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Referencia número: HY-169432

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TET-13

TET-13 is a positive allosteric modulator of GABA_A 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).

Para uso exclusivo en investigación. No vendemos a pacientes.

Fòrmula: C₁₅H₁₆N₂O₃S
Peso molecular:304.36

Almacenamiento:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (275 KB)

TET-13 Chemical Structure

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Actividad biológica
- Descripciòn
- In Vitro
- In Vivo
Chemical Information
Pureza y Documentación
Referencias
Calculators
Help & FAQs
Classifications
Bioz

Actividad biológica

Descripciòn

In Vitro

TET-13 (1 mg/mL, 0-30 min) is rapidly metabolized in SD rat plasma with a half-life T_1/2 of 0.48 min^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

TET-13 (1.2 mg/kg for mice, 1.725 mg/kg for rats, i.v.) shows potent anesthetic effects in both mice and rats (ED₅₀: 0.48 mg/kg and 0.69 mg/kg, respectively), with a faster recovery than Etomidate^[1].
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.

Animal Model:

Mice, rats^[1]
Dosage:

2.5 ×ED₅₀ (ED₅₀: 0.48 mg/kg (mice) and 0.69 mg/kg, (rats))
Administration:

Intravenous injection (i.v.)
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

Peso molecular 304.36
Fòrmula C₁₅H₁₆N₂O₃S
SMILES

COC(CSC(C1=CN=CN1[C@H](C)C2=CC=CC=C2)=O)=O
Envío

Room temperature in continental US; may vary elsewhere.
Almacenamiento

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureza y Documentación

Select Batch:

Pureza: 99.98%

Assay: 99.98%

ee.: 99.98%

Ficha de datos (275 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instrucciones de manejo (2659 KB)

Referencias

[1]. Zhu, et al. Discovery of thioetomidate derivatives as rapid recovery hypnotics without adrenocortical suppression. Bioorganic chemistry. 2024, 154, 107997. [Content Brief]

Calculators

Calculadora de molaridad

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculadora de dilución

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Bioz

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MOQ

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100 mg

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