Date published: 2026-5-7

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CYP7B1 Inhibitors

CYP7B1 inhibitors belong to a specific chemical class of compounds that target and inhibit the activity of the cytochrome P450 enzyme CYP7B1. Cytochrome P450 enzymes are a superfamily of heme-containing proteins involved in the metabolism of various endogenous and exogenous compounds in the body. CYP7B1, in particular, plays a crucial role in the metabolism of steroid hormones, including bile acids and neuroactive steroids. By inhibiting this enzyme, CYP7B1 inhibitors can modulate the production and breakdown of these steroids, potentially leading to alterations in their physiological effects. Structurally, CYP7B1 inhibitors can be diverse, often possessing complex molecular frameworks. Researchers have identified several synthetic and naturally occurring compounds with inhibitory effects on CYP7B1. These inhibitors are typically characterized by functional groups and chemical moieties that allow them to interact with the active site of the CYP7B1 enzyme, impeding its catalytic activity. The mechanism of action of CYP7B1 inhibitors involves competitive or non-competitive inhibition. Competitive inhibitors compete with the substrate for the active site of the enzyme, while non-competitive inhibitors bind to a distinct site, leading to conformational changes that decrease the enzyme's catalytic efficiency.The discovery and development of CYP7B1 inhibitors have been driven by the aim to gain a deeper understanding of steroid metabolism and its impact on various physiological processes. By selectively inhibiting CYP7B1, researchers can explore the role of specific steroid metabolites in different tissues and systems. These inhibitors have been invaluable tools in basic research to uncover the complex interplay of steroid hormones in health and disease.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Cbz-Glycine hydrazide

5680-83-1sc-353130
sc-353130A
1 g
5 g
$116.00
$399.00
(0)

Carbamazepine (CBZ) is an antiepileptic agent that also inhibits CYP7B1 as a metabolic pathway. Similar to 4-MA, its primary use is not as a CYP7B1 inhibitor, but it has been studied for research purposes.

Lithocholic acid

434-13-9sc-215262
sc-215262A
10 g
25 g
$100.00
$272.00
1
(1)

Lithocholic acid, a bile acid, can inhibit CYP7B1, and its role as a natural inhibitor of the enzyme has been studied.

GW 4064

278779-30-9sc-218577
5 mg
$95.00
13
(1)

GW 4064 is a synthetic compound known as a selective farnesoid X receptor (FXR) agonist, but it has also been shown to inhibit CYP7B1 in some studies.

24-Nor Ursodeoxycholic Acid

99697-24-2sc-478796
1 mg
$401.00
(0)

Norursodeoxycholic acid, another bile acid derivative, has been shown to inhibit CYP7B1 activity.

Isoliquiritigenin

961-29-5sc-255222
10 mg
$316.00
1
(1)

Isoliquiritigenin is a natural flavonoid found in licorice root, and it has been investigated for its inhibitory effects on CYP7B1.