Droxidopa
| Clinical data | |
|---|---|
| Trade names | Northera, Dops |
| Other names | 3,4-Dihydroxyphenylserine; 3,4-threo-DOPS; L-threo-Dihydroxyphenylserine; L-DOPS; L-threo-DOPS; Threo-DOPS; β,3-Dihydroxytyrosine; (–)-threo-3-(3,4-Dihydroxyphenyl)-L-serine; SM-5688 |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a614025 |
| License data | |
| Routes of administration | By mouth |
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| Pharmacokinetic data | |
| Bioavailability | 90% |
| Metabolism | Liver |
| Metabolites | Norepinephrine |
| Elimination half-life | 1.5 hours |
| Excretion | Kidney |
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| ECHA InfoCard | 100.215.254 |
| Chemical and physical data | |
| Formula | C9H11NO5 |
| Molar mass | 213.189 g·mol−1 |
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Droxidopa, also known as L-threo-dihydroxyphenylserine (L-DOPS) and sold under the brand names Northera and Dops among others, is sympathomimetic medication which is used in the treatment of hypotension (low blood pressure) and for other indications.[1][2] It is taken by mouth.[1]
Side effects of droxidopa include headache, dizziness, nausea, and hypertension, among others.[1] Droxidopa is a synthetic amino acid precursor which acts as a prodrug to the neurotransmitter norepinephrine (noradrenaline).[3] Hence, it acts as a non-selective agonist of the α- and β-adrenergic receptors. Unlike norepinephrine, but similarly to levodopa (L-DOPA), droxidopa is capable of crossing the protective blood–brain barrier (BBB).[3]
Droxidopa was first described by 1971.[4][5] It was approved for use in Japan in 1989[6] and was introduced in the United States in 2014.[1][7]
- ^ a b c d "Northera (droxidopa) capsules - Prescribing Information" (PDF). Food and Drug Administration. February 10, 2017.
- ^ "Sumitomo Pharma/Lundbeck". AdisInsight. 2023-11-05. Retrieved 2024-09-01.
- ^ a b Goldstein DS (2006). "L-Dihydroxyphenylserine (L-DOPS): a norepinephrine prodrug". Cardiovascular Drug Reviews. 24 (3–4): 189–203. doi:10.1111/j.1527-3466.2006.00189.x. PMID 17214596.
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