期刊
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 23, 期 23, 页码 6481-6485出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2013.09.023
关键词
nAChR; Carbachol; Ligand; Affinity; Carbamoyl; Oxazolidinone
资金
- Italian PRIN [2009R7WCZS]
- CNR Research Project on Aging
- Regione Lombardia Project NUTEC [30263049]
- fondazione Giancarla Vollaro
A series of acetylcholine carbamoyl analogues, cyclised at the carbamate moiety or at the cationic head or at both, were tested for binding affinity at muscarinic and neuronal nicotinic receptors (nAChRs). While no muscarinic affinity was found, submicromolar K-i values, similar to that of carbachol, were measured at alpha(4)beta(2) nAChRs for the enantiomers of 5-dimethylaminomethyl- and 5-trimethylammoniomethyl-2-oxazolidinone, 2 and 2a, and for (S)-N-methylprolinol carbamate (S)-3. Methylation of oxazolidinone nitrogen of 2 and 2a and of N-methylprolinol nitrogen of (S)-3 and, even more, hybridization of cyclic carbamate substructure (oxazolidinone) with cyclic cationic head (N-methylpyrrolidine) markedly lower the nicotinic affinity. Docking results were consistent with SAR analysis highlighting the interaction capabilities of (R)-2a and (S)-3 and the negative effect of intracyclic nitrogen methylation and of double cyclisation. (C) 2013 Elsevier Ltd. All rights reserved.
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