Tetrahydropapaveroline

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==Description==
==Description==
A leukomaine (animal alkaloid) formed in brain and liver from dopamine and L-dopa; it may be implicated in psychiatric problems.
A leukomaine (animal alkaloid) formed in brain and liver from dopamine and L-dopa; it may be implicated in psychiatric problems.
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The inhibitory effects of tetrahydropapaveroline on serotonin biosynthesis in serotonin-producing murine mastocytoma P815 cells were investigated. Tetrahydropapaveroline decreased serotonin content in a concentration-dependent manner in P815 cells and showed 44.9% reduction of serotonin content at a concentration of 5.0 μM for 24 h.(Kim et al, 2002)
==General Properties==
==General Properties==

Current revision

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Tetrahydropapaveroline
Systematic (IUPAC) name
1-[(3,4-dihydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol
Identifiers
CAS number  ?
ATC code  ?
PubChem 18519
Chemical data
Formula C16H17NO4
Mol. mass 287.31048
SMILES eMolecules & PubChem
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

?

Legal status
Routes  ?

[edit] Description

A leukomaine (animal alkaloid) formed in brain and liver from dopamine and L-dopa; it may be implicated in psychiatric problems.

The inhibitory effects of tetrahydropapaveroline on serotonin biosynthesis in serotonin-producing murine mastocytoma P815 cells were investigated. Tetrahydropapaveroline decreased serotonin content in a concentration-dependent manner in P815 cells and showed 44.9% reduction of serotonin content at a concentration of 5.0 μM for 24 h.(Kim et al, 2002)

[edit] General Properties

*Molecular Weight

287.31048

*Molecular Formula

C16H17NO4

*IUPAC NAME

1-[(3,4-dihydroxyphenyl)methyl]-1,2,3,4-tetrahydroisoquinoline-6,7-diol

*Canonical Smiles

C1CNC(C2=CC(=C(C=C21)O)O)CC3=CC(=C(C=C3)O)O

*Isomeric Smiles

N/A

*XLogP

1.3

*Topological Polar Surface Area

93

[edit] External Links

Link to BIAdb Database