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β3-AR agonist 2 是一种有效的选择性 β3 肾上腺素能受体 (β3-adrenergic receptor，β3-AR) 激动剂， EC50 为 8 nM

Citicoline产品描述：Citicoline is an intermediate in the synthesis of phosphatidylcholine, a component of cell membranes. Citicoline exerts neuroprotective effects.In Vitro: To determine the potential neuroprotective activity of Citicoline ａnd Homotaurine, treated retinal cells are treated with increasing concentrations of Citicoline or Homotaurine for 24 hours. 1?μM, 10?μM ａnd 100?μM of Citicoline or Homotaurine are used to investigate whether may contribute to a reduced cell viability in retinal cells. Retinal cells are well preserved in Citicoline- or Homotaurine-treated cultures, with no evidence of toxicity or significant loss of viability after treatments. 100?μM of Citicoline is not harmful to retinal neuroglial cells in vitro ａnd 100?μM of Homotaurine is an effective concentration to enhance neuroprotection in a model of experimental glaucoma. Therefore, this concentration of Citicoline ａnd Homotaurine is used for all subsequent experiments. To evaluate whether cotreatment with Citicoline ａnd Homotaurine is able to induce a synergistic neuroprotective effect against glutamate excitotoxicity, retinal cell cultures are exposed to Citicoline 100?μM, Homotaurine 100?μM, ａnd Citicoline+Homotaurine 100?μM, 24 hours before glutamate treatment. In the presence of 100?μM Citicoline, a significant increase in cell viability is observed^[1].In Vivo: Administration of Citicoline in a dose of 1000 mg/kg produces more pronounced increase in the threshold of clonic seizures ａnd tonic phase of seizures with lethal outcome (by 18.54 ａnd 50.08% respectively, in comparison with the control). The anticonvulsant effect is most pronounced after injection of Citicoline in a dose of 1000 mg/kg^[2].
产品链接：www.medchemexpress.com/Citicoline.html

研究领域：Others

靶点：Others

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