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Structure

3,5-Diiodo-L-thyronine

CAS
1041-01-6
Catalog Number
ACM1041016-2
Category
Main Products
Molecular Weight
525.08
Molecular Formula
C15H13I2NO4

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Specification

Synonyms
Diiodothyronine
IUPAC Name
(2S)-2-Amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]propanoic acid
Canonical SMILES
C1=CC(=CC=C1O)OC2=C(C=C(C=C2I)CC(C(=O)O)N)I
InChI
InChI=1S/C15H13I2NO4/c16-11-5-8(7-13(18)15(20)21)6-12(17)14(11)22-10-3-1-9(19)2-4-10/h1-6,13,19H,7,18H2,(H,20,21)/t13-/m0/s1
InChI Key
ZHSOTLOTTDYIIK-ZDUSSCGKSA-N
Boiling Point
559.4±50.0 °C
Melting Point
255-260 °C
Flash Point
292.1 °C
Density
2.095±0.06 g/cm³
Appearance
Solid
Storage
Keep in dark place, sealed in dry, store in freezer, under -20 °C
Complexity
365
EC Number
213-867-7
Exact Mass
524.89340
Hazard Statements
Xn
Isomeric SMILES
C1=CC(=CC=C1O)OC2=C(C=C(C=C2I)C[C@@H](C(=O)O)N)I
Monoisotopic Mass
524.89340
pKa
2.15±0.30(Predicted)
Refractive Index
1.726
Safety Description
24/25
Topological Polar Surface Area
92.8 Ų
WGK Germany
3

Physiological Effects of 3,5-Diiodo-L-Thyronine in Dietary Supplements

Hernandez A. Endocrinology, 2015, 156(1), 5-7.

3,5-Diiodo-L-thyronine (T2) is a thyroid hormone (TH) metabolite that has found its way into the formulations of many drugs. 3,5-Diiodo-L-thyronine was observed to have rapid induction of hepatic oxygen consumption and oxidative capacity and was therefore used as a metabolic inducer. Outlined below are some of the physiological effects that T2 may have as a dietary supplement ingredient.
Physiological Effects of 3,5-Diiodo-L-Thyronine
· T2 has positive effects on mitochondrial function, fat mass, lipid metabolism, and insulin resistance, supporting the use of T2 to enhance metabolism.
· Although T2's ability to increase metabolism is unquestionable, it is unclear which conditions allow its safe and effective use in humans.
· The researchers used an obese mouse model to analyze the physiological effects of T2. These effects include inhibition of the HPT axis, reductions in fat mass, serum leptin, and cholesterol, and increases in lean body mass, food intake, and hepatic expression of TH-dependent genes related to lipid metabolism.
· In addition, studies have shown that in addition to increasing metabolism and reducing fat mass, T2 administration can lead to HPT axis suppression, increased food intake, and cardiac hypertrophy.

July 21, 2024


Highly Effective in Regulating Gene Activity
3,5-Diiodo-L-thyronine from Alfa Chemistry to be a highly effective product in regulating gene activity. The off-white solid compound is easy to work with and has provided promising results in my studies related to homeostasis, lipid metabolism, and insulin resistance. I have also found it to be useful in the early detection and treatment of congenital or drug-induced hypothyroidism. Overall, I highly recommend this product for anyone conducting research in the field of thyroid hormones and gene regulation.

Upstream Synthesis Route 1

  • 178877-78-6
  • 1041-01-6

Reference: [1] Synthetic Communications, 2013, vol. 43, # 10, p. 1439 - 1446

Upstream Synthesis Route 2

  • 54337-43-8
  • 300-39-0
  • 1041-01-6

Reference: [1] Tetrahedron Letters, 1997, vol. 38, # 40, p. 6965 - 6968

Upstream Synthesis Route 3

  • 623-05-2
  • 1041-01-6

Reference: [1] Tetrahedron Letters, 1997, vol. 38, # 40, p. 6965 - 6968

Downstream Synthesis Route 1

  • 1041-01-6
  • 51-48-9

Reference: [1]Patent: WO2015/151013,2015,A1 .Location in patent: Page/Page column 14

Downstream Synthesis Route 2

  • 1041-01-6
  • 6893-02-3

Reference: [1]Biochemical Journal,1953,vol. 53,p. 645,647
[2]Biochemical Journal,1953,vol. 53,p. 645,647
[3]Biochemical Journal,1953,vol. 53,p. 645,647
[4]Organic Process Research and Development,2014,vol. 18,p. 1175 - 1180
[5]Patent: JP5833222,2015,B2

* For details of the synthesis route, please refer to the original source to ensure accuracy.

Alfa Chemistry

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