15 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Oxime Ethers of (E)-11-Isonitrosostrychnine as Highly Potent Glycine Receptor Antagonists.

The German University In Cairo
Ensemble-based virtual screening for cannabinoid-like potentiators of the human glycine receptora1 for the treatment of pain.

University of Pittsburgh
Australian marine sponge alkaloids as a new class of glycine-gated chloride channel receptor modulator.

The University of Queensland
Pharmacological characteristics and binding modes of caracurine V analogues and related compounds at the neuronal alpha7 nicotinic acetylcholine receptor.

University of Copenhagen
Ircinialactams: subunit-selective glycine receptor modulators from Australian sponges of the family Irciniidae.

The University of Queensland
Structural Basis for Molecular Recognition of Cannabinoids by Inhibitory Cys-Loop Channels.

Universidad de Buenos Aires
Probing the pharmacophore of ginkgolides as glycine receptor antagonists.

University of Copenhagen
C-2-Linked Dimeric Strychnine Analogues as Bivalent Ligands Targeting Glycine Receptors.

The German University In Cairo
11-Aminostrychnine and

The German University In Cairo
Applications of parallel synthetic lead hopping and pharmacophore-based virtual screening in the discovery of efficient glycine receptor potentiators.

Amgen
Modulation of Glycine-Mediated Spinal Neurotransmission for the Treatment of Chronic Pain.

Albany College of Pharmacy and Health Sciences
Progress in the discovery of small molecule modulators of the Cys-loop superfamily receptors.

Amgen
Pharmacological property optimization for allosteric ligands: A medicinal chemistry perspective.

Intellisyn Pharma
Pharmacologically active compounds

The University of Liverpool
Atomoxetine increases extracellular levels of norepinephrine and dopamine in prefrontal cortex of rat: a potential mechanism for efficacy in attention deficit/hyperactivity disorder.

Eli Lilly