Published May 31, 2022
| Version v1
Journal article
Restricted
Pimarane, abietane, and labdane diterpenoids from Euphorbia pekinensis Rupr. and their anti-tumor activities
Creators
- 1. * & Key Laboratory of Shaanxi Administration of Traditional Chinese Medicine for TCM Compatibility, and Shaanxi Key Laboratory of New Drugs and Chinese Medicine
Description
Chen, Yan-Yan, Zeng, Xiao-Tao, Xu, Ding-Qiao, Yue, Shi-Jun, Fu, Rui-Jia, Yang, Xue, Liu, Zhao-Xi, Tang, Yu-Ping (2022): Pimarane, abietane, and labdane diterpenoids from Euphorbia pekinensis Rupr. and their anti-tumor activities. Phytochemistry (113113) 197: 1-8, DOI: 10.1016/j.phytochem.2022.113113, URL: http://dx.doi.org/10.1016/j.phytochem.2022.113113
Files
Restricted
The record is publicly accessible, but files are restricted to users with access.
Linked records
Additional details
Identifiers
- LSID
- urn:lsid:plazi.org:pub:B601FFECFF8CFF91FFACFFF3EC40BF63
References
- Benabdelaziz, I., G´omez-Ruiz, S., Benkhaled, M., Carralero, S., Schenker, P., Salm, A., Gertsch, J., Haba, H., 2018. New cycloartane-type ester triterpenes from Euphorbia pterococca and biological evaluation. Fitoterapia 127, 271-278. https://doi:10.10 16/j.fitote.2018.02.027.
- Block, S., Baccelli, C., Tinant, B., Van Meervelt, L., Rozenberg, R., Habib Jiwan, J.L., Llabres, G., De Pauw-Gillet, M.C., Quetin-Leclercq, J., 2004. Diterpenes from the leaves of Croton zambesicus. Phytochemistry 65, 1165-1171. https://doi.org/ 10.1016/j.phytochem.2004.02.023.
- Crespi-Perellino, N., Garofano, L., Arlandini, E., Pinciroli, V., 1996. Identification of new diterpenoids from Euphorbia calyptrata. Cell Cult. J. Nat. Prod. 59, 773-776. https://doi.org/10.1021/np960127v.
- Duarte, N., Lage, H., Ferreira, M.J., 2008. Three new jatrophane polyesters and antiproliferative constituents from Euphorbia tuckeyana. Planta Med. 74, 61-68. https://doi.org/10.1055/s-2007-993765.
- Duarte, N., Varga, A., Cherepnev, G., Radics, R., Molnar, J., Ferreira, M.J., 2007. Apoptosis induction and modulation of P-glycoprotein mediated multidrug resistance by new macrocyclic lathyrane-type diterpenoids. Bioorg. Med. Chem. 15, 546-554. https://doi.org/10.1016/j.bmc.2006.09.028.
- El-Bassuony, A.A., 2007. Antibacterial activity of new polyester diterpenes from Euphorbia guyoniana. Asian J. Chem. 19, 4553-4562.
- Hou, P., Zeng, Y., Ma, B., Bi, K., Chen, X., 2013. A new cytotoxic cembrane diterpene from the roots of Euphorbia pekinensis Rupr. Fitoterapia 90, 10-13. https://doi.org/ 10.1016/j.fitote.2013.07.004.
- Kong, L., Li, Y., Wu, X., MIn, Z., 2002. Cytotoxic diterpenoids from Euphorbia pekinensis. Planta Med. 68, 249-252. https://doi.org/10.1055/s-2002-23132.
- Liaw, C.C., Huang, H.T., Liu, H.K., Lin, Y.C., Zhang, L.J., Wei, W.C., Shen, C.C., Wu, C.L., Huang, C.Y., Kuo, Y.H., 2022. Cucurbitane-type triterpenoids from the vines of Momordica charantia and their anti-inflammatory, cytotoxic, and antidiabetic activity. Phytochemistry 195, 113026. https://doi.org/10.1016/j. phytochem.2021.113026.
- Oh, S., Oh, H.W., Lee, H.R., Yoon, S.Y., Oh, S.R., Ko, Y.E., Yoo, N., Jeong, J., Kim, J.W., 2016. Ingenane-type diterpene compounds from Euphorbia kansui modulate IFN-γ production through NF-κB activation. J. Sci. Food Agric. 96, 2635-2640. https://doi. org/10.1002/jsfa.7380.
- Shizuri, Y., Kosemuras, S., Yamamuras, H., Ohba, H., Ito, M., Saito, Y., 1983. Isolation and structures of helioscopinolides, new diterpenes from Euphorbia Helioscopia. L. Chem. Lett. 12, 65-68.
- Tao, W.W., Duan, J.A., Tang, Y.P., Yang, N.Y., Li, J.P., Qian, Y.F., 2013. Casbane diterpenoids from the roots of Euphorbia pekinensis. Phytochemistry 94, 249-253. https://doi.org/10.1016/j.phytochem.2013.06.009.
- Tian, R.Y., Lu, Y., Chen, D.F., 2016. Four new diterpenoids from the roots of Euphorbia pekinensis. Chem. Biodivers. 13, 1404-1409. https://doi.org/10.1002/ cbdv.201600091.
- Valente, C., Pedro, M., Duarte, A., Nascimento, M.S.J., Abreu, P.M., Ferreira, M.-J., 2004. Bioactive diterpenoids, a new jatrophane and two ent-abietanes, and other constituents from Euphorbia pubescens. J. Nat. Prod. 67, 902-904. https://doi.org/ 10.1021/np0400048.
- Vasas, A., Hohmann, J., 2014. Euphorbia diterpenes: isolation, structure, biological activity, and synthesis (2008-2012). Chem. Rev. 114, 8579-8612. https://doi.org/ 10.1021/cr400541j.
- Wei, W.J., Song, Q.Y., Zheng, Z.Q., Yao, X., Li, Y., Gao, K., 2018. Phytotoxic ent- Isopimarane-Type Diterpenoids from Euphorbia hylonoma. J. Nat. Prod. 81, 2381-2391. https://doi.org/10.1021/acs.jnatprod.8b00365.
- Xu, Y., Tang, P., Zhu, M., Wang, Y., Sun, D., Li, H., Chen, L., 2021. Diterpenoids from the genus Euphorbia: structure and biological activity (2013-2019). Phytochemistry 190, 112846. https://doi.org/10.1016/j.phytochem.2021.112846.
- Yan, X.L., Huang, J.L., Tang, Y.Q., Tang, G.H., Yin, S., 2020. Euphopanes A-C, three new diterpenoids from Euphorbia pekinensis. Nat. Prod. Res. 1-8 https://doi.org/ 10.1080/14786419.2020.1765342.
- Yan, X.L., Sang, J., Chen, S.X., Li, W., Tang, G.H., Gan, L.S., Yin, S., 2019. Euphorkanlide A, a highly modified ingenane diterpenoid with a C(24) appendage from Euphorbia kansuensis. Org. Lett. 21, 4128-4131. https://doi.org/10.1021/acs.orglett.9b01315.
- Yu, W.W., Ma, J.T., He, J., Li, Z.H., Liu, J.K., Feng, T., 2022. Cadinane sesquiterpenoids from the fungus Antrodiella albocinnamomea and their inhibitory activity against nitric oxide production. Phytochemistry 196, 113018. https://doi.org/10.1016/j. phytochem.2021.113081.