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Published July 31, 2022 | Version v1
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Abietane diterpenes from the twigs and leaves of Cephalotaxus oliveri Mast. with antitumor activity

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  • 1. ** & * & Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, And School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical

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Jiang, Chunyu, Yang, Mengyue, Zhao, Chunxue, Liu, Fangshen, Yang, Hangao, Li, Zhanlin, Han, Tong, Lin, Bin, Li, Dahong, Hua, Huiming (2022): Abietane diterpenes from the twigs and leaves of Cephalotaxus oliveri Mast. with antitumor activity. Phytochemistry (113187) 199: 1-8, DOI: 10.1016/j.phytochem.2022.113187, URL: http://dx.doi.org/10.1016/j.phytochem.2022.113187

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urn:lsid:plazi.org:pub:3F76D8348F76FF921425FFFDFFDFFFD9

Cites
Publication: 10.1080/14786419.2017.1343323 (DOI)
Publication: 10.1016/0031-9422(90)80044-H (DOI)
Publication: 10.1021/np50060a002 (DOI)
Publication: 10.1021/np040219h (DOI)
Publication: 10.1016/j.phytol.2020.01.005 (DOI)
Publication: 10.1080/14786419.2017.1314280 (DOI)
Publication: 10.1021/acs.jafc.0c01347 (DOI)
Publication: 10.2174/1381612826666200331082917 (DOI)
Publication: 10.1016/0031-9422(88)80134-1 (DOI)
Publication: 10.1039/c4np00110a (DOI)
Publication: 10.1016/j.ejmech.2014.10.023 (DOI)
Publication: 10.1016/0031-9422(92)80282-J (DOI)
Publication: 10.1039/C4RA10665B (DOI)
Publication: 10.1016/j.phytochem.2021.112939 (DOI)
Publication: 10.1021/acs.jnatprod.0c01180 (DOI)
Publication: 10.1016/S0040-4020(03)00883-4 (DOI)
Publication: 10.1080/14786410802267510 (DOI)
Publication: 10.1016/j.bmcl.2013.10.040 (DOI)
Publication: 10.1016/j.cclet.2014.03.024 (DOI)
Publication: 10.1016/0031-9422(93)85463-2 (DOI)
Publication: 10.1016/j.bioorg.2020.104445 (DOI)
Publication: 10.3390/plants10010175 (DOI)
Publication: 10.1039/C7RA13309J (DOI)
Publication: 10.1016/S0031-9422(00)94837-4 (DOI)
Publication: 10.1016/j.phytochem.2019.02.008 (DOI)
Publication: 10.1021/acs.jnatprod.6b00802 (DOI)
Publication: 10.1016/s1875-5364(11)60060-5 (DOI)
Has part
Figure: 10.5281/zenodo.8237246 (DOI)
Figure: 10.5281/zenodo.8237248 (DOI)
Figure: 10.5281/zenodo.8237250 (DOI)
Figure: 10.5281/zenodo.8237252 (DOI)
Figure: 10.5281/zenodo.8237254 (DOI)
Figure: 10.5281/zenodo.8237256 (DOI)

References

  • Ahmed, A., Li, W., Zhang, J.S., Sam, P.H., Zou, Y.H., Tang, G.H., Yin, S., 2018. A new bisabolane sesquiterpenoid and a new abietane diterpenoid from Cephalotaxus sinensis. Nat. Prod. Res. 32, 175-181. https://doi.org/10.1080/ 14786419.2017.1343323.
  • Ara, I., Siddiqui, B.S., Faizi, S., Siddiqui, S., 1990. Tricyclic diterpenoids from root bark of Azadzrachta indica. Phytochemistry 29, 911-914. https://doi.org/10.1016/0031- 9422(90)80044-H.
  • Ara, I., Siddiqui, B.S., Faizi, S., Siddiqui, S., 1988. Tricyclic diterpenoids from the stem bark of Azadzrachta indica. J. Nat. Prod. 51, 1054-1061. https://doi.org/10.1021/ np50060a002.
  • Bai, J., Ito, N., Sakai, J., Kitabatake, M., Fujisawa, H., Bai, L., Dai, J.G., Zhang, S.J., Hirose, K., Tomida, A., Tsuruo, T., Ando, M., 2005. Taxoids and abietanes from callus cultures of Taxus cuspidata. J. Nat. Prod. 68, 497-501. https://doi.org/ 10.1021/np040219h.
  • Chen, B.S., Wang, S.X., Liu, G.Q., Bao, L., Huang, Y., Zhao, R.L., Liu, H.W., 2020a. Anti-inflammatory diterpenes and steroids from peels of the cultivated edible mushroom Wolfiporia cocos. Phytochem. Lett. 36, 11-16. https://doi.org/10.1016/j. phytol.2020.01.005.
  • Chen, X.J., Ni, L., Bao, M.F., Wang, L., Cai, X.H., 2017. Abietane diterpenoids from Cephalotaxus lanceolata. Nat. Prod. Res. 31, 2473-2478. https://doi.org/10.1080/ 14786419.2017.1314280.
  • Chen, X.L., Luo, Q.Y., Hu, W.Y., Chen, J.J., Zhang, R.P., 2020b. Abietane diterpenoids with antioxidative damage activity from Rosmarinus officinalis. J. Agric. Food Chem. 68, 5631-5640. https://doi.org/10.1021/acs.jafc.0c01347.
  • Etsassala, N., Cupido, C.N., Iwuoha, E.I., Hussein, A.A., 2020. Abietane diterpenes as potential candidates for the management of type 2 diabetes. Curr. Pharmaceut. Des. 26, 2885-2891. https://doi.org/10.2174/1381612826666200331082917.
  • Feliciano, A.S., Medarde, M., Lopez, J.L., Miguel, J.M., Puebla, P., Barrero, A.F., 1988. Terpenoids from leaves of Juniperus thurifera. Phytochemistry 27, 2251. https://doi. org/10.1016/0031-9422(88)80134-1.
  • Gonz´alez, M.A., 2015. Aromatic abietane diterpenoids: their biological activity and synthesis. Nat. Prod. Rep. 32, 684-704. https://doi.org/10.1039/c4np00110a.
  • Gonzalez, M.A., 2014. Synthetic derivatives of aromatic abietane diterpenoids and their biological activities. Eur. J. Med. Chem. 87, 834-842. https://doi.org/10.1016/j. ejmech.2014.10.023.
  • Gonzalez, A.G., Andres, L.S., Aguiar, Z.E., Luis, J.G., 1992. Diterpenes from Salua mellifera and their biogenetic significance. Phytochemistry 31, 1297-1305. https:// doi.org/10.1016/0031-9422(92)80282-J.
  • He, Y.R., Shen, Y.H., Shan, L., Yang, X., Wen, B., Ye, J., Yuan, X., Li, H.L., Xu, X.K., Zhang, W.D., 2015. Diterpenoid lanceolatins A-G from Cephalotaxus lanceolata and their anti-inflammatory and anti-tumor activities. RSC Adv. 5, 4126-4134. https:// doi.org/10.1039/C4RA10665B.
  • Jiang, C.Y., Xue, J.J., Yuan, Y.Z., Li, Y.Z., Zhao, C.X., Jing, Q.X., Zhang, X., Yang, M.Y., Han, T., Bai, J., Li, Z.L., Li, D.H., Hua, H.M., 2021. Progress in structure, synthesis and biological activity of natural cephalotane diterpenoids. Phytochemistry 192, 112939. https://doi.org/10.1016/j.phytochem.2021.112939.
  • Kadir, A., Zheng, G., Zheng, X., Jin, P., Maiwulanjiang, M., Gao, B., Aisa, H.A., Yao, G., 2021. Structurally diverse diterpenoids from the roots of Salvia deserta based on nine different skeletal types. J. Nat. Prod. 84, 1442-1452. https://doi.org/10.1021/acs. jnatprod.0c01180.
  • Li, A., She, X.G., Zhang, J.Y., Wu, T.X., Pan, X.F., 2003. Synthesis of C-7 oxidized abietane diterpenes from racemic ferruginyl methyl ether. Tetrahedron 59, 5737-5741. https://doi.org/10.1016/S0040-4020(03)00883-4.
  • Li, W.H., Chang, S.T., Chang, S.C., Chang, H.T., 2008. Isolation of antibacterial diterpenoids from Cryptomeria japonica bark. Nat. Prod. Res. 22, 1085-1093. https:// doi.org/10.1080/14786410802267510.
  • Li, S., Wang, P., Deng, G., Yuan, W., Su, Z., 2013. Cytotoxic compounds from invasive giant salvinia (Salvinia molesta) against human tumor cells. Bioorg. Med. Chem. Lett 23, 6682-6687. https://doi.org/10.1016/j.bmcl.2013.10.040.
  • Long, H.P., Li, F.S., Xu, K.P., Yang, Z.B., Li, J., Peng, J., Tan, G.S., 2014. Bioactive compounds from Selaginella involven Spring that protect PC-12 cells. Chin. Chem. Lett. 25, 805-808. https://doi.org/10.1016/j.cclet.2014.03.024.
  • Luis, J.G., Andres, L.S., 1993. C-16 Hydroxylated abitane diterpene from Salvia malufera. Phytochemistry 33, 635-638. https://doi.org/10.1016/0031-9422(93)85463-2.
  • Ma, G.L., Guo, N., Wang, X.L., Li, J., Jin, Z.X., Han, Y., Dong, S.Z., Xiong, J., Hu, J.F., 2020. Cytotoxic secondary metabolites from the vulnerable conifer Cephalotaxus oliveri and its associated endophytic fungus Alternaria alternate Y-4-2. Bioorg. Chem. 105, 104445. https://doi.org/10.1016/j.bioorg.2020.104445.
  • Ndjoubi, K.O., Sharma, R., Badmus, J.A., Jacobs, A., Jordaan, A., Marnewick, J., Warner, D.F., Hussein, A.A., 2021. Antimycobacterial, cytotoxic, and antioxidant activities of abietane diterpenoids isolated from Plectranthus madagascariensis. Plants 10, 175. https://doi.org/10.3390/plants10010175.
  • Perard-Viret, J., Quteishat, L., Alsalim, R., Royer, J., Dumas, F., 2017. Cephalotaxus alkaloids, alkaloids. Chem. Biol. 78, 205-352.
  • Pu, D.B., Wang, T., Zhang, X.J., Gao, J.B., Zhang, R.H., Li, X.N., Wang, Y.M., Li, X.L., Wang, H.Y., Xiao, W.L., 2018. Isolation, identification and bioactivities of abietane diterpenoids from Premna szemaoensis. RSC Adv. 8, 6425-6435. https://doi.org/ 10.1039/C7RA13309J.
  • Su, W.C., Fang, J.M., Cheng, Y.S., 1994. Abietanes and kauranes from leaves of Cryptomeria japonica. Phytochemistry 35, 1279-1284. https://doi.org/10.1016/ S0031-9422(00)94837-4.
  • Tu, W.C., Qi, Y.Y., Ding, L.F., Yang, H., Liu, J.X., Peng, L.Y., Song, L.D., Gong, X., Wu, X. D., Zhao, Q.S., 2019. Diterpenoids and sesquiterpenoids from the stem bark of Metasequoia glyptostroboides. Phytochemistry 161, 86-96. https://doi.org/10.1016/j. phytochem.2019.02.008.
  • Xiao, S., Ding, J., 2017. Chemical constituents from the twigs and leaves of the endangered plant Cephalotaxus oliveri. J. Chin. Med. Mater. 40, 2594-2597.
  • Zhang, Y., Li, Y., Ye, J.H., Zhang, J.J., Zou, J., Pan, L.T., 2019. The abietane type diterpenes from Isodon (Bl.) Hassk. Chin. J. Ethnomed. Ethnopharmacy 28, 40-47.
  • Zhao, J.X., Fan, Y.Y., Xu, J.B., Gan, L.S., Xu, C.H., Ding, J., Yue, J.M., 2017. Diterpenoids and lignans from Cephalotaxus fortunei. J. Nat. Prod. 80, 356-362. https://doi.org/ 10.1021/acs.jnatprod.6b00802.
  • Zhao, W., Pu, J.X., Du, X., Su, J., Li, X.N., Yang, J.H., Xue, Y.B., Li, Y., Sun, H.D., 2011. Cytotoxic diterpenoids from Isodon adenolomus. Chin. J. Nat. Med. 9, 253-258. https://doi.org/10.1016/s1875-5364(11)60060-5.