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  2. Dihydrotestosterone - Wikipedia

    en.wikipedia.org/wiki/Dihydrotestosterone

    Dihydrotestosterone (DHT, 5α-dihydrotestosterone, 5α-DHT, androstanolone or stanolone) is an endogenous androgen sex steroid and hormone primarily involved in the growth and repair of the prostate and the penis, as well as the production of sebum and body hair composition.

  3. 5β-Dihydrotestosterone - Wikipedia

    en.wikipedia.org/wiki/5β-Dihydrotestosterone

    5β-Dihydrotestosterone (5β-DHT), also known as 5β-androstan-17β-ol-3-one or as etiocholan-17β-ol-3-one, is an etiocholane (5β-androstane) steroid as well as an inactive metabolite of testosterone formed by 5β-reductase in the liver and bone marrow [1] [2] and an intermediate in the formation of 3α,5β-androstanediol and 3β,5β-androstanediol (by 3α-and 3β-hydroxysteroid ...

  4. 5,6-Dihydroxytryptamine - Wikipedia

    en.wikipedia.org/wiki/5,6-dihydroxytryptamine

    5,6-Dihydroxytryptamine (5,6-DHT) is a monoaminergic neurotoxin and tryptamine derivative related to serotonin (5-hydroxytryptamine) and 5,7-dihydroxytryptamine (5,7-DHT). [ 1 ] [ 2 ] [ 3 ] It is a relatively selective serotonergic neurotoxin , but also acts as a dopaminergic and noradrenergic neurotoxin at higher doses.

  5. Androsterone - Wikipedia

    en.wikipedia.org/wiki/Androsterone

    Androsterone is a metabolite of testosterone and dihydrotestosterone (DHT). In addition, it can be converted back into DHT via 3α-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase , bypassing conventional intermediates such as androstanedione and testosterone, and as such, can be considered to be a metabolic intermediate in ...

  6. 5α-Reductase inhibitor - Wikipedia

    en.wikipedia.org/wiki/5α-reductase_inhibitor

    In vitro and animal models suggest subsequent 3α-reduction of DHT, 5α-DHP and DHDOC lead to neurosteroid metabolites with effect on cerebral function. These neurosteroids , which include allopregnanolone , tetrahydrodeoxycorticosterone (THDOC), and 3α-androstanediol , act as potent positive allosteric modulators of GABA A receptors , and ...

  7. Discovery and development of 5α-reductase inhibitors - Wikipedia

    en.wikipedia.org/wiki/Discovery_and_development...

    Dutasteride, however, is a so-called dual inhibitor with both 5α-R1 and 5α-R2 inhibition. IC50 for 5α-R1 is 7 nM but 6 nM for 5α-R2. As mentioned above, it reduces DHT > 90% overall, or precisely 94.7% and for intraprostatic DHT the reduction is 97-99%. Dutasteride has also been found to inhibit 5α-R3, in vitro, with IC50=0.33 nM. [6]

  8. List of human hormones - Wikipedia

    en.wikipedia.org/wiki/List_of_human_hormones

    5-DHT or DHT is a male reproductive hormone that targets the prostate gland, bulbourethral gland, seminal vesicles, penis and scrotum and promotes growth/mitosis/cell maturation and differentiation. Testosterone is converted to 5-DHT by 5alpha-reductase, usually with in the target tissues of 5-DHT because of the need for high concentrations of ...

  9. Androstanedione - Wikipedia

    en.wikipedia.org/wiki/Androstanedione

    Androstanedione, also known as 5α-androstanedione or as 5α-androstane-3,17-dione, is a naturally occurring androstane (5α-androstane) steroid and an endogenous metabolite of androgens like testosterone, dihydrotestosterone (DHT), dehydroepiandrosterone (DHEA), and androstenedione. [1] It is the C5 epimer of etiocholanedione (5β ...