19 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
Synthesis of beta-spiro[pyrrolidinoindolines], their binding to the glycine receptor, and in vivo biological acitivity.

TBA
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
Synthesis of heteroaromatic tropeines and heterogeneous binding to glycine receptors.

Hungarian Academy of Sciences
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
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
Heterocyclic inhibitors of monocarboxylate transporter

The Scripps Research Institute
Aminoindane-, aminotetrahydronaphthalene- and aminobenzocyclobutane-derived PRMT5-inhibitors

Ctxt
Heteroaromatic compounds as BTK inhibitors

Boehringer Ingelheim International
Synthesis, thymidine phosphorylase inhibition and molecular modeling studies of 1,3,4-oxadiazole-2-thione derivatives.

Comsats Institute of Information Technology
Splicing factor SF3b as a target of the antitumor natural product pladienolide.

Eisai
Discovery of begacestat, a Notch-1-sparing gamma-secretase inhibitor for the treatment of Alzheimer's disease.

Wyeth Research