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dextroamphetamine

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dextroamphetamine
INN: Dexamfetamine
Clinical data
Pronunciation/ˌdɛkstræmˈfɛtəmn/
Trade namesDexedrine, others
Other namesd-Amphetamine, (S)-Amphetamine, S(+)-Amphetamine
AHFS/Drugs.comMonograph
MedlinePlusa605027
License data
Pregnancy
category
  • AU: B3
Dependence
liability
Physical: None
Psychological: Moderate
Addiction
liability
Moderate – high
Routes of
administration
By mouth, transdermal, intravenous, insufflation, rectal
Drug classStimulant
ATC code
Legal status
Legal status
Pharmacokinetic data
BioavailabilityOral: ~90%
Protein binding15–40%
MetabolismCYP2D6, DBH, FMO3
Onset of actionIR dosing: 0.5–1.5 hours
XR dosing: 1.5–2 hours
Elimination half-life9–11 hours
pH-dependent: 7–34 hours
Duration of actionIR dosing: 3–6 hours
XR dosing: 8–12 hours
ExcretionKidney (45%); urinary pH-dependent
Identifiers
  • (2S)-1-Phenylpropan-2-amine
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC9H13N
Molar mass135.21 g·mol−1
3D model (JSmol)
ChiralityDextrorotatory enantiomer
Density0.913 g/cm3
Boiling point201.5 °C (394.7 °F)
Solubility in water20mg per ml
  • C[C@@H](Cc1ccccc1)N
  • InChI=InChI=1S/C9H13N/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7,10H2,1H3/t8-/m0/s1 ☒N
  • Key:KWTSXDURSIMDCE-QMMMGPOBSA-N checkY
 ☒NcheckY (what is this?)  (verify)


Főnév

dextroamphetamine (tsz. dextroamphetamines)

  1. (gyógyszertan) dextroamfetamin