Date published: 2025-12-11

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DHRS2 Inhibitors

DHRS2 inhibitors belong to a specific class of chemical compounds that have garnered interest in the field of biochemistry and cellular metabolism. DHRS2, also known as dehydrogenase/reductase SDR family member 2, is a member of the short-chain dehydrogenase/reductase (SDR) superfamily of enzymes. Enzymes in this superfamily are involved in a wide range of cellular processes, including the metabolism of steroids, lipids, and other small molecules. DHRS2, in particular, plays a role in the reduction of various substrates, including retinoids, steroids, and xenobiotics, through its NADPH-dependent dehydrogenase activity. DHRS2 inhibitors are chemical compounds designed to interact with DHRS2, potentially modulating its enzymatic activity and affecting the metabolism of its substrates.

The mechanism of action of DHRS2 inhibitors typically involves their binding to specific sites or domains within the DHRS2 enzyme. This interaction can lead to changes in DHRS2's ability to catalyze the reduction of its substrates, potentially influencing the cellular levels of biologically active molecules and metabolic pathways in which DHRS2 is involved. Consequently, DHRS2 inhibitors may have implications for understanding the regulation of cellular metabolism, the detoxification of xenobiotics, and the synthesis of biologically active compounds in various tissues and cellular contexts. They provide valuable tools for investigating the roles of DHRS2 in cellular physiology and its impact on metabolic processes that are essential for maintaining normal cellular functions and overall organismal health. The study of DHRS2 inhibitors contributes to advancing our understanding of enzymatic reactions and metabolic pathways, shedding light on the complex molecular mechanisms that govern cellular metabolism and the regulation of small molecule substrates.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Retinoic Acid, all trans

302-79-4sc-200898
sc-200898A
sc-200898B
sc-200898C
500 mg
5 g
10 g
100 g
$65.00
$319.00
$575.00
$998.00
28
(1)

High levels of retinoic acid can trigger feedback inhibition mechanisms that may downregulate DHRS2 expression as a means to balance retinoid metabolism.

13-cis-Retinoic acid

4759-48-2sc-205568
sc-205568A
100 mg
250 mg
$74.00
$118.00
8
(1)

A retinoic acid analog that can disrupt normal retinoid signaling and potentially downregulate DHRS2 through negative feedback loops.

Citral

5392-40-5sc-252620
1 kg
$212.00
(1)

Known to modulate retinoid pathways, could potentially decrease DHRS2 expression by altering retinoid signaling.

Bisphenol A

80-05-7sc-391751
sc-391751A
100 mg
10 g
$300.00
$490.00
5
(0)

An endocrine disruptor that could interfere with steroid metabolism, potentially affecting the expression of DHRS2.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$149.00
$470.00
$620.00
$1199.00
$2090.00
33
(3)

An HDAC inhibitor that can alter gene expression, potentially leading to decreased DHRS2 expression through epigenetic changes.

Ketoconazole

65277-42-1sc-200496
sc-200496A
50 mg
500 mg
$62.00
$260.00
21
(1)

An antifungal agent that inhibits steroid synthesis enzymes, which could indirectly affect DHRS2 expression.

Methotrexate

59-05-2sc-3507
sc-3507A
100 mg
500 mg
$92.00
$209.00
33
(5)

An antimetabolite that can impact cell growth and proliferation, potentially downregulating DHRS2 expression.

4-Hydroxyphenylretinamide

65646-68-6sc-200900
sc-200900A
5 mg
25 mg
$104.00
$315.00
(0)

A synthetic retinoid that can affect retinoid signaling and potentially decrease DHRS2 expression.

Dexamethasone

50-02-2sc-29059
sc-29059B
sc-29059A
100 mg
1 g
5 g
$76.00
$82.00
$367.00
36
(1)

A synthetic corticosteroid that may influence retinoid metabolism and the expression of enzymes like DHRS2.

Aminoglutethimide

125-84-8sc-207280
sc-207280A
sc-207280B
sc-207280C
1 g
5 g
25 g
100 g
$41.00
$143.00
$530.00
$2020.00
2
(1)

Blocks steroid synthesis and could indirectly reduce DHRS2 expression by altering retinoid metabolism.