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デキストロチロキシン

Structure via PubChem · Public domain (PubChem)

EntityQ5268499· pop 11· linked from 145 articles

デキストロチロキシン

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Also known as Choloxin®, D-T4, D-thyroxine, O-(4-hydroxy-3,5-diiodophenyl)-3,5-diiodo-D-tyrosine, DT4, Dextrothyroxine, O-(4-Hydroxy-3,5-diiodophenyl)-3,5-diiodo-D-tyrosine

Dextrothyroxine (trade name Choloxin) is a dextrorotary isomer of thyroxine. It saw research as a cholesterol-lowering drug 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.

Chemical data

Formula
C15H11I4NO4
Molecular weight
776.87 g/mol
IUPAC name
(2R)-2-azaniumyl-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoate

via PubChem

Drug data · ChEMBL

Max clinical phase
Approved
Molecule type
Small molecule
First approval
1967
Admin. routes
oral
Indications
cardiovascular disease, Down syndrome

via ChEMBL · EBI

Research

309 papers

via PubMed

Wikidata facts

Subclass of
thyroxine
Mass
776.6867
Has use
medication
Show 5 more facts
chemical formula
C₁₅H₁₁I₄NO₄
medical condition treated
coronary artery disease
canonical SMILES
C1=C(C=C(C(=C1I)OC2=CC(=C(C(=C2)I)O)I)I)CC(C(=O)O)N
isomeric SMILES
C1=C(C=C(C(=C1I)OC2=CC(=C(C(=C2)I)O)I)I)C[C@H](C(=O)O)N
defined daily dose
4
Sources (3)

via Wikidata · CC0

Article · 日本語

デキストロチロキシン(Dextrothyroxine)は、チロキシンのD-異性体(右旋性)である。コレステロールを下げる薬として研究されたが、心臓の副作用の為に中止された。肝リパーゼを増加させ、トリグリセリドの利用率を高め、血清中のの濃度を低下させる。左旋性のL-チロキシンは、内因性の甲状腺ホルモンであると同時に、甲状腺ホルモン補充療法に用いられる医薬品である。

Abstract from DBpedia / Wikipedia · CC BY-SA