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  2. L-DOPA - Wikipedia

    en.wikipedia.org/wiki/L-DOPA

    [3] [4] In some plant families (of the order Caryophyllales), l-DOPA is the central precursor of a biosynthetic pathway that produces a class of pigments called betalains. [5] l-DOPA can be manufactured and in its pure form is sold as a drug with the INN Tooltip International Nonproprietary Name levodopa. Trade names include Sinemet, Pharmacopa ...

  3. Levodopa - Wikipedia

    en.wikipedia.org/wiki/Levodopa

    Levodopa crosses the protective blood–brain barrier, whereas dopamine itself cannot. [3] [4] Thus, levodopa is used to increase dopamine concentrations in the treatment of Parkinson's disease, Parkinsonism, dopamine-responsive dystonia and Parkinson-plus syndrome. The therapeutic efficacy is different for different kinds of symptoms.

  4. Dopamine agonist - Wikipedia

    en.wikipedia.org/wiki/Dopamine_agonist

    The synthesis of dopamine consists of three stages. The synthesis process starts with an amino acid, called L-tyrosine. In the second stage L-DOPA (levodopa) is formed by adding a phenol group to the benzene ring of L-tyrosine. The formation of L-DOPA from L-tyrosine is catalyzed by the enzyme tyrosine hydroxylase.

  5. Neurotransmitter prodrug - Wikipedia

    en.wikipedia.org/wiki/Neurotransmitter_prodrug

    Levodopa (L-DOPA), a prodrug of dopamine which is used to treat Parkinson's disease and certain other conditions. A neurotransmitter prodrug, or neurotransmitter precursor, is a drug that acts as a prodrug of a neurotransmitter. A variety of neurotransmitter prodrugs have been developed and used in medicine.

  6. List of human blood components - Wikipedia

    en.wikipedia.org/wiki/List_of_human_blood_components

    Needed for nerve cells, red blood cells, and to make DNA 6-14 × 10 −10: 1-10 × 10 −10: Cocarboxylase: 7-9 × 10 −8: Complement system: C1q 5.8-7.2 × 10 −5: C1r 2.5-3.8 × 10 −5: C1s (C1 esterase) 2.5-3.8 × 10 −5: C2 2.2-3.4 × 10 −5: C3( b1C-globulin) 8-15.5 × 10 −4: factor B (C3 proactivator) 2-4.5 × 10 −4: C4 (b1E ...

  7. Aromatic L-amino acid decarboxylase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Aromatic_L-amino_acid_de...

    Administration can prevent common side-effects, such as nausea and vomiting, as a result of interaction with D 2 receptors in the vomiting center (or cheomoreceptor trigger zone) located outside the blood–brain barrier. [2] Examples of extracerebral decarboxylase inhibitors include carbidopa and benserazide.

  8. List of dopaminergic drugs - Wikipedia

    en.wikipedia.org/wiki/List_of_dopaminergic_drugs

    This is a list of dopaminergic drugs. These are pharmaceutical drugs , naturally occurring compounds and other chemicals that influence the function of the neurotransmitter dopamine . Dopamine receptor ligands

  9. Aromatic L-amino acid decarboxylase - Wikipedia

    en.wikipedia.org/wiki/Aromatic_L-amino_acid_de...

    These cells include melanin-pigmented cells that are typically designated as catecholaminergic and may also be serotonergic. Significant localization of dopaminergic cells that are also immunoreactive for AADC is reported in the substantia nigra, ventral tegmental area, and the mesencephalic reticular formation. Unlike previous reports on ...

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