1 Xiao WL, Li RT, Huang SX, Pu JX, Sun HD. Triterpenoids from the Schisandraceae family. Nat Prod Rep. 2008;25:871-91. 2 Shi YM, Xiao WL, Pu JX, Sun HD. Triterpenoids from the Schisandraceae family:an update. Nat Prod Rep. 2015;32:367-410. 3 Yang P, Li J, Sun L, Yao M, Zhang X, Xiao WL, et al. Elucidation of the structure of pseudorubriflordilactone B by chemical synthesis. J Am Chem Soc. 2020;142:13701-8. 4 Liang CQ, Shi YM, Luo RH, Li XY, Gao ZH, Li XN, et al. Kadcoccitones A and B, two new 6/6/5/5-fused tetracyclic triterpenoids from Kadsura coccinea. Org Lett. 2012;14:6362-5. 5 Liang CQ, Shi YM, Li XY, Luo RH, Li Y, Zheng YT, et al. Kadcotriones A-C:tricyclic triterpenoids from Kadsura coccinea. J Nat Prod. 2013;76:2350-4. 6 Hu ZX, Shi YM, Wang WG, Li XN, Du X, Liu M, et al. Kadcoccinones A-F, new biogenetically related lanostane-type triterpenoids with diverse skeletons from Kadsura coccinea. Org Lett. 2015;17:4616-9. 7 Liang CQ, Shi YM, Wang WG, Hu ZX, Li Y, Zheng YT, et al. Kadcoccinic acids A-J, triterpene acids from Kadsura coccinea. J Nat Prod. 2015;78:2067-73. 8 Yang YP, Jian YQ, Liu YB, Ismail M, Xie QL, Yu HH, et al. Triterpenoids from Kadsura coccinea with their anti-inflammatory and inhibited proliferation of rheumatoid arthritis-fibroblastoid synovial cells activities. Front Chem. 2021;9:808870. 9 Xu HC, Hu K, Sun HD, Puno PT. Four 14(13→12)-abeolanostane triterpenoids with 6/6/5/6-fused ring system from the roots of Kadsura coccinea. Nat Prod Bioprospect. 2019;9:165-73. 10 Xu HC, Hu K, Shi XH, Tang JW, Li XN, Sun HD, et al. Synergistic use of NMR computation and quantitative interproton distance analysis in the structural determination of neokadcoccitane A, a rearranged triterpenoid featuring an aromatic ring D from Kadsura coccinea. Org Chem Front. 2019;6:1619-26. 11 Pu JX, Xiao WL, Lu Y, Li RT, Li HM, Zhang L, et al. Kadlongilactones A and B, two novel triterpene dilactones from Kadsura longipedunculata possessing a unique skeleton. Org Lett. 2005;7:5079-82. 12 Zanardi MM, Marcarino MO, Sarotti AM. Redefining the impact of Boltzmann analysis in the stereochemical assignment of polar and flexible molecules by NMR calculations. Org Lett. 2020;22:52-6. 13 Xia JN, Hu K, Su XZ, Tang JW, Li XN, Sun HD, et al. Discovery of ent-kaurane diterpenoids, characteristic metabolites of Isodon species, from an endophytic fungal strain Geopyxis sp. XY93 inhabiting Isodon parvifolia. Fitoterapia. 2022;158:105160. |