We report the first pharmacological tool agonist for in vitro characterization of the orphan receptor GPR132, preliminary structure–activity relationships based on 32 analogs and a suggested binding mode from docking.M.A.S. was supported by a research scholarship from the Drug Research Academy and Novo Nordisk A/S. D.E.G. and H.B.-O. gratefully acknowledge financial support by the Carlsberg Foundation. D.E.G. and D.S.P. gratefully acknowledges financial support by the Lundbeck Foundation. Nils Nyberg is acknowledged for help with NMR spectroscopy. NMR equipment used in this work was purchased via a grant from The Lundbeck Foundation (R77-A6742).This is the accepted manuscript. The final version is available at http://pubs.rsc.org/en/Content...
G protein-coupled receptors (GPCRs) are therapeutically significant proteins and are targeted by ove...
grantor: University of TorontoG protein-coupled receptors (GPCRs) are integral membrane pr...
G protein-coupled receptors (GPCRs), which are modulated by a variety of endogenous and synthetic li...
The GPR139 receptor is an orphan G-protein-coupled receptor (GPCR) mainly found in the central nervo...
GPR139 is an orphan G protein-coupled receptor expressed in the brain, in particular in the habenula...
The poorly characterized G-protein-coupled receptor GPR35 has been suggested as a potential explorat...
The orphan G protein coupled receptor GPR35 has emerged as a therapeutic target in a number of disea...
The G-protein-coupled receptor 39 (GPR39) is a G-protein-coupled receptor activated by Zn<sup>2+</su...
G protein coupled receptors (GPCR) are the largest family of membrane receptors and currently the mo...
Over 100 orphan G protein-coupled receptors (GPCRs) are yet to be paired with their endogenous ligan...
G protein coupled receptors (GPCR) are the largest family of membrane receptors and currently the mo...
Background and Purpose GPR35 is a poorly characterized G protein-coupled receptor at which kynurenic...
The G protein-coupled receptor GPR17, a dualistic receptor that responds to nucleotides and cysteiny...
Acknowledgements: This work was funded through BBSRC research grants to DN (BB/W020718/1) and to GL ...
GPCRs are the most successful pharmaceutical targets in history. Nevertheless, the pharmacology of m...
G protein-coupled receptors (GPCRs) are therapeutically significant proteins and are targeted by ove...
grantor: University of TorontoG protein-coupled receptors (GPCRs) are integral membrane pr...
G protein-coupled receptors (GPCRs), which are modulated by a variety of endogenous and synthetic li...
The GPR139 receptor is an orphan G-protein-coupled receptor (GPCR) mainly found in the central nervo...
GPR139 is an orphan G protein-coupled receptor expressed in the brain, in particular in the habenula...
The poorly characterized G-protein-coupled receptor GPR35 has been suggested as a potential explorat...
The orphan G protein coupled receptor GPR35 has emerged as a therapeutic target in a number of disea...
The G-protein-coupled receptor 39 (GPR39) is a G-protein-coupled receptor activated by Zn<sup>2+</su...
G protein coupled receptors (GPCR) are the largest family of membrane receptors and currently the mo...
Over 100 orphan G protein-coupled receptors (GPCRs) are yet to be paired with their endogenous ligan...
G protein coupled receptors (GPCR) are the largest family of membrane receptors and currently the mo...
Background and Purpose GPR35 is a poorly characterized G protein-coupled receptor at which kynurenic...
The G protein-coupled receptor GPR17, a dualistic receptor that responds to nucleotides and cysteiny...
Acknowledgements: This work was funded through BBSRC research grants to DN (BB/W020718/1) and to GL ...
GPCRs are the most successful pharmaceutical targets in history. Nevertheless, the pharmacology of m...
G protein-coupled receptors (GPCRs) are therapeutically significant proteins and are targeted by ove...
grantor: University of TorontoG protein-coupled receptors (GPCRs) are integral membrane pr...
G protein-coupled receptors (GPCRs), which are modulated by a variety of endogenous and synthetic li...