Title of article :
Novel 2,5-disubstituted-1H-pyrroles with high affinity for the dopamine D3 receptor: N-benzyl modifications
Author/Authors :
Izzy Boyfield، نويسنده , , Martyn C. Coldwell، نويسنده , , Michael S. Hadley، نويسنده , , Maureen A. M. Healy، نويسنده , , Christopher N. Johnson، نويسنده , , David J. Nash، نويسنده , , Graham J. Riley، نويسنده , , Emma E. Scott، نويسنده , , Stephen A. Smith، نويسنده , , Geoffrey Stemp، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1997
Pages :
4
From page :
327
To page :
330
Abstract :
A series of 2,5-disubstituted-1H-pyrroles (4 – 26) has been prepared where the conformational requirements of the N-ethyl, N-benzyl side-chain of 1 and the effect of introducing substituents into the benzyl group have been investigated. The (R)-α-methylbenzyl 6 and aminoindane 10 side-chains retained high affinity for the dopamine D3 receptor, although neither showed the selectivity of 2-phenylazacycloheptane 2.
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
1997
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
788562
Link To Document :
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