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Filtered Search Results
TARGETMOL CHEMICALS INC Mephenytoin 10MG
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Also available in 1 mL, 1 mg, 2 mg, 5 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Mephenytoin (Phenantoin) is an anticonvulsant and a substrate of CYP2C19 and CYP2B6. Purity 99.72%
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Pfaltz & Bauer Glycoluril 100G | 496-46-8
Glycoluril 100G | 496-46-8
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TARGETMOL CHEMICALS INC S-Mephenytoin 5MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Also available in 1 mL, 1 mg, 10 mg, 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. (S)-Mephenytoin ((+)-Mephenytoin) is an anticonvulsant that serves as a substrate of the cytochrome P450 (CYP) isoform CYP2C19 and is used to analyze cytochrome P450 metabolism.
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Apexbio Technology LLC Phenytoin 57-41-0 10mM (in 1mL DMSO)
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Phenytoin (57-41-0) is a small-molecule inhibitor targeting voltage-gated sodium channels It is designed to inhibit sodium channel activity thereby regulating neuronal excitability and electrical signaling Phenytoin exerts its biological activity primarily through the stabilization and inhibition of voltage-gated sodium channels by reducing repetitive neuronal firing In in vitro studies Phenytoin demonstrates inhibitory activity with reported IC50 values typically ranging from 40 to 60 M depending upon experimental protocols and neuronal models applied Based on these pharmacological properties Phenytoin holds research potential in neurological studies including epilepsy pathogenesis and sodium channel-targeted therapeutic mechanism evaluation
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Medchemexpress LLC 2-Ethylhexyl diphenyl phosphate | 1241-94-7 | 94.3% | 362.41 | 50 MG
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2-Ethylhexyl diphenyl phosphate is an organophosphate flame retardant (OPFR) and acts as a PPARG agonist with an EC20 of 2.04 μM. It also demonstrates inhibitory activity on ERRγ transcriptional activity with an IC50 of 1.3 μM. This compound has been shown to upregulate 3β-HSD1, human chorionic gonadotropin (hCG), and progesterone secretion. It can be utilized in studies pertaining to female reproduction and fetal development.
- Organophosphate flame retardant (OPFR).
- PPARG agonist (EC20: 2.04 μM).
- Inhibits ERRγ transcriptional activity (IC50: 1.3 μM).
- Upregulates 3β-HSD1, human chorionic gonadotropin (hCG), and progesterone secretion.
- Applicable for studies in female reproduction and fetal development.
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Medchemexpress LLC R-mephenytoin | 71140-51-7 | MFCD00272651 | 99.6% | 218.25 g/mol | C12H14N2O2 | 5MG
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(R)-Mephenytoin is the R-enantiomer of mephenytoin, an anticonvulsant compound used in pharmacological and biochemical research. It is supplied as a high-purity analytical reagent for laboratory use (CAS 71140-51-7; molecular weight 218.25 g/mol). Not for human or clinical use.
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Medchemexpress LLC 5-phenylimidazolidine-2,4-dione | 89-24-7 | MFCD00037881 | ≥97.0% | 176.18 g/mol | C9H8N2O2 | 100MG
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5-Phenylhydantoin (CAS 89-24-7) is a small-molecule research compound described as having antiepileptic activity and reported hypolipidemic properties. It is supplied for research use only and is typically provided as a solid with high purity suitable for biochemical and pharmacological studies.
- High purity: ≥97.0%.
- Molecular formula: C9H8N2O2.
- Molecular weight: 176.18 g/mol.
- Physical form: solid powder or crystals.
- Research applications: anticonvulsant and lipid metabolism studies.
- Available in small-scale packs for lab use.
- Not for human consumption; research use only.
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eMolecules FMOC-N N-DIMETHYL-L-ASPA 250MG
5000190695 FMOC-N N-DIMETHYL-L-ASPA 250MG
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Medchemexpress LLC Phenytoin (5,5-diphenylhydantoin) | 57-41-0 | 99.9% | 1 G
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Phenytoin (5,5-Diphenylhydantoin) is a potent Voltage-gated Na+ channels (VGSCs) blocker. It has antiepileptic activity and reduces breast tumor growth and metastasis in mice. This product is for research use only and not sold to patients.
- Potent voltage-gated Na+ channels (VGSCs) blocker
- Has antiepileptic activity
- Reduces breast tumor growth and metastasis in mice
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eMolecules EMOLECULES INC
5000190691 1-9H-FLUOREN-9-YL-3-OX 100MG
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Medchemexpress LLC S-Adenosyl-L-methionine-13C dihydrochloride | 29908-03-0 | 98.64% | 20 MG
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S-Adenosyl-L-methionine-13C dihydrochloride is the 13C labeled version of S-Adenosyl-L-methionine, an orally active methyl group donor and dietary supplement. It has potent antidepressant effects and exhibits anti-proliferative, pro-apoptotic, and anti-metastatic roles in cancers, with potential for research in cancer, liver disease, and osteoarthritis.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Molecular Weight: 508.81
- Appearance: Solid
- Color: Off-white to light yellow
- Solubility: In H2O: 50 mg/mL (98.27 mM; requires ultrasonic assistance)
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Medchemexpress LLC S-Adenosyl-L-methionine | 29908-03-0 | 99.96% | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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S-Adenosyl-L-methionine is an orally active methyl group donor and dietary supplement with potent antidepressant effects. It plays anti-proliferative, pro-apoptotic, and anti-metastatic roles in cancers. This compound has potential for research in cancer, liver disease, and osteoarthritis.
- Induces cell apoptosis and promotes cell cycle arrest
- Decreases cell migration
- Protects anticancer effects of 5-FU
- Prevents ASD-like behaviors in mice
- Shows antiepileptic, memory-enhancing, and antioxidant properties
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Medchemexpress LLC Mephenytoin | 50-12-4 | 99.9% | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Mephenytoin is an anticonvulsant and a substrate for CYP2C19 and CYP2B6. It is for research use only. In preclinical studies, orally administered Mephenytoin reduced maternal weight gain and increased offspring mortality at 200 mg/kg in pregnant Sprague-Dawley CD rats. Additionally, Mephenytoin significantly reduced serum cholesterol and triglyceride levels in mice, suggesting a hypolipidemic effect.
- Anticonvulsant compound.
- Acts as a substrate for CYP2C19 and CYP2B6.
- Reduced maternal weight gain in preclinical studies at higher doses.
- Demonstrated hypolipidemic effect in mice by reducing serum cholesterol and triglyceride levels.
- Intended for research use only.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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NC3933232 TEBIDEUTOREXANT CAS 1637681-55
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eMolecules N-FMOC-2-METHYL-L-ASPARTI 0.5G
5000188302 N-FMOC-2-METHYL-L-ASPARTI 0.5G
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