Zhang LB. 2004. Huperziaceae and lycopodiaceae. In: Zhang XC (ed) Fl. Reipubl. Popularis Sin. 6(3):63.
Pharmacopoeia Commission of People’s Republic of China (2025) Pharmacopoeia of the People’s Republic of China (Part 1). Chin Med Sci Technol Press, Beijing, p 190
Li JS, Zhang YW, Cao Y, Yang L, Yang HY, Lian AQ, Song D, Xu HX (2017) Analysis on external application of herbs regularity for pain in neck, shoulders, waist and legs. Tianjin J Trad Chin Med 34(12):849–853. https://doi.org/10.11656/j.issn.1672-1519.2017.12.16
Sun Y, Yan J, Meng H, He CL, Yi P, Qiao Y, Qiu MH (2008) A new alkaloid from Lycopodium japonicum thunb. Helv Chim Acta 91(11):2107–2109. https://doi.org/10.1002/hlca.200890225
Wang X, Wang FQ, Wu J, Chen SQ, Jiang CS, Yang SP, Wang C, Cai YS (2022) Japonisine A, a fawcettimine-type Lycopodium alkaloid with an unusual skeleton from Lycopodium japonicum Thunb. Fitoterapia. https://doi.org/10.1016/j.fitote.2021.105069
Wang XJ, Li L, Si YK, Yu SS, Ma SG, Bao XQ, Zhang D, Qu J, Liu YB, Li Y (2013) Nine new lycopodine-type alkaloids from Lycopodium japonicum Thunb. Tetrahedron 69(30):6234–6240. https://doi.org/10.1016/j.tet.2013.05.028
Wang XJ, Yu DQ, Yu SS (2014) Two new triterpenoids from Lycopodium japonicum thunb. Chin J Chem 32(10):1007–1010. https://doi.org/10.1002/cjoc.201400456
Yan J, Zhang XM, Li ZR, Zhou L, Chen JC, Sun LR, Qiu MH (2005) Three new triterpenoids from Lycopodium japonicum Thunb. Helv Chim Acta 88(2):240–244. https://doi.org/10.1002/hlca.200590004
Ren Q, Xu KP, Liu Y, Zou ZX, Tan GS (2020) Chemical constituents from Lycopodii Herba. Central South Pharm 18(03):466–469. https://doi.org/10.7539/j.issn.1672-2981.2020.03.025
Jo A, Een Kim C, Lee M (2020) Serratane triterpenoids isolated from Lycopodium clavatum by bioactivity-guided fractionation attenuate the production of inflammatory mediators. Bioorg Chem 96:103632. https://doi.org/10.1016/j.bioorg.2020.103632
Article CAS PubMed Google Scholar
Liu J, Nian H, Xu Y, Wu TJ, Sun YC, Shao YT, Hang J (2019) Anti-inflammatory effect and mechanism of shenjincao alkaloids on adjuvant arthritis rats. Drug Eval Res 42(05):869–872
Xie Z, Liu Y, Luo Q, Wang Q, Min YB, Liu L, Zheng DK (2025) New Lycopodium alkaloids with neuroprotective activities from Lycopodium japonicum Thunb. Nat Prod Res 39(4):718–724. https://doi.org/10.1080/14786419.2023.2288242
Article CAS PubMed Google Scholar
Halldorsdottir ES, Jaroszewski JW, Olafsdottir ES (2010) Acetylcholinesterase inhibitory activity of lycopodane-type alkaloids from the Icelandic Lycopodium annotinum ssp. alpestre. Phytochemistry 71(2–3):149–157. https://doi.org/10.1016/j.phytochem.2009.10.018
Article CAS PubMed Google Scholar
Zou JX, You XM, Wang GH (2010) Determination of the content of α-obscurine in Herba Lycopodii by high performance liquid chromatography (HPLC). J Chinese Med Mater 33(06):934–936. https://doi.org/10.13863/j.issn1001-4454.2010.06.035
Wu J, Wang H, Ma Y, Jiang J, Zhan R, Chen Y (2015) Isolation of a new lycodine alkaloid from Lycopodium japonicum. Nat Prod Res 29(8):735–738. https://doi.org/10.1080/14786419.2014.984184
Article CAS PubMed Google Scholar
Zhang R, Feng XC, Xu YZ, Xu BH (2024) Quality evaluation of Lycopodium japonicum from different producing areas. China Pharm 35(22):2732–2738. https://doi.org/10.6039/j.issn.1001-0408.2024.22.05
Zhu JH, He JG, Xie H, Qiu XY, Xiao YH, Lei YJ (2000) Authentication of Lycopodium japonicum Thunb. and its adulterant Palhinhaea cernuum L. J Chin Med Mater. https://doi.org/10.13863/j.issn1001-4454.2000.10.007
Xu GJ, Cui XM, Wang ZY (1989) Recent advances of pharmacognosy in China. Chin Trad Herbal Drugs 20(09):39–47
Pan L, Kim M, Liu TZ, Si ZH, Han ZZ, Gu LH, Yang L, Wang ZT (2024) Rapid authentication of five medicinal seeds from Cruciferae family based on high-performance thin-layer chromatography. JPC-J Planar Chromatogr-Mod TLC 37(4):319–330. https://doi.org/10.1007/s00764-024-00309-9
Do TKT, Schmid M, Phanse M, Charegaonkar A, Sprecher H, Obkircher M, Reich E (2021) Development of the first universal mixture for use in system suitability tests for high-performance thin layer chromatography. J Chromatogr A 1638:461830. https://doi.org/10.1016/j.chroma.2020.461830
Article CAS PubMed Google Scholar
Schmid M, Do TKT, Trettin I, Reich E (2022) Applicability of the Universal Mixture for describing system suitability and quality of analytical data in routine normal phase high performance thin layer chromatography methods. J Chromatogr A 1666:462863. https://doi.org/10.1016/j.chroma.2022.462863
Article CAS PubMed Google Scholar
Pharmacopoeia Commission of People’s Republic of China (2025) Pharmacopoeia of the People’s Republic of China (Part 4). Chin Med Sci Technol Press, Beijing, p 567
Gu L, Jiang Y, Han Y, Yang L, Wang Z (2023) A TLC-direct bioassay method for detection of anti-lipid peroxidation constituents from fruits of Perilla frutescens. LWT-Food Sci Technol 182:114779. https://doi.org/10.1016/j.lwt.2023.114779
Feng YF, Guo XL, Han L (2005) Study on chemical constituents of volatile oils from lycopodii herb. J Guangdong Pharm Univ. https://doi.org/10.16809/j.cnki.1006-8783.2005.05.001
Ma D, Gu X, Wang X, Liu Y, Di X (2019) Pharmacokinetic studies of three alkaloids in rats after intragastrical administration of Lycopodii Herba extract by LC-MS/MS. Molecules 24(10):1930. https://doi.org/10.3390/molecules24101930
Article CAS PubMed PubMed Central Google Scholar
Hu PF, Gross ML, Yuan SQ, Wei TT, Lu YQ (1992) Mass-spectrometric differentiation of Huperzinine, N N-dimethylhuperzine-A and N-methylhuperzine-B. Organic Mass Spectrometr 27(2):99–104. https://doi.org/10.1002/oms.1210270206
Ayer WA, Kasitu GC (1989) Some new Lycopodium alkaloids. Can J Chem 67(6):1077–1086. https://doi.org/10.1139/v89-163
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