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Supplier NameMedChemExpress (MCE)
Contactsales
Tel609-228-6898
Mobile609-228-6898
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Emailsales@medchemexpress.com; tech@medchemexpress.com
Websitehttp://www.medchemexpress.com/
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Product NameL-DOPA
SynonymsL-DOPA
Levodopa
H-Tyr(3-OH)-OH
L-3-Hydroxytyrosine
3-HYDROXY-L-TYROSINE
3-Hydroxy-L-tyrosine
3,4-L-DIHYDROXYPHENYLALANINE

Synonyms

L-DOPA
Levodopa
H-Tyr(3-OH)-OH
L-3-Hydroxytyrosine
3-HYDROXY-L-TYROSINE
3-Hydroxy-L-tyrosine
3,4-L-DIHYDROXYPHENYLALANINE
3,4-DIHYDROXY-L-PHENYLALANINE
3,4-Dihydroxyphenyl-L-alanine
L-3-(3,4-Dihydroxyphenyl)alanine
3,4-Dihydroxyphenylalanine(form2)
3-(3,4-DIHYDROXYPHENYL)-L-ALANINE
L-DOPA 3,4-L-Dihydroxyphenylalanine
BETA-(3,4-DIHYDROXYPHENYL)-L-ALANINE
2-amino-3-(3,4-dihydroxyphenyl)propanoicacid
CAS59-92-7
EINECS200-445-2
Chemical FormulaC9H11NO4
Molecular Weight197.19
inchiInChI=1/C9H11NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6,11-12H,3,10H2,(H,13,14)/t6-/m0/s1
Package200 mg;1 g
PriceEmail to quote
DescriptionsL-DOPA

L-DOPA

MedChemExpress (MCE)

HY-N0304

59-92-7

Levodopa

Descriptions

L-DOPA

L-DOPA

MedChemExpress (MCE)

HY-N0304

59-92-7

Levodopa
3,4-Dihydroxyphenylalanine

99.98%

4°C, stored under nitrogen *The compound is unstable in solutions, freshly prepared is recommended.

Room temperature in continental US
may vary elsewhere.

L-DOPA (Levodopa) is an orally active metabolic precursor of neurotransmitters dopamine. L-DOPA can cross the blood-brain barrier and is converted into dopamine in the brain. L-DOPA has anti-allodynic effects and the potential for Parkinson's disease.

L-DOPA can be used to create movement disorder models. In adult common marmosets, after oral administration of L-DOPA (20/5 mg/kg), the Tmax in plasma is 30 minutes, and the Tmax in striatal extracellular fluid (ECF) is 60-90 minutes. The mean Cmax of L-DOPA in plasma is 20.3 μM, while the mean Cmax in striatal ECF is 442.9 nM, representing about 2.2% of the plasma level[6]. .f12{ font-size: 12px
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} Induction of dyskinesia model[5] Background L-DOPA-induced dyskinesia results from a pulsatile stimulation of brain dopamine (DA) receptors, triggering a complex cascade of molecular and synaptic alterations within the basal ganglia[5]. Specific Mmodeling Methods Mice: C57Bl/6 mice • male • 8 weeks (period: 21 days)Administration: 20 mg/kg • ip • once daily for 21 days Note (1) sustained unilateral 6-OHDA injections in the striatum before starting treatment.(2) Injection volume is 10mL/kg body weight. Modeling Indicators Behavioral changes: Shows developed abnormal involuntary movements (AIMs) affecting the head, trunk and forelimb on the side contralateral to the lesion. Correlated Product(s): Oxidopamine hydrochloride (HY-B1081) Opposite Product(s): Oxidopamine hydrobromide (HY-B1081A)

Human Endogenous Metabolite

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[1]. Hyland K, et al. Aromatic L-amino acid decarboxylase deficiency: diagnostic methodology. Clin Chem. 1992 Dec
38(12):2405-10.
[Content Brief]

[2]. Merims D, et al. Dopamine dysregulation syndrome, addiction and behavioral changes in Parkinson's disease. Parkinsonism Relat Disord. 2008
14(4):273-80. Epub 2007 Nov 7.
[Content Brief]

[3]. Perez-Pardo P, et al. Additive Effects of Levodopa and a Neurorestorative Diet in a Mouse Model of Parkinson's Disease. Front Aging Neurosci. 2018 Aug 3
10:237.
[Content Brief]

[4]. Park HJ, et al. Anti-allodynic effects of levodopa in neuropathic rats. Yonsei Med J. 2013 Mar 1
54(2):330-5.
[Content Brief]

[5]. M Lundblad, et al. Pharmacological validation of a mouse model of l-DOPA-induced dyskinesia. Exp Neurol. 2005 Jul
194(1):66-75.
[Content Brief]

[6]. Jie Zhang, et al. Pharmacokinetics of L-dopa in plasma and extracellular fluid of striatum in common marmosets. Brain Res. 2003 Dec 12
993(1-2):54-8.
[Content Brief]

Supplier Websitehttp://www.medchemexpress.com/L-DOPA.html
Last Update2025-10-14 16:03:33
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