Date published: 2025-11-25

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CYP1B1 Inhibitors

CYP1B1 inhibitors belong to a distinct chemical class known for their ability to modulate the enzymatic activity of cytochrome P450 1B1 (CYP1B1), a member of the cytochrome P450 superfamily of enzymes. These inhibitors play a crucial role in research aimed at understanding the intricate metabolic pathways of various endogenous and exogenous compounds. CYP1B1, primarily found in extrahepatic tissues such as the eye, liver, and reproductive organs, participates in the metabolism of numerous substrates, including polycyclic aromatic hydrocarbons, and steroid hormones. The chemical class of CYP1B1 inhibitors encompasses a diverse range of small molecules, often designed with specific structural features that facilitate their interaction with the active site of the CYP1B1 enzyme. Structurally, CYP1B1 inhibitors exhibit considerable variation, with diverse functional groups and scaffolds contributing to their inhibitory properties. These inhibitors act by binding to the active site of the CYP1B1 enzyme, thereby impeding its enzymatic activity. This binding interference can result in a variety of effects, influencing the metabolism and disposition of substrates that are metabolized by CYP1B1. Researchers often employ CYP1B1 inhibitors as tools in studies investigating the role of this enzyme in xenobiotic metabolism and endogenous compound regulation. By selectively inhibiting CYP1B1, researchers can gain insights into the broader implications of its activity on biological processes. Additionally, CYP1B1 inhibitors can serve as valuable probes to dissect the complex network of cytochrome P450-mediated metabolism, shedding light on interactions between the enzyme and various substrates. In conclusion, the chemical class of CYP1B1 inhibitors constitutes a diverse array of compounds instrumental in deciphering the multifaceted functions of the CYP1B1 enzyme and its involvement in the metabolism of a range of biologically important compounds.

Items 1 to 10 of 13 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

TMS

24144-92-1sc-203708
sc-203708A
10 mg
50 mg
$162.00
$417.00
(0)

TMS exhibits unique interactions with CYP1B1, characterized by its ability to form stable complexes through hydrogen bonding and hydrophobic interactions. Its structural conformation allows for effective substrate positioning, enhancing catalytic efficiency. The compound's reactivity is influenced by electron-donating groups, which modulate the enzyme's active site dynamics. Additionally, TMS demonstrates distinct reaction kinetics, showcasing a balance between substrate affinity and competitive inhibition, ultimately shaping metabolic pathways.

Lumaricoxib

220991-20-8sc-205736
sc-205736A
100 mg
250 mg
$140.00
$280.00
(0)

Lumiracoxib is a nonsteroidal anti-inflammatory drug (NSAID) that has been studied for its potential to inhibit CYP1B1 activity. It competitively inhibits the enzyme, suggesting its potential for modulating CYP1B1 substrate metabolism.

Alizarin

72-48-0sc-214519
sc-214519A
1.5 g
100 g
$21.00
$50.00
(0)

Alizarin interacts with CYP1B1 through specific π-π stacking and electrostatic interactions, facilitating its binding to the enzyme's active site. This compound exhibits unique conformational flexibility, allowing it to adapt to varying substrate environments, which influences its metabolic fate. The presence of functional groups alters the electron density, impacting the enzyme's catalytic activity. Alizarin's distinct kinetic profile reveals a nuanced interplay between substrate turnover and enzyme regulation, shaping its biochemical pathways.

Ellagic Acid, Dihydrate

476-66-4sc-202598
sc-202598A
sc-202598B
sc-202598C
500 mg
5 g
25 g
100 g
$57.00
$93.00
$240.00
$713.00
8
(1)

Ellagic acid is a polyphenol found in fruits and nuts. It exhibits inhibitory effects on CYP1B1, potentially aiding in reducing the activation of procarcinogens and supporting chemoprevention.

Fisetin

528-48-3sc-276440
sc-276440A
sc-276440B
sc-276440C
sc-276440D
50 mg
100 mg
500 mg
1 g
100 g
$51.00
$77.00
$102.00
$153.00
$2856.00
7
(1)

Fisetin is a naturally occurring polyphenol found in fruits and vegetables. It has demonstrated inhibitory effects on CYP1B1, which could help suppress the activation of procarcinogens.

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
$150.00
$286.00
$479.00
$1299.00
$8299.00
$915.00
22
(1)

Sulforaphane is a compound present in cruciferous vegetables like broccoli. Studies have explored its potential to inhibit CYP1B1, thereby reducing the bioactivation of specific carcinogens.

Resveratrol

501-36-0sc-200808
sc-200808A
sc-200808B
100 mg
500 mg
5 g
$60.00
$185.00
$365.00
64
(2)

Resveratrol, a polyphenol in grapes, berries, and red wine, has been suggested to possess inhibitory properties against CYP1BThis could contribute to its potential as a chemopreventive agent.

Quercetin

117-39-5sc-206089
sc-206089A
sc-206089E
sc-206089C
sc-206089D
sc-206089B
100 mg
500 mg
100 g
250 g
1 kg
25 g
$11.00
$17.00
$108.00
$245.00
$918.00
$49.00
33
(2)

Quercetin, a flavonoid in various plant-based foods, can inhibit CYP1B1-mediated metabolism of certain procarcinogens. This action might lead to reduced activation of these compounds.

Indole-3-carbinol

700-06-1sc-202662
sc-202662A
sc-202662B
sc-202662C
sc-202662D
1 g
5 g
100 g
250 g
1 kg
$38.00
$60.00
$143.00
$306.00
$1012.00
5
(1)

Found in cruciferous vegetables, indole-3-carbinol inhibits CYP1B1, potentially decreasing the activation of carcinogens and aiding in cancer prevention.

Eugenol

97-53-0sc-203043
sc-203043A
sc-203043B
1 g
100 g
500 g
$31.00
$61.00
$214.00
2
(1)

Eugenol, a phenolic compound in clove oil and other plants, exhibits potential as a CYP1B1 inhibitor. This effect could have implications for cancer prevention.