Forest Research Institute Malaysia (FRIM). Flora of Malaysia i-Newsletter Part 3. 2013:1969–1969. https://www.mybis.gov.my/art/1985. Accessed 21 Dec 2022.
He RR, Wang M, Li YF, Dai Y, Duan YH, Yao XS, et al. Effects of Sarcandra glabra extract on immune activity in restraint stress mice. Zhongguo Zhongyao Zazhi. 2009;34:100–3.
Liu CP, Liu JX, Gu JY, Liu F, Li JH, Yang B, et al. Combination effect of three main constituents from Sarcandra glabra inhibits oxidative stress in the mice following acute lung injury: a role of MAPK-NF-κB pathway. Front Pharmacol. 2021;11:2082. https://doi.org/10.3389/fphar.2020.580064.
Yang XR, Tanaka N, Tsuji D, Lu FL, Yan XJ, Itoh K, et al. Sarcaglabrin A, a conjugate of C15 and C10 terpenes from the aerial parts of Sarcandra glabra. Tetrahedron Lett. 2020;61: 151916. https://doi.org/10.1016/j.tetlet.2020.151916.
Zeng YL, Liu JY, Zhang Q, Qin XH, Li ZL, Sun GJ, et al. The traditional uses, phytochemistry and pharmacology of Sarcandra glabra (Thunb.) Nakai, a Chinese herb with potential for development: review. Front Pharmacol. 2021;12:652926. https://doi.org/10.3389/fphar.2021.652926.
Article CAS PubMed PubMed Central Google Scholar
Chloranthaceae VB. Flora Malesiana—series 1. Spermatophyta. 1984;10:123–44.
Verdcourt B. Notes on Malesian Chloranthaceae. Kew Bull. 1985;40:213–24. https://doi.org/10.2307/4108497.
Vossen HAM, Wessel M, editors. Plant resources of South-East Asia, No 16, Stimulants. Leiden: Backhuys Publishers; 1999. https://doi.org/10.2307/4118801.
Swamy BGL, Bailey IW. Sarcandra, A vesselless genus of the Chloranthaceae. J Arnold Arbor. 1950;31:128.
Zhou B, Liu KY, Chang J, Cheng CQ. Advances on chemical constituents and pharmacological activities of Sarcandra glabra. Chin J Mod Appl Pharm. 2009;6:982–6.
Zhang H, Zhao P, Zhang YY, Huang XX, Song SJ. Chemical constituents and pharmacological properties of Sarcandra glabra (Thunb.) Nakai. Asian J Trad Med. 2019;14:237–46.
Ludwiczuk A, Skalicka-Woźniak K, Georgiev MI. Terpenoids. In: Badal S, Delgoda RBT, editors. Pharmacognosy: fundamentals. Applications and Strategy, Boston: Academic Press; 2017. p. 233–66. https://doi.org/10.1016/B978-0-12-802104-0.00011-1.
Cocker W, McMurry TBH. Stereochemical relationships in the eudesmane (selinane) group of sesquiterpenes. Tetrahedron. 1960;8:181–204. https://doi.org/10.1016/0040-4020(60)80028-2.
Li Y, Zhang DM, Li JB, Yu SS, Li Y, Luo YM. Hepatoprotective sesquiterpene glycosides from Sarcandra glabra. J Nat Prod. 2006;69:616–20. https://doi.org/10.1021/np050480d.
Article CAS PubMed Google Scholar
Zhu LP, Li Y, Yang JZ, Zuo L, Zhang DM. Two new sesquiterpene lactones from Sarcandra glabra. J Asian Nat Prod Res. 2008;10:541–5. https://doi.org/10.1080/10286020801966773.
Article CAS PubMed Google Scholar
Hu XR, Yang JS, Xu XD. Three novel sesquiterpene glycosides of Sarcandra glabra. Chem Pharm Bull. 2009;57:418–20. https://doi.org/10.1248/cpb.57.418.
He XF, Yin S, Ji YC, Su ZS, Geng MY, Yue JM. Sesquiterpenes and dimeric sesquiterpenoids from Sarcandra glabra. J Nat Prod. 2010;73:45–50. https://doi.org/10.1021/np9006469.
Article CAS PubMed Google Scholar
Teng F, Zhong HM, Chen CX, Liu HY. Four new eudesmane sesquiterpenoid lactones from Chloranthus serratus. Helv Chim Acta. 2009;92:1298–303. https://doi.org/10.1002/hlca.200800450.
Do TO, Pham TK, Hang NTB, Pham HY, Tran HH, Nguyen XC, et al. Two new sesquiterpenes from Sarcandra glabra. Nat Prod Commun. 2010;5:1717–20.
Wang C, Li Y, Li CJ, Yu SS, Zhang DM. Three new compounds from Sarcandra glabra. Chinese Chem Lett. 2012;23:823–6. https://doi.org/10.1016/j.cclet.2012.05.007.
Hu XR, Wu HF, Zhang XP, Yang JS, Dai Z, Lin RC, et al. A new sesquiterpene lactone from Sarcandra glabra. Nat Prod Res. 2013;27:1197–201. https://doi.org/10.1080/14786419.2012.722084.
Article CAS PubMed Google Scholar
Ni G, Zhang H, Liu HC, Yang SP, Geng MY, Yue JM. Cytotoxic sesquiterpenoids from Sarcandra glabra. Tetrahedron. 2013;69:564–9. https://doi.org/10.1016/j.tet.2012.11.023.
Yaermaimaiti S, Wang P, Luo J, Li RJ, Kong LY. Sesquiterpenoids from the seeds of Sarcandra glabra and the potential anti-inflammatory effects. Fitoterapia. 2016;111:7–11. https://doi.org/10.1016/j.fitote.2016.03.020.
Article CAS PubMed Google Scholar
Li YT, Li SF, Lei C, You JQ, Huang JC, Hou AJ. Dimeric sesquiterpenoids and anti-inflammatory constituents of Sarcandra glabra. Bioorg Chem. 2022;124: 105821. https://doi.org/10.1016/j.bioorg.2022.105821.
Article CAS PubMed Google Scholar
Wang YY, Li QR, Chi J, Li JX, Kong LY, Luo J. Sesquiterpenoids from the leaves of Sarcandra glabra. Chin J Nat Med. 2022;20:215–20. https://doi.org/10.1016/S1875-5364(21)60102-4.
Article CAS PubMed Google Scholar
Takeda Y, Yamashita H, Matsumoto T, Terao H, Chloranthalactone F. A sesquiterpenoid from the leaves of Chloranthus glaber. Phytochemistry. 1993;33:713–5. https://doi.org/10.1016/0031-9422(93)85480-F.
Wong KC, Tan MS, Ali DMH, Teoh SG, Osman H, Tan SK. Essential oil of the leaves of Sarcandra glabra (Thunb.) Nakai. J Essent Oil Res. 2009;21:71–3. https://doi.org/10.1080/10412905.2009.9700114.
Yue GZ, Yang L, Yuan CC, Du B, Liu B. Progress in total syntheses of lindenane-type sesquiterpenoids and their dimers. Chin J Org Chem. 2013;33:90–100. https://doi.org/10.6023/cjoc201207003.
Liao SG, Yue JM. Dimeric sesquiterpenoids. In: Kinghorn AD, Falk H, Gibbons S, Kobayashi J, editors. Prog Chem Org Nat Prod, vol. 101. Cham: Springer International Publishing; 2016. p. 1–112. https://doi.org/10.1007/978-3-319-22692-7_1.
Uchida M, Kusano G, Kondo Y, Takemoto T, Nozoe S. Two new sesquiterpenoids from Chloranthus glaber Makino. Heterocycles. 1978;9:139–44. https://doi.org/10.3987/r-1978-02-0139.
Okamura H, Nakashima N, Iwagawa T, Nakayama N, Nakatani M. The structures of two lindenane sesquiterpene glucosides from Chloranthus glaber. Chem Lett. 1994;23:1541–2. https://doi.org/10.1246/cl.1994.1541.
Tsui WY, Brown GD. Cycloeudesmanolides from Sarcandra glabra. Phytochemistry. 1996;43:819–21. https://doi.org/10.1016/0031-9422(96)00352-4.
Chi J, Wei SS, Gao HL, Xu DQ, Zhang LN, Yang L, et al. Diverse chemosensitizing 8,9-secolindenane-type sesquiterpenoid oligomers and monomers from Sarcandra glabra. J Org Chem. 2019;84:9117–26. https://doi.org/10.1021/acs.joc.9b00986.
Article CAS PubMed Google Scholar
Wang C, Zhu LP, Yang JZ, Li CJ, Zhang DM. Chemical constituents from Sarcandra glabra. China J Chin Mater Medicaedica. 2010;35:714–7. https://doi.org/10.4268/cjcmm20100612.
Li X, Zhang YF, Yang L, Feng Y, Liu YM, Zeng X. Sesquiterpenoids from the whole plant of Sarcandra glabra. Yaoxue Xuebao. 2011;46:1349–51.
Zheng XF, Liu HY, Zhong HM. Chemical constituents from Sarcandra glabra. Nat Prod Res Dev. 2014;26:1221–4.
Wang P, Luo J, Zhang YM, Kong LY. Sesquiterpene dimers esterified with diverse small organic acids from the seeds of Sarcandra glabra. Tetrahedron. 2015;71:5362–70. https://doi.org/10.1016/j.tet.2015.05.112.
Wang P, Li RJ, Liu RH, Jian KL, Yang MH, Yang L, et al. Sarglaperoxides A and B, sesquiterpene-normonoterpene conjugates with a peroxide bridge from the seeds of Sarcandra glabra. Org Lett. 2016;18:832–5. https://doi.org/10.1021/acs.orglett.6b00112.
Article CAS PubMed Google Scholar
Wang YY, Cui ZR, Chi J, Tang PF, Zhang MH, Li JX, et al. Sarcaglarols A–D, lindenane−monoterpene heterodimers from Sarcandra glabra based on molecular networks. Chin J Chem. 2021;39:129–36. https://doi.org/10.1002/cjoc.202000456.
Sun YP, Wang YY, Li YQ, Wang SY, Zhang DY, Kong LY, et al. Sarcaglarone A, a lindenane-monoterpene heterodimer from the seeds of Sarcandra glabra. Org Biomol Chem. 2022;20:9222–7. https://doi.org/10.1039/d2ob01830f.
Article CAS PubMed Google Scholar
Sun YP, Chi J, Zhang LJ, Wang SY, Chen ZH, Zhang H, et al. Sarglaromatics A-E: a class of naphthalene-like architecture fused norlindenane sesquiterpene dimers from Sarcandra glabra. J Org Chem. 2022;87:4323–32. https://doi.org/10.1021/acs.joc.2c00014.
Article CAS PubMed Google Scholar
Xiao LG, Li P, Yan H, Ni W, He L, Liu HY. Sarcanolides C-E: Three new lindenane sesquiterpenoid dimers with anti-inflammatory activities from Sarcandra glabra. Org Biomol Chem. 2022;20:1320–6. https://doi.org/10.1039/d1ob02417e.
Comments (0)