243 Results for "

Anti-epileptic

" in MedChemExpress (MCE) Product Catalog:
Products (243)

243 Results for "Anti-epileptic" in MCE Product Catalog:

584
584 Publications Verification
Cat. No.: HY-10583
CAS No.: 129830-38-2
Purity:  99.94%
Target:  

Organoid ROCK

Research Areas:  

Neurological Disease Cancer

Y-27632 dihydrochloride is an orally active and ATP-competitive ROCK (Rho-kinase) inhibitor (ROCK-I Ki=220 nM; ROCK-II Ki=300 nM). Y-27632 dihydrochloride shows antiepileptic effects .
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428
428 Cited Publications
Cat. No.: HY-10583R
CAS No.: 129830-38-2
Research Areas:  

Cancer

Y-27632 dihydrochloride (Standard) is the analytical standard of Y-27632 dihydrochloride. Y-27632 dihydrochloride is an orally active and ATP-competitive ROCK (Rho-kinase) inhibitor (ROCK-I Ki=220 nM; ROCK-II Ki=300 nM). Y-27632 dihydrochloride shows antiepileptic effects .
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9
9 Cited Publications
Cat. No.: HY-B0122
CAS No.: 97240-79-4
Synonyms: McN 4853; RWJ 17021
Topiramate (McN 4853) is a broad-spectrum antiepileptic agent. Topiramate is a GluR5 receptor antagonist. Topiramate produces its antiepileptic effects through enhancement of GABAergic activity, inhibition of kainate/AMPA receptors, inhibition of voltage-sensitive sodium and calcium channels, increases in potassium conductance, and inhibition of carbonic anhydrase .
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7
7 Cited Publications
Cat. No.: HY-B0495
CAS No.: 84057-84-1
Synonyms: LTG; BW430C
Research Areas:  

Neurological Disease Cancer

Lamotrigine (BW430C) is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine selectively blocks voltage-gated Na + channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine can be used for the research of epilepsy, focal seizure, et al .
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7
7 Cited Publications
Cat. No.: HY-110032
CAS No.: 113170-86-8
Synonyms: LTG isethionate; BW430C isethionate
Research Areas:  

Neurological Disease Cancer

Lamotrigine (BW430C) isethionate is a potent and orally active anticonvulsant or antiepileptic agent. Lamotrigine isethionate selectively blocks voltage-gated Na + channels, stabilizing presynaptic neuronal membranes and inhibiting glutamate release. Lamotrigine isethionate can be used for the research of epilepsy, focal seizure, et al .
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6
6 Cited Publications
Cat. No.: HY-B0448
CAS No.: 57-41-0
Synonyms: 5,5-Diphenylhydantoin
Research Areas:  

Neurological Disease Cancer

Phenytoin (5,5-Diphenylhydantoin) is a potent Voltage-gated Na + channels (VGSCs) blocker. Phenytoin has antiepileptic activity and reduces breast tumour growth and metastasis in mice .
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6
6 Cited Publications
Cat. No.: HY-B0448A
CAS No.: 630-93-3
Synonyms: 5,5-Diphenylhydantoin sodium salt
Research Areas:  

Neurological Disease Cancer

Phenytoin sodium (5,5-Diphenylhydantoin sodium salt) is a potent Voltage-gated Na + channels (VGSCs) blocker. Phenytoin has antiepileptic activity and reduces breast tumour growth and metastasis in mice .
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6
6 Cited Publications
Cat. No.: HY-B0033
CAS No.: 1391054-02-6
Synonyms: γ-Vinyl-GABA hydrochloride
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Vigabatrin hydrochloride (γ-Vinyl-GABA hydrochloride), a inhibitory neurotransmitter GABA vinyl-derivative, is an orally active and irreversible GABA transaminase inhibitor. Vigabatrin hydrochloride is an antiepileptic agent, which acts by increasing GABA levels in the brain by inhibiting the catabolism of GABA by GABA transaminase .
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6
6 Cited Publications
Cat. No.: HY-15399
CAS No.: 68506-86-5
Purity:  ≥98.0%
Synonyms: γ-Vinyl-GABA
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Vigabatrin (γ-Vinyl-GABA), an inhibitory neurotransmitter GABA vinyl-derivative, is an orally active and irreversible GABA transaminase inhibitor. Vigabatrin is an antiepileptic agent, which acts by increasing GABA levels in the brain by inhibiting the catabolism of GABA by GABA transaminase .
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4
4 Cited Publications
Cat. No.: HY-B0774
CAS No.: 112665-43-7
Synonyms: AA 2414
Seratrodast (AA 2414), an orally active antiasthmatic agent, is a thromboxane A2 receptor (TP) antagonist and ferroptosis inhibitor. Seratrodast reduces lipid ROS production, modulates the systemic xc-/GSH/GPX4 axis, and inhibits JNK phosphorylation and p53 expression. Seratrodast exhibits anti-asthmatic and anti-epileptic activity .
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3
3 Cited Publications
Cat. No.: HY-107515
CAS No.: 198419-91-9
Purity:  ≥99.0%
Target:  

mGluR

Research Areas:  

Neurological Disease

LY367385 is a highly selective and potent mGluR1a antagonist. LY367385 has an IC50 of 8.8 μM for inhibiting of quisqualate-induced phosphoinositide (PI) hydrolysis, compared with >100 μM for mGlu5a. LY367385 has neuroprotective, anticonvulsant and antiepileptic effects .
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3
3 Cited Publications
Cat. No.: HY-107515A
CAS No.: 2829282-00-8
Purity:  99.47%
Target:  

mGluR

Research Areas:  

Neurological Disease

LY367385 hydrochloride is a highly selective and potent mGluR1a antagonist. LY367385 hydrochloride has an IC50 of 8.8 μM for inhibiting of quisqualate-induced phosphoinositide (PI) hydrolysis, compared with >100 μM for mGlu5a. LY367385 hydrochloride has neuroprotective, anticonvulsant and antiepileptic effects .
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2
2 Cited Publications
Cat. No.: HY-109009
CAS No.: 1294000-61-5
Purity:  99.65%
Synonyms: UCB-0942
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

Padsevonil (UCB0942) is a potent antiepileptic agent that selectively acts on presynaptic and postsynaptic targets. Padsevonil binds to synaptic vesicular protein 2 (SV2) with high affinity. Padsevonil is also a positive allosteric modulator and partial agonist of GABAAR, with high potency against α1 and α5 receptors. Padsevonil has antiepileptic effects in a variety of rodent models .
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2
2 Cited Publications
Cat. No.: HY-108316
CAS No.: 61-56-3
Purity:  98.89%
Target:  

Carbonic Anhydrase

Research Areas:  

Neurological Disease

Sultiame is a carbonic anhydrase inhibitor, widely used as an antiepileptic agent.
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2
2 Cited Publications
Cat. No.: HY-B1730
CAS No.: 86-34-0
Phensuximide is an orally active succinimide antiepileptic and anticonvulsant agent. Phensuximide inhibits cyclic AMP and cyclic GMP accumulation in depolarized brain tissue. Phensuximide can be used for the study of seizure and petit mal .
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2
2 Cited Publications
Cat. No.: HY-B0106
CAS No.: 102767-28-2
Synonyms: UCB L059
Target:  

DNA Methyltransferase

Research Areas:  

Neurological Disease Cancer

Levetiracetam, an antiepileptic agent, binds the synaptic vesicle protein SV2A. Levetiracetam enhances Temozolomide effect on glioblastoma stem cell proliferation and apoptosis. Levetiracetam modulates HDAC levels ultimately silencing MGMT, thus increasing Temozolomide effectiveness. A chemosensitizer agent .
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2
2 Cited Publications
Cat. No.: HY-B0437
CAS No.: 959-24-0
Synonyms: MJ 1999
Sotalol hydrochloride (MJ 1999) is an orally active, non-selective β-adrenergic receptor blocker. Sotalol hydrochloride is a potent antiarrhythmic agent that can be used for the research of pediatric arrhythmias. Sotalol hydrochloride blocks β-receptors, and potassium KCNH2 channels. Antiepileptic Agent .
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2
2 Cited Publications
Cat. No.: HY-122114
CAS No.: 325457-89-4
Purity:  99.27%
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

ICA-27243 is a selective, potent and orally active KCNQ2/Q3 potassium channel opener with an EC50 of 0.38 μM. ICA-27243 is less effective at activating KCNQ4 and KCNQ3/Q5. ICA-27243 has antiepileptic and anticonvulsant effects .
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1
1 Cited Publications
Cat. No.: HY-B1378
CAS No.: 77-67-8
Target:  

Calcium Channel

Research Areas:  

Neurological Disease Cancer

Ethosuximide, a widely prescribed anti-epileptic agent, improves the phenotypes of multiple neurodegenerative disease models and blocks the low voltage activated T-type calcium channel.
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1
1 Cited Publications
Cat. No.: HY-N2124
CAS No.: 174972-79-3
Parishin B is a multi-target biological agent with anti-epileptic, anti-fascioliasis and anti-breast cancer lung metastasis activities . Parishin B regulates the gene/protein activities of ACLY, unc13c, γ-aminobutynergic system, pro-inflammatory system, antioxidant system, monoaminergic system, ferroptosis-related pathways, as well as GST, CatL, Trx and TRIB3 . Parishin B modulates energy-lipid metabolism, synaptic function, neurotransmitter balance, neuroinflammation, oxidative stress, parasite detoxification/invasion processes, as well as apoptosis, cell cycle, proliferation and metastasis of cancer cells [1][2][3]. Parishin B can be used for related research of epilepsy, fascioliasis and breast cancer lung metastasis [3].
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