Published November 30, 2021
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Cephalotaxine-type alkaloids from the seeds of Cephalotaxus fortunei and their cytotoxic activities
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Zhu, Li, Gong, Li-Jie, Zhu, Dong-Rong, Zhu, Jiang-Min, Li, Yin, Kong, Ling-Yi, Luo, Jian-Guang (2021): Cephalotaxine-type alkaloids from the seeds of Cephalotaxus fortunei and their cytotoxic activities. Phytochemistry (112903) 191: 1-8, DOI: 10.1016/j.phytochem.2021.112903, URL: http://dx.doi.org/10.1016/j.phytochem.2021.112903
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- urn:lsid:plazi.org:pub:2259AD7CFFA8FF8FDC429E10FFE77A5A
References
- Abdelkafi, H., Nay, B., 2012. Natural products from Cephalotaxus sp.: chemical diversity and synthetic aspects. Nat. Prod. Rep. 29, 845-869. https://doi.org/10.1039/ C2NP20037F.
- Bocar, M., Jossang, A., Bodo, B., 2003. New alkaloids from Cephalotaxus fortunei. J. Nat. Prod. 66, 152-154. https://doi.org/10.1021/np0203178.
- Fitzgerald, J.S., Johns, S.R., Lamberton, J.A., Sioumis, A.A., 1969. Alkaloids of Schelhammera pedunculata (liliaceae). Aust. J. Chem. 22, 2187-2201. https://doi. org/10.1071/CH9692203.
- Gurel, G., Blaha, G., Moore, B., P, A Steitz, T., 2009. U2504 determines the species specificity of the A-site cleft antibiotics: the structures of tiamulin, homoharringtonine, and bruceantin bound to the ribosome. J. Mol. Biol. 389, 146-156. https://doi.org/10.1016/j.jmb.2009.04.005.
- He, Y.R., Shen, Y.H., Li, B., Li, B., Lu, L., Tian, J.M., Zhang, W.D., 2013. Alkaloids from Cephalotaxus lanceolata and their cytotoxicities. Chem. Biodivers. 10, 584-595. https://doi.org/10.1002/cbdv.201200105.
- Kouam, S.F., Kusari, S., Lamshoft ยจ, M., Tatuedom, O.K., Spiteller, M., 2012. Sapelenins G- J, acyclic triterpenoids with strong anti-inflammatory activities from the bark of the Cameroonian medicinal plant Entandrophragma cylindricum. Phytochemistry 83, 79-86 https://doi.org/j.phytochem.2012.06.004.
- Li, H.X., Wen, Y.H., Wang, F.F., Wu, P., Wei, X.Y., 2015. Cephalofortunone, a structurally unique Cephalotaxus alkaloid from Cephalotaxus fortune Hook. f.. Tetrahedron Letters 56, 5735-5737. https://doi.org/10.1016/j.tetlet.2015.08.071.
- Ling, T.T., Lang, W.H., Maier, J., Centurion, M.Q., Rivas, F., 2019. Cytostatic and cytotoxic natural products against cancer cell models. Molecules 24. https://doi.org/ 10.3390/molecules24102012, 2012/1-2012/15.
- Mei, K.K., Wang, G.K., Cai, H.P., Luo, Z.H., 2019. Cephalounei A, a new cephalotaxus alkaloid from the powdered stems of Cephalotaxus fortune. Hook. f. Rec. Nat. Prod. 13 (6), 506-511. https://doi.org/10.25135/rnp.19.02.1197.
- Morita, H., Yoshinaga, M., Kobayash, J., 2002. Cephalezomines G, H, J, K, L, and M, new alkaloids from Cephalotaxus harringtonia var. nana. Tetrahedron 58, 5489-5495. https://doi.org/10.1002/chin.200243238.
- Ni, L., Schinnerl, J., Bao, M.F., Zhang, B.J., Wu, J., Cai, X.H., 2016a. Two key biogenetic intermediates of Cephalotaxus alkaloids from Cephalotaxus oliveri and C. lanceolata. Tetrahedron Lett. 57, 5201-5204. https://doi.org/10.1016/j.tetlet.2016.10.026.
- Ni, L., Zhong, X.H., Cai, J., Bao, M.F., Zhang, B.J., Wu, J., Cai, X.H., 2016b. Five new alkaloids from Cephalotaxus lanceolata and C. fortunei car. Alpine. Nat. Prod. Bioprospect. 6, 149-154. https://doi.org/10.1007/s13659-016-0093-7.
- Paudler, W.W., Kerley, G.I., McKay, J., 1963. The alkaloids of Cephalotaxus drupacea and Cephalotaxus fortunei. J. Org. Chem. 28, 2194-2197. https://doi.org/10.1021/ jo01044a010.
- Paudler, W.W., McKay, J., 1973. The structures of some of the minor alkaloids of cephalotaxus fortunei. J. Org. Chem. 38, 2110-2112. https://doi.org/10.1021/ jo00951a040.
- Pearson, W.H., Kropf, J.E., Choy, A.L., Lee, I.Y., Kampf, J.W., 2007. Approach to the homoerythrina alkaloids using a tandem N-Alkylation/Azomethine ylide cycloaddition. J. Org. Chem. 72, 4135-4148. https://doi.org/10.1021/jo0703799.
- Powell, R.G., Weisleder, D., Smith, C.R., Rohwedder, W.K., 1970. Structures of harringtonine, isoharringtonine, and homoharringtonine. Tetrahedron Lett. 11, 815-818. https://doi.org/10.1016/S0040-4039(01)97839-6.
- Powell, R.G., 1972. Structures of homoerythrina alkaloids from cephalotaxus harringtonia. Phytochemistry 11, 1467-1472. https://doi.org/10.1016/S0031-9422(00)90102-X.
- Powell, R.G., Madrigal, R.V., Smith, C.R., Mikolajczak, K.L., 1974. Alkaloids of Cephalotaxus harringtonia var. drupacea. 11-Hydroxycephalotaxine and Drupacine. J. Org. Chem. 39, 676-680. https://doi.org/10.1021/jo00919a020.
- Takano, I., Yasuda, I., Nishijima, M., Yanagi, Y., Takeya, K., Itokwa, H., 1997. Ester-type cephalotaxus alkaloids from cephalotaxus harringtonia var. Drupacea. Phytochemistry 44, 735-738. https://doi.org/10.1016/S0031-9422(96)00574-2.
- Taniguchi, T., Yokoyama, S., Ishibashi, H., 2009. Asymmetric total synthesis and revised structure of cephalezomine. H. J. Org. Chem. 74, 7592-7594 https://doi.org/ 101021/acs.joc.7b01231.
- Zhang, Y., Chen, C., Zhang, Y.L., Kong, L.Y., Luo, J.G., 2018. Target discovery of cytotoxic withanolides from Physalis angulata var. villosa via reactivity-based screening. J. Pharmaceut. Biomed. Anal. 151, 194-199. https://doi.org/10.1016/j. jpba.2017.12.047.