L-Thyroxine
Based on 13 publication(s) in Google Scholar
L-Thyroxine (Levothyroxine; T4) is a synthetic hormone for the research of hypothyroidism. DIO enzymes convert biologically active thyroid hormone (Triiodothyronine,T3) from L-Thyroxine (T4).
For research use only. We do not sell to patients.
- Purity: 98.43%
- CAS No.: 51-48-9
- Formula: C15H11I4NO4
- Molecular Weight:776.87
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Publications Citing Use of MedChemExpress (MCE) L-Thyroxine
More- Cell. 2026 Apr 2;189(7):2007-2023.e20. [Abstract]
- Nat Immunol. 2024 Apr;25(4):659-670. [Abstract]
- Cell Rep Med. 2023 Jun 20;4(6):101061. [Abstract]
- EMBO J. 2024 Aug;43(15):3090-3115. [Abstract]
- Europace. 2026 Mar 30;28(4):euag047. [Abstract]
- J Drug Deliv Sci Technol. 2023 Sep 28, 105008.
- Stem Cell Rev Rep. 2021 Jun;17(3):999-1013. [Abstract]
- Sci Rep. 2022 Jul 4;12(1):11259. [Abstract]
- Clin Exp Med. 2025 Dec 20. [Abstract]
- Dis Model Mech. 2024 Aug 14:dmm.050748. [Abstract]
- Mol Brain. 2021 Jan 27;14(1):25. [Abstract]
- Ther Deliv. 2025 Oct 30:1-15. [Abstract]
- Aalto University. 2026.
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In Vivo Efficacy Study
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In Vivo Efficacy Study
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Histological Imaging/Staining
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In Vivo Imaging
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In Vivo Efficacy Study
All Endogenous Metabolite Isoforms
More
Biological Activity
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Human Endogenous Metabolite |
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| HEK293 | IC50 |
4.9 μM
Compound: Levothyroxine
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Inhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in bilirubin glucuronidation by LC-MS/MS method
Inhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in bilirubin glucuronidation by LC-MS/MS method
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[PMID: 21030469] |
| HEK293 | IC50 |
5.6 μM
Compound: Levothyroxine
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Inhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in estradiol 3-glucuronidation by LC-MS/MS method
Inhibition of human recombinant UGT1A1 expressed in HEK293 cells assessed as reduction in estradiol 3-glucuronidation by LC-MS/MS method
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[PMID: 21030469] |
| HEK-293T | EC50 |
12 μM
Compound: T4
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Agonist activity at recombinant human pFA-CMV fused PPARgamma expressed in HEK293T cells transfected with pFR-luciferase plasmid and pRL-SV40 plasmid incubated for 14 to 16 hrs by dual glo luciferase reporter gene assay
Agonist activity at recombinant human pFA-CMV fused PPARgamma expressed in HEK293T cells transfected with pFR-luciferase plasmid and pRL-SV40 plasmid incubated for 14 to 16 hrs by dual glo luciferase reporter gene assay
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[PMID: 32356658] |
| HEK-293T | EC50 |
15.4 μM
Compound: T4
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Agonist activity at recombinant human pFA-CMV fused RXRalpha LBD expressed in HEK293T cells transfected with pFR-luciferase plasmid and pRL-SV40 plasmid incubated for 14 to 16 hrs by dual glo luciferase reporter gene assay
Agonist activity at recombinant human pFA-CMV fused RXRalpha LBD expressed in HEK293T cells transfected with pFR-luciferase plasmid and pRL-SV40 plasmid incubated for 14 to 16 hrs by dual glo luciferase reporter gene assay
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[PMID: 32356658] |
| HepG2 | EC50 |
100 μM
Compound: Levothyroxine
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Activation of human PXR expressed in human HepG2 (DPX-2) cells assessed as induction of CYP3A4 after 24 hrs by luminescent analysis
Activation of human PXR expressed in human HepG2 (DPX-2) cells assessed as induction of CYP3A4 after 24 hrs by luminescent analysis
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[PMID: 20966043] |
| MDCK | IC50 |
8 μM
Compound: Thyroxine
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TP_TRANSPORTER: inhibition of Triiodothyronine uptake in OATP4C1-expressing MDCK cells
TP_TRANSPORTER: inhibition of Triiodothyronine uptake in OATP4C1-expressing MDCK cells
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[PMID: 14993604] |
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 51-48-9
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Appearance Solid
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Molecular Weight 776.87
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Formula C15H11I4NO4
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Color White to light yellow
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SMILES
N[C@@H](CC1=CC(I)=C(C(I)=C1)OC2=CC(I)=C(O)C(I)=C2)C(O)=O
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Synonyms
Levothyroxine; T4
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Structure Classification
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Publications (13)
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Journal Impact Factor
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Most Recent
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Cell
Restoring circadian rhythms in the hypothalamic paraventricular nucleus reverses aging biomarkers and extends lifespan in male mice. [Abstract]2026 Apr 2;189(7):2007-2023.e20. PMID: 41785851 -
Nat Immunol
2024 Apr;25(4):659-670. PMID: 38499799 -
Cell Rep Med
2023 Jun 20;4(6):101061. PMID: 37267943 -
EMBO J
Whole-body replacement of larval myofibers generates permanent adult myofibers in zebrafish. [Abstract]2024 Aug;43(15):3090-3115. PMID: 38839992
L-Thyroxine purchased from MedChemExpress. Usage Cited in: EMBO J. 2024 Aug;43(15):3090-3115. [Abstract]
Timeline and three different Thyroxine hormone (T4) treatment schemes. RT-qPCR analysis of the whole-animal myofiber loss for each of the schemes.
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Europace
Fto-mediated m6A demethylation of Lox drives atrial fibrosis and promotes atrial fibrillation in a murine model of hyperthyroidism. [Abstract]2026 Mar 30;28(4):euag047. PMID: 41812233 -
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Stem Cell Rev Rep
2021 Jun;17(3):999-1013. PMID: 33389681 -
Sci Rep
The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice. [Abstract]2022 Jul 4;12(1):11259. PMID: 35788623
L-Thyroxine purchased from MedChemExpress. Usage Cited in: Sci Rep. 2022 Jul 4;12(1):11259. [Abstract]
Growth curve of male wild type (WT), Slc26a7+/−, Slc26a7−/−, and Slc26a7-/− mice receiving L-Thyroxine (drinking water containing 0.39 mg/L L-Thyroxine) replacement from day 21 with a low iodine diet. Note that Slc26a7−/− mice without thyroid hormone replacement did not survive.
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Clin Exp Med
2025 Dec 20. PMID: 41420729 -
Dis Model Mech
2024 Aug 14:dmm.050748. PMID: 39139065 -
Mol Brain
iTRAQ-based proteomic profiling reveals protein alterations after traumatic brain injury and supports thyroxine as a potential treatment. [Abstract]2021 Jan 27;14(1):25. PMID: 33504361
L-Thyroxine purchased from MedChemExpress. Usage Cited in: Mol Brain. 2021 Jan 27;14(1):25. [Abstract]
Effects of L-Thyroxine on histopathology post-TBI. a Brain sections stained with cresyl violet were shown on the left. Lesion volume was calculated from the sections.
L-Thyroxine purchased from MedChemExpress. Usage Cited in: Mol Brain. 2021 Jan 27;14(1):25. [Abstract]
Brain water content of traumatized hemisphere increased 1 day post-TBI, whereas L-Thyroxine alleviates edema.
L-Thyroxine purchased from MedChemExpress. Usage Cited in: Mol Brain. 2021 Jan 27;14(1):25. [Abstract]
BBB integrity was reflected by detecting the extravasation of EB dye (n = 3 per group).
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Ther Deliv
Excipient adjusting rheological properties of silica-based injectable hydrogel composites for controlled drug delivery. [Abstract]2025 Oct 30:1-15. PMID: 41168137 -
Solvent & Solubility
DMSO : 233.33 mg/mL (300.35 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
1M NaOH : 5 mg/mL (6.44 mM; ultrasonic and warming and adjust pH to 11 with NaOH and heat to 60°C)
H2O : < 0.1 mg/mL (insoluble)
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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
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. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.08 mg/mL (2.68 mM); Clear solution
This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.08 mg/mL (2.68 mM); Clear solution
This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Please enter your animal formula composition:
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%DMSO +
Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
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%+
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+%Tween-80 + +
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%Saline +
The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
Working solution concentration: 0.22 mg/mL
Method for preparing stock solution: mg drug dissolved in μL DMSO. Stock solution concentration: mg/mL.
1. Take μL DMSO stock solution;
2. Add μL .
μL , mix evenly;
3. Then add μL Tween 80, mix evenly;
4. Then add μL
Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
Protocol
Rats[2]
Sprague-Dawley female rats (N=22) are used. Non-pregnant rats are divided into four groups: 1) control, 2) hypothyroidism, 3) hypothyroidism treated with low doses of L-Thyroxine (20 μg/kg/day) and 4) with high doses of L-Thyroxine (100 μg/kg/day). Control rats (group 1) are fed with standard diet, while the intervention rats are fed with iodine-free diet for 12 weeks to induce hypothyroidism (groups 2-4) which is continued for four more weeks to allow screening of hypothyroid status and L-Thyroxine-treatment. Food and water (iodine-free diet) are available ad libitum. The hypothyroid group treated with low (group 3) or high doses of L-Thyroxine (group 4) are injected intraperitoneally every 24 h with respectively 20 μg/kg/day and 100 μg/kg/day. Blood samples are collected for thyroid function screening at week 12 and 16 following the initiation of either the control or iodine-free diet. Hysterectomy is performed under general anesthesia (isoflurane 2%) at the end of the treatment and the two uterine horns are placed in physiological Krebs' solution until isometric tension measurements within no more than 1 h.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Purity & Documentation
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Data Sheet (276 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
[1]. Arici M, et al. Association between genetic polymorphism and levothyroxine bioavailability in hypothyroid patients. Endocr J. 2018 Mar 28;65(3):317-323. [Content Brief]
[2]. Corriveau S, et al. Levothyroxine treatment generates an abnormal uterine contractility patterns in an in vitro animalmodel. J Clin Transl Endocrinol. 2015 Sep 9;2(4):144-149. [Content Brief]
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. 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 |
|---|---|---|---|---|---|
| 1M NaOH / DMSO | 1 mM | 1.2872 mL | 6.4361 mL | 12.8722 mL | 32.1804 mL |
| 5 mM | 0.2574 mL | 1.2872 mL | 2.5744 mL | 6.4361 mL | |
| DMSO | 10 mM | 0.1287 mL | 0.6436 mL | 1.2872 mL | 3.2180 mL |
| 15 mM | 0.0858 mL | 0.4291 mL | 0.8581 mL | 2.1454 mL | |
| 20 mM | 0.0644 mL | 0.3218 mL | 0.6436 mL | 1.6090 mL | |
| 25 mM | 0.0515 mL | 0.2574 mL | 0.5149 mL | 1.2872 mL | |
| 30 mM | 0.0429 mL | 0.2145 mL | 0.4291 mL | 1.0727 mL | |
| 40 mM | 0.0322 mL | 0.1609 mL | 0.3218 mL | 0.8045 mL | |
| 50 mM | 0.0257 mL | 0.1287 mL | 0.2574 mL | 0.6436 mL | |
| 60 mM | 0.0215 mL | 0.1073 mL | 0.2145 mL | 0.5363 mL | |
| 80 mM | 0.0161 mL | 0.0805 mL | 0.1609 mL | 0.4023 mL | |
| 100 mM | 0.0129 mL | 0.0644 mL | 0.1287 mL | 0.3218 mL |