Please use this identifier to cite or link to this item: https://doi.org/10.1021/jm9019068
Title: "carba"-analogues of fentanyl are opioid receptor agonists
Authors: Weltrowska, G.
Chung, N.N.
Lemieux, C.
Guo, J.
Lu, Y. 
Wilkes, B.C.
Schiller, P.W.
Issue Date: 8-Apr-2010
Citation: Weltrowska, G., Chung, N.N., Lemieux, C., Guo, J., Lu, Y., Wilkes, B.C., Schiller, P.W. (2010-04-08). "carba"-analogues of fentanyl are opioid receptor agonists. Journal of Medicinal Chemistry 53 (7) : 2875-2881. ScholarBank@NUS Repository. https://doi.org/10.1021/jm9019068
Abstract: There is evidence to indicate that the Asp residue in the third transmembrane helix (TMH) of opioid receptors forms a salt bridge with the positively charged nitrogen of endogenous and exogenous opioid ligands. To further examine the role of this electrostatic interaction in receptor binding and activation, we synthesized "carba"-analogues of a published fentanyl analogue containing a 3-(guanidinomethyl)-benzyl group in place of the phenyl moiety attached to the ethylamido group (C. Dardonville et al., Bioorg. Med. Chem. 2006, 14, 6570-6580 (1)), in which the piperidine ring nitrogen was replaced with a carbon. As expected, the resulting cis and trans isomers (8a and 8b) showed reduced μ and - opioid receptor binding affinities as compared to 1 but, surprisingly, retained opioid full agonist activity with about half the potency of leucine-enkephalin in the guinea pig ileum assay. In conjunction with performed receptor docking studies, these results indicate that the electrostatic interaction of the protonated nitrogen in the piperidine ring of fentanyl analogues with the Asp residue in the third TMH is not a conditio sine qua non for opioid receptor activation. © 2010 American Chemical Society.
Source Title: Journal of Medicinal Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/75379
ISSN: 00222623
DOI: 10.1021/jm9019068
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