The 2-amino-benzoylthiophene derivatives LUF 5468 [(2-amino-4-ethyl-5-methyl-3-thienyl)[3-(trifluoromethyl)phenyl]methanone] and LUF 5484 [(2-amino-4,5,6,7-tetrahydrobenzo[b]thiophen-3-yl)(3,4-dichlorophenyl)methanone] have been shown to allosterically enhance the adenosine A1 receptor agonist binding. We report a thermodynamic analysis of the agonist affinity obtained at human adenosine A1 receptors, in the presence and absence of LUF 5468 and LUF 5484. Moreover, an analysis of the temperature dependence for association and dissociation rates of N6-cyclohexyladenosine (CHA) binding was performed in the absence and presence of LUF 5484. Thermodynamic data were obtained by affinity measurements performed at different temperatures followed by van’t Hoff analysis. The results indicate that the agonist binding is always totally entropy-driven, and that the modulators contribute to decrease the DGj, DHj and DSj values. It is concluded that the enhancers are able to increase the non-bonded interactions of the binding site with agonists as CHA, N6-cyclopentlyladenosine (CPA), 2V-methyl-N6-cyclopentyladenosine (MeCPA) and 2-chloro-2Vmethyl-N6-cyclopentyladenosine (MeCCPA).

Temperature dependence of the affinity enhancement of selective adenosine A1 receptor agonism: a thermodynamic analysis.

DALPIAZ, Alessandro;PAVAN, Barbara;
2002

Abstract

The 2-amino-benzoylthiophene derivatives LUF 5468 [(2-amino-4-ethyl-5-methyl-3-thienyl)[3-(trifluoromethyl)phenyl]methanone] and LUF 5484 [(2-amino-4,5,6,7-tetrahydrobenzo[b]thiophen-3-yl)(3,4-dichlorophenyl)methanone] have been shown to allosterically enhance the adenosine A1 receptor agonist binding. We report a thermodynamic analysis of the agonist affinity obtained at human adenosine A1 receptors, in the presence and absence of LUF 5468 and LUF 5484. Moreover, an analysis of the temperature dependence for association and dissociation rates of N6-cyclohexyladenosine (CHA) binding was performed in the absence and presence of LUF 5484. Thermodynamic data were obtained by affinity measurements performed at different temperatures followed by van’t Hoff analysis. The results indicate that the agonist binding is always totally entropy-driven, and that the modulators contribute to decrease the DGj, DHj and DSj values. It is concluded that the enhancers are able to increase the non-bonded interactions of the binding site with agonists as CHA, N6-cyclopentlyladenosine (CPA), 2V-methyl-N6-cyclopentyladenosine (MeCPA) and 2-chloro-2Vmethyl-N6-cyclopentyladenosine (MeCCPA).
2002
Dalpiaz, Alessandro; Pavan, Barbara; NGO NGOS, F. L.; Franchetti, P.; Ijzerman, A. P.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1201123
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