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α-Methyl-3,5,3'-triiodothyropropionic acid, also known as 3,5,3'-triiodothyronine (T3), is a naturally occurring hormone derived from the thyroid gland. It plays a crucial role in regulating the body's metabolism, affecting protein synthesis, and influencing the breakdown of fats and carbohydrates. T3 is structurally similar to thyroxine (T4), another thyroid hormone, but with a methyl group replacing the outer ring's hydroxyl group. This difference allows T3 to be more biologically active than T4, as it can directly bind to nuclear receptors and exert its effects without the need for conversion. The chemical formula for α-methyl-3,5,3'-triiodothyropropionic acid is C15H12I3NO4, and it is essential for maintaining normal growth, development, and overall health.

35456-56-5

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35456-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35456-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,5 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35456-56:
(7*3)+(6*5)+(5*4)+(4*5)+(3*6)+(2*5)+(1*6)=125
125 % 10 = 5
So 35456-56-5 is a valid CAS Registry Number.

35456-56-5Downstream Products

35456-56-5Relevant academic research and scientific papers

α-Methylated Analogues of Triiodothyroalkanoic Acids: Synthesis and Biological Activity

Zenker, N.,Ekpe, A. E.,Hubbard, L. S.

, p. 548 - 552 (2007/10/02)

Three novel thyroid hormone analogues: α-methyl-3,5,3'-triiodothyroacetic acid, α-methyl-3,5,3'-triiodothyropropionic acid and α-methyl-3,5,3',5'-tetraiodothyropropionic acid were synthesized.The hepatic thyroid receptor affinity of these analogues was compared to that other available thyroid analogues.The ability of these compounds to increase the activity of two hepatic enzymes and to lower blood cholesterol was compared to that of L-triiodothyronine. α-Methyl-3,5,3'-triiodothyroacetic acid was shown to have less nuclear binding affinity, less enzyme inducing ability, but more blood cholesterol lowering ability than triiodothyroacetic acid. α-Methyl-3,5,3',5'-tetraiodothyropropionic acid showed less nuclear binding affinity and less enzyme-inducing activity than α-methyl-3,5,3'-triiodothyropropionic acid.

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