Azepines
Apexbio Technology LLC Carbamazepine 298-46-4 50mg
Carbamazepine (CAS 298-46-4) is a tricyclic compound that functions primarily as a voltage-gated sodium channel blocker By stabilizing the inactivated state of sodium channels it reduces neuronal excitability and inhibits repetitive firing of action potentials Carbamazepine is widely utilized in research to model and investigate mechanisms of anticonvulsant activity synaptic transmission modulation and ion channel pharmacology Its established action on sodium channels makes it a valuable tool for studies involving neuronal hyperexcitability and related neurological disorders
Selleck Chemical LLC Oxcarbazepine S1391-10mg
Oxcarbazepine (GP47680) inhibits the binding of [3H]BTX to sodium channels with IC50 of 160 M and also inhibits the influx of 22Na into rat brain synaptosomes with IC50 about 100 M
Medchemexpress LLC Carbamazepine 10,11-epoxide | 36507-30-9 | 99.1% | 252.27 | 25 MG
Carbamazepine 10,11-epoxide is an orally active metabolite of Carbamazepine. This compound exhibits an anticonvulsant effect and is suitable for research related to seizures.
- Orally active metabolite
- Anticonvulsant effect
- Suitable for research of seizures
Medchemexpress LLC Carbamazepine-(Ph)d8 | 1538624-35-9 | 98.7% | 1 MG
Carbamazepine-(Ph)d8 is a deuterium-labeled compound intended for research use only. It can be used as a tracer or an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS. Deuteration, the incorporation of stable heavy isotopes into drug molecules, has gained attention for its potential to affect the pharmacokinetic and metabolic profiles of drugs.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
Selleck Chemical LLC Carbamazepine S1693-1g
Carbamazepine (Carbatrol NSC 169864) is a sodium channel blocker with IC50 of 131 M in rat brain synaptosomes
Cayman Chemical CarbamazepIn 5g
A sodium channel inhibitor; preferentially inhibits inactivated Nav1.7 and Nav1.3 channels (IC50s = 406 and 900 µM, respectively) over resting (closed) Nav1.7 and Nav1.3 channels in whole-cell patch-clamp assays using HEK293 cells (IC50s = 1,584 and 2,464 µM, respectively); inhibits sodium currents in a rat sciatic nerve patch-clamp assay ex vivo at 100 µM; reduces dopamine levels in the striatum and hippocampus, as well as L-DOPA levels in the striatum, in rats at 100 mg/kg; reduces amphetamine-induced hyperactivity in mice at 0.5% w/w in the diet; reduces immobility time in the forced swim test in mice at 0.75% w/w in the diet
eMolecules 108724-15-8 | HEXAHYDRO-1H-AZEPIN-4-AMINE 2HCL | AstaTech | MFCD29058558 | 187.110 | C6H16Cl2N2 | 95.000 | Cl.Cl.NC1CCCNCC1 | 1g | 391059339
HEXAHYDRO-1H-AZEPIN-4-AMINE 2HCL | AstaTech | 108724-15-8 | MFCD29058558 | 187.110 | C6H16Cl2N2 | 95.000 | Cl.Cl.NC1CCCNCC1 | 1g | 391059339
TARGETMOL CHEMICALS INC OXCARBAZEPINE 100MG
Also available in 5 mg 10 mg 25 mg 50 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Oxcarbazepine (GP 47680) is an Anti-epileptic Agent. The physiologic effect of oxcarbazepine is by means of Decreased Central Nervous System Disorganized Electrical Activity. purity: 99%
Medchemexpress LLC Carbamazepine | 298-46-4 | 99.95% | 236.27 | 100 MG
Carbamazepine is an orally active pressure-sensitive sodium ion channel blocker with an IC50 of 131 μM. It blocks voltage-gated Na+, Ca2+, and K+ channels and is also a HDAC inhibitor (IC50: 2 μM). Carbamazepine is an anticonvulsant and can be used for research of epilepsy and neuropathic pain.
- Orally active pressure-sensitive sodium ion channel blocker
- Blocks voltage-gated Na+, Ca2+, and K+ channels
- Acts as a HDAC inhibitor
- Anticonvulsant properties
- Useful for research into epilepsy
- Useful for research into neuropathic pain
Selleck Chemical LLC Carbamazepine-50mg
Carbamazepine (Carbatrol, NSC 169864) is a sodium channel blocker with IC50 of 131 μM in rat brain synaptosomes.
Cayman Chemical CondurItol B epoxIde 50mg
An irreversible inhibitor of GBA (IC50 = 9 μM); does not inhibit non-lysosomal glucosylceramidase or cytosolic β-glucosidase
Medchemexpress LLC Carbamazepine 10,11-epoxide | 36507-30-9 | 99.14% | 252.27 | 50 MG
Carbamazepine 10,11-epoxide is an orally active metabolite of Carbamazepine. It has an anticonvulsant effect and can be used for the research of seizures.
- Orally active metabolite
- Has anticonvulsant effect
- Suitable for research of seizures
Medchemexpress LLC Conduritol B epoxide | 6090-95-5 | MFCD00077326 | 99.9% | 162.14 g/mol | C6H10O5 | 1 ML
Conduritol B epoxide is an irreversible covalent inhibitor of acid β-glucosidase (GCase) used to block GCase activity in biochemical and cellular studies. It is supplied in solid form and as a 10 mM solution in DMSO for convenient preparation and dosing in research assays.
- Irreversible covalent inhibitor of acid β-glucosidase (GCase).
- Useful for biochemical and cellular assays investigating lysosomal function.
- Available as solid and as a 10 mM solution in DMSO for convenience.
- High reported purity and defined molecular weight for reproducible results.
- Stable under recommended storage conditions to preserve activity.
Medchemexpress LLC Carbamazepine 10,11 epoxide-d10 | 1219804-16-6 | 99.0% | 262.33 | 1 MG
Carbamazepine 10,11 epoxide-d10 is a deuterium labeled version of Carbamazepine 10,11 epoxide, intended for research use. It serves as a valuable tool in quantitative analysis for various scientific applications.
- Functions as a tracer
- Suitable as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS