Sone-214 ((exclusive)) -
Sone-214 is a highly selective and potent inhibitor of the c-MET signaling pathway. By binding to the ATP-binding site of the c-MET receptor, Sone-214 effectively blocks the activation of downstream signaling pathways, thereby inhibiting the downstream effects of c-MET signaling. Specifically, Sone-214 has been shown to prevent the recruitment of p85 subunit of PI3K to c-MET, leading to a reduction in the activation of the PI3K/AKT signaling cascade and the subsequent suppression of cell growth and survival pathways.
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SONE‑214 is a next‑generation STING‑targeting small molecule designed to trigger a type I interferon‑dominant response while minimizing the pro‑inflammatory NF‑κB cascade that often leads to systemic toxicity in earlier STING agonists (e.g., DMXAA, ADU‑S100).
No weight loss > 5 % at the highest tested dose (60 mg/kg). Serum ALT/AST ≤ 1.2× baseline. Histopathology showed only mild, transient splenic hyperplasia (consistent with IFN response).
The c-MET signaling pathway is a key regulator of cellular growth, survival, and motility in response to its ligand, hepatocyte growth factor (HGF). Aberrant activation of c-MET has been implicated in the development and progression of numerous cancers, leading to tumor aggression, chemotherapy resistance, and poor patient outcomes. The c-MET pathway has also been linked to the epithelial-to-mesenchymal transition (EMT) process, which enables cancer cells to acquire migratory and invasive properties, further complicating cancer treatment.