Tetrahydropapaveroline
| Names | |
|---|---|
| IUPAC name
1-[(3,4-dihydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol | |
| Other names
Norlaudanosoline; Tetrahydroxypapaveroline | |
| Identifiers | |
3D model (JSmol) |
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| ECHA InfoCard | 100.158.898 |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C16H17NO4 | |
| Molar mass | 287.315 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Tetrahydropapaveroline, also known as norlaudanosoline, is a tetrahydroisoquinoline alkaloid.
It can be formed in trace amounts in the brain by a condensation reaction of dopamine and dopaldehyde (a metabolite of dopamine).
It inhibits dopamine uptake within the cerebral cortex.