| Weight | 153.181 g/mol |
|---|---|
| Formula | C8H11NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
dopamine
Intropin · Dopamine Hydrochloride · Hydroxytyramine
62-31-7, 50444-17-2, 51-61-6
Score:
#95 in Neuroscience
,
#494 in Biology
,
#519 in Chemistry
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- Regional studies of catecholamines in the rat brain. I. The disposition of [3H]norepinephrine, [3H]dopamine and [3H]dopa in various regions of the brain. (Journal of Neurochemistry, 1966)
- Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats (Proceedings of the National Academy of Sciences of the United States of America, 1988)
- Multiple receptors for dopamine. (Nature, 1979)
- Predictive Reward Signal of Dopamine Neurons (Journal of Neurophysiology, 1998)
- What is the role of dopamine in reward: hedonic impact, reward learning, or incentive salience? (Brain Research Reviews, 1998)
- Dopamine Receptors: From Structure to Function (Physiological Reviews, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Intropin
- Dopamine Hydrochloride
- Hydroxytyramine
- 3,4-Dihydroxyphenethylamine
- 4-(2-Aminoethyl)-1,2-benzenediol
- 3,4 Dihydroxyphenethylamine
-
SMILESC1=CC(=C(C=C1CCN)O)O
-
InChIKeyVYFYYTLLBUKUHU-UHFFFAOYSA-N
- Pubchem - dopamine
- Wikipedia - dopamine
Dopamine (DA, a contraction of 3,4-dihydroxyphenethylamine) is an organic chemical of the catecholamine and phenethylamine families that plays several important roles in the brain and body. It is an amine synthesized by removing a carboxyl group from a molecule of its precursor chemical L-DOPA, which is synthesized in the brain and kidneys. Dopamine is also synthesized in plants and most animals.
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