2. Membrane Transporter/Ion Channel Neuronal Signaling Metabolic Enzyme/Protease
  3. GABA Receptor Endogenous Metabolite
  4. Tetrahydrodeoxycorticosterone

Tetrahydrodeoxycorticosterone  (Synonyms: Tetrahydro-11-deoxycorticosterone)

Cat. No.: HY-113346 Purity: ≥98.0%
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Tetrahydrodeoxycorticosterone, an neurosteroid, is a potent positive allosteric modulator (PAM) of GABAA receptor. Tetrahydrodeoxycorticosterone has potent neuroinhibitory properties.

For research use only. We do not sell to patients.

Tetrahydrodeoxycorticosterone Chemical Structure

Tetrahydrodeoxycorticosterone Chemical Structure

CAS No. : 567-03-3

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1 mg USD 230 In-stock
5 mg USD 580 In-stock
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Based on 1 publication(s) in Google Scholar

Other Forms of Tetrahydrodeoxycorticosterone:

Tetrahydrodeoxycorticosterone Related Antibodies

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  • Biological Activity

  • Purity & Documentation

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Description

Tetrahydrodeoxycorticosterone, an neurosteroid, is a potent positive allosteric modulator (PAM) of GABAA receptor. Tetrahydrodeoxycorticosterone has potent neuroinhibitory properties[1][2].

IC50 & Target

Human Endogenous Metabolite

 

In Vitro

The endogenous neurosteroid Tetrahydrodeoxycorticosterone (THDOC) at physiological concentrations selectively enhances tonic currents mediated by αβδ receptors[1].
In hippocampus, 10 nM Tetrahydrodeoxycorticosterone reduces neuronal excitability by augmenting tonic αβδ receptor currents. In thalamocortical neurons, although 100 nM Tetrahydrodeoxycorticosterone enhances tonic currents, 10 nM Tetrahydrodeoxycorticosterone does not[1].

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

Tetrahydrodeoxycorticosterone Related Antibodies
In Vivo

Concentrations of Tetrahydrodeoxycorticosterone (THDOC) in brain tissue from mice with hepatic encephalopathy (HE) resulting from toxic liver injury are sufficient to induce sedation in animals of the same species[2].

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

334.49

Formula

C21H34O3
CAS No.
Appearance

Solid

Color

White to off-white

SMILES

C[C@@]12[C@@H](C(CO)=O)CC[C@@]1([H])[C@]3([H])CC[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC2
Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Solvent & Solubility
In Vitro: 

DMSO : 100 mg/mL (298.96 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.9896 mL 14.9481 mL 29.8963 mL
5 mM 0.5979 mL 2.9896 mL 5.9793 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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

Mass
=
Concentration
×
Volume
×
Molecular Weight *

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

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start)

C1

×
Volume (start)

V1

=
Concentration (final)

C2

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Volume (final)

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
Purity & Documentation
References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.9896 mL 14.9481 mL 29.8963 mL 74.7407 mL
5 mM 0.5979 mL 2.9896 mL 5.9793 mL 14.9481 mL
10 mM 0.2990 mL 1.4948 mL 2.9896 mL 7.4741 mL
15 mM 0.1993 mL 0.9965 mL 1.9931 mL 4.9827 mL
20 mM 0.1495 mL 0.7474 mL 1.4948 mL 3.7370 mL
25 mM 0.1196 mL 0.5979 mL 1.1959 mL 2.9896 mL
30 mM 0.0997 mL 0.4983 mL 0.9965 mL 2.4914 mL
40 mM 0.0747 mL 0.3737 mL 0.7474 mL 1.8685 mL
50 mM 0.0598 mL 0.2990 mL 0.5979 mL 1.4948 mL
60 mM 0.0498 mL 0.2491 mL 0.4983 mL 1.2457 mL
80 mM 0.0374 mL 0.1869 mL 0.3737 mL 0.9343 mL
100 mM 0.0299 mL 0.1495 mL 0.2990 mL 0.7474 mL
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Tetrahydrodeoxycorticosterone Related Classifications

Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Tetrahydrodeoxycorticosterone567-03-3Tetrahydro-11-deoxycorticosteroneGABA ReceptorEndogenous MetaboliteGamma-aminobutyric acid Receptorγ-Aminobutyric acid ReceptorGABAAneurosteroidneuroinhibitorysedationInhibitorinhibitorinhibit

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