| Weight | 176.175 g/mol |
|---|---|
| Formula | C9H8N2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
pemoline (2152-34-3)
Cylert · Lilly Brand of Pemoline · PemADD
Score:
#72 in Neurology
,
#357 in Neuroscience
,
#1620 in Biology
,
#1908 in Chemistry
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- Sigma-Aldrich - pemoline83.00 - 322.50 USD
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- Fatigue therapy in multiple sclerosis Results of a doubleblind, randomized, parallel trial of amantadine, pemoline, and placebo (Neurology, 1995)
- Relative Efficacy of Long-Acting Stimulants on Children With Attention Deficit-Hyperactivity Disorder: A Comparison of Standard Methylphenidate, Sustained-Release Methylphenidate, Sustained-Release Dextroamphetamine, and Pemoline (Pediatrics, 1990)
- A doubleblind, randomized, crossover trial of pemoline in fatigue associated with multiple sclerosis (Neurology, 1992)
- PHARMACOLOGY OF METHYLPHENIDATE, AMPHETAMINE ENANTIOMERS AND PEMOLINE IN ATTENTION-DEFICIT HYPERACTIVITY DISORDER (Human Psychopharmacology-clinical and Experimental, 1997)
- The Effects of Amantadine and Pemoline on Cognitive Functioning in Multiple Sclerosis (JAMA Neurology, 1996)
- Magnesium Pemoline: Enhancement of Learning and Memory of a Conditioned Avoidance Response (Science, 1966)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Cylert
- Lilly Brand of Pemoline
- PemADD
- Phenoxazole
- Abbott Brand of Pemoline
- Tradon
- Pemoline Compounds
- Pemoline Magnesium
- Mallinckrodt Brand of Pemoline
- Phenylisohydantoin
-
SMILESC1=CC=C(C=C1)C2C(=O)N=C(O2)N
-
InChIKeyNRNCYVBFPDDJNE-UHFFFAOYSA-N
- Pubchem - pemoline
- Wikipedia - pemoline
Pemoline is a stimulant drug of the 4-oxazolidinone class. It was first synthesized in 1913 but its activity was not discovered until the 1930s. Under the names Betanamin, Cylert, Tradon, and Ceractiv it was used as a medication to treat attention-deficit hyperactivity disorder (ADHD) and narcolepsy.
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Reactant
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pemoline
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