Date published: 2026-1-23

1-800-457-3801

SCBT Portrait Logo
Seach Input

RAR β Inhibitors

Santa Cruz Biotechnology now offers a broad range of RAR β inhibitors for use in various applications. These inhibitors are crucial tools in scientific research, particularly in the fields of developmental biology, cancer research, and neurobiology. RAR β inhibitors target the retinoic acid receptor beta (RAR β), a nuclear receptor involved in regulating gene expression during cell differentiation and development. By modulating the activity of RAR β, researchers can explore the roles of retinoic acid signaling pathways in various biological processes. This control is vital for studying gene expression regulation, embryonic development, and tissue differentiation. Moreover, RAR β inhibitors serve as important molecular probes, enabling scientists to dissect complex cellular mechanisms and understand the effects of altered retinoid signaling. The versatility of RAR β inhibitors makes them indispensable in experimental design, allowing researchers to uncover new insights into cellular function and organismal development. View detailed information on our available RAR β inhibitors by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

LE 135

155877-83-1sc-204053
sc-204053A
10 mg
50 mg
$168.00
$707.00
5
(1)

LE 135 acts as a selective RAR beta inhibitor, distinguished by its unique ability to form stable complexes with the receptor through intricate van der Waals forces and electrostatic interactions. This compound exhibits a notable influence on the receptor's allosteric sites, altering its conformational dynamics and impacting downstream signaling cascades. Its specific molecular design facilitates targeted engagement, allowing for nuanced modulation of cellular responses and regulatory mechanisms.

CD 2665

170355-78-9sc-293988
sc-293988A
10 mg
50 mg
$360.00
$1400.00
2
(1)

CD 2665 functions as a selective RAR beta inhibitor, characterized by its capacity to disrupt receptor dimerization through specific hydrogen bonding and hydrophobic interactions. This compound uniquely alters the receptor's ligand-binding affinity, leading to distinct modulation of gene expression pathways. Its kinetic profile reveals a rapid association and slower dissociation, enhancing its effectiveness in fine-tuning receptor activity and influencing transcriptional regulation.