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  2. Steroid - Wikipedia

    en.wikipedia.org/wiki/Steroid

    Steroid isolation, depending on context, is the isolation of chemical matter required for chemical structure elucidation, derivitzation or degradation chemistry, biological testing, and other research needs (generally milligrams to grams, but often more [86] or the isolation of "analytical quantities" of the substance of interest (where the ...

  3. Corticosteroid - Wikipedia

    en.wikipedia.org/wiki/Corticosteroid

    In general, corticosteroids are grouped into four classes, based on chemical structure. Allergic reactions to one member of a class typically indicate an intolerance of all members of the class. This is known as the "Coopman classification". [43] [44] The highlighted steroids are often used in the screening of allergies to topical steroids. [45]

  4. Corticosterone - Wikipedia

    en.wikipedia.org/wiki/Corticosterone

    Corticosterone, also known as 17-deoxycortisol and 11β,21-dihydroxyprogesterone, [1] is a 21-carbon steroid hormone of the corticosteroid type produced in the cortex of the adrenal glands. In the very rare case of congenital adrenal hyperplasia due to 17α-hydroxylase deficiency cortisol production is blocked. [2]

  5. Glucocorticoid - Wikipedia

    en.wikipedia.org/wiki/Glucocorticoid

    The name "glucocorticoid" is a portmanteau (glucose + cortex + steroid) and is composed from its role in regulation of glucose metabolism, synthesis in the adrenal cortex, and its steroidal structure (see structure below).

  6. Anabolic steroid - Wikipedia

    en.wikipedia.org/wiki/Anabolic_steroid

    Structural aspects of androgens and anabolic steroids; Classes Androgen Structure Chemical name Features Testosterone 4-Hydroxytestosterone a: 4-Hydroxytestosterone – Androstenediol a: 5-Androstenediol (androst-5-ene-3β,17β-diol) Prohormone Androstenedione a: 4-Androstenedione (androst-4-ene-3,17-dione) Prohormone Boldenone: 1 ...

  7. Steroid hormone - Wikipedia

    en.wikipedia.org/wiki/Steroid_hormone

    A variety of synthetic steroids and sterols have also been contrived. Most are steroids, but some nonsteroidal molecules can interact with the steroid receptors because of a similarity of shape. Some synthetic steroids are weaker or stronger than the natural steroids whose receptors they activate. [8] Some examples of synthetic steroid hormones:

  8. Gonane - Wikipedia

    en.wikipedia.org/wiki/Gonane

    Gonane is a significant chemical compound in the family of steroids because its structure comprises four hydrocarbon rings fused together, consisting of three cyclohexane units and one cyclopentane, which is often referred to as the "steroid nucleus" and serves as the parent compound for steroids.

  9. Sterol - Wikipedia

    en.wikipedia.org/wiki/Sterol

    [2] [3] The most familiar type of animal sterol is cholesterol, which is vital to the structure of the cell membrane, and functions as a precursor to fat-soluble vitamins and steroid hormones. While technically alcohols, sterols are classified by biochemists as lipids (fats in the broader sense of the term).