918423-39-9Relevant articles and documents
Elucidation of the bioactive conformation of the N-substituted trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine class of μ-opioid receptor antagonists
Le Bourdonnec, Bertrand,Goodman, Allan J.,Michaut, Mathieu,Ye, Hai-Fen,Graczyk, Thomas M.,Belanger, Serge,Herbertz, Torsten,Yap, Glenn P. A.,DeHaven, Robert N.,Dolle, Roland E.
, p. 7278 - 7289 (2007/10/03)
The series of trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidines have been widely investigated as opioid receptor antagonists. One of our research goals was to explore the bioactive conformation of the N-phenethyl trans-3,4-dimethyl-4-(3-hydroxyphenyl)pipe
Synthesis and structure-activity relationships of a new series of 2α-substituted trans-4,5-dimethyl-4-(3-hydroxyphenyl)piperidine as μ-selective opioid antagonists
Le Bourdonnec, Bertrand,Goodman, Allan J.,Michaut, Mathieu,Ye, Hai-Fen,Graczyk, Thomas M.,Belanger, Serge,DeHaven, Robert N.,Dolle, Roland E.
, p. 864 - 868 (2007/10/03)
Structure-activity relationships at the 2α-position of the piperidine ring of the trans-4,5-dimethyl-4-(3-hydroxyphenyl)piperidine μ-opioid antagonist series were investigated. This study showed that only small linear alkyl groups (methyl, propyl) are tol