| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10587788 | Bioorganic & Medicinal Chemistry Letters | 2013 | 5 Pages |
Abstract
Inhibition of the signal transducer and activator of transcription 3 (STAT3) signaling pathway has been considered a novel therapeutic strategy to treat human cancers that harbor aberrantly-active STAT3. In this study, a series of small molecules were identified as novel inhibitors of STAT3 signaling pathway through virtual screening. A tricyclic scaffold containing compound, 6, was identified as an inhibitor of IL-6/STAT3 signaling with an IC50 of 26.68 μM. In addition, this compound inhibited Tyr705 phosphorylation of STAT3 and had no obvious effect on upstream tyrosine kinases. Thus, compound 6 is a potential lead structure and valuable for further drug development.
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Authors
Mingming Zhang, Weiliang Zhu, Ning Ding, Wei Zhang, Yingxia Li,
