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  2. Woman Shares Simple DIY Treat Recipe for Dogs With ... - AOL

    www.aol.com/woman-shares-simple-diy-treat...

    This dog mom shared a quick and easy recipe that requires no cooking. You simply blend up the ingredients in a blender, pour them into treat molds, then freeze them. At the end she gives one to ...

  3. Enantiopure drug - Wikipedia

    en.wikipedia.org/wiki/Enantiopure_drug

    An enantiopure drug is a pharmaceutical that is available in one specific enantiomeric form. Most biological molecules (proteins, sugars, etc.) are present in only one of many chiral forms, so different enantiomers of a chiral drug molecule bind differently (or not at all) to target receptors. Chirality can be observed when the geometric ...

  4. Kinetic resolution - Wikipedia

    en.wikipedia.org/wiki/Kinetic_resolution

    In organic chemistry, kinetic resolution is a means of differentiating two enantiomers in a racemic mixture.In kinetic resolution, two enantiomers react with different reaction rates in a chemical reaction with a chiral catalyst or reagent, resulting in an enantioenriched sample of the less reactive enantiomer. [1]

  5. Racemic mixture - Wikipedia

    en.wikipedia.org/wiki/Racemic_mixture

    In chemistry, a racemic mixture or racemate (/ r eɪ ˈ s iː m eɪ t, r ə-, ˈ r æ s ɪ m eɪ t / [1]) is one that has equal amounts of left- and right-handed enantiomers of a chiral molecule or salt. Racemic mixtures are rare in nature, but many compounds are produced industrially as racemates.

  6. 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.

  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

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