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  2. Enantiopure drug - Wikipedia

    en.wikipedia.org/wiki/Enantiopure_drug

    The desired enantiomer is known as an eutomer while the undesired enantiomer is known as the distomer. [2] When equal amounts of both enantiomers are found in a mixture, the mixture is known as a racemic mixture. If a mixture for a drug does not have a 1:1 ratio of its enantiomers it is a candidate for an enantiopure drug.

  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. Chirality - Wikipedia

    en.wikipedia.org/wiki/Chirality

    Chirality is also seen in the study of facial asymmetry and is known as aurofacial asymmetry. [35] Schema of the development of the axial twist in vertebrates. According to the Axial Twist theory, vertebrate animals develop into a left-handed chirality. Due to this, the brain is turned around and the heart and bowels are turned by 90°. [36]

  5. Chiral inversion - Wikipedia

    en.wikipedia.org/wiki/Chiral_inversion

    Chiral inversion is the process of conversion of one enantiomer of a chiral molecule to its mirror-image version with no other change in the molecule. [1] [2] [3] [4]Chiral inversion happens depending on various factors (viz. biological-, solvent-, light-, temperature- induced, etc.) and the energy barrier energy barrier associated with the stereogenic element present in the chiral molecule. 2 ...

  6. Stereoisomerism - Wikipedia

    en.wikipedia.org/wiki/Stereoisomerism

    Pure enantiomers also exhibit the phenomenon of optical activity and can be separated only with the use of a chiral agent. In nature, only one enantiomer of most chiral biological compounds, such as amino acids (except glycine, which is achiral), is present. Enantiomers differ by the direction they rotate polarized light: the amount of a chiral ...

  7. List of human cell types - Wikipedia

    en.wikipedia.org/wiki/List_of_human_cell_types

    The Human Cell Atlas project, which started in 2016, had as one of its goals to "catalog all cell types (for example, immune cells or brain cells) and sub-types in the human body". [13] By 2018, the Human Cell Atlas description based the project on the assumption that "our characterization of the hundreds of types and subtypes of cells in the ...

  8. Eudysmic ratio - Wikipedia

    en.wikipedia.org/wiki/Eudysmic_ratio

    A racemic mixture is an equal mixture of both enantiomers, which may be easier to manufacture than a single enantiomeric form. Indacrinone Enantiomers. It is often the case that only a single one of the enantiomers contains all of the wanted bioactivity, the distomer is often less active, has no desired activity or may even be toxic. [6]

  9. Amphetamine - Wikipedia

    en.wikipedia.org/wiki/Amphetamine

    The half-lives of amphetamine enantiomers differ and vary with urine pH. [3] At normal urine pH, the half-lives of dextroamphetamine and levoamphetamine are 9–11 hours and 11–14 hours, respectively. [3] Highly acidic urine will reduce the enantiomer half-lives to 7 hours; [17] highly alkaline urine will increase the half-lives up to 34 ...