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Cat. No. Product Name Target Signaling Pathways
T68599 Orphenadrine

Orphenadrine (free base)

Sodium Channel; NMDAR; AChR Membrane transporter/Ion channel; Neuroscience
Orphenadrine 是一种非竞争性的 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,以浓度依赖性方式抑制克隆的 HERG 通道,在 HEK 细胞中产生0.85μM 的 IC。Orphenadrine 是中枢和外周毒蕈碱受体的拮抗剂,通过孔残基 Y652或 F656突变阻断衰减。 Orphenadrine 具有抗痉挛、镇痛和抗胆碱能活性,对在体外和体内对谷氨酸神经毒性具有保护作用。Orphenadrine 对钠离子通道具有抑制作用,可用来治疗帕金森。
T70487 Tofenacin (free base)

Tofenacin (free base) is an antidepressant drug with a tricyclic-like structure. It acts as a serotonin-norepinephrine reuptake inhibitor, and based on its close relation to orphenadrine, may also possess anticholinergic and antihistamine properties. Tofenacin is also the major active metabolite of orphenadrine and likely plays a role in its beneficial effects against depressive symptoms seen in Parkinson's disease patients.

化合物

Orphenadrine
Cat.No: T68599
Synonym: Orphenadrine (free base)
Target: Sodium Channel, NMDAR, AChR
Tofenacin (free base)
Cat.No: T70487
Synonym:
Target:
TargetMol Loading
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