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  2. Enantiopure drug - Wikipedia

    en.wikipedia.org/wiki/Enantiopure_drug

    If a mixture for a drug does not have a 1:1 ratio of its enantiomers it is a candidate for an enantiopure drug. Advances in industrial chemical processes have made it economical for pharmaceutical manufacturers to take drugs that were originally marketed as a racemic mixture and market the individual enantiomers, either by specifically ...

  3. Racemic mixture - Wikipedia

    en.wikipedia.org/wiki/Racemic_mixture

    In chemistry, a racemic mixture or racemate ... A sample with only a single enantiomer is an enantiomerically pure or enantiopure compound. [3] Etymology

  4. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    The herbicide mecoprop is a racemic mixture, with the (R)-(+)-enantiomer ("Mecoprop-P", "Duplosan KV") possessing the herbicidal activity. [25] Another example is the antidepressant drugs escitalopram and citalopram. Citalopram is a racemate [1:1 mixture of (S)-citalopram and (R)-citalopram]; escitalopram [(S)-citalopram] is a pure enantiomer ...

  5. Homochirality - Wikipedia

    en.wikipedia.org/wiki/Homochirality

    Many drugs are available as both a racemic mixture (equal amounts of both chiralities) and an enantiopure drug (only one chirality). Depending on the manufacturing process, enantiopure forms can be more expensive to produce than stereochemical mixtures. [9]: 168 Chiral preferences can also be found at a macroscopic level.

  6. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Chiral drugs that are equimolar (1:1) mixture of enantiomers are called racemic drugs and these are obviously devoid of optical rotation. The most commonly encountered stereogenic unit, [2] that confers chirality to drug molecules are stereogenic center. Stereogenic center can be due to the presence of tetrahedral tetra coordinate atoms (C,N,P ...

  7. Enantiomeric excess - Wikipedia

    en.wikipedia.org/wiki/Enantiomeric_excess

    A non-racemic mixture of two enantiomers will have a net optical rotation. It is possible to determine the specific rotation of the mixture and, with knowledge of the specific rotation of the pure enantiomer, the optical purity can be determined. [2] optical purity (%) = ⁠ [α] obs / [α] max ⁠ × 100

  8. Chiral resolution - Wikipedia

    en.wikipedia.org/wiki/Chiral_resolution

    Chiral resolution, or enantiomeric resolution, [1] is a process in stereochemistry for the separation of racemic mixture into their enantiomers. [2] It is an important tool in the production of optically active compounds, including drugs. [3] Another term with the same meaning is optical resolution.

  9. Category:Enantiopure drugs - Wikipedia

    en.wikipedia.org/wiki/Category:Enantiopure_drugs

    Pages in category "Enantiopure drugs" The following 136 pages are in this category, out of 136 total. This list may not reflect recent changes. ...