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Chemodex
3,4-Dihydroxy-L-phenylalanine
Product Details | |
---|---|
Synonyms | 3-(3,4-Dihydroxyphenyl)-L-alanine; L-DOPA; 3-Hydroxy-L-tyrosine; Levodopa |
Product Type | Chemical |
Properties | |
Formula |
C9H11NO4 |
MW | 197.19 |
CAS | 59-92-7 |
Source/Host Chemicals | Synthetic |
Purity Chemicals | ≥98% |
Appearance | White to off-white powder. |
Solubility | Soluble in water (5-10mM), acidic and basic solutions. |
Identity | Determined by NMR. |
Declaration | Manufactured by Chemodex. |
Other Product Data |
Click here for Original Manufacturer Product Datasheet |
InChi Key | WTDRDQBEARUVNC-LURJTMIESA-N |
Smiles | OC1=C(O)C=CC(C[C@H](N)C(O)=O)=C1 |
Shipping and Handling | |
Shipping | AMBIENT |
Short Term Storage | +20°C |
Long Term Storage | +20°C |
Handling Advice | Protect from light and moisture. |
Use/Stability | Stable for at least 2 years after receipt when stored at +20°C. |
Documents | |
MSDS | Download PDF |
Product Specification Sheet | |
Datasheet | Download PDF |
Metabolic precursor of the neurotransmitters dopamine, norepinephrine (noradrenaline), and epinephrine (adrenaline), which are collectively known as catecholamines. This amino acid is produced from L-tyrosine by tyrosine hydroxylase and metabolized by catechol-O-methyl transferase (COMT). L-DOPA is capable of crossing the blood brain barrier where it is converted to dopamine. Formulations containing L-DOPA have been used to increase dopamine concentrations in the brain as a treatment for Parkinson’s disease and stroke recovery. Mediates neurotrophic factor release by the brain and CNS. Used for the treatment of Parkinson’s disease and dopamine-responsive dystonia. In addition it is used, as a cell adhesion molecule in serum-free cultures of anchorage-dependent mammalian cells, to prevent surfaces from fouling by bonding antifouling polymers to a susceptible substrate or to stain melanocytes.
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