[1] HUFFMAN J. Cannabimimetic Indoles, Pyrroles, and Indenes: Structure–Activity Relationships and Receptor Interactions[C]. 1900: 0. DOI:
10.1007/978-1-59745-503-9_3[2] RURI KIKURA-HANAJIRI Yukihiro G Nahoko Uchiyama. Survey of current trends in the abuse of psychotropic substances and plants in Japan[J]. Legal Medicine, 2011, 13 3: Pages 109-115. DOI:
10.1016/j.legalmed.2011.02.003[3] SEBASTIAN DRESEN. Monitoring of herbal mixtures potentially containing synthetic cannabinoids as psychoactive compounds[J]. Journal of Mass Spectrometry, 2010, 45 10: 1186-1194. DOI:
10.1002/jms.1811[4] LISA K BRENTS. Phase I hydroxylated metabolites of the K2 synthetic cannabinoid JWH-018 retain in vitro and in vivo cannabinoid 1 receptor affinity and activity.[J]. PLoS ONE, 2011: e21917. DOI:
10.1371/journal.pone.0021917[5] LISA K. BRENTS . Monohydroxylated metabolites of the K2 synthetic cannabinoid JWH-073 retain intermediate to high cannabinoid 1 receptor (CB1R) affinity and exhibit neutral antagonist to partial agonist activity[J]. Biochemical pharmacology, 2012, 83 7: Pages 952-961. DOI:
10.1016/j.bcp.2012.01.004