HU大麻素列表

维基媒体列表条目

耶路撒冷希伯來大學Hebrew University)的拉斐尔·梅舒朗研究小组合成了上百种大麻素,其中一些是[1]

大麻素及其Ki值(Ki是化合物对大麻素1型受体(CB1)或大麻素2型受体(CB2)的结合亲和力)
名称 类别 分子式 Ki/nM (CB1) Ki/nM (CB2) 选择性 结构
HU-210 二苯并吡喃 C25H38O3 0.23 CB1
HU-211 二苯并吡喃 C25H38O3 CB2
HU-239 二苯并吡喃 C25H36O4
HU-243 二苯并吡喃 C25H40O3
HU-308 联苯 C27H42O3
HU-320 联苯 C25H36O4
HU-331 联苯 C21H28O3
HU-336 二苯并吡喃 C21H28O3
HU-345 二苯并吡喃 C21H24O3
HU-474 联苯[2] C21H29FO2
HU-910 联苯[2] C27H42O3 1400[3] 6[3] CB2

参见

参考文献

  1. ^ Howlett, AC; Champion, TM; Wilken, GH; Mechoulam, R. Stereochemical effects of 11-OH-delta 8-tetrahydrocannabinol-dimethylheptyl to inhibit adenylate cyclase and bind to the cannabinoid receptor. Neuropharmacology. February 1990, 29 (2): 161–5. PMID 2158635. S2CID 28602221. doi:10.1016/0028-3908(90)90056-W. 
  2. ^ 2.0 2.1 Dos Santos Pereira, M; Maitan Santos, B; Gimenez, R; Guimarães, FS; Raisman-Vozari, R; Del Bel, E; Michel, PP. The two synthetic cannabinoid compounds 4'-F-CBD and HU-910 efficiently restrain inflammatory responses of brain microglia and astrocytes.. Glia. 2024-03, 72 (3): 529–545. PMID 38013496. doi:10.1002/glia.24489. 
  3. ^ 3.0 3.1 Horváth, B; Magid, L; Mukhopadhyay, P; Bátkai, S; Rajesh, M; Park, O; Tanchian, G; Gao, RY; Goodfellow, CE; Glass, M; Mechoulam, R; Pacher, P. A new cannabinoid CB2 receptor agonist HU-910 attenuates oxidative stress, inflammation and cell death associated with hepatic ischaemia/reperfusion injury.. British journal of pharmacology. 2012-04, 165 (8): 2462–78. PMID 21449982. doi:10.1111/j.1476-5381.2011.01381.x.