoxic activities. Phytochemistry 182, 112596. https://doi.org/10.1016/j.phytochem.2020.112596.
- Liu, J.Q., Wang, C.F., Li, Y., Luo, H.R., Qiu, M.H., 2012. Isolation and bioactivity evaluation of terpenoids from the medicinal fungus Ganoderma sinense. Planta Med. 78, 368-376. https://doi.org/10.1055/s-0031-1280441.
- Liu, X.T., Winkler, A.L., Schwan, W.R., Volk, T.J., Rott, M., Monte, A., 2010. Antibacterial compounds from mushrooms II: lanostane triterpenoids and an ergostane steroid with activity against Bacillus cereus isolated from Fomitopsis pinicola. Planta Med. 76, 464-466. https://doi.org/10.1055/s-0029-1186227. Muszy´nska, B., Fijalkowska, A., Sulkowska Ziaja, K., Wlodarczyk, A., Kaczmarczyk, P., Nogaj, E., Pietka, J., 2020. Fomitopsis officinalis: a species of arboreal mushroom with promising biological and medicinal properties. Chem. Biodivers. 17, 210-213. https://doi.org/10.1002/cbdv.202000213.
- Nukaya, H., Yamashiro, H., Fukazawa, H., Ishida, H., Tsuji, K., 1996. Isolation of inhibitors of TPA-induced mouse ear edema from Hoelen, Poria cocos. Chem. Pharm. Bull. 44, 847-849. https://doi.org/10.1248/cpb.44.847.
- Peng, X.R., Su, H.G., Liu, J.H., Huang, Y.J., Yang, X.Z., Li, Z.R., Qiu, M.H., 2019. C30 and C31 Triterpenoids and triterpene sugar esters with cytotoxic activities from edible mushroom Fomitopsis pinicola (Sw. Ex Fr.) krast. J. Agric. Food Chem. 67, 10330-10341. https://doi.org/10.1021/acs.jafc.9b04530.
- R¨osecke, J., K¨onig, W.A., 1999. Steroids from the fungus Fomitopsis pinicola. Phytochemistry 52, 1621-1627. https://doi.org/10.1016/S0031-9422(99)00349-0.
- R¨osecke, J., K¨onig, W.A., 2000. Constituents of the fungi Daedalea quercina and Daedaleopsis confragosa var. tricolor. Phytochemistry 54, 757-762. https://doi.org/ 10.1016/S0031-9422(00)00130-8.
- Shi, Z., Bao, H., Feng, S., 2017. Antitumor activity and structure-activity relationship of seven lanostane-type triterpenes from Fomitopsis pinicola and F. officinalis. China J. Chin. Mater. Med. 42, 915-922. https://doi.org/10.19540/j.cnki. cjcmm.20170121.017.
- Tai, T., Akahori, A., Shingu, T., 1993. Triterpenes of Poria cocos. Phytochemistry 32, 1239-1244. https://doi.org/10.1016/S0031-9422(00)95099-4.
- Tohtahon, Z., Xue, J., Han, J., Liu, Y., Hua, H., Yuan, T., 2017. Cytotoxic lanostane triterpenoids from the fruiting bodies of Piptoporus betulinus. Phytochemistry 143, 98-103. https://doi.org/10.1016/j.phytochem.2017.07.013.
- Wang, Y.G., Ma, Q.G., Tian, J., Ren, J., Wang, A.G., Ji, T.F., Su, Y.L., 2016. Hepatoprotective triterpenes from the gum resin of Boswellia carterii. Fitoterapia 109, 266-273. https://doi.org/10.1016/j.fitote.2015.12.018.
- Zhao, J., Yang, Y., Yu, M., Yao, K., Luo, X., Qi, H., Luo, Y., 2018. Lanostane-type C31 triterpenoid derivatives from the fruiting bodies of cultivated Fomitopsis palustris. Phytochemistry 152, 10-21. https://doi.org/10.1016/j.phytochem.2018.04.012.