| Weight | 287.315 g/mol |
|---|---|
| Formula | C16H17NO4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Tetrahydropapaveroline (10139-29-4, 4747-99-3)
Score:
#7 in Multidisciplinary scientific
,
#1067 in Neuroscience
,
#2323 in Biochemistry
,
#4624 in Biology
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- Alcohol drinking: abnormal intake caused by tetrahydropapaveroline in brain (Science, 1977)
- Tetrahydropapaveroline: formation in vivo and in vitro in rat brain. (Life Sciences, 1974)
- Preference for alcohol evoked by tetrahydropapaveroline (THP) chronically infused in the cerebral ventricle of the rat (Pharmacology, Biochemistry and Behavior, 1977)
- Naloxone alters alcohol drinking induced in the rat by tetrahydropapaveroline (THP) infused ICV. (Pharmacology, Biochemistry and Behavior, 1982)
- Buspirone alters alcohol drinking induced in rats by tetrahydropapaveroline injected into brain monoaminergic pathways (Alcohol, 1988)
- TETRAHYDROPAPAVEROLINE: AN ALKALOID METABOLITE OF DOPAMINE IN VITRO (Journal of Pharmacology and Experimental Therapeutics, 1970)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNC(C2=CC(=C(C=C21)O)O)CC3=CC(=C(C=C3)O)O
-
InChIKeyABXZOXDTHTTZJW-UHFFFAOYSA-N
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Synthesis
dopamine
+
Reactant
(Alkylation of primary amines)
Pyrocatechol
+
Reactant
(Friedel-Crafts alkylation)
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