Weight | 135.21 g/mol |
---|---|
Formula | C9H13N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
Levamfetamine (156-34-3, 41820-21-7)
Amphetamine · Amphetamine Sulfate · Levoamphetamine
Score:
#793 in Neuroscience
,
#3480 in Biology
,
#4354 in Chemistry
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- Enduring Changes in Brain and Behavior Produced by Chronic Amphetamine Administration: A Review and Evaluation of Animal Models of Amphetamine Psychosis (Brain Research Reviews, 1986)
- Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter (Nature, 1996)
- Amphetamine and apomorphine responses in the rat following 6-OHDA lesions of the nucleus accumbens septi and corpus striatum (Brain Research, 1975)
- DOPAMINERGIC NEURONS: EFFECT OF ANTIPSYCHOTIC DRUGS AND AMPHETAMINE ON SINGLE CELL ACTIVITY (Journal of Pharmacology and Experimental Therapeutics, 1973)
- Factors that predict individual vulnerability to amphetamine self-administration (Science, 1989)
- A circuitry model of the expression of behavioral sensitization to amphetamine-like psychostimulants (Brain Research Reviews, 1997)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Amphetamine
- Amphetamine Sulfate
- Levoamphetamine
- Phenamine
- Phenopromin
- Fenamine
- Centramina
- Amphetamine Sulfate (2:1)
- Desoxynorephedrin
- levo-Amphetamine
- l-Amphetamine
- l Amphetamine
- Mydrial
- levo Amphetamine
- Thyramine
- Amfetamine
-
SMILESCC(CC1=CC=CC=C1)N
-
InChIKeyKWTSXDURSIMDCE-UHFFFAOYSA-N
- Pubchem - Levamfetamine
- Wikipedia - R(-)amphetamine
Levoamphetamine is a central nervous system (CNS) stimulant known to increase wakefulness and concentration in association with decreased appetite and fatigue. Pharmaceuticals that contain levoamphetamine are currently indicated and prescribed for the treatment of attention deficit hyperactivity disorder (ADHD), obesity, and narcolepsy in some countries. Levoamphetamine is the levorotatory stereoisomer of the amphetamine molecule.
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