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  2. Absolute configuration - Wikipedia

    en.wikipedia.org/wiki/Absolute_configuration

    Examples of absolute configuration of some carbohydrates and amino acids according to Fischer projection (D/L system) and Cahn–Ingold–Prelog priority rules (R/S system) The R/S system is an important nomenclature system for denoting enantiomers. This approach labels each chiral center R or S according to a system by which its substituents ...

  3. Enantiomer - Wikipedia

    en.wikipedia.org/wiki/Enantiomer

    There are three common naming conventions for specifying one of the two enantiomers (the absolute configuration) of a given chiral molecule: the R/S system is based on the geometry of the molecule; the (+)- and (−)- system (also written using the obsolete equivalents d- and l-) is based on its optical rotation properties; and the D/L system is based on the molecule's relationship to ...

  4. (R)-1-Aminoindane - Wikipedia

    en.wikipedia.org/wiki/(R)-1-Aminoindan

    R)-1-Aminoindane is a 1-aminoindane derivative. [1] It is specifically the (R)-enantiomer of 1-aminoindane, which is a racemic mixture of (R)- and (S)-enantiomers. [8] 1-Aminoindane is structurally related to 2-aminoindan. [1] A number of derivatives of 1- and 2-aminoindane are known. [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. 1-Aminoindane - Wikipedia

    en.wikipedia.org/wiki/1-aminoindane

    It is a racemic mixture of (R)- and (S)-enantiomers. [6] The (R)-enantiomer is -1-aminoindan, which has pharmacological activity and is an active metabolite of the antiparkinsonian agent rasagiline. [2] [4] [5] A number of notable 1-aminoindane derivatives exist. These include the following:

  7. Indacrinone - Wikipedia

    en.wikipedia.org/wiki/Indacrinone

    As indicated earlier, the (R)- enantiomer is the pharmacologically active diuretic. Like most other diuretics, the (R)-isomer possesses an undesirable side-effect of retaining uric acid. But the (S)-enantiomer, the distomer , has the property of assisting uric acid secretion (uricosuric effect), and, therefore, antagonizing the undesirable side ...

  8. AOL

    search.aol.com

    The search engine that helps you find exactly what you're looking for. Find the most relevant information, video, images, and answers from all across the Web.

  9. Esketamine - Wikipedia

    en.wikipedia.org/wiki/Esketamine

    Esketamine, sold under the brand names Spravato (for depression) and Ketanest (for anesthesia) among others, [10] [12] is the S(+) enantiomer of ketamine. [5] [13] It is a dissociative hallucinogen drug used as a general anesthetic and as an antidepressant for treatment of depression.