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Bioorganic & Medicinal Chemistry|December 8, 2004
Synthesis and receptor assay of aromatic-ethynyl-aromatic derivatives with potent mGluR5 antagonist activityDavid Alagille, Ronald M Baldwin, Bryan L Roth, et al.
Bioorganic & Medicinal Chemistry Letters|August 3, 2005
SAR of psilocybin analogs: discovery of a selective 5-HT 2C agonistHoward Sard, Govindaraj Kumaran, Cynthia Morency, et al.
Bioorganic & Medicinal Chemistry Letters|February 3, 2005
Functionalization at position 3 of the phenyl ring of the potent mGluR5 noncompetitive antagonists MPEPDavid Alagille, Ronald M Baldwin, Bryan L Roth, et al.
The Journal of Biological Chemistry|December 24, 2008
Ribosomal S6 kinase 2 directly phosphorylates the 5-hydroxytryptamine 2A (5-HT2A) serotonin receptor, thereby modulating 5-HT2A signalingRyan T Strachan, Douglas J Sheffler, Belinda Willard, et al.
Assay and Drug Development Technologies|March 21, 2012
An automated electrophysiological assay for differentiating Ca(v)2.2 inhibitors based on state dependence and kineticsAndrew M Swensen, Wende Niforatos, Timothy A Vortherms, et al.
Journal of Medicinal Chemistry|July 22, 2017
A Simple Representation of Three-Dimensional Molecular StructureSeth D Axen, Xi-Ping Huang, Elena L Cáceres, et al.
Bioorganic & Medicinal Chemistry|January 17, 2012
Multi-receptor drug design: Haloperidol as a scaffold for the design and synthesis of atypical antipsychotic agentsKwakye Peprah, Xue Y Zhu, Suresh V K Eyunni, et al.
Bioorganic & Medicinal Chemistry Letters|April 20, 2006
Evaluation of the eutomer of 4-{3-(4-chlorophenyl)-3-hydroxypyrrolidin-1-yl}-1-(4-fluorophenyl)butan-1-one, {(+)-SYA 09}, a pyrrolidine analog of haloperidolSeth Y Ablordeppey, Margaret Lyles-Eggleston, Barbara Bricker, et al.
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