18 articles for thisTarget
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Functional characterization of the human multidrug transporter, ABCG2, expressed in insect cells.

Hungarian Academy of Sciences
Design, synthesis, pharmacological evaluation, and structure-activity study of novel endomorphin analogues with multiple structural modifications.

Hungarian Academy of Sciences
Synthesis of heteroaromatic tropeines and heterogeneous binding to glycine receptors.

Hungarian Academy of Sciences
Validation of high-affinity binding sites for succinic acid through distinguishable binding of gamma-hydroxybutyric acid receptor-specific NCS 382 antipodes.

Hungarian Academy of Sciences
New endomorphin analogues containing alicyclic beta-amino acids: influence on bioactive conformation and pharmacological profile.

Hungarian Academy of Sciences
Beta-methyl substitution of cyclohexylalanine in Dmt-Tic-Cha-Phe peptides results in highly potent delta opioid antagonists.

Hungarian Academy of Sciences
Discovery of selective fragment-sized immunoproteasome inhibitors.

Hungarian Academy of Sciences
The impact of binding site waters on the activity/selectivity trade-off of Janus kinase 2 (JAK2) inhibitors.

Hungarian Academy of Sciences
Deltorphin II analogues with 6-hydroxy-2-aminotetralin-2-carboxylic acid in position 1.

Hungarian Academy of Sciences
Conformationally constrained deltorphin analogs with 2-aminotetralin-2-carboxylic acid in position 3.

Hungarian Academy of Sciences
Synthesis of tropeines and allosteric modulation of ionotropic glycine receptors.

Hungarian Academy of Sciences
Inhibition of the LOX enzyme family members with old and new ligands. Selectivity analysis revisited.

Hungarian Academy of Sciences
Discovery of d-amino acid oxidase inhibitors based on virtual screening against the lid-open enzyme conformation.

Hungarian Academy of Sciences
Discovery of isatin and 1H-indazol-3-ol derivatives as d-amino acid oxidase (DAAO) inhibitors.

Hungarian Academy of Sciences