Synthesis and pharmacological profile of a series of 1-substituted-2-carbonyl derivatives of diphenidol:: Novel M4 muscarinic receptor antagonists

被引:7
|
作者
Varoli, Lucilla [1 ]
Angeli, Piero [2 ]
Buccioni, Michela [2 ]
Burnelli, Silvia [1 ]
Fazio, Nicola [3 ]
Marucci, Gabriella [2 ]
Recanatini, Maurizio [1 ]
Spampinato, Santi
机构
[1] Univ Bologna, Dept Pharmaceut Sci, I-40126 Bologna, Italy
[2] Univ Camerino, Dept Chem Sci, I-62032 Camerino, Italy
[3] Univ Bologna, Dept Pharmacol, I-40126 Bologna, Italy
关键词
muscarinic antagonists; subtype selectivity; diphenidol derivatives; binding studies; functional studies; cAMP;
D O I
10.2174/157340608783789211
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Novel 2-carbonyl analogues of diphenidol (1) - bearing lipophylic 1-substituents (2) - were synthesized starting from previously investigated diphenidol derivatives acting as M-2-selective muscarinic antagonists. These compounds were tested for receptor binding affinity versus human muscarinic M-1-M-5 receptors stably expressed in CHO-K1 cells. Their activity in functional assays carried out on CHO-K1 cells expressing human M-4 receptors (CHO-hM(4)) and on classical models of M-1-M-3 receptors, in guinea pig and rabbit tissue preparations, was also evaluated. Compound 2d showed an affinity of pKi = 7.73 at the human M-4-receptor subtype with selectivity ratios ranging from 31-fold (M-4/M-5) to 60-fold (M-4/M-2). Interestingly this compound, in CHO-hM(4) cells, blocked the inhibition of forskolin-activated cAMP accumulation produced by carbachol (IC50= 61 nM) whereas it was a weak muscarinic antagonist in functional tests carried out in guinea-pig and rabbit tissue expressing M-1 (pK(b) = 5.96), M-2 (pK(b) = 6.43) and M-3 (pK(b) = 6.09) receptors. In conclusion, the modifications performed in this work on reference compounds led us to obtain surprisingly a M-4 selective antagonist. Considering the therapeutic indications for M-4 selective antagonists, compound 2d may serve as a novel lead compound for further optimization.
引用
收藏
页码:121 / 128
页数:8
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