Dextrothyroxine |
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| Trade names | Choloxin |
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| Other names | D-3,5,3',5'-tetraiodothyronine |
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| AHFS/Drugs.com | Multum Consumer Information |
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| ATC code | |
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(2R)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoic acid
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| ECHA InfoCard | 100.000.094 |
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| Formula | C15H11I4NO4 |
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| Molar mass | 776.874 g·mol−1 |
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| 3D model (JSmol) | |
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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) is a dextrorotary isomer of thyroxine.[1] It saw research as a cholesterol-lowering drug[2] but was pulled due to cardiac side-effects. It increases hepatic lipase which in turn improves utilization of triglycerides and decreases levels of lipoprotein(a) in blood serum.[3]
References
- ^ "Dextrothyroxine (Code C61719)". NCI Thesaurus. National Cancer Institute. 2011-11-14. Retrieved 2020-01-28.
- ^ Bantle JP, Hunninghake DB, Frantz ID, Kuba K, Mariash CN, Oppenheimer JH (September 1984). "Comparison of effectiveness of thyrotropin-suppressive doses of D- and L-thyroxine in treatment of hypercholesterolemia". The American Journal of Medicine. 77 (3): 475–81. doi:10.1016/0002-9343(84)90107-4. PMID 6475988.
- ^ Bommer C, Werle E, Walter-Sack I, Keller C, Gehlen F, Wanner C, et al. (January 1998). "D-thyroxine reduces lipoprotein(a) serum concentration in dialysis patients". Journal of the American Society of Nephrology. 9 (1): 90–6. doi:10.1681/ASN.V9190. PMID 9440092.
Lipid-lowering agents (C10) |
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| GI tract | | Cholesterol absorption inhibitors, NPC1L1 | |
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| Bile acid sequestrants/resins (LDL) | |
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| Liver | | Statins (HMG-CoA reductase, LDL) | |
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| Niacin and derivatives (HDL and LDL) | |
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| MTTP inhibitors (VLDL) |
- Dirlotapide
- Lomitapide
- Mitratapide
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| ATP citrate lyase inhibitors (LDL) | |
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| Thyromimetics (VLDL) | |
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| Blood vessels | | PPAR agonists (LDL) | |
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| CETP inhibitors (HDL) |
- Anacetrapib†
- Dalcetrapib§
- Evacetrapib§
- Obicetrapib†
- Torcetrapib§
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| PCSK9 inhibitors (LDL) |
- Alirocumab
- Bococizumab
- Enlicitide†
- Evolocumab
- Inclisiran
- Lerodalcibep
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| ANGPTL3 inhibitors (LDL/HDL) | |
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| Combinations |
- Amlodipine/atorvastatin
- Bempedoic acid/ezetimibe
- Ezetimibe/atorvastatin
- Ezetimibe/rosuvastatin
- Ezetimibe/simvastatin
- Fenofibrate/pravastatin
- Fenofibrate/simvastatin
- Niacin/laropiprant
- Niacin/lovastatin
- Niacin/simvastatin
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| Other |
- Alipogene tiparvovec
- Azacosterol
- Azalanstat
- Benfluorex‡
- Darapladib§
- Lapaquistat§
- Magnesium pyridoxal 5-phosphate glutamate
- Meglutol
- Mipomersen
- Olezarsen
- Omega−3-acid ethyl esters
- Plozasiran
- Policosanol
- Probucol
- Tiadenol
- Triparanol‡
- Volanesorsen
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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Thyroid hormone receptor modulators |
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Receptor (ligands) | | THRTooltip Thyroid hormone receptor | | Agonists | |
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Thyromimetics (selective agonists) |
- Elunetirom (ABX-002, MA-JD21)
- Eprotirome (KB-2115)
- KB-141
- KB-2611
- KB-130015
- MB-07344
- MB-07811
- Resmetirom
- Sobetirome (GC-1, GRX-431)
- VK-0214
- VK-2809
- ZYT1
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| Antagonists |
- 1-850
- NH3
- Tetraiodothyroacetic acid (Tetrac)
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Transporter (blockers) | NISTooltip Sodium-iodide symporter |
- Inhibitors: Cyanogenic glycosides
- Perchlorates (e.g., potassium perchlorate)
- Pertechnetates (e.g., sodium pertechnetate)
- Thiocyanates
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Enzyme (inhibitors) | | TPOTooltip Thyroid peroxidase | |
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| DIOTooltip Iodothyronine deiodinase | |
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| Others | |
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- See also: Receptor/signaling modulators
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