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ProxyBind: A compendium of binding sites for proximity-induced pharmacology.

  • Read more about ProxyBind: A compendium of binding sites for proximity-induced pharmacology.

An open source plant kinase chemogenomics set.

  • Read more about An open source plant kinase chemogenomics set.

Distal extracellular teneurin region (teneurin C-terminal associated peptide; TCAP) possesses independent intracellular calcium regulating actions, in vitro: A potential antagonist of corticotropin-releasing factor (CRF).

  • Read more about Distal extracellular teneurin region (teneurin C-terminal associated peptide; TCAP) possesses independent intracellular calcium regulating actions, in vitro: A potential antagonist of corticotropin-releasing factor (CRF).

Autoantigenic properties of the aminoacyl tRNA synthetase family in idiopathic inflammatory myopathies.

  • Read more about Autoantigenic properties of the aminoacyl tRNA synthetase family in idiopathic inflammatory myopathies.

Discovery of 3-Amino-1H-pyrazole-Based Kinase Inhibitors to Illuminate the Understudied PCTAIRE Family.

  • Read more about Discovery of 3-Amino-1H-pyrazole-Based Kinase Inhibitors to Illuminate the Understudied PCTAIRE Family.

MSC-1186, a Highly Selective Pan-SRPK Inhibitor Based on an Exceptionally Decorated Benzimidazole-Pyrimidine Core.

  • Read more about MSC-1186, a Highly Selective Pan-SRPK Inhibitor Based on an Exceptionally Decorated Benzimidazole-Pyrimidine Core.

Skeletal muscle metabolism and contraction performance regulation by teneurin C-terminal-associated peptide-1.

  • Read more about Skeletal muscle metabolism and contraction performance regulation by teneurin C-terminal-associated peptide-1.

The future of chemical probes is diversity.

  • Read more about The future of chemical probes is diversity.

Development of a Potent Cyclic Peptide Inhibitor of the nNOS/PSD-95 Interaction.

  • Read more about Development of a Potent Cyclic Peptide Inhibitor of the nNOS/PSD-95 Interaction.

Systematic Design of Adenosine Analogs as Inhibitors of a Clostridioides difficile-Specific DNA Adenine Methyltransferase Required for Normal Sporulation and Persistence.

  • Read more about Systematic Design of Adenosine Analogs as Inhibitors of a Clostridioides difficile-Specific DNA Adenine Methyltransferase Required for Normal Sporulation and Persistence.

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