15 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Benzylpiperidine variations on histamine H3 receptor ligands for improved drug-likeness.
Johann Wolfgang Goethe University
Evaluation of structure-derived pharmacophore of soluble epoxide hydrolase inhibitors by virtual screening.
Johann Wolfgang Goethe University
Structure-activity relationship of nonacidic quinazolinone inhibitors of human microsomal prostaglandin synthase 1 (mPGES 1).
Johann Wolfgang Goethe University
Acidic elements in histamine H(3) receptor antagonists.
Johann Wolfgang Goethe University
Azole derivatives as histamine H3 receptor antagonists, part I: thiazol-2-yl ethers.
Johann Wolfgang Goethe University
Azole derivatives as histamine H3 receptor antagonists, part 2: C-C and C-S coupled heterocycles.
Johann Wolfgang Goethe University
2,4-Diaminopyrimidines as histamine H4 receptor ligands--Scaffold optimization and pharmacological characterization.
Johann Wolfgang Goethe University
NVP-BHG712: Effects of Regioisomers on the Affinity and Selectivity toward the EPHrin Family.
Johann Wolfgang Goethe University
Hybrid approach for the design of highly affine and selective dopamine D(3) receptor ligands using privileged scaffolds of biogenic amine GPCR ligands.
Johann Wolfgang Goethe University
Shifting the selectivity of pyrido[2,3-d]pyrimidin-7(8H)-one inhibitors towards the salt-inducible kinase (SIK) subfamily.
Johann Wolfgang Goethe University
Structure-Based Design of Selective Salt-Inducible Kinase Inhibitors.
Johann Wolfgang Goethe University
Synthesis of thieno[2,3-b]pyridinones acting as cytoprotectants and as inhibitors of [3H]glycine binding to the N-methyl-D-aspartate (NMDA) receptor.
Johann Wolfgang Goethe University
Development of a Selective Dual Discoidin Domain Receptor (DDR)/p38 Kinase Chemical Probe.
Johann Wolfgang Goethe University
Selective targeting of the αC and DFG-out pocket in p38 MAPK.
Johann Wolfgang Goethe University