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BindingDB contains 3.1M data for 1.3M Compounds and 9.6K Targets. Of those, 1.5M data for 698K Compounds and 4.7K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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19 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Oxime Ethers of (E)-11-Isonitrosostrychnine as Highly Potent Glycine Receptor Antagonists.EBI
The German University In Cairo
Ensemble-based virtual screening for cannabinoid-like potentiators of the human glycine receptora1 for the treatment of pain.EBI
University of Pittsburgh
Synthesis of beta-spiro[pyrrolidinoindolines], their binding to the glycine receptor, and in vivo biological acitivity.EBI
TBA
Australian marine sponge alkaloids as a new class of glycine-gated chloride channel receptor modulator.EBI
The University of Queensland
Pharmacological characteristics and binding modes of caracurine V analogues and related compounds at the neuronal alpha7 nicotinic acetylcholine receptor.EBI
University of Copenhagen
Ircinialactams: subunit-selective glycine receptor modulators from Australian sponges of the family Irciniidae.EBI
The University of Queensland
Synthesis of heteroaromatic tropeines and heterogeneous binding to glycine receptors.EBI
Hungarian Academy of Sciences
Probing the pharmacophore of ginkgolides as glycine receptor antagonists.EBI
University of Copenhagen
C-2-Linked Dimeric Strychnine Analogues as Bivalent Ligands Targeting Glycine Receptors.EBI
The German University In Cairo
11-Aminostrychnine and EBI
The German University In Cairo
Modulation of Glycine-Mediated Spinal Neurotransmission for the Treatment of Chronic Pain.EBI
Albany College of Pharmacy and Health Sciences
Progress in the discovery of small molecule modulators of the Cys-loop superfamily receptors.EBI
Amgen
Pharmacological property optimization for allosteric ligands: A medicinal chemistry perspective.EBI
Intellisyn Pharma
Heterocyclic inhibitors of monocarboxylate transporterBDB
The Scripps Research Institute
Aminoindane-, aminotetrahydronaphthalene- and aminobenzocyclobutane-derived PRMT5-inhibitorsBDB
Ctxt
Heteroaromatic compounds as BTK inhibitorsBDB
Boehringer Ingelheim International
Synthesis, thymidine phosphorylase inhibition and molecular modeling studies of 1,3,4-oxadiazole-2-thione derivatives.BDB
Comsats Institute of Information Technology
Splicing factor SF3b as a target of the antitumor natural product pladienolide.BDB
Eisai
Discovery of begacestat, a Notch-1-sparing gamma-secretase inhibitor for the treatment of Alzheimer's disease.BDB
Wyeth Research