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  2. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    In chemistry, an enantiomer (/ɪˈnænti.əmər, ɛ-, ... A common chiral case is the point group C 1, meaning no symmetries, which is the case for lactic acid.

  3. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    By definition, molecules that are stereoisomers of each other represent the same structural isomer. ... Enantiomers, also known as ... (chemistry). For instance, by ...

  4. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    In chemistry, chirality usually refers to molecules. Two mirror images of a chiral molecule are called enantiomers or optical isomers. Pairs of enantiomers are often designated as "right-", "left-handed" or, if they have no bias, "achiral". As polarized light passes through a chiral molecule, the plane of polarization, when viewed along the ...

  5. Chirality (chemistry) - Wikipedia

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

    Two enantiomers of a generic amino acid that are chiral (S)-Alanine (left) and (R)-alanine (right) in zwitterionic form at neutral pH. In chemistry, a molecule or ion is called chiral (/ ˈ k aɪ r əl /) if it cannot be superposed on its mirror image by any combination of rotations, translations, and some conformational changes.

  6. Enantiomeric excess - Wikipedia

    en.wikipedia.org/wiki/Enantiomeric_excess

    This has led to informal use the two terms as interchangeable, especially because optical purity was the traditional way of measuring enantiomeric excess. However, other methods such as chiral column chromatography and NMR spectroscopy can now be used for measuring the amount of each enantiomer individually.

  7. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Since there is a frequent large pharmacokinetic and pharmacodynamic differences between enantiomers of a chiral drug it is not surprising that enantiomers may result in stereoselective toxicity. They can reside in the pharmacologically active enantiomer (eutomer) or in the inactive one (distomer).

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  9. 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.