PMID

Data

Article Title

Organization

STAT6 phosphorylation inhibitors block eotaxin-3 secretion in bronchial epithelial cells.

Massachusetts General Hospital

Synthesis and evaluation of 2-{[2-(4-hydroxyphenyl)-ethyl]amino}pyrimidine-5-carboxamide derivatives as novel STAT6 inhibitors.

Astellas Pharm

Novel 7H-pyrrolo[2,3-d]pyrimidine derivatives as potent and orally active STAT6 inhibitors.

Astellas Pharma

Identification of 4-benzylamino-2-[(4-morpholin-4-ylphenyl)amino]pyrimidine-5-carboxamide derivatives as potent and orally bioavailable STAT6 inhibitors.

Astellas Pharma

Discovery of a Potent and Selective STAT5 PROTAC Degrader with Strong Antitumor Activity

University of Michigan

Total Synthesis, Structure Reassignment, and Biological Evaluation of the Anti-Inflammatory Macrolactone 13-Hydroxy-14-deoxyoxacyclododecindione.

Johannes Gutenberg-University

Total Synthesis and Biological Evaluation of the Anti-Inflammatory (13

Johannes Gutenberg-University

SD-91 as A Potent and Selective STAT3 Degrader Capable of Achieving Complete and Long-Lasting Tumor Regression.

University of Michigan

Targeting the Src Homology 2 (SH2) Domain of Signal Transducer and Activator of Transcription 6 (STAT6) with Cell-Permeable, Phosphatase-Stable Phosphopeptide Mimics Potently Inhibits Tyr641 Phosphorylation and Transcriptional Activity.

Rice University