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  2. 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 ...

  3. 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

  4. Enantiopure drug - Wikipedia

    en.wikipedia.org/wiki/Enantiopure_drug

    The two enantiomers have inverse effects on the rate of glucose metabolism in the frontal cortex. [ 22 ] Dihydroxy-3, 4 phenylalanine (Dopa): Dopa is a racemic mixture where one enantiomer, L-Dopa, is used as a treatment for Parkinson's Disease, and the other enantiomer, D-Dopa is considered to be toxic.

  5. Chiral analysis - Wikipedia

    en.wikipedia.org/wiki/Chiral_analysis

    The enantiomer forming the more stable complex will have less energy and stay longer in the stationary phase compared to the less stable complex with higher energy. The success of chiral separation basically depends in manipulating the subtle energy differences between the reversibly formed non-covalent transient diastereomeric complexes.

  6. Enantiomeric excess - Wikipedia

    en.wikipedia.org/wiki/Enantiomeric_excess

    in what is known as the Horeau effect [3] the relationship between mole based ee and optical rotation based ee can be non-linear i.d. in the succinic acid example the optical activity at 50% ee is lower than expected. the specific rotation of enantiopure 1-phenylethanol can be enhanced by the addition of achiral acetophenone as an impurity. [4]

  7. Racemization - Wikipedia

    en.wikipedia.org/wiki/Racemization

    Of note, the L form of amino acids and the D form of sugars (primarily glucose) are usually the biologically reactive form. This is due to the fact that many biological molecules are chiral and thus the reactions between specific enantiomers produce pure stereoisomers. [5] Also notable is the fact that all amino acid residues exist in the L form.

  8. Management of tuberculosis - Wikipedia

    en.wikipedia.org/wiki/Management_of_tuberculosis

    Management of tuberculosis refers to techniques and procedures utilized for treating tuberculosis (TB), or simply a treatment plan for TB.. The medical standard for active TB is a short course treatment involving a combination of isoniazid, rifampicin (also known as Rifampin), pyrazinamide, and ethambutol for the first two months.

  9. File:Negative enantiomer of ethambutol.png - Wikipedia

    en.wikipedia.org/wiki/File:Negative_enantiomer...

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