13 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Rational design and synthesis of 4-substituted 2-pyridin-2-ylamides with inhibitory effects on SH2 domain-containing inositol 5'-phosphatase 2 (SHIP2).

University of Toyama
Discovery and evaluation of novel SHIP-1 inhibitors.

Purdue University
NVP-BHG712: Effects of Regioisomers on the Affinity and Selectivity toward the EPHrin Family.

Johann Wolfgang Goethe University
Inhibition of the EphA2-Sam/Ship2-Sam Association through Peptide Ligands: Studying the Combined Effect of Charge and Aromatic Character.

Institute of Biostructures and Bioimaging
Discovery of aurones bearing two amine functionalities as SHIP2 inhibitors with insulin-sensitizing effect in rat myotubes.

Universiti Sains Malaysia
Allosteric Site on SHIP2 Identified Through Fluorescent Ligand Screening and Crystallography: A Potential New Target for Intervention.

University of East Anglia
Regioisomeric Family of Novel Fluorescent Substrates for SHIP2.

School of Biological Sciences, Uea
Identification of crizotinib derivatives as potent SHIP2 inhibitors for the treatment of Alzheimer's disease.

Korea Institute of Science and Technology
Heterocyclic inhibitors of monocarboxylate transporter

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

Ctxt
ORA1, a zebrafish olfactory receptor ancestral to all mammalian V1R genes, recognizes 4-hydroxyphenylacetic acid, a putative reproductive pheromone.

German Institute of Human Nutrition Potsdam-Rehbruecke
Chromane compounds

Comentis
Pharmacological and functional comparison of the polo-like kinase family: insight into inhibitor and substrate specificity.

Abbott Laboratories