Hemisynthesis and preliminary evaluation of novel endocannabinoid analogues
Three new endocannabinoid analogues in which amide moiety was replaced either by oxomethylene group or ester moiety with simultaneous substitution of both α-hydrogens with methyl groups were synthesized and their abilities to interact with CB1-receptor and FAAH were investigated. © 2003 Elsevier Science Ltd. All rights reserved.