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Bioorg Med Chem Lett
; 13(12): 1977-80, 2003 Jun 16.
Article
in English
| MEDLINE
| ID: mdl-12781177
ABSTRACT
Three new endocannabinoid analogues in which amide moiety was replaced either by oxomethylene group or ester moiety with simultaneous substitution of both alpha-hydrogens with methyl groups were synthesized and their abilities to interact with CB1-receptor and FAAH were investigated.