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L-DOPA methyl ester (hydrochloride)

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    L-<wbr/>DOPA methyl ester (hydro<wbr>chloride)
  • L-<wbr/>DOPA methyl ester (hydro<wbr>chloride)
Cat No: 16149
Biochemicals - More Biochemicals
Cayman

L-DOPA (Item No. 13248) is a metabolic precursor of dopamine that is capable of crossing the blood brain barrier to act as a dopamine D1 receptor agonist. It is produced from L-tyrosine by trysosine hydroxylase. In the brain, L-DOPA is converted to dop...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • 3-hydroxy-L-tyrosine, methyl ester, monohydrochloride
Correlated keywords:
  • dopamine neurotransmitters locomotion Parkinson’s diseases strokes receptors agonists L DOPA LDOPA metabolic precursors blood brains barriers D1 L-tyrosine tyrosine hydroxylases enzymes aromatic L-amino aminos acids decarboxylase concentrations recovery methyl esters hydrochloride HCl derivatives neutral solubility soluble compounds 52618-24-3 7101-51-1 levomet melevodopa methyl 3-Hydroxy-L-tyrosine ST41769 ST-41769
Product Overview:
L-DOPA (Item No. 13248) is a metabolic precursor of dopamine that is capable of crossing the blood brain barrier to act as a dopamine D1 receptor agonist. It is produced from L-tyrosine by trysosine hydroxylase. In the brain, L-DOPA is converted to dopamine by the enzyme aromatic L-amino acid decarboxylase. It is conventionally used to increase dopamine concentrations in the brain as a treatment for Parkinson’s disease and stroke recovery.{17819} L-DOPA methyl ester is a neutral derivative of L-DOPA formulated for increased solubility compared to the parent compound.{26614}
Size 500 mg
Shipping dry ice
CAS Number 1421-65-4
Molecular Formula C10H13NO4 • HCl
SMILES OC1=C(O)C=CC(C[C@H](N)C(OC)=O)=C1.Cl
Molecular Weight 247,7
Formulation A crystalline solid
Purity ≥98%
Custom Code 2907.29
UNSPSC code 12352100

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Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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