Date published: 2025-11-22

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RAR gamma Inhibitors

Santa Cruz Biotechnology now offers a broad range of RAR gamma inhibitors for use in various applications. RAR gamma inhibitors are crucial tools in scientific research, particularly in the study of gene regulation, cellular differentiation, and developmental biology. Retinoic acid receptors (RARs), including the gamma subtype, are nuclear receptors that regulate the expression of genes involved in numerous biological processes. Inhibiting these receptors allows researchers to dissect the pathways and mechanisms controlled by retinoic acid signaling, providing insights into how these pathways influence cell fate and function. RAR gamma inhibitors are valuable in exploring the roles of retinoic acid in embryogenesis, tissue regeneration, and the modulation of immune responses. Additionally, they are utilized in the development of new research models to study diseases linked to dysregulation of retinoic acid pathways, such as certain cancers and developmental disorders. By using these inhibitors, scientists can better understand the intricacies of cellular processes and develop innovative approaches to manipulate gene expression for experimental purposes. View detailed information on our available RAR gamma inhibitors by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

CD 2665

170355-78-9sc-293988
sc-293988A
10 mg
50 mg
$238.00
$974.00
2
(1)

CD 2665 functions as a selective RAR gamma modulator, characterized by its unique ability to stabilize receptor dimers through specific hydrogen bonding interactions. This compound exhibits a distinctive hydrophobic core that facilitates enhanced binding affinity, promoting effective signal transduction. Its structural rigidity contributes to slower reaction kinetics, allowing for prolonged receptor activation. Additionally, CD 2665's unique steric properties influence its interaction with co-regulators, further diversifying its biological impact.

BMS 453

166977-43-1sc-311294
10 mg
$189.00
1
(1)

BMS 453 acts as a selective RAR gamma modulator, distinguished by its capacity to engage in unique electrostatic interactions that enhance receptor affinity. This compound features a flexible molecular framework, allowing for dynamic conformational changes that optimize binding efficiency. Its specific isomeric forms exhibit varied reactivity profiles, influencing downstream signaling pathways. Furthermore, BMS 453's solubility characteristics facilitate its interaction with lipid membranes, impacting cellular uptake and distribution.

Bexarotene

153559-49-0sc-217753
sc-217753A
10 mg
100 mg
$54.00
$245.00
6
(1)

Bexarotene is a synthetic retinoid and RARγ agonist, primarily used in cancer therapy. Although traditionally considered an activator, the dual nature of retinoids can lead to context-dependent actions. In certain cellular environments or concentrations, Bexarotene may exhibit inhibitory effects on RARγ, possibly through interference with co-regulatory proteins or induction of negative feedback loops.

MM 11253

345952-44-5sc-361255
sc-361255A
10 mg
50 mg
$468.00
$2000.00
2
(1)

MM11253 is a chemical compound with reported inhibitory effects on RARγ. Its potential as an RARγ inhibitor suggests interference with retinoic acid-mediated signaling pathways. MM11253 provides researchers with a tool to explore the specific contributions of RARγ to cellular processes and to decipher its role in development, differentiation, and disease.

CD 1530

107430-66-0sc-203871
sc-203871A
10 mg
50 mg
$204.00
$816.00
(1)

CD1530 is a synthetic retinoid with reported inhibitory effects on RARγ. As a potential RARγ inhibitor, CD1530 may interfere with retinoic acid binding, modulating downstream signaling cascades associated with RARγ activity. This compound serves as a valuable pharmacological tool for researchers aiming to dissect the specific contributions of RARγ to cellular processes and explore its implications in various contexts, including development, differentiation, and disease.