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Cat. No. | Product Name | Target | Signaling Pathways |
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T1413 |
Pentetrazol
Metrazole,Pentylenetetrazole,Pentylenetetrazol,戊四唑,PTZ,pentamethylenetetrazol,Cardiazol |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Pentetrazol 是一种 GABA(A) 受体拮抗剂,具有中枢神经系统和呼吸兴奋剂的活性。 | |||
T22171 |
WWL123
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MAGL | Metabolism |
WWL123 是一种有效的选择性 ABHD6 抑制剂,IC50 为 430 nM。WWL123 可穿过血脑屏障并抑制脑实质中的 ABHD6。WWL123 阻断 ABHD6 在 Pentylenetetrazole (PTZ)诱导的 R6/2 小鼠癫痫样发作和自发性癫痫发作中发挥抗癫痫作用。 | |||
T25764 |
LY 81067
Lilly-81067,LY81067,Lilly81067,Lilly 81067,LY-81067 |
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LY 81067是一种新型抗惊厥化合物,可有效预防戊四唑和苦防己毒素诱导的小鼠惊厥。它通过结合到苦防己素结合位点或其附近来发挥其抗惊厥作用。 | |||
T81674 |
NIR-FP
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NIR-FP是一款用于超氧阴离子(O2-)检测的近红外荧光探针,具备高灵敏度和高选择性。由于O2-是活性氧种(ROS)的关键前体,此探针能有效动态监测由超氧阴离子引发的铁死亡介导的癫痫模型。这些模型包括红藻氨酸诱导的慢性癫痫模型、Pentylenetetrazole诱导的急性癫痫模型以及毛果芸香碱诱导的癫痫模型。 | |||
T16948 |
Suclofenide
PB385,Neosulfalepsine,琥氯非尼 |
Others | Others |
Suclofenide 是一种苯磺酰胺衍生物,可作为抗惊厥和抗癫痫剂。在临床前模型中,它对小鼠电击和戊四唑诱导的惊厥表现出强大的抗惊厥活性。亚致死毒性表现为嗜睡、肌阵挛抽搐和腹泻。 | |||
T37950 |
2-(Isopentylamino)naphthalene-1,4-dione
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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 tr... | |||
T70292 |
DDPM-2571 HCl
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DDPM-2571 is a highly potent and in vivo active inhibitor of GABA transporter subtype 1 with anticonvulsant, anxiolytic, antidepressant and antinociceptive properties. DDPM-2571 was quickly distributed into the brain and was highly effective in the prevention of chemically-induced seizures (pentylenetetrazole and pilocarpine models) and 6-Hz convulsions. It demonstrated significant anxiolytic-like and antidepressant-like properties. DDPM-2571 had antinociceptive properties, both in the hot plate... | |||
T37215 |
5α,6β-Dihydroxycholestanol
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5α,6β-Dihydroxycholestanol is an oxysterol metabolite of cholesterol formed from conversion of cholesterol epoxides by 5,6-epoxysterol hydrolase. It inhibits NMDA-mediated calcium influx in HEK293 cells expressing NR1/NR2B NMDA receptors in a concentration-dependent manner. It also binds to voltage-gated sodium (Nav) channels and decreases action potentials in hippocampal neurons in vitro when used at a concentration of 10 uM. It increases survival of spinal cord motoneurons, cortical neurons, a... | |||
T35755 |
Avermectin B1a aglycone
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Avermectin B1a aglycone is an aglycone form of the anthelmintic and insecticide avermectin B1a . It hyperpolarizes P. crassipes muscle fibers with a minimum active concentration (MAC) value of 0.1 μM. Avermectin B1a aglycone decreases survival of C. elegans (MAC = 0.1 μM). In vivo, avermectin B1a aglycone prevents seizures induced by pentylenetetrazole in mice (ED50 = 43.9 mg/kg) without inducing deficits in rotarod performance. | |||
T37847 |
Zonisamide-13C2,15N
Zonisamide-13C2,15N |
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Zonisamide-13C2,15N is intended for use as an internal standard for the quantification of zonisamide by GC- or LC-MS. Zonisamide 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... | |||
T37194 |
5α-Androst-16-en-3α-ol
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5α-Androst-16-en-3α-ol is a steroid pheromone that has been found in boar testes and human male axillary sweat and has diverse biological activities.1,2It enhances GABA-activated currents in primary mouse cerebellar granule cells (EC50= 0.4 μM).25α-Androst-16-en-3α-ol (0.1-1 μM) increases the amplitude of GABA-activated currents in HEK293 cells expressing human α1β2γ2and α2β2γ2subunit-containing GABAAreceptors.In vivo, 5α-androst-16-en-3α-ol (5-10 mg/kg) decreases immobility time in the forced s... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T0983 |
Penicillamine
青霉胺,d-penicillamin,Dimethyl Cysteine,D-青霉胺,Artamine,D-(-)-Penicillamine |
Antibiotic | Microbiology/Virology |
Penicillamine (Artamine) 是一种 penicillin 的代谢降解产物,是一种螯合剂,可作用于威尔逊氏病。 | |||
TMS1461 |
Qingyangshengenin B
青阳参甙元B,青阳参苷元B,Otophylloside B |
Beta Amyloid | Neuroscience |
Qingyangshengenin B (Otophylloside B) 是一种分离自 Qingyangshen 的 C-21 甾体苷。它能够在 mRNA 水平上抑制 Aβ 的表达来减少 Aβ 的沉积,对 Aβ 的毒性有保护作用。它具有抗癫痫作用。 | |||
T20493 |
Palmitone
NSC-953,NSC953,NSC 953 |
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In the CA3 hippocampal region, Palmitone against pentylenetetrazole-caused neuronal damage. | |||
TN4722 |
Otophylloside F
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Others | Others |
Otophylloside F can suppress the seizure-like locomotor activity caused by pentylenetetrazole in zebrafish. |