TET-13
TET-13 is a positive allosteric modulator of GABAA receptor with an EC50 of 5.65 μM, lower than that of Etomidate (EC50: 9.29 μM). TET-13 shows potent anesthetic effects in both mice and rats (ED50: 0.48 mg/kg and 0.69 mg/kg, respectively).
For research use only. We do not sell to patients.
- Formula: C15H16N2O3S
- Molecular Weight:304.36
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
TET-13 (1 mg/mL, 0-30 min) is rapidly metabolized in SD rat plasma with a half-life T1/2 of 0.48 min[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
TET-13 (1.38 mg/kg, i.v.) shows little inhibition on cortisone of rat serum, indicating it has no effect on cortisol biosynthesis[1].
TET 13 (22 mg/kg/h) continuous infusion induces shorter recovery times and walking times than Etomidate in rats at 0.5, 1 and 2 hours[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Mice, rats[1]
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Dosage:2.5 ×ED50 (ED50: 0.48 mg/kg (mice) and 0.69 mg/kg, (rats))
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Administration:Intravenous injection (i.v.)
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Result:Exhibited faster recovery compared to Etomidate (the times to walk: 27.88 s and 107.80 s, respectively) in mice.
Showed the incidence of myoclonus is 100% in mice.
Showed faster onset time (3.04 s) than etomidate in rats.
Showed the incidence of myoclonus was 0 % in rats.
Chemical Information
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Molecular Weight 304.36
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Formula C15H16N2O3S
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SMILES
COC(CSC(C1=CN=CN1[C@H](C)C2=CC=CC=C2)=O)=O
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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)