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  2. Levoamphetamine - Wikipedia

    en.wikipedia.org/wiki/Levoamphetamine

    [12] [note 2] [45] With very large doses, ranging from 270 to 640 mg, the potency ratios of dextroamphetamine and levoamphetamine in stimulating locomotor activity and inducing amphetamine psychosis in humans have ranged from 1:1 to 2:1 in a couple studies. [12] The differences in potency and dopamine versus norepinephrine release between ...

  3. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    This is the origin of the D/L and R/S notations, and the employment of prefixes levo-and dextro-in common names. The prefix ar-, from the Latin recto (right), is applied to the right-handed version; es-, from the Latin sinister (left), to the left-handed molecule. Example: ketamine, arketamine, esketamine. [13]

  4. Racemic mixture - Wikipedia

    en.wikipedia.org/wiki/Racemic_mixture

    A single Adderall dose combines the neutral sulfate salts of dextroamphetamine and amphetamine, with the dextro isomer of amphetamine saccharate and D/L-amphetamine aspartate monohydrate. The original Benzedrine was a racemic mixture, and isolated dextroamphetamine was later introduced to the market as Dexedrine.

  5. Dextroamphetamine - Wikipedia

    en.wikipedia.org/wiki/Dextroamphetamine

    A 2018 systematic review and network meta-analysis of 50 trials involving 12 different psychosocial interventions for amphetamine, methamphetamine, or cocaine addiction found that combination therapy with both contingency management and community reinforcement approach had the highest efficacy (i.e., abstinence rate) and acceptability (i.e ...

  6. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Louis Pasteur - pioneering stereochemist. Chirality can be traced back to 1812, when physicist Jean-Baptiste Biot found out about a phenomenon called "optical activity." [10] Louis Pasteur, a famous student of Biot's, made a series of observations that led him to suggest that the optical activity of some substances is caused by their molecular asymmetry, which makes nonsuperimposable mirror ...

  7. D-DOPA - Wikipedia

    en.wikipedia.org/wiki/D-DOPA

    Levo- and dextro- rotation refer to a molecule's ability to rotate planes of polarized light in one or the other direction. Whereas L -DOPA is moderately effective in the treatment of Parkinson's disease (PD) and dopamine-responsive dystonia (DRD) by stimulating the production of dopamine in the brain, D -DOPA is biologically inactive.

  8. Adderall - Wikipedia

    en.wikipedia.org/wiki/Adderall

    Adderall and Mydayis [11] are trade names [note 2] for a combination drug containing four salts of amphetamine.The mixture is composed of equal parts racemic amphetamine and dextroamphetamine, which produces a (3:1) ratio between dextroamphetamine and levoamphetamine, the two enantiomers of amphetamine. [13]

  9. Chirality (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Chirality_(chemistry)

    dextro- and levo-rotation (the clockwise and counterclockwise optical rotation of plane-polarized light) uses similar notation, but shouldn't be confused. Chiral ligands confer chirality to a metal complex, as illustrated by metal- amino acid complexes.

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