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  2. Ethambutol - Wikipedia

    en.wikipedia.org/wiki/Ethambutol

    (S,S)-(+)-Ethambutol is powerful and selective antitubercular drug.It is a typical example of an old drug that was introduced for clinical use in its unichiral form. . Ethambutol contains two constitutionally symmetrical chiral centers in its structure and exists in three stereoisomeric forms, the enantiomeric pair (+)-(S,S)- and (−)-(R,R)-ethambutol, along with the achiral stereoisomer called m

  3. Chiral drugs - Wikipedia

    en.wikipedia.org/wiki/Chiral_drugs

    Ethambutol enantiomers The antitubercular agent Ethambutol contains two constitutionally symmetrical stereogenic centers in its structure and exists in three stereoisomeric forms. An enantiomeric pair (S,S)- and (R,R)-ethambutol, along with the achiral stereoisomer called meso -form, it holds a diastereomeric relationship with the optically ...

  4. Enantiopure drug - Wikipedia

    en.wikipedia.org/wiki/Enantiopure_drug

    In 1848, Louis Pasteur became the first scientist to discover chirality and enantiomers while he was working with tartaric acid. During the experiments, he noticed that there were two crystal structures produced but these structures looked to be non-superimposable mirror images of each other; this observation of isomers that were non-superimposable mirror images became known as enantiomers.

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  6. 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 ...

  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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  9. Is Tofu Actually Healthy? Nutritionists Weigh In - AOL

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    Non-organic tofu may contain the herbicide glyphosate, depending on the brand, and residual exposure could pose health risks just like other non-organic plant-based foods, Manaker says, noting it ...