| Weight | 423.422 g/mol |
|---|---|
| Formula | C19H25N3O8 |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 9 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 7 |
Duodopa (57308-51-7)
Score:
#148 in Neurology
,
#663 in Neuroscience
,
#2954 in Biology
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- Subacute Axonal Neuropathy in Parkinson's Disease with Cobalamin and Vitamin B6 Deficiency Under Duodopa Therapy (Movement Disorders, 2010)
- Reversible encephalopathy and axonal neuropathy in Parkinson's disease during duodopa therapy (Movement Disorders, 2009)
- Duodopa treatment for advanced Parkinson's disease: a review of efficacy and safety. (Parkinsonism & Related Disorders, 2012)
- Comparison of subthalamic nucleus deep brain stimulation and Duodopa in the treatment of advanced Parkinson's disease (Movement Disorders, 2011)
- Reducing uncertainty in value-based pricing using evidence development agreements: the case of continuous intraduodenal infusion of levodopa/carbidopa (Duodopa) in Sweden. (Applied Health Economics and Health Policy, 2010)
- Prospective assessment of peripheral neuropathy in Duodopatreated parkinsonian patients (Acta Neurologica Scandinavica, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(CC1=CC(=C(C=C1)O)O)(C(=O)O)NN.C1=CC(=C(C=C1CC(C(=O)O)N)O)O
-
InChIKeyIVTMXOXVAHXCHI-UHFFFAOYSA-N
- Pubchem - Duodopa
- Wikipedia - Carbidopa/levodopa
L-DOPA (), also known as levodopa () or L-3,4-dihydroxyphenylalanine is an amino acid that is made and used as part of the normal biology of humans, some animals and plants. Some animals and humans make it via biosynthesis from the amino acid L-tyrosine. L-DOPA is the precursor to the neurotransmitters dopamine, norepinephrine (noradrenaline), and epinephrine (adrenaline), which are collectively known as catecholamines.
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