Biaryl piperidines as potent and selective delta opioid receptor ligands
作者:Spiros Liras、Stanton F. McHardy、Martin P. Allen、Barb E. Segelstein、Steven D. Heck、Dianne K. Bryce、Anne W. Schmidt、Michelle Vanase-Frawley、Ernesto Callegari、Stafford McLean
DOI:10.1016/j.bmcl.2009.11.113
日期:2010.1
The design and synthesis of novel opiates are reported. Based on the message-address principle a novel class of 4,4- and 3,3-biaryl piperidines was designed and synthesized. Biologicalevaluation confirmed that these compounds exhibit highaffinity and selectivity for the delta opioid receptor. Key structure–activity relationships that influence affinity, selectivity, functional activity and clearance
The present invention relates to compounds of the formula I,
wherein Z1, Z2, R1, R2 and R3 are defined as in the specification, pharmaceutical compositions containing such compounds the use of such compounds to treat neurological and gastrointestinal disorders.
4,4-BIARYLPIPERIDINE DERIVATIVES WITH OPIOID RECEPTOR ACTIVITY
申请人:Pfizer Products Inc.
公开号:EP1112255A1
公开(公告)日:2001-07-04
US6720336B2
申请人:——
公开号:US6720336B2
公开(公告)日:2004-04-13
[EN] 4,4-BIARYLPIPERIDINE DERIVATIVES WITH OPIOID RECEPTOR ACTIVITY<br/>[FR] DERIVES DE 4,4-BIARYLPIPERIDINE POSSEDANT UNE ACTIVITE DE RECEPTEUR OPIOIDE
申请人:PFIZER PROD INC
公开号:WO2000014066A1
公开(公告)日:2000-03-16
The present invention relates to compounds of formula (I), wherein Z?1, Z2, R1, R2 and R3¿ are defined as in the specification, pharmaceutical compositions containing such compounds, the use of such compounds to treat neurological and gastrointestinal disorders.