What Is T4 LEVOTHYROXINE 400MCGS / ML | 60ML?
Levothyroxine is a synthetic analog of the thyroid hormone, thyroxine (T4). It is an FDA-approved drug that is sold under the brand name synthroid. It is primarily indicated for the treatment of hypothyroidism, a condition in which the thyroid gland is unable to produce sufficient quantities of thyroxine (T4 or tetraiodothyronine).
Plus, it can also be used in combination with surgery and radiation therapy to address thyroid cancer. Currently, it is being researched for its effect on multiple sclerosis and non-alcoholic fatty liver disease (NAFLD). At Pinnacle Peptides, levothyroxine for sale is exclusively available for research and educational institutions.
Structure Of T4 LEVOTHYROXINE 400MCGS / ML | 60ML

From Pubchem
IUPAC Name: (2S)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl] propanoic acid
Synonyms: L-thyroxine, levothyroxin, 51-48-9, thyroxine, thyroxin
Molecular Formula: C15H11I4NO4
Molecular Weight: 776.87 g/mol
Sequence: Ala-Glu-Asp-Gly
CAS number: 51-48-9
PubChem CID: 5819
Mechanism Of T4 LEVOTHYROXINE 400MCGS / ML | 60ML
Levothyroxine mimics the function of thyroxine (T4), an endogenous hormone produced by the thyroid gland. After it is absorbed by the gastrointestinal tract, it undergoes a transformation in liver cells and is converted to its active form, L-triiodothyronine (T3). T3, in turn, binds to thyroid receptors located in the cell nucleus. This, in turn, activates downstream signaling that influences gene expression and protein synthesis, leading to enhanced metabolic effects, such as increased thermogenesis and oxygen consumption.
Pre-Clinical/Clinical Research
1. Congenital Hypothyroidism
Congenital hypothyroidism is characterized by a deficiency of thyroid hormone in newborns. It is a fatal condition that requires prompt diagnosis to prevent irreversible neurological damage. Research suggests that immediate treatment of levothyroxine (L-T4) upon diagnosis, preferably within the first two weeks after birth, successfully reduces the risk of intellectual deficits and optimizes neurodevelopment [2].
Furthermore, T4 is considered a preferred treatment for congenital hypothyroidism [2]. One study concluded that combination treatment with T4 plus T3 didn’t show any significant advantage over T4 therapy in patients with congenital hypothyroidism [4].
The effective treatment of congenital hypothyroidism typically involves a single morning dose of oral levothyroxine[3]. However, an initial study in adult patients suggested that levothyroxine administration in the evening might yield at least an equal, if not better, therapeutic effect compared to morning administration [5].
2. Polycystic ovary syndrome (PCOS)
According to the guidelines of the American Thyroid Association, hypothyroid women aiming for pregnancy should modify their levothyroxine dosage to attain a TSH level within the range of the lower reference limit and 2.5 mIU/L. However, there is insufficient evidence to establish whether levothyroxine supplementation enhances fertility in anti-TPO antibody-positive women with subclinical hypothyroidism who are trying to conceive naturally [6].
In a small case-control study, levothyroxine treatment in women with polycystic ovary syndrome (PCOS) and subclinical hypothyroidism (SCH) demonstrated no significant impact based on multivariate analysis. The T4 treatment did not alter serum metabolic markers, including LDL and HDL cholesterol, triglycerides, glucose, and insulin [7].
3. Multiple Sclerosis
Multiple sclerosis (MS) is an autoimmune disease characterized by the demyelination of nerves. Stats show that approximately 70% of individuals with MS experience impaired and demyelinated visual systems. Oligodendrocyte progenitor cells (OPC) play an important role in the generation of oligodendrocytes, which are responsible for the myelination of nerve fibers. Research shows that the effectiveness of this process depends on various factors including thyroid hormones [8].
According to one study in male Wistar rats’, intraperitoneal administration of levothyroxine at doses of 50 and 100 μg/kg effectively prevented impairments in visual evoked potentials induced by lysolecithin. However, the lower levothyroxine dose (20 μg/kg) did not exhibit any effects [9]. These findings suggest that higher doses of thyroid hormones have more favorable effects on the healing process following demyelination induced by lysolecithin injection.
4. Nonalcoholic Fatty Liver Disease (NAFLD)
Nonalcoholic fatty liver disease (NAFLD) is characterized by the accumulation of extrahepatic fat in the absence of excessive alcohol consumption. The rising prevalence of NAFLD is contributing to a growing need for liver transplantation. As levothyroxine has been shown to reduce body weight and serum lipid levels, it might alleviate the negative side effects of NAFLD[10].
One study found that levothyroxine replacement therapy had a positive impact on NAFLD patients with subclinical hypothyroidism (SCH). It reduced the prevalence of NAFLD and lowered hepatic enzyme levels in serum. The results of the study suggest that thyroxine supplementation could be an effective treatment to manage NAFLD in patients with SCH [11].
Summary
Levothyroxine is a synthetic levo-isomer analog of the thyroxine hormone produced by the thyroid gland. Researchers show that it is an effective drug for the treatment of hypothyroidism, multiple sclerosis and nonalcoholic fatty liver disease. Despite being FDA-approved, it is still being tested to determine its efficacy in other clinical conditions. At Pinnacle Peptides, we offer levothyroxine purchase solely for research. Only buy levothyroxine if you are a qualified researcher.
References
- Rousset, B., et al., Thyroid hormone synthesis and secretion. 2015.
- Goldis., S.A.B.M. Congenital Hypothyroidism. 2023; Available from:
- Bernal, J., Thyroid hormones and brain development. Vitamins & Hormones, 2005. 71: p. 95-122.
- Cassio, A., et al., Treatment for congenital hypothyroidism: thyroxine alone or thyroxine plus triiodothyronine? Pediatrics, 2003. 111(5): p. 1055-1060.
- Bolk, N., et al., Effects of evening vs morning thyroxine ingestion on serum thyroid hormone profiles in hypothyroid patients. Clinical endocrinology, 2007. 66(1): p. 43-48.
- Alexander, E.K., et al., 2017 Guidelines of the American Thyroid Association for the diagnosis and management of thyroid disease during pregnancy and the postpartum. Thyroid, 2017. 27(3): p. 315-389.
- Kowalczyk, K., et al., The influence of treated and untreated subclinical hypothyroidism on metabolic profile in women with polycystic ovary syndrome. International Journal of Endocrinology, 2021. 2021.
- Calzà, L., M. Fernandez, and L. Giardino, Cellular approaches to central nervous system remyelination stimulation: thyroid hormone to promote myelin repair via endogenous stem and precursor cells. Journal of molecular endocrinology, 2009. 44(1): p. 13-23.
- Payghani, C., et al., Effects of levothyroxine on visual evoked potential impairment following local injections of lysolecithin into the rat optic chiasm. International Journal of Preventive Medicine, 2018. 9.
- Zhao, M., et al., A worthy finding: decrease in total cholesterol and low-density lipoprotein cholesterol in treated mild subclinical hypothyroidism. Thyroid, 2016. 26(8): p. 1019-1029.
- Liu, L., et al., Benefits of levothyroxine replacement therapy on nonalcoholic fatty liver disease in subclinical hypothyroidism patients. International Journal of Endocrinology, 2017. 2017.
T4 LEVOTHYROXINE 400MCG/ML | 60ML
| Molecular Formula | Molecular Weight | CAS Number | SKU |
|---|---|---|---|
| C15H11I4NO4 | 776.87 g/mol | 51-48-9 | T4-400MCG-60ML |
T4 Levothyroxine is a synthetic form of L-thyroxine, functioning predominantly as a prohormone requiring enzymatic conversion to T3 by iodothyronine deiodinase enzymes (DIO1, DIO2, DIO3) prior to nuclear receptor engagement.
An essential research tool for investigating the enzymatic cascade governing iodothyronine activation. Research applications include cell-free deiodinase enzyme kinetics assays, characterisation of iodothyronine membrane transporter proteins, and comparative binding studies examining differential TR binding affinities of T4 versus T3.
Manufactured in the USA by Pinnacle Peptides. Verified for concentration accuracy. For laboratory research use only. Store at room temperature away from direct light.
WARNING: For research purposes only. Not for human or animal consumption. Not intended to diagnose, treat, cure, or prevent any disease. For use by qualified research professionals only.
