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3,3'',5-Triiodo-L-thyronine Sodium Salt

Promotes adipogenic differentiation of MSCs; also thyroid hormone (T3) analog CAS# 55-06-1

3,3'',5-Triiodo-L-thyronine Sodium Salt

2D Structure

Catalog No. BCN1419----Order now to get a substantial discount!

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3,3'',5-Triiodo-L-thyronine Sodium Salt: 5mg $6 In Stock
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Quality Control of 3,3'',5-Triiodo-L-thyronine Sodium Salt

3D structure

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3,3'',5-Triiodo-L-thyronine Sodium Salt

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Chemical Properties of 3,3'',5-Triiodo-L-thyronine Sodium Salt

Cas No. 55-06-1 SDF Download SDF
PubChem ID 23666110 Appearance Powder
Formula C15H11I3NNaO4 M.Wt 672.96
Type of Compound Miscellaneous Storage Desiccate at -20°C
Synonyms T3 Sodium salt; Sodium L-3,3',5-triiodothyronine; Liothyronine sodium
Solubility DMSO : ≥ 42 mg/mL (62.41 mM)
*"≥" means soluble, but saturation unknown.
Chemical Name sodium;(2S)-2-amino-3-[4-(4-hydroxy-3-iodophenoxy)-3,5-diiodophenyl]propanoate
SMILES C1=CC(=C(C=C1OC2=C(C=C(C=C2I)CC(C(=O)[O-])N)I)I)O.[Na+]
Standard InChIKey SBXXSUDPJJJJLC-YDALLXLXSA-M
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Biological Activity of 3,3'',5-Triiodo-L-thyronine Sodium Salt

DescriptionThe administration of 3,3'',5-Triiodo-L-thyronine Sodium Salt (T3) elicited a vasodilatation in C57BL/6 mice even at the lowest concentration (10(-9)M), a maximal relaxation of more than 50% was observed with the concentrations between 10(-9) and 10(-8)M.
TargetsEstrogen receptor | Antifection | Progestogen receptor
In vivo

Vascular function of the mesenteric artery isolated from thyroid hormone receptor-α knockout mice.[Pubmed: 25500991]

J Vasc Res. 2014;51(5):350-9.

This study evaluated the consequences of thyroid hormone receptor-α (TRα) disruption on vascular reactivity.
METHODS AND RESULTS:
The activity of superior mesenteric arteries isolated from TRα knockout mice generated in the SV129 background (TRα(0/0)SV) or in a pure C57BL/6 background (TRα(0/0)C57) was compared to that of their corresponding wild-type strains (SV129 or C57BL/6 mice). The wild-type SV129 mice exhibited an impaired acetylcholine (Ach)-induced mesenteric artery relaxation compared to C57BL/6 mice, associated with greater responses to angiotensin II (AII) and phenylephrine (PE). The disruption of TRα decreased the vascular response to sodium nitroprusside and PE in both the SV129 and C57BL/6 genetic backgrounds. Responses to Ach and AII were also blunted, but only in TRα(0/0)C57 mice. The administration of 3,3'',5-Triiodo-L-thyronine Sodium Salt (T3) elicited a vasodilatation in C57BL/6 mice even at the lowest concentration (10(-9)M); a maximal relaxation of more than 50% was observed with the concentrations between 10(-9) and 10(-8)M. However, the response to T3 was nearly absent in TRα(0/0)C57 mice.
CONCLUSIONS:
TRα is essential for the control of vascular tone, particularly in thyroid hormone-mediated relaxation. The difference in response to Ach observed between the two wild-type mice should be taken into account for interpreting the vascular responses of genetically engineered mice.

3,3'',5-Triiodo-L-thyronine Sodium Salt Dilution Calculator

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Preparing Stock Solutions of 3,3'',5-Triiodo-L-thyronine Sodium Salt

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.486 mL 7.4299 mL 14.8597 mL 29.7194 mL 37.1493 mL
5 mM 0.2972 mL 1.486 mL 2.9719 mL 5.9439 mL 7.4299 mL
10 mM 0.1486 mL 0.743 mL 1.486 mL 2.9719 mL 3.7149 mL
50 mM 0.0297 mL 0.1486 mL 0.2972 mL 0.5944 mL 0.743 mL
100 mM 0.0149 mL 0.0743 mL 0.1486 mL 0.2972 mL 0.3715 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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Background on 3,3'',5-Triiodo-L-thyronine Sodium Salt

Liothyronine Sodium is the most potent form of thyroid hormone acting on the body to increase the basal metabolic rate, affect protein synthesis.

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References on 3,3'',5-Triiodo-L-thyronine Sodium Salt

Vascular function of the mesenteric artery isolated from thyroid hormone receptor-alpha knockout mice.[Pubmed:25500991]

J Vasc Res. 2014;51(5):350-9.

OBJECTIVE: This study evaluated the consequences of thyroid hormone receptor-alpha (TRalpha) disruption on vascular reactivity. METHODS: The activity of superior mesenteric arteries isolated from TRalpha knockout mice generated in the SV129 background (TRalpha(0/0)SV) or in a pure C57BL/6 background (TRalpha(0/0)C57) was compared to that of their corresponding wild-type strains (SV129 or C57BL/6 mice). RESULTS: The wild-type SV129 mice exhibited an impaired acetylcholine (Ach)-induced mesenteric artery relaxation compared to C57BL/6 mice, associated with greater responses to angiotensin II (AII) and phenylephrine (PE). The disruption of TRalpha decreased the vascular response to sodium nitroprusside and PE in both the SV129 and C57BL/6 genetic backgrounds. Responses to Ach and AII were also blunted, but only in TRalpha(0/0)C57 mice. The administration of 3,3'5-triiodo-L-thyronine sodium salt (T3) elicited a vasodilatation in C57BL/6 mice even at the lowest concentration (10(-9)M); a maximal relaxation of more than 50% was observed with the concentrations between 10(-9) and 10(-8)M. However, the response to T3 was nearly absent in TRalpha(0/0)C57 mice. CONCLUSION: TRalpha is essential for the control of vascular tone, particularly in thyroid hormone-mediated relaxation. The difference in response to Ach observed between the two wild-type mice should be taken into account for interpreting the vascular responses of genetically engineered mice.

Description

Liothyronine sodium is an active form of thyroid hormone, which binds to β1 thyroid hormone receptor (TRβ1), and activates its activity.

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