|Chemical and physical data|
|Molar mass||288.387 g/mol|
|3D model (JSmol)|
Upon systemic administration, regardless of route of administration, DHED has been found to rapidly and selectively convert into estradiol in the brain, whereas no such conversion occurs in the rest of the body. Moreover, DHED itself possesses no estrogenic activity, requiring transformation into estradiol for its estrogenicity. As such, the drug shows selective estrogenic effects in the brain (e.g., alleviation of hot flashes, neuroprotection) that are said to be identical to those of estradiol, whereas estrogenic effects elsewhere in the body are not observed.
DHED has been proposed as a possible novel estrogenic treatment for neurological and psychiatric conditions associated with hypoestrogenism (e.g., menopausal hot flashes, depression, cognitive decline, Alzheimer's disease, and stroke) that uniquely lacks potentially detrimental estrogenic side effects in the periphery.
- Merchenthaler I, Lane M, Sabnis G, Brodie A, Nguyen V, Prokai L, Prokai-Tatrai K (2016). "Treatment with an orally bioavailable prodrug of 17β-estradiol alleviates hot flushes without hormonal effects in the periphery". Sci Rep. 6: 30721. doi:10.1038/srep30721. PMC . PMID 27477453.
- Prokai L, Nguyen V, Szarka S, Garg P, Sabnis G, Bimonte-Nelson HA, McLaughlin KJ, Talboom JS, Conrad CD, Shughrue PJ, Gould TD, Brodie A, Merchenthaler I, Koulen P, Prokai-Tatrai K (2015). "The prodrug DHED selectively delivers 17β-estradiol to the brain for treating estrogen-responsive disorders". Sci Transl Med. 7 (297): 297ra113. doi:10.1126/scitranslmed.aab1290. PMC . PMID 26203081.
- Tschiffely AE, Schuh RA, Prokai-Tatrai K, Prokai L, Ottinger MA (2016). "A comparative evaluation of treatments with 17β-estradiol and its brain-selective prodrug in a double-transgenic mouse model of Alzheimer's disease". Horm Behav. 83: 39–44. doi:10.1016/j.yhbeh.2016.05.009. PMID 27210479.
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