Title of article :
Redefining the structure–activity relationships of 2,6-methano-3-benzazocines. Part 6: Opioid receptor binding properties of cyclic variants of 8-carboxamidocyclazocine Original Research Article
Author/Authors :
Mark P. Wentland، نويسنده , , Xufeng Sun، نويسنده , , Dana J. Cohen، نويسنده , , Jean M. Bidlack، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
12
From page :
5653
To page :
5664
Abstract :
A series of 7,8- and 8,9-fused pyrimidinone, aminopyrimidine and pyridone derivatives of 8-carboxamidocyclazocine (8-CAC) have been prepared and evaluated in opioid receptor binding assays. Targets were designed to corroborate a pharmacophore hypothesis regarding the bioactive conformation of the carboxamide of 8-CAC. In addition to the results from this study strongly supporting this pharmacophore hypothesis, a number of novel compounds with high affinity to opioid receptors have been identified.
Keywords :
SAR , Opioid , Pharmacophore hypothesis
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2008
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1304372
Link To Document :
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