| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
TTNPB | 71441-28-6 | sc-203303 sc-203303A sc-203303B | 10 mg 25 mg 50 mg | $210.00 $347.00 $640.00 | 20 | |
TTNPB functions as a potent retinoic acid receptor (RAR) agonist, exhibiting high affinity for RAR subtypes. Its unique molecular structure allows for selective binding, triggering conformational changes that enhance receptor dimerization and transcriptional activity. The compound's ability to modulate gene expression is influenced by its interaction with coactivators and corepressors, leading to distinct regulatory pathways. This specificity in molecular interactions underscores its role in cellular differentiation and development. | ||||||
4-Hydroxyphenylretinamide | 65646-68-6 | sc-200900 sc-200900A | 5 mg 25 mg | $104.00 $315.00 | ||
4-Hydroxyphenylretinamide acts as a selective retinoic acid receptor (RAR) modulator, characterized by its unique ability to stabilize receptor conformations. This compound engages in specific hydrogen bonding and hydrophobic interactions, facilitating enhanced receptor-ligand dynamics. Its kinetic profile reveals a rapid association and dissociation with RARs, influencing downstream signaling pathways. The compound's distinct structural features promote unique gene regulatory mechanisms, impacting cellular processes. | ||||||
AC-41848 | 400856-69-1 | sc-252347 | 5 mg | $107.00 | ||
AC-41848 functions as a retinoic acid receptor (RAR) modulator, distinguished by its capacity to selectively alter receptor activity through unique allosteric interactions. This compound exhibits a remarkable affinity for specific binding sites, leading to conformational changes that enhance receptor stability. Its reaction kinetics demonstrate a nuanced balance between activation and inhibition, influencing transcriptional regulation and cellular signaling pathways in a distinct manner. | ||||||
LG 100754 | 180713-37-5 | sc-361231 sc-361231A | 5 mg 25 mg | $137.00 $555.00 | ||
LG 100754 acts as a retinoic acid receptor (RAR) modulator, characterized by its ability to engage in selective molecular interactions that fine-tune receptor dynamics. This compound showcases unique binding affinities that induce specific conformational shifts, promoting receptor resilience. Its kinetic profile reveals a sophisticated interplay between agonistic and antagonistic effects, thereby modulating gene expression and influencing various cellular processes with precision. | ||||||