D-DOPA
From Wikipedia, the free encyclopedia
| D-DOPA | |
|---|---|
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(R)-2-Amino-3-(3,4-dihydroxyphenyl)propanoic acid |
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| Identifiers | |
| CAS number | 5796-17-8 |
| PubChem | 92222 |
| ChemSpider | 83260 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C9H11NO4 |
| Molar mass | 197.19 g mol−1 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references |
D-DOPA (D-3,4-dihydroxyphenylalanine; Dextrodopa) is similar to L-DOPA (Levodopa), but with opposite chirality. Levo- and dextro- rotation reference a molecule's ability to rotate planes of polarized light in either direction. Whereas L-DOPA is moderately effective in the treatment of Parkinson's disease (PD), D-DOPA is biologically inactive.
[edit] See also
- L-DOPA (Levodopa; Sinemet, Parcopa, Atamet, Stalevo, Madopar, Prolopa, etc.)
- L-DOPS (Droxidopa)
- Methyldopa (Aldomet, Apo-Methyldopa, Dopamet, Novomedopa, etc.)
- Dopamine (Intropan, Inovan, Revivan, Rivimine, Dopastat, Dynatra, etc.)
- Norepinephrine (Noradrenaline; Levophed, etc.)
- Epinephrine (Adrenaline; Adrenalin, EpiPen, Twinject, etc.)
[edit] References
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