172 Results for "

Anticonvulsant agent

" in MedChemExpress (MCE) Product Catalog:
Products (172)

172 Results for "Anticonvulsant agent" in MCE Product Catalog:

25
25 Publications Verification
Cat. No.: HY-B1302
CAS No.: 6151-40-2
Quinidine hydrochloride monohydrate is an orally active antiarrhythmic agent. Quinidine hydrochloride monohydrate reduces the expression level of P-gp, inhibits P-gp-mediated efflux, increases the intracellular accumulation of P-gp substrates, induces PARP cleavage and Caspase-3 activation, and elevates the proportion of Apoptotic cells at the sub-G1 phase. Quinidine hydrochloride monohydrate exerts sustained block and open-channel block effects on IK(f). Quinidine hydrochloride monohydrate alters the urinary metabolic ratio of Amphetamine, modulates the Pentylenetetrazol-induced seizure threshold, and regulates the anticonvulsant effect of Dextromethorphan. Quinidine hydrochloride monohydrate can be used in studies related to uterine sarcoma and seizures .
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24
24 Cited Publications
Cat. No.: HY-B1751
CAS No.: 56-54-2
Quinidine (15% dihydroquinidine) is an orally active antiarrhythmic agent. Quinidine (15% dihydroquinidine) reduces the expression level of P-gp, inhibits P-gp-mediated efflux, increases the intracellular accumulation of P-gp substrates, induces PARP cleavage and Caspase-3 activation, and elevates the proportion of Apoptotic cells at the sub-G1 phase. Quinidine (15% dihydroquinidine) exerts sustained block and open-channel block effects on IK(f). Quinidine (15% dihydroquinidine) alters the urinary metabolic ratio of Amphetamine, modulates the Pentylenetetrazol-induced seizure threshold, and regulates the anticonvulsant effect of Dextromethorphan. Quinidine (15% dihydroquinidine) can be used in studies related to uterine sarcoma and seizures .
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16
16 Cited Publications
Cat. No.: HY-B0211
CAS No.: 1744-22-5
Synonyms: PK 26124
Research Areas:  

Neurological Disease Cancer

Riluzole is an anticonvulsant agent and belongs to the family of use-dependent Na + channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM.
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16
16 Cited Publications
Cat. No.: HY-B0211A
CAS No.: 850608-87-6
Synonyms: PK 26124 hydrochloride
Research Areas:  

Neurological Disease Cancer

Riluzole hydrochloride is an anticonvulsant agent and belongs to the family of use-dependent Na + channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM.
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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-103392
CAS No.: 49763-96-4
Purity:  99.99%
Synonyms: BCX2600
Target:  

Cytochrome P450

Research Areas:  

Neurological Disease

Stiripentol (STP) is an anticonvulsant agent, which can inhibit N-demethylation of CLB to NCLB mediatated by CYP3A4 (noncompetitively) and CYP2C19 (competitively) with Ki of 1.59±0.07 and 0.516±0.065 μM and IC50 of 1.58 and 3.29 μM, respectively.
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4
4 Cited Publications
Cat. No.: HY-129105
CAS No.: 533-45-9
Purity:  98.65%
Research Areas:  

Neurological Disease

Chlormethiazole is an potent and orally active GABAA agonist . Chlormethiazole inhibits cytochrome P450 isoforms: CYP2A6 and CYP2E1 in human liver microsomes. Chlormethiazole is an anticonvulsant agent and has the potential for treating convulsive status epilepticus .
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4
4 Cited Publications
Cat. No.: HY-A0296
CAS No.: 6001-74-7
Synonyms: Clomethiazole hydrochloride
Target:  

Cytochrome P450

Research Areas:  

Neurological Disease

Clomethiazole hydrochloride is a potent and orally active GABAA agonist . Clomethiazole hydrochloride inhibits cytochrome P450 isoforms: CYP2A6 and CYP2E1 in human liver microsomes. Clomethiazole hydrochloride is an anticonvulsant agent and has the potential for treating convulsive status epilepticus .
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2
2 Cited Publications
Cat. No.: HY-B0339
CAS No.: 125-33-7
Primidone is the orally active inhibitor for TRPM3 (IC50 = 0.6 μM), RIP kinase and voltage-gated sodium channel, and the antagonist for GABA receptor. Primidone can be used as the analgesic and anticonvulsant agent .
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2
2 Cited Publications
Cat. No.: HY-B1274
CAS No.: 58473-74-8
Synonyms: trans-3-Bromo-N-ethylcinnamamide
Cinromide is an anticonvulsant agent. Cinromide inhibits epithelial neutral amino acid transporter B 0AT1 (SLC6A19) with an IC50 of 0.5 μM .
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2
2 Cited Publications
Cat. No.: HY-B1642
CAS No.: 86-35-1
Synonyms: Peganone
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Ethotoin (Peganone) is an orally active anticonvulsant agent used in epilepsy research, Ethotoin is a hydantoin, similar to phenytoin .
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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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1
1 Cited Publications
Cat. No.: HY-100379
CAS No.: 92262-58-3
Purity:  99.42%
Synonyms: TV1901
Target:  

Sodium Channel Fungal

Research Areas:  

Neurological Disease

Valrocemide (TV1901) is a promising antiepileptic agent candidate that shows a broad spectrum of anticonvulsant activity.
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Cat. No.: HY-B0246S
CAS No.: 132183-78-9
Synonyms: CBZ-d10; NSC 169864-d10
Carbamazepine-d10 is the deuterium labeled Carbamazepine. Carbamazepine (CBZ), a sodium channel blocker, is an anticonvulsant agent .
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Cat. No.: HY-A0092
CAS No.: 127-48-0
Synonyms: 3,5,5,-Trimethyloxazolidine-2,4-dione
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Trimethadione (3,5,5,-Trimethyloxazolidine-2,4-dione) is an oxazolidinedione anticonvulsant agent widely used against absences seizures. Trimethadione also is a T-type calcium channel blocker which has antihyperalgesic effects .
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Cat. No.: HY-B0246S2
CAS No.: 1538624-35-9
Synonyms: CBZ-d8; NSC 169864-d8
Carbamazepine-d8 is the deuterium labeled Carbamazepine. Carbamazepine, a sodium channel blocker, is an anticonvulsant agent, with an IC50 of 131 μM .
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Cat. No.: HY-123193
CAS No.: 65617-86-9
Synonyms: Pro-diazepam
Target:  

Drug Intermediate

Research Areas:  

Neurological Disease

Avizafone (Pro-diazepam), a pro-drug of Diazepam, is an anticonvulsant agent. Avizafone can be used as an antidote of nerve agent poisoning. In vivo, Avizafone is rapidly hydrolyzed by aminopeptidase to produce lysine and diazepam. Avizafone has research areas including neurological disease, such as epilepsy .
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Cat. No.: HY-115366
CAS No.: 112415-83-5
Purity:  98.86%
Research Areas:  

Neurological Disease

Soluflazine is a nucleoside transport inhibitor with anticonvulsant action. Soluflazine can be used as an antiepileptic agent .
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Cat. No.: HY-152358
CAS No.: 7103-27-7
Research Areas:  

Others

N3-Methyl-2’-O-methyluridine is a uridine analogue. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents .
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