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Carbamazepine
CAS No. : 298-46-4
MCE 国际站:Carbamazepine
产品活性:Carbamazepine 是一种具有口服活性的压敏钠离子通道阻断剂,IC50 为 131 μM。Carbamazepine 可阻断电压门控 Na+、Ca2+ 和 K+ 通道,也是一种 HDAC 抑制剂 (IC50: 2 μM)。Carbamazepine 是一种抗惊厥试剂,可用于癫痫和神经性疼痛的研究。
研究领域:Membrane Transporter/Ion Channel | Autophagy | Neuronal Signaling | Epigenetics | Cell Cycle/DNA Damage
作用靶点:Sodium Channel | Autophagy | Mitophagy | Potassium Channel | Calcium Channel | HDAC
In Vitro: Carbamazepine (0-500 μM, 10 days) inhibits pre-adipocyte differentiation (10 days) and triglyceride accumulation (7 days) in 3T3-L1, 3T3-F442A and T37i cells.
Carbamazepine (5-20 μM, 15 min before LPS) inhibits LPS-induced production of NO and iNOS protein, and phosphorylation of Akt in microglial (BV-2) cells.
Carbamazepine (20 μM, 15 min before LPS) inhibits LPS-induced COX-2 expression and TNF-α production in microglial (BV-2) cells.
In Vivo: Carbamazepine (250 mg/kg, p.o.) promotes liver regeneration and survival in partial hepatectomy (PHx) treated mice.
Carbamazepine (0.25%-0.75% for ICR mice, 0.5% and 0.75% for C57bl/6 mice with, in food (w/w)) shows mood-stabilising effects in mice.
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