CYP17A1 activators belong to a class of chemical compounds that target and modulate the activity of the enzyme cytochrome P450 17A1, also known as CYP17A1. This enzyme plays a crucial role in the biosynthesis of steroids within the human body, specifically in the pathways responsible for the production of androgens and glucocorticoids. CYP17A1 catalyzes two distinct reactions: the conversion of pregnenolone and progesterone into their respective 17-hydroxy derivatives, which are intermediates in the androgen biosynthesis pathway, and the subsequent conversion of these intermediates into dehydroepiandrosterone (DHEA) and cortisol, which are important in the glucocorticoid biosynthesis pathway. CYP17A1 activators are compounds that enhance the enzyme's activity, primarily in the context of androgen biosynthesis.
The activation of CYP17A1 can have significant physiological implications, particularly in conditions where androgen production needs to be regulated. By modulating CYP17A1 activity, these activators can impact the balance of androgenic hormones in the body, leading to increased levels of androgens such as testosterone. This, in turn, can have a range of effects on various bodily functions, including sexual development, muscle growth, and overall hormonal balance. Understanding the mechanisms by which CYP17A1 activators operate and their effects on androgen levels is of interest in various fields, such as endocrinology and reproductive medicine, as it can shed light on hormonal imbalances and contribute to our understanding of conditions related to androgen excess or deficiency. Additionally, research into CYP17A1 activators may have broader implications for the development of novel compounds in the future.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Rifampicin | 13292-46-1 | sc-200910 sc-200910A sc-200910B sc-200910C | 1 g 5 g 100 g 250 g | $97.00 $328.00 $676.00 $1467.00 | 6 | |
Rifampicin can induce CYP17A1 expression by activating pregnane X receptor (PXR), which regulates steroid metabolism. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $91.00 $139.00 $374.00 | 36 | |
Dexamethasone may elevate CYP17A1 levels through glucocorticoid receptor-mediated transcriptional activation. | ||||||
Clotrimazole | 23593-75-1 | sc-3583 sc-3583A | 100 mg 1 g | $42.00 $57.00 | 6 | |
Clotrimazole can induce CYP17A1 possibly by interacting with steroidogenic regulatory elements in the gene promoter. | ||||||
Omeprazole | 73590-58-6 | sc-202265 | 50 mg | $67.00 | 4 | |
Omeprazole may upregulate CYP17A1 expression by activating nuclear receptors involved in P450 enzyme regulation. | ||||||
Mifepristone | 84371-65-3 | sc-203134 | 100 mg | $61.00 | 17 | |
Mifepristone may increase CYP17A1 levels by antagonizing glucocorticoid receptors and modifying transcription. | ||||||
5-Pregnen-3β-ol-20-one-16α-carbonitrile | 1434-54-4 | sc-227010 | 50 mg | $69.00 | 3 | |
This compound is known to induce CYP17A1 by acting as a ligand for the PXR receptor. | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-207495A sc-207495B sc-207495C sc-207495 sc-207495E sc-207495D | 5 mg 10 mg 25 mg 1 g 10 g 250 mg | $153.00 $292.00 $489.00 $1325.00 $8465.00 $933.00 | 22 | |
DL-Sulforaphane can induce the expression of CYP17A1 through the activation of the Nrf2 signaling pathway. | ||||||