17 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
Organization
Structure-Activity Relationships of Small Molecule Autotaxin Inhibitors with a Discrete Binding Mode.

University of Strathclyde
Investigation of a Bicyclo[1.1.1]pentane as a Phenyl Replacement within an LpPLA

University of Strathclyde
Development of Autotaxin Inhibitors: An Overview of the Patent and Primary Literature.

University of Strathclyde
Doing the methylene shuffle--further insights into the inhibition of mitotic kinesin Eg5 with S-trityl L-cysteine.

University of Strathclyde
6-Acetyl-7,7-dimethyl-5,6,7,8-tetrahydropterin is an activator of nitric oxide synthases.

University of Strathclyde
Synthesis and Evaluation of Small Molecule Inhibitors of the Androgen Receptor N-Terminal Domain.

University of Strathclyde
M4 agonists/5HT7 antagonists with potential as antischizophrenic drugs: serominic compounds.

University of Strathclyde
Structure-Based Design of a Novel Class of Autotaxin Inhibitors Based on Endogenous Allosteric Modulators.

University of Strathclyde
Discovery of the first potent and selective α

University of Strathclyde
Hi-JAK-ing the ubiquitin system: The design and physicochemical optimisation of JAK PROTACs.

University of Strathclyde
A fragment-like approach to PYCR1 inhibition.

University of Strathclyde
Optimization of Potent ATAD2 and CECR2 Bromodomain Inhibitors with an Atypical Binding Mode.

University of Strathclyde
Novel tacrine analogues for potential use against Alzheimer's disease: potent and selective acetylcholinesterase inhibitors and 5-HT uptake inhibitors.

University of Strathclyde
Discovery of ( S)-3-(3-(3,5-Dimethyl-1 H-pyrazol-1-yl)phenyl)-4-(( R)-3-(2-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)ethyl)pyrrolidin-1-yl)butanoic Acid, a Nonpeptidic α

University of Strathclyde
Discovery of Tetrahydroquinoxalines as Bromodomain and Extra-Terminal Domain (BET) Inhibitors with Selectivity for the Second Bromodomain.

University of Strathclyde
Emergence of Small-Molecule Non-RGD-Mimetic Inhibitors for RGD Integrins.

University of Strathclyde
Inhibitory Kappa B Kinaseα (IKKα) Inhibitors That Recapitulate Their Selectivity in Cells against Isoform-Related Biomarkers.

University of Strathclyde