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Cell|February 6, 2018
5-HT2C Receptor Structures Reveal the Structural Basis of GPCR PolypharmacologyYao Peng, John D McCorvy, Kasper Harpsøe, et al.Plos One|March 11, 2016
In Vitro and In Vivo Characterization of the Alkaloid NuciferineMartilias S Farrell, John D McCorvy, Xi-Ping Huang, et al.Nature|May 4, 2019
Publisher Correction: Structural basis of ligand recognition at the human MT1 melatonin receptorBenjamin Stauch, Linda C Johansson, John D McCorvy, et al.Angewandte Chemie (International Ed. in English)|March 3, 2015
A potent, selective and cell-active allosteric inhibitor of protein arginine methyltransferase 3 (PRMT3)H Ümit Kaniskan, Magdalena M Szewczyk, Zhengtian Yu, et al.Nature Neuroscience|July 8, 2020
Deschloroclozapine, a potent and selective chemogenetic actuator enables rapid neuronal and behavioral modulations in mice and monkeysYuji Nagai, Naohisa Miyakawa, Hiroyuki Takuwa, et al.Nature Biotechnology|October 27, 2015
Comprehensive characterization of the Published Kinase Inhibitor SetJonathan M Elkins, Vita Fedele, Marta Szklarz, et al.Biorxiv : the Preprint Server for Biology|May 25, 2026
Toward a Random Background for Ligand OptimizationXinyu Xu, Olivier Mailhot, Galen J Correy, et al.Nature|May 21, 2026
De novo design of miniproteins targeting GPCRsEdin Muratspahić, David Feldman, David E Kim, et al.Nature|September 28, 2022
Bespoke library docking for 5-HT2A receptor agonists with antidepressant activityAnat Levit Kaplan, Danielle N Confair, Kuglae Kim, et al.Nature Chemical Biology|July 12, 2011
A chemical probe selectively inhibits G9a and GLP methyltransferase activity in cellsMasoud Vedadi, Dalia Barsyte-Lovejoy, Feng Liu, et al.Pageof 43