dhea

Dehydroepiandrosterone 是一种类固醇激素。它通过多种信号传导途径介导其作用，并通过转化成雄激素和雌激素衍生物（例如，雄激素，雌激素，7α和7β DHEA (Prasterone)，以及7α和7β表雄甾酮衍生物）在特异性受体上起作用。

Dehydroisoandrosterone 3-acetate (Prasterone acetate) 是一种雄性激素 雌性激素的前体物质，是一种由肾上腺皮质产生的主要 C19 类固醇，能够调节脊椎动物的攻击性行为。

16α-hydroxy Dehydroepiandrosterone (16α-OH-DHEA) 是一种存在于大脑中的神经类固醇，是胎盘雌三醇生物合成的前体。

Dehydroepiandrosterone-2,2,3,4,4,6-d6 是 Dehydroepiandrosterone 的氘代化合物。Dehydroepiandrosterone 的 CAS 号为 53-43-0。Dehydroepiandrosterone 是一种类固醇激素。它通过多种信号传导途径介导其作用，并通过转化成雄激素和雌激素衍生物（例如，雄激素，雌激素，7α和7β DHEA (Prasterone)，以及7α和7β表雄甾酮衍生物）在特异性受体上起作用。

7-keto Dehydroepiandrosterone Acetate 是一种天然化合物，可作为天然产物对照品，其 CAS 号为 1449-61-2。

7-keto Dehydroepiandrosterone 是一种天然化合物，可作为天然产物对照品，其 CAS 号为 566-19-8。

16α-Bromoepiandrosterone (BEA) 是一种与 DHEA 相关的水溶性合成甾醇，可用于研究 II 型糖尿病和非糖尿病结核感染。

Dehydroepiandrosterone sulfate (PB-005) 影响神经元的迁移、树突的分枝和新突触的形成。

17a-Hydroxypregnenolone 是一种孕烷类固醇, 是形成脱氢表雄酮的激素原。17a-Hydroxypregnenolone 是一种神经调节剂。

16α-Hydroxydehydroepiandrosterone-d5 (16α-Hydroxy-DHEA-d5) 是 16α-Hydroxydehydroepiandrosterone 的氘代形式。

16α-Hydroxyetiocholanolone is a metabolite of 16α-hydroxydehydroisoandrosterone (16α-DHEA) and androstenedione.1,2 1.Lai, E.Y., and Solomon, S.The in vivo metabolism of 16ɑ-hydroxydehydroisoandrosterone in manBiochemistry6(7)2040-2052(1967) 2.Christakoudi, S., Cowan, D.A., Christakudis, G., et al.21-hydroxylase deficiency in the neonate - trends in steroid anabolism and catabolism during the first weeks of lifeJ. Steroid Biochem. Mol. Biol.138334-347(2013)

N-Acyl ethanolamines (NAEs) have diverse biological actions that are strongly affected by the associated acyl group. Docosahexaenoyl ethanolamide (DHEA) has potential signaling roles in cancer, inflammation, and neurological development and functioning. At least some of DHEA's effects are mediated through cannabinoid (CB) receptors, while some NAEs also act as vanilloid receptor agonists and voltage-gated K+ channel blockers. (R)-(+)-Docosahexaenyl-1'-hydroxy-2'-propylamide is a homolog of DHEA, characterized by the addition of an (R)-α-methyl group at the methylene carbon adjacent to the amide nitrogen. A similar modification of arachidonoyl ethanolamide to produce R-1 methanandamide imparts higher affinity for the CB receptor as well as improved metabolic stability. The physiological actions of this compound have not been evaluated.

Efonidipine(NZ-105)盐酸盐是T 型和L 型钙离子通道双重阻断剂。

5β-Androstan-3β-ol-17-one（3β-Etiocholanolone；5β-Epiandrosterone），为5β还原型类固醇，主要是脱氢表雄酮（DHEA）的关键代谢物之一。在C57BL KsJ基因型糖尿病（db db）小鼠中，该化合物显示出显著的降糖效果，并且具有对神经元的抑制活性。

5-Androstenetriol, a steroid and active metabolite of dehydroepiandrosterone (DHEA), demonstrates significant therapeutic effects. Administered at 0.75 mg 25 g body weight, it mitigates radiation-induced mortality and facilitates hematopoietic recovery from surviving stem cells in mice. Moreover, a dosage of 40 mg kg enhances survival rates in rats subjected to surgical trauma-induced sepsis. Additionally, elevated urinary levels of 5-androstenetriol are observed in women suffering from androgenic alopecia.

17a-Hydroxypregnenolone-d3 是 17a-Hydroxypregnenolone 的氘代化合物。17a-Hydroxypregnenolone 的 CAS 号为 387-79-1。17a-Hydroxypregnenolone 是一种孕烷类固醇, 是形成脱氢表雄酮的激素原。17a-Hydroxypregnenolone 是一种神经调节剂。