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Filtered Search Results
Medchemexpress LLC (1R,2R)-N1,N2-Dibenzylcyclohexane-1,2-diamine | 143443-23-6 | MFCD29919494 | 97.7% | 294.44 g·mol⁻¹ | C20H26N2 | 250 MG
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(1R,2R)-N1,N2-Dibenzylcyclohexane-1,2-diamine is a chiral diamine used primarily as a synthetic intermediate in the preparation of pharmaceutical and fine chemical compounds. It is intended for research and development applications such as route scouting, asymmetric synthesis, and medicinal chemistry studies.
- Chiral diamine with defined (1R,2R) stereochemistry.
- Drug intermediate for synthesis of active pharmaceutical compounds.
- High purity (≈97.7%) suitable for analytical and synthetic use.
- Molecular formula C20H26N2 and molecular weight 294.44 g·mol⁻¹.
- Available in multiple small-scale pack sizes for research use.
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Medchemexpress LLC Conduritol B epoxide | 6090-95-5 | MFCD00077326 | 99.9% | 162.14 g/mol | C6H10O5 | 1 ML
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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.
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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
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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
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Sigma Aldrich Fine Chemicals Biosciences Epinastine hydrochloride United States Pharmacopeia (USP) Reference Standard | 108929-04-0 | MFCD00933434 | 250MG
Epinastine hydrochloride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 285.77 | 108929-04-0 | MFCD00933434 | 250MG
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eMolecules 1713477-43-0 | 2,7-Dimethyl-1H-purin-6(7H)-one | Ambeed | MFCD26938318 | 164.168 | C7H8N4O | 97.000 | Cc1nc2ncn(C)c2c(=O)[nH]1 | 5g | 847282773
2,7-Dimethyl-1H-purin-6(7H)-one | Ambeed | 1713477-43-0 | MFCD26938318 | 164.168 | C7H8N4O | 97.000 | Cc1nc2ncn(C)c2c(=O)[nH]1 | 5g | 847282773
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Apexbio Technology LLC Carbamazepine 298-46-4 50mg
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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
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Medchemexpress LLC Oxcarbazepine | 28721-07-5 | 99.9% | C15H12N2O2 | 5 MG
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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
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Medchemexpress LLC Carbamazepine | 298-46-4 | 99.95% | 236.27 | 100 MG
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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
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Apexbio Technology LLC Oxcarbazepine 28721-07-5 50mg
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Oxcarbazepine (CAS 28721-07-5) is a small molecule that modulates voltage-gated sodium channels a critical target in neuronal excitability studies It impedes the association of [3H]batrachotoxin ([3H]BTX) with sodium channels demonstrating an IC50 of 160 M and restricts sodium ion influx as indicated by inhibition of 22Na uptake into rat brain synaptosomes with an IC50 of approximately 100 M These properties make oxcarbazepine valuable for investigating sodium channel function and regulation in neuropharmacology and for exploring mechanisms underlying neuronal signaling and excitotoxicity
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eMolecules 84030-20-6 | 1,3,4,6,7,8-Hexahydro-1-methyl-2H-pyrimido[1,2-a]pyrimidine | Combi-Blocks | MFCD00043004 | 153.229 | C8H15N3 | 95.000 | CN1CCCN2CCCN=C12 | 1g | 528673218
1,3,4,6,7,8-Hexahydro-1-methyl-2H-pyrimido[1,2-a]pyrimidine | Combi-Blocks | 84030-20-6 | MFCD00043004 | 153.229 | C8H15N3 | 95.000 | CN1CCCN2CCCN=C12 | 1g | 528673218
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000695645 N-CBZ-1 2 3 6-TETRAH 25G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000756838 OXCARBAZEPINE IMPURI 500MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000759196 OXCARBAZEPINE IMPURI 250MG
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eMolecules 84030-20-6 | 7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene | AA Blocks LLC | MFCD00043004 | 153.229 | C8H15N3 | 0.000 | CN1CCCN2CCCN=C12 | 25g | 784379262
7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene | AA Blocks LLC | 84030-20-6 | MFCD00043004 | 153.229 | C8H15N3 | 0.000 | CN1CCCN2CCCN=C12 | 25g | 784379262
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000784250 OXCARBAZEPINE IMPURI 50G
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