Date published: 2026-4-24

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CYP17A1 Activators

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.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Rifampicin

13292-46-1sc-200910
sc-200910A
sc-200910B
sc-200910C
1 g
5 g
100 g
250 g
$97.00
$328.00
$676.00
$1467.00
6
(1)

Rifampicin can induce CYP17A1 expression by activating pregnane X receptor (PXR), which regulates steroid metabolism.

Dexamethasone

50-02-2sc-29059
sc-29059B
sc-29059A
100 mg
1 g
5 g
$91.00
$139.00
$374.00
36
(1)

Dexamethasone may elevate CYP17A1 levels through glucocorticoid receptor-mediated transcriptional activation.

Clotrimazole

23593-75-1sc-3583
sc-3583A
100 mg
1 g
$42.00
$57.00
6
(2)

Clotrimazole can induce CYP17A1 possibly by interacting with steroidogenic regulatory elements in the gene promoter.

Omeprazole

73590-58-6sc-202265
50 mg
$67.00
4
(1)

Omeprazole may upregulate CYP17A1 expression by activating nuclear receptors involved in P450 enzyme regulation.

Mifepristone

84371-65-3sc-203134
100 mg
$61.00
17
(1)

Mifepristone may increase CYP17A1 levels by antagonizing glucocorticoid receptors and modifying transcription.

5-Pregnen-3β-ol-20-one-16α-carbonitrile

1434-54-4sc-227010
50 mg
$69.00
3
(1)

This compound is known to induce CYP17A1 by acting as a ligand for the PXR receptor.

D,L-Sulforaphane

4478-93-7sc-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
(1)

DL-Sulforaphane can induce the expression of CYP17A1 through the activation of the Nrf2 signaling pathway.