electroshock seizure

Lvguidingan 是一种抗惊厥药。

Cyclamic acid sodium (Cyclohexylsulfamicacidsodium) 是一种碳酸酐酶抑制剂，是食品和药品中使用最广泛的人工甜味剂之一。Cyclamic acid sodium 在最大电休克惊厥发作模型显示出中等的抗惊厥活性。Cyclamic acid sodium 可用于研究癌症。

(R)-AS-1 是一种选择性激动性氨基酸转运体2 (EAAT2) 的正向异构调节剂，其EC50为11 nM。(R)-AS-1 以60和90 mg/kg剂量显著增加小鼠的自发运动活动。在最大电休克 (MES)、戊四氮 (PTZ) 和电流刺激 (32或44 mA) 所引发的小鼠癫痫模型中，(R)-AS-1 显示出抗癫痫活性，ED50分别为66.3、36.3、15.6和41.6 mg/kg。此化合物可应用于神经疾病的研究。

Anticonvulsant agent 7 (Compound 19) 是一种口服活性广谱抗惊厥剂，在MES (最大电休克) 和6 Hz癫痫模型中展现了卓越的抗惊厥活性。

H3R antagonist 8 是一种选择性的非咪唑组胺H3 receptor拮抗剂 (IC50= 0.35 μM)，同时表现出对hERG通道的阻断活性 (IC50= 0.67 μM)。通过对H3受体的拮抗作用，H3R antagonist 8 能有效抑制癫痫发作。在最大电休克癫痫 (MES) 模型中，该化合物可以减少小鼠的强直后肢伸展 (THLE) (ED50= 20.21 mg/kg)，并减少AB株斑马鱼幼虫中由戊四唑 (PTZ) 诱导的总移动距离。H3R antagonist 8 可用于癫痫研究。

Zonisamide-13C2,15N is intended for use as an internal standard for the quantification of zonisamide by GC- or LC-MS. Zonisamide (T0267) is an antiepileptic agent.1 It selectively inhibits the repeated firing of sodium channels (IC50 = 2 μg/ml)in mouse embryo spinal cord neurons and inhibits spontaneous channel firing when used at concentrations greater than 10 μg/ml.2 In rat cerebral cortex neurons,zonisamide (1-1,000 μM)inhibits T-type calcium channels with a maximum reduction of 60% of the calcium current.3 Zonisamide (T0267)inhibits H. pylori recombinant carbonic anhydrase (CA)and the human CA isoforms I,II,and V with Ki values of 218,56,35,and 21 nM,respectively.4,5 In mice,it has anticonvulsant activity against maximal electroshock seizure (MES)and pentylenetetrazole-induced maximal,but not minimal,seizures (ED50s = 19.6,9.3,and >500 mg/kg,respectively). Zonisamide (T0267) (40 mg/kg,p.o.)prevents MPTP-induced decreases in the levels of dopamine ,but not homovanillic acid or dihydroxyphenyl acetic acid ,and increases MPTP-induced decreases in the dopamine turnover rate in mouse striatum in a model of Parkinson's disease.6 Formulations containing zonisamide have been used in the treatment of partial seizures in adults with epilepsy.

2-(Isopentylamino)naphthalene-1,4-dione is a vitamin K analog.1It inhibits spasms induced by pentylenetetrazole and tonic hindlimb extension induced by maximal electroshock (MES) in mice (ED50s = 349.2 and 108.1 mg/kg, respectively). It also protects mice against seizures in the 6 Hz psychomotor seizure test (ED50s = 152.7 and 263.7 mg/kg at stimulus intensities of 32 and 44 mA, respectively). 1.Li, X., Himes, R.A., Prosser, L.C., et al.Discovery of the first vitamin K analogue as a potential treatment of pharmacoresistant seizuresJ. Med. Chem.63(11)5865-5878(2020)

Sodium cyclamate-D4是Sodium cyclamate (T38808)的氘代化合物。Sodium cyclamate的CAS号为139-05-9。Cyclamic acid sodium是一种碳酸酐酶抑制剂，是食品和药品中使用最广泛的人工甜味剂之一。Cyclamic acid sodium在最大电休克惊厥发作模型显示出中等的抗惊厥活性。Cyclamic acid sodium可用于研究癌症。

Cyclamic acid sodium (Standard) 是 Cyclamic acid sodium 的标准品，适用于定量分析、质量控制及生化实验等相关研究。Cyclamic acid sodium (Cyclohexylsulfamicacidsodium) 是一种碳酸酐酶抑制剂，是食品和药品中使用最广泛的人工甜味剂之一。Cyclamic acid sodium 在最大电休克惊厥发作模型显示出中等的抗惊厥活性。Cyclamic acid sodium 可用于研究癌症。