SePP
SePP is a blood-brain barrier-permeable NMDAR antagonist and dopamine/norepinephrine reuptake inhibitor, with a Ki of 28.7 nM for rat NMDAR. SePP exerts anticonvulsant effects. SePP can be used in research related to fragile X syndrome.
For research use only. We do not sell to patients.
- Formula: C17H21NSe
- Molecular Weight:318.32
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
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NMDA Receptor 28.7 nM (Ki) |
SePP (multiple concentrations; 2 h) potently binds to rat forebrain NMDARs with a Ki of 28.7 nM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| Species | Dose | Route | Plasma Concentration |
|---|---|---|---|
| Mice[1] | 10 mg/kg | i.p. | 387.5 ng/mL |
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:FVB.129P2-Pde6b+ Tyrc‑ch Fmr1tm1Cgr/J (Fmr1 knockout, 4 male and 4 female, postnatal day 23-25, audiogenic seizure induction)[1]
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Dosage:10 mg/kg
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Administration:i.p.; single dose
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Result:Abolished wild running and jumping (WRJ), tonic-clonic seizure (TCS), and respiratory arrest (RA) in all treated mice, with statistically significant differences compared to vehicle controls (P < 0.0001 for WRJ and TCS, P = 0.0013 for RA).
Exhibited normal behaviors including exploring, rearing, grooming, and interacting with cage-mates during testing.
Chemical Information
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Molecular Weight 318.32
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Formula C17H21NSe
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SMILES
C1(CC(N2CCCCC2)C3=CC=C[Se]3)=CC=CC=C1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)