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Clinical data | |
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Trade names | Cylert, others |
Other names | Pheniminooxazolidinone; Phenylisohydantoin; Phenylpseudohydantoin; Phenilone; 2-Imino-5-phenyl-4-oxazolidinone; 2-Amino-5-phenyl-1,3-oxazol-4(5H)-one |
AHFS/Drugs.com | Micromedex Detailed Consumer Information |
Routes of administration | By mouth[1][2] |
Drug class | Stimulant; Dopamine reuptake inhibitor; Dopamine releasing agent |
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Pharmacokinetic data | |
Protein binding | ≤50%[2][1] |
Metabolism | Liver[2] |
Metabolites | Various[2] |
Elimination half-life | 7–12 hours[1][2] |
Excretion | Mainly urine[2] |
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.016.763 |
Chemical and physical data | |
Formula | C9H8N2O2 |
Molar mass | 176.175 g·mol−1 |
3D model (JSmol) | |
Chirality | Racemic mixture |
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Pemoline, formerly sold under the brand name Cylert among others, is a stimulant medication which was used in the treatment of attention deficit hyperactivity disorder (ADHD) and narcolepsy,[2]- it has since been discontinued in most countries due to rare but serious liver toxicity.[4][5] The medication was taken by mouth.[2]
Common side effects include insomnia, decreased appetite, abdominal pain, irritability, and headaches,[1][2] while rare cases of serious liver damage requiring liver transplantation or causing death have been reported.[6][7] As a stimulant, Pemoline acts as a selective dopamine reuptake inhibitor and releasing agent[1][8][2][9] via indirect agonism of dopamine receptors.[10] In addition, it shows little activity with respect to norepinephrine, thus minimal to no cardiovascular or sympathomimetic effects in comparison to many other stimulants.[1][8][2]
Pemoline was first synthesized in 1913, but its stimulant activity was not discovered until the 1930s, nor used for ADHD until 1975.[11][12][1] Between 1997 and 2005, many countries, including the United States, withdrew the drug due to liver toxicity.[13][7][14] However, it remains available in Japan for the treatment of narcolepsy at lower doses than those used for ADHD.[5] Pemoline is a schedule IV controlled substance in the United States due to structural and functional similarity to other stimulants, and potential for misuse.[15][16] but is noted to have less misuse potential than other stimulant drugs.[1]
PatrickMarkowitz1997
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