Azepines
Medchemexpress LLC Carbamazepine 10,11-epoxide | 36507-30-9 | 99.1% | 252.27 | 10 MG
Carbamazepine 10,11-epoxide is an orally active metabolite of Carbamazepine. It exhibits an anticonvulsant effect, making it suitable for research related to seizures. This compound is provided as an off-white to light yellow solid.
- Orally active metabolite
- Exhibits anticonvulsant properties
- Useful for seizure research
- High purity (99.14%)
- Supplied as an off-white to light yellow solid
Medchemexpress LLC Carbamazepine 10,11 epoxide-d10 | 1219804-16-6 | 99.0% | 262.33 | 5 MG
Carbamazepine 10,11 epoxide-d10 is the deuterium labeled Carbamazepine 10,11 epoxide.
- This compound can be used as a tracer.
- This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
- Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.
Cayman Chemical CondurItol B epoxIde 50mg
An irreversible inhibitor of GBA (IC50 = 9 μM); does not inhibit non-lysosomal glucosylceramidase or cytosolic β-glucosidase
Accela Chembio Inc N-boc-hexahydro-1h-azepin-4-one | 1g | 188975-88-4 | MFCD03788435 | 97+% | Shelf Life: 1800 Days | Light Sensitive/air Sensitive/nitrogen Or Argon/+4
N-boc-hexahydro-1h-azepin-4-one | 1g | 188975-88-4 | MFCD03788435 | 97+% | Shelf Life: 1800 Days | Light Sensitive/air Sensitive/nitrogen Or Argon/+4
Medchemexpress LLC 1-Boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester | 286961-14-6 | 99.8% | 309.21 | 100 G
1-Boc-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
- For research use only
- Suitable for laboratory chemicals and manufacture of substances
- Supplied as a solid appearance
- Stable under recommended storage conditions
Medchemexpress LLC Methoctramine tetrah 5mg | 104807-46-7 | 728.75 g/mol | C36H66Cl4N4O2 | 5 MG
Methoctramine tetrahydrochloride is the tetrahydrochloride salt of methoctramine, a selective M2 muscarinic receptor antagonist used in pharmacological research to probe M2 receptor-mediated signaling and cardiovascular responses. The compound is provided as a solid with high purity and documented storage and solubility properties.
- Selective M2 muscarinic receptor antagonist.
- Intended for research use in pharmacology and cardiovascular studies.
- Tetrahydrochloride salt; white to off-white solid.
- Purity: 97%.
- Molecular weight: 728.75 g/mol; formula: C36H66Cl4N4O2.
- Solubility: water 20 mg/mL (may require ultrasonic).
- Storage: -20°C sealed; in solution -80°C (6 months), -20°C (1 month).
- Typical laboratory pack size: 5 mg.
Medchemexpress LLC Oxcarbazepine (Standard) | 28721-07-5 | 99.9% | C₁₅H₁₂N₂O₂ | 5 MG
Oxcarbazepine (Standard) is the analytical standard of Oxcarbazepine, intended for research and analytical applications. It acts as a sodium channel blocker and significantly inhibits glioblastoma cell growth, inducing apoptosis or G2/M arrest in glioblastoma cell lines. It exhibits anti-cancer and anticonvulsant effects.
- Analytical standard grade
- Acts as a sodium channel blocker
- Significantly inhibits glioblastoma cell growth
- Induces apoptosis or G2/M arrest in glioblastoma cell lines
- Exhibits anti-cancer effects
- Exhibits anticonvulsant effects
- Commonly used as a reference standard for assays in qualitative, quantitative, and methodological research experiments such as HPLC, GC, and MS.
Medchemexpress LLC Oxcarbazepine | 28721-07-5 | 99.9% | C15H12N2O2 | 5 MG
Oxcarbazepine is a sodium channel blocker that significantly inhibits glioblastoma cell growth and induces apoptosis or G2/M arrest in glioblastoma cell lines. It exhibits anti-cancer and anticonvulsant effects. In vitro, it significantly inhibits glioblastoma cell growth with IC50 values of 12.35 μg/mL for U87 cell lines and 9.45 μg/mL for T98 cell lines.
- Sodium channel blocker
- Inhibits glioblastoma cell growth
- Induces apoptosis or G2/M arrest in glioblastoma cell lines
- Exhibits anti-cancer effects
- Exhibits anticonvulsant effects
- Protects against generalized tonic-clonic seizures
Medchemexpress LLC Oxcarbazepine-d4 | 1020719-71-4 | C15H8D4N2O2 | 2.5 MG
Oxcarbazepine-d4 is a deuterium-labeled version of Oxcarbazepine, which acts as a sodium channel blocker. It significantly inhibits glioblastoma cell growth, inducing apoptosis or G2/M arrest in glioblastoma cell lines. This compound exhibits both anti-cancer and anticonvulsant effects.
- Deuterium labeled oxcarbazepine
- Acts as a sodium channel blocker
- Molecular weight: 256.29
- Formula: C15H8D4N2O2
- Can be utilized as a tracer
- Can serve as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Incorporated into drug molecules for quantitation during drug development
- Potential to influence pharmacokinetic and metabolic profiles of drugs