A Comprehensive Review of Ephedrine Analogues: Varieties, Abuse and Synthesis Methodologies
DOI: https://doi.org/10.62517/jmhs.202405117
Author(s)
Wu Tianqi
Affiliation(s)
School of Narcotics Control and Public Order Studies, Criminal Investigation Police University of China, Shenyang, Liaoning, China
Abstract
Ephedrine analogues include ephedrine and its derivatives, which can be categorized into natural and synthetic types depending on their sources. Natural analogues primarily originate from Ephedra plants such as ephedrine, pseudoephedrine, norephedrine, norpseudoephedrine, methylephedrine and methylpseudoephedrine. Synthetic analogues are obtained through chemical modifications to achieve specific purposes. The review delves into the abuse issues and potential hazards associated with ephedrine analogues, introduces various methods ranging from traditional extraction techniques of ephedrine analogues to modern chemical and biosynthesis technologies. This aids researchers, regulatory bodies, and the public in better understanding the sources and applications of ephedrine and its analogues, providing an important reference for subsequent research and regulation of ephedrine analogues.
Keywords
Ephedrine; Ephedrine Analogues; Abuse; Synthesis Methodologies
References
[1]Nagai N. Ephedra vulgaris Rich. var. helvetica Hook. et Thomps[J]. Pharm. Ztg, 1887, 32: 700.
[2]Li Li. Research progress on Ephedra and its active ingredients [J]. Journal of Xinjiang Medical University, 2003(6): 606-608.
[3]Zhang B M, Wang Z B, Xin P, et al. Phytochemistry and pharmacology of genus Ephedra[J]. Chinese Journal of Natural Medicines, 2018, 16(11): 811-828.
[4]Luo Lei, Mu Xiaoqing, Wu Tao, et al. One-pot synthesis of ephedrine hydrochloride [J]. Journal of Shanghai Jiaotong University (Science), 2021, 42(8).
[5]Zhao Shujin, Yuan Jin. Reasons for and reflections on the suspension of phenylethanolamine[J]. Chinese Journal of Hospital Pharmacy, 2001(10): 51-52.
[6]Xu Boping, Shi Hongfei, Xu Chengxin. Research progress on psychoactive components and extraction detection in Chaetoceros[J]. Forensic Science, 2024, 49(1).
[7]Liu Weiguo, Liu Xingjun, Jiang Xiaowei. Research progress on pharmacological effects of methylephedrine[C]. Annual Aerospace Nursing Conference, 2006.
[8]Liu Bo. GC/MS examination of methylephedrine in drug-related cases[J]. Forensic Science, 2012, 2012(1).
[9]Li Hangqi, Lan Hui, Zhuang Shun, et al. Examination research on chloroephedrine[J]. Forensic Science, 2015, 40(6): 477-479.
[10]Gaddum J H. Ephedrine[J]. BMJ, 1938, 1(4030): 713-717.
[11]Hou Ping, Yang Li, Liu Ning, et al. Effects of ephedrine, β-asarone and pseudoephedrine on calcium ion concentration in rat cardiomyocytes and calcium channels in cell membranes[J]. Journal of China Medical University, 2013, 42(03): 201-203+216.
[12]Chait L D. Factors influencing the reinforcing and subjective effects of ephedrine in humans[J]. Psychopharmacology, 1994, 113: 381-387.
[13]Xiao Kun. Causes and countermeasures of methcathinone spread in a city in Shanxi[J]. Journal of Guangxi Police College, 2018, 31(5).
[14]Jacobs I, Pasternak H, Bell D G. Effects of Ephedrine, Caffeine, and Their Combination on Muscular Endurance:[J]. Medicine & Science in Sports & Exercise, 2003, 35(6): 987-994.
[15]Zhu B, Conlan X, Cao J, et al. Case studies on illegal production of ephedrine/pseudoephedrine within Fujian China[J]. Forensic Science International, 2020, 312: 110326.
[16]Online World Drug Report 2023 - Latest data and trend analysis[EB/OL]. United Nations : Office on Drugs and Crime.
[17]Shi Liancheng, Ye Chen, Li Xiao. Research progress on ephedrine alkaloids[J]. Guide to Chinese Medicine, 2012, 10(10).
[18]Li Li, Chen Jian. Improvement of ephedrine alkaloid extraction process[J]. Journal of Xinjiang Medical University, 2003, 2003(6).
[19]Ji Yong, Chen Jie. Brief chemical synthesis methods of ephedrine alkaloids[C]. Communist Party of Shenyang Municipal Committee, Shenyang Municipal People's Government, 2010: 548-553.
[20]Ling Haiqiu, Mao Peihong, Jin Xiang, et al. Research on microbial production of ephedrine and pseudoephedrine[J]. Biotechnology, 2009, 19(4): 94-95.
[21]Ling Haiqiu, Jin Xiang, Mao Peihong, et al. Characteristics of biotransformation of ephedrine by recombinant yeast and the influence of L-Phe on its synthesis[J]. Biotechnology, 2010, 20(4).
[22]Lee Y C, Chen Y Y, Lin J S, et al. Stereoselective synthesis of (1R, 2S)-norephedrine by recombinant whole-cell biocatalysts coupling acetohydroxyacid synthase I and ω-transaminase[J]. Process biochemistry, 2018, 73: 74-81.