D-dopa
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| D-dopa | |
| Systematic (IUPAC) name | |
| (R)-2-amino-3-(3,4-dihydroxyphenyl)-propanoic acid | |
| Synonyms | |
| Dextrodopa
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| Identifiers | |
| PubChem | 92222 |
| Chemical data | |
| Formula | C9H11NO4 |
| Molar mass | 197.188 |
| Complete data | |
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Ongoing Trials on D-dopa at Clinical Trials.gov Clinical Trials on D-dopa at Google
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US National Guidelines Clearinghouse on D-dopa
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Directions to Hospitals Treating D-dopa Risk calculators and risk factors for D-dopa
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D-DOPA (Dextrodopa) is similar to L-DOPA (levodopa, 3,4-dihydroxy-L-phenylalanine), but differs in its property of dextrorotation. Levo- and dextro- rotation reference a molecules ability to rotate planes of polarized light in either direction.
While L-Dopa is moderately effective against the loss of natural dopamine in Parkinson's disease, D-Dopa is biologically inactive. D- dopa is L- Dopa's enantiomer. See L-DOPA for more information about DOPA in general.
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
