An endogenous catecholamine
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Dopamine (hydrochloride)

Item No. 21992

Technical Information
Formal Name
4-(2-aminoethyl)-1,2-benzenediol, monohydrochloride
CAS Number
62-31-7
Synonyms
  • DA
  • KW 3160
  • 3-hydroxy Tyramine
Molecular Formula
C8H11NO2 • HCl
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 1 mg/mlPBS (pH 7.2): 5 mg/ml
SMILES
OC1=C(O)C=CC(CCN)=C1.Cl
InChi Code
InChI=1S/C8H11NO2.ClH/c9-4-3-6-1-2-7(10)8(11)5-6;/h1-2,5,10-11H,3-4,9H2;1H
InChi Key
CTENFNNZBMHDDG-UHFFFAOYSA-N
Shipping & Storage Information
Storage
Room temperature
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Dopamine is an endogenous catecholamine neurotransmitter synthesized from the amino acid L-tyrosine that acts as an agonist at dopamine receptors (D1-5).1 Dopamine is mainly synthesized in the substantia nigra and ventral tegmental area, and is a precursor in norepinephrine and epinephrine biosynthesis. Dopamine-containing neurons in the brain are involved in reward-motivated behavior, motor control, and hormone release. Dopamine is also synthesized in the adrenal glands where it exerts peripheral paracrine functions including control of vasodilation, sodium excretion, insulin production, gastrointestinal motility, and the activity of lymphocytes.2,3 Loss or damage of dopaminergic neurons in the substantia nigra is associated with Parkinson’s disease.4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Missale, C., Nash, S.R., Robinson, S.W., et alDopamine receptors: From structure to function. Physiol. Rev. 78(1), 190-225 (1998).

    2. Hayaishi, O. Molecular genetic studies on sleep-wake regulation, with special emphases on the prostaglandin D2 system. J. Appl. Physiol. 92(2), 863-868 (2015).

    3. Garza, J.H.H., and Carr, D.J.J. Neuroendocrine peptide receptors on cells of the immune system. Chem. Immunol. 69, 132-154 (1997).

    4. Angeles, D.C., Ho, P., Dymock, B.W., et alAntioxidants inhibit neuronal toxicity in Parkinson’s disease-linked LRRK2. Ann. Clin. Transl. Neurol. 3(4), 288-294 (2016).