Dextrothyroxine
Dextrothyroxine
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Systematic (IUPAC) name |
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(2R)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoic acid |
Clinical data |
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Trade names |
Choloxin |
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AHFS/Drugs.com |
Multum Consumer Information |
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- US: B (No risk in non-human studies)
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Identifiers |
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51-49-0 |
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C10AX01 |
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PubChem |
CID 8730 |
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DrugBank |
DB00509 |
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ChemSpider |
8402 |
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UNII |
4W9K63FION |
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ChEBI |
CHEBI:30659 |
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ChEMBL |
CHEMBL559 |
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Synonyms |
D-3,5,3',5'-tetraiodothyronine |
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Chemical data |
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Formula |
C15H11I4NO4 |
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776.87 g/mol |
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SMILES
- O=C(O)[C@H](N)Cc2cc(I)c(Oc1cc(I)c(O)c(I)c1)c(I)c2
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InChI=1S/C15H11I4NO4/c16-8-4-7(5-9(17)13(8)21)24-14-10(18)1-6(2-11(14)19)3-12(20)15(22)23/h1-2,4-5,12,21H,3,20H2,(H,22,23)/t12-/m1/s1
Key:XUIIKFGFIJCVMT-GFCCVEGCSA-N
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Dextrothyroxine (trade name Choloxin) saw research as an cholesterol-lowering drug[1][2] but was pulled due to cardiac side-effects. It also increases hepatic lipase which in turn improves utilization of triglycerides, improving apolipoprotein E cholesterol particles.
See also
References
- ↑ Bantle, J. P.; Hunninghake, D. B.; Frantz, I. D.; Kuba, K.; Mariash, C. N.; Oppenheimer, J. H. (1984). "Comparison of effectiveness of thyrotropin-suppressive doses of D- and L-thyroxine in treatment of hypercholesterolemia". The American journal of medicine 77 (3): 475–481. doi:10.1016/0002-9343(84)90107-4. PMID 6475988.
- ↑ Bommer, C.; Werle, E.; Walter-Sack, I.; Keller, C.; Gehlen, F.; Wanner, C.; Nauck, M.; März, W.; Wieland, H.; Bommer, J. (1998). "D-thyroxine reduces lipoprotein(a) serum concentration in dialysis patients". Journal of the American Society of Nephrology : JASN 9 (1): 90–96. PMID 9440092.
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| Liver | | |
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| Niacin and derivatives ( HDL and LDL) | |
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| Description |
- Vitamins
- Cofactors
- Metal metabolism
- Fats
- metabolism
- intermediates
- lipoproteins
- Sugars
- Glycolysis
- Glycogenesis and glycogenolysis
- Fructose and galactose
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| Disease |
- Vitamins
- Carbohydrate
- Lipid
- Metals
- Other
- Symptoms and signs
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| Treatment |
- Drugs
- Vitamins
- Mineral supplements
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