Weight | 337.463 g/mol |
---|---|
Formula | C22H27NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 8 |
Amineptine (57574-09-1)
amineptin hydrochloride · S 1694 · amineptin sodium salt
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- Amisulpride versus Amineptine and Placebo for the Treatment of Dysthymia (Neuropsychobiology, 1999)
- Biochemical and pharmacological studies on amineptine (S 1694) and (+)amphetamine in the rat (Journal of Pharmacy and Pharmacology, 1977)
- Changes in [3H]5-HT uptake and [3H]imipramine binding in platelets after chlorimipramine in healthy volunteers: Comparison with maprotiline and amineptine (Biological Psychiatry, 1987)
- Dopamine agonist amineptine prevents the antidepressant effect of sleep deprivation (Psychiatry Research-neuroimaging, 1996)
- Amineptine, a tricyclic antidepressant, inhibits the mitochondrial oxidation of fatty acids and produces microvesicular steatosis of the liver in mice. (Journal of Pharmacology and Experimental Therapeutics, 1988)
- Genetic predisposition to drug hepatotoxicity: Role in hepatitis caused by amineptine, a tricyclic antidepressant (Hepatology, 1989)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - amineptin hydrochloride
- S 1694
- amineptin sodium salt
- 10,11-dihydrodibenzo(a,d)cyclohept-5-enyl-7-aminoheptanoic acid
- amineptin
- Survector
-
SMILESC1CC2=CC=CC=C2C(C3=CC=CC=C31)NCCCCCCC(=O)O
-
InChIKeyONNOFKFOZAJDHT-UHFFFAOYSA-N
- Pubchem - Amineptine
- Wikipedia - amineptine hydrochloride
Amineptine, sold under the brand name Survector among others, is an atypical antidepressant of the tricyclic antidepressant (TCA) family. It acts as a selective and mixed dopamine reuptake inhibitor and releasing agent, and to a lesser extent as a norepinephrine reuptake inhibitor. Amineptine was developed by the French Society of Medical research in the 1960s.
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