Names | |
---|---|
IUPAC name
1-[(3,4-dihydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol
| |
Other names
Norlaudanosoline; Tetrahydroxypapaveroline
| |
Identifiers | |
3D model (
JSmol)
|
|
ECHA InfoCard | 100.158.898 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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).
|
Tetrahydropapaveroline (norlaudanosoline) is a benzyltetrahydroisoquinoline alkaloid. [1]
It can be formed in trace amounts in the brain by a condensation reaction of dopamine and dopaldehyde (a metabolite of dopamine). [1] [2]
It inhibits dopamine uptake within the cerebral cortex. [3]
Names | |
---|---|
IUPAC name
1-[(3,4-dihydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol
| |
Other names
Norlaudanosoline; Tetrahydroxypapaveroline
| |
Identifiers | |
3D model (
JSmol)
|
|
ECHA InfoCard | 100.158.898 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
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).
|
Tetrahydropapaveroline (norlaudanosoline) is a benzyltetrahydroisoquinoline alkaloid. [1]
It can be formed in trace amounts in the brain by a condensation reaction of dopamine and dopaldehyde (a metabolite of dopamine). [1] [2]
It inhibits dopamine uptake within the cerebral cortex. [3]