Peng H, Caroline MP (2013) Flora of China 11. Science Press, Beijing, p 124. http://www.iplant.cn/foc/pdf/Chloranthaceae.pdf

Chen C, Zeng HT, He XQ, Yuan YJ, Yu JB (2018) Scientific research on selection of medicinal herbs of Chloranthaceae based on materia medica theory. China J Chin Mater Med 43:3036–3040. https://doi.org/10.19540/j.cnki.cjcmm.20180528.003

Article  Google Scholar 

Editorial Committee of the State Administration of Traditional Chinese Medicine (1999) Zhonghua Materia Medica (Chinese medicine). pp 196–197. https://zy.yaozh.com/zhbc/zhbc-my-0127.pdf

Chi J, Xu WJ, Wei SS, Wang XB, Li JX, Gao HL, Kong LY, Luo J (2019) Chlotrichenes A and B, two lindenane sesquiterpene dimers with highly fused carbon skeletons from Chloranthus holostegius. Org Lett 21:789–792. https://doi.org/10.1021/acs.orglett.8b04046

Article  CAS  PubMed  Google Scholar 

Luo J, Zhang DY, Tang PF, Wang N, Zhao S, Kong LY (2023) Chemistry and bioactivity of lindenane sesquiterpenoids and their oligomers. Nat Prod Rep 41:25–58. https://doi.org/10.1039/d3np00022b

Article  CAS  Google Scholar 

Shen CP, Luo JG, Yang MH, Kong LY (2017) Sesquiterpene dimers from the roots of Chloranthus holostegius with moderate anti-inflammatory activity. Phytochemistry 137:117–122. https://doi.org/10.1016/j.phytochem.2017.02.016

Article  CAS  PubMed  Google Scholar 

Yang SP, Gao ZB, Wu Y, Hu GY, Yue JM (2008) Chlorahololides C-F: a new class of potent and selective potassium channel blockers from Chloranthus holostegius. Tetrahedron 64:2027–2034. https://doi.org/10.1016/j.tet.2007.12.057

Article  CAS  Google Scholar 

Yang SP, Gao ZB, Wang FD, Liao SG, Chen HD, Zhang CR, Hu GY, Yue JM (2007) Chlorahololides A and B, two potent and selective blockers of the potassium channel isolated from Chloranthus holostegius. Org Lett 9:903–906. https://doi.org/10.1021/ol0700759

Article  CAS  PubMed  Google Scholar 

Wang SY, Li YQ, Wang XL, Zhang XQ, Xu F, Ying P, Kong LY, Luo J (2023) Fortunilides M-O, anti-inflammatory lindenane sesquiterpenoid dimers from Chloranthus fortunei. Fitoterapia 168:105547. https://doi.org/10.1016/j.fitote.2023.105547

Article  CAS  PubMed  Google Scholar 

Wang SY, Sun YP, Li YQ, Xu WJ, Li QQ, Mu YB, Kong LY, Luo J (2023) Rearranged lindenane sesquiterpenoid trimers from Chloranthus fortunei: target discovery and biomimetic conversion. J Org Chem 88:347–354. https://doi.org/10.1021/acs.joc.2c02372

Article  CAS  PubMed  Google Scholar 

Li JX, Cui ZR, Li YY, Han CH, Zhang YQ, Tang PF, Cui LT, Zhang H, Luo J, Kong LY (2022) Chlospicenes A and B, cyclopropane cracked lindenane sesquiterpenoid dimers with anti-nonalcoholic steatohepatitis activity from Chloranthus henryi. Chin Chem Lett 33:4257–4260. https://doi.org/10.1016/j.cclet.2022.01.084

Article  CAS  Google Scholar 

Li JX, Chi J, Tang PF, Sun YP, Lu WJ, Xu WJ, Wang YY, Luo J, Kong LY (2022) Spirolindemers A and B, lindenane sesquiterpenoid oligomers equipped with oxaspiro[4.5]decane from Chloranthus henryi. Chin J Chem 40:603–608. https://doi.org/10.1002/cjoc.202100743

Article  CAS  Google Scholar 

Kim SY, Kashiwada Y, Kawazoe K, Murakami K, Sun HD, Li SL, Takaishi Y (2011) Spicachlorantins G-J, new lindenane sesquiterpenoid dimers from the roots of Chloranthus spicatus. Chem Pharm Bull 59:1281–1284. https://doi.org/10.1248/cpb.59.1281

Article  CAS  Google Scholar 

Ran XH, Teng F, Chen CX, Wei G, Hao XJ, Liu HY (2010) Chloramultiols A-F, lindenane-type sesquiterpenoid dimers from Chloranthus multistachys. J Nat Prod 73:972–975. https://doi.org/10.1021/np900764n

Article  CAS  PubMed  Google Scholar 

Zhou B, Wu Y, Dalal S, Merino EF, Liu QF, Xu CH, Yuan T, Ding J, Kingston DGI, Cassera MB, Yue JM (2017) Nanomolar antimalarial agents against chloroquine-resistant Plasmodium falciparum from medicinal plants and their structure-activity relationships. J Nat Prod 80:96–107. https://doi.org/10.1021/acs.jnatprod.6b00744

Article  CAS  PubMed  Google Scholar 

Yang XR, Tanaka N, Tsuji D, Lu FL, Yan XJ, Itoh K, Li DP, Kashiwada Y (2020) Sarcaglabrin A, a conjugate of C15 and C10 terpenes from the aerial parts of Sarcandra glabra. Tetrahedron Lett 61:151916. https://doi.org/10.1016/j.tetlet.2020.151916

Article  CAS  Google Scholar 

Yang SP, Yue JM (2006) Chloramultilide A, a highly complex sesquiterpenoid dimmer from Chloranthus multistachys. Tetrahedron Lett 47:1129–1132. https://doi.org/10.1016/j.tetlet.2005.12.023

Article  CAS  Google Scholar 

Wang P, Li RJ, Liu RH, Jian KL, Yang MH, Yang L, Kong LY, Luo J (2016) Sarglaperoxides A and B, sesquiterpene-normonoterpene conjugates with a peroxide bridge from the seeds of Sarcandra glabra. Org Lett 18:832–835. https://doi.org/10.1021/acs.orglett.6b00112

Article  CAS  PubMed  Google Scholar 

Kawabata J, Fukushi E, Mizutani J (1995) Sesquiterpene dimers from Chloranthus japonicus. Phytochemistry 39:121–125. https://doi.org/10.1016/0031-9422(94)00865-Q

Article  CAS  Google Scholar 

Xiao ZY, Wang XC, Zhang GP, Huang ZL, Hu LH (2010) Terpenoids from roots of Chloranthus spicatus. Helv Chim Acta 93:803–810. https://doi.org/10.1002/hlca.200900299

Article  CAS  Google Scholar 

Hua W, Wang XL, Li QQ, Li YQ, Cui LT, Li YY, Kong LY, Luo J (2023) Rare noreudesmane sesquiterpenoids from the fruits of Dysoxylum densiflorum. Fitoterapia 166:105462. https://doi.org/10.1016/j.fitote.2023.105462

Article  CAS  PubMed  Google Scholar 

Wang YY, Li QR, Chi J, Li JX, Kong LY, Luo J (2022) Sesquiterpenoids from the leaves of Sarcandra glabra. Chin J Nat Med 20:215–220. https://doi.org/10.1016/S1875-5364(21)60102-4

Article  CAS  PubMed  Google Scholar