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Journal of Medicinal Chemistry|July 12, 2024
Ligand-Directed Labeling of the Adenosine A<sub>1</sub> Receptor in Living CellsEleonora Comeo, Joëlle Goulding, Chia-Yang Lin, et al.Nature Communications|February 25, 2016
The role of kinetic context in apparent biased agonism at GPCRsCarmen Klein Herenbrink, David A Sykes, Prashant Donthamsetti, et al.ACS Chemical Biology|July 25, 2019
Molecular Determinants of the Intrinsic Efficacy of the Antipsychotic AripiprazoleCarmen Klein Herenbrink, Ravi Verma, Herman D Lim, et al.European Journal of Medicinal Chemistry|July 9, 2023
Design, synthesis and evaluation of novel 2-phenyl-3-(1H-pyrazol-4-yl)pyridine positive allosteric modulators for the M<sub>4</sub> mAChRManuela Jörg, Emma T van der Westhuizen, Yao Lu, et al.Journal of Medicinal Chemistry|June 29, 2019
Novel Human Aminopeptidase N Inhibitors: Discovery and Optimization of Subsite Binding InteractionsJisook Lee, Natalie B Vinh, Nyssa Drinkwater, et al.Biochemical Pharmacology|January 13, 2018
The structural determinants of the bitopic binding mode of a negative allosteric modulator of the dopamine D<sub>2</sub> receptorChristopher J Draper-Joyce, Mayako Michino, Ravi Kumar Verma, et al.European Journal of Medicinal Chemistry|January 26, 2016
Potent dual inhibitors of Plasmodium falciparum M1 and M17 aminopeptidases through optimization of S1 pocket interactionsNyssa Drinkwater, Natalie B Vinh, Shailesh N Mistry, et al.Journal of Medicinal Chemistry|March 16, 2021
Development and Application of Subtype-Selective Fluorescent Antagonists for the Study of the Human Adenosine A<sub>1</sub> Receptor in Living CellsEleonora Comeo, Phuc Trinh, Anh T Nguyen, et al.ACS Chemical Neuroscience|December 15, 2018
6-Phenylpyrimidin-4-ones as Positive Allosteric Modulators at the M<sub>1</sub> mAChR: The Determinants of Allosteric ActivityManuela Jörg, Emma T van der Westhuizen, Elham Khajehali, et al.Journal of Molecular Recognition : JMR|January 26, 2016
Solution NMR characterization of apical membrane antigen 1 and small molecule interactions as a basis for designing new antimalarialsBankala Krishnarjuna, San Sui Lim, Shane M Devine, et al.Pageof 15