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  2. Equianalgesic - Wikipedia

    en.wikipedia.org/wiki/Equianalgesic

    An equianalgesic chart can be a useful tool, but the user must take care to correct for all relevant variables such as route of administration, cross tolerance, half-life and the bioavailability of a drug. [5] For example, the narcotic levorphanol is 4–8 times stronger than morphine, but also has a much longer half-life. Simply switching the ...

  3. 11β-Hydroxysteroid dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/11β-Hydroxysteroid...

    11β-Hydroxysteroid dehydrogenase (HSD-11β or 11β-HSD) enzymes catalyze the conversion of inert 11 keto-products to active cortisol, or vice versa, [1] thus regulating the access of glucocorticoids to the steroid receptors. The human genome encodes two distinct HSD-11β isozymes (HSD-11β Type 1 and HSD-11β Type 2) on distinct genes.

  4. Cortisone - Wikipedia

    en.wikipedia.org/wiki/Cortisone

    Cortisone is a pregnene (21-carbon) steroid hormone. It is a naturally-occurring corticosteroid metabolite that is also used as a pharmaceutical prodrug . Cortisol is converted by the action of the enzyme corticosteroid 11-beta-dehydrogenase isozyme 2 into the inactive metabolite cortisone, particularly in the kidneys.

  5. Topical hydrocortisone - Wikipedia

    en.wikipedia.org/wiki/Topical_hydrocortisone

    The strength of topical hydrocortisone products ranges from 0.1% to 2.5%, which means there could be 1 mg to 25 mg hydrocortisone in 1g of the products. [12] Some formulations for topical hydrocortisone include hydrocortisone 0.5% cream or ointment, hydrocortisone 1% cream or ointment, and hydrocortisone 2.5% cream or ointment. [34]

  6. Corticosteroid - Wikipedia

    en.wikipedia.org/wiki/Corticosteroid

    Corticosteroids are a class of steroid hormones that are produced in the adrenal cortex of vertebrates, as well as the synthetic analogues of these hormones.Two main classes of corticosteroids, glucocorticoids and mineralocorticoids, are involved in a wide range of physiological processes, including stress response, immune response, and regulation of inflammation, carbohydrate metabolism ...

  7. 11-Deoxycortisol - Wikipedia

    en.wikipedia.org/wiki/11-Deoxycortisol

    11-Deoxycortisol in mammals has limited glucocorticoid activity, but it is the direct precursor of the major mammalian glucocorticoid, cortisol. [15] As a result, the level of 11-deoxycortisol is measured to diagnose impaired cortisol synthesis, to find out the enzyme deficiency that causes impairment along the pathway to cortisol, and to differentiate adrenal disorders.

  8. Hydroxycorticosteroids - Wikipedia

    en.wikipedia.org/wiki/Hydroxycorticosteroids

    Steroid skeleton. Carbons 18 and above can be absent. Hydroxycorticosteroids (OHCSs) are corticosteroids that have an additional hydroxy (-OH) group. There are two main positions where the hydroxy group may be added: at carbon atom 11, and at carbon atom 17.

  9. List of corticosteroid esters - Wikipedia

    en.wikipedia.org/wiki/List_of_corticosteroid_esters

    Hydrocortisone buteprate (hydrocortisone 17α-butyrate 21-propionate) Hydrocortisone butyrate (hydrocortisone 17α-butyrate) Hydrocortisone 21-butyrate; Hydrocortisone cypionate (hydrocortisone cyclopentanepropionate) Hydrocortisone phosphate; Hydrocortisone succinate (hydrocortisone hemisuccinate) Hydrocortisone tebutate; Hydrocortisone valerate