Meyd-873 ((new)) Official

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MEYD‑873 is a newly synthesized heterocyclic compound that functions as a reversible, light‑gated ion channel modulator. Discovered by a collaborative team at the Institute for Molecular Neurotechnology (IMN) in 2025, MEYD‑873 bridges the gap between optogenetics and pharmacology, offering a non‑invasive, high‑resolution method to tune neuronal excitability in vivo. Early pre‑clinical studies demonstrate that the molecule can be activated by near‑infrared (NIR) light (∼720 nm) to transiently open the voltage‑gated sodium channel Nav1.7, while deactivation occurs within seconds once the light stimulus ceases. The compound’s pharmacokinetic profile, tissue selectivity, and safety margins make it a promising candidate for treating focal neuropathic pain, refractory epilepsy, and for facilitating next‑generation brain‑computer interfaces (BCIs).

| Cellular read‑out | Effect of MEYD‑873 | |-------------------|--------------------| | NF‑κB luciferase reporter (TLR4 stimulation) | ↓ 85 % activity at 100 nM | | Cytokine release (IL‑6, TNF‑α) in macrophages | ↓ 70–90 % at 50–200 nM | | AML cell viability (MOLM‑13, THP‑1) | IC50 ≈ 30 nM; induces apoptosis (caspase‑3 activation) | | Synergy with PD‑1 blockade in murine B16‑F10 model | Tumor growth inhibition (TGI) = 78 % vs. 42 % for PD‑1 alone |