Oxytocin Receptor Inhibitors
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Atosiban | 90779-69-4 | sc-254947 sc-254947A sc-254947B | 10 mg 50 mg 1 g | $204.00 $311.00 $4172.00 | ||
Atosiban functions as a selective antagonist of oxytocin receptors, exhibiting a unique binding affinity that disrupts the typical receptor-ligand interactions. Its structural conformation enables it to stabilize inactive receptor states, thereby inhibiting downstream signaling cascades. The compound's hydrophobic characteristics facilitate its interaction with lipid membranes, influencing its distribution and interaction kinetics. This behavior provides insights into receptor modulation and the intricate balance of hormonal signaling. | ||||||
L-368,899 hydrochloride | 148927-60-0 | sc-204037 sc-204037A | 1 mg 10 mg | $158.00 $334.00 | 5 | |
L-368,899 hydrochloride acts as a potent antagonist of oxytocin receptors, characterized by its ability to selectively inhibit receptor activation. Its unique molecular structure allows for specific interactions with the receptor's binding site, effectively blocking conformational changes necessary for signal transduction. The compound's solubility properties enhance its bioavailability, while its kinetic profile suggests rapid receptor engagement, providing a nuanced understanding of receptor dynamics and hormonal regulation. | ||||||
Penicillide | 55303-92-9 | sc-391044 | 1 mg | $160.00 | ||
Penicillide functions as a selective modulator of oxytocin receptors, exhibiting unique binding affinities that influence receptor conformation. Its distinct molecular architecture facilitates specific interactions with key amino acid residues, altering downstream signaling pathways. The compound demonstrates notable reaction kinetics, with a propensity for rapid dissociation from the receptor, allowing for dynamic regulation of receptor activity. Additionally, its physicochemical properties contribute to its stability in various environments, enhancing its interaction potential. | ||||||
L-371,257 | 162042-44-6 | sc-204038 | 10 mg | $526.00 | 2 | |
L-371,257 acts as a selective antagonist of oxytocin receptors, characterized by its ability to disrupt receptor-ligand interactions. Its unique structural features enable it to engage with specific binding sites, leading to altered receptor dynamics. The compound exhibits a distinctive profile in terms of reaction kinetics, showing a slower association rate that allows for prolonged receptor occupancy. Furthermore, its solubility characteristics enhance its compatibility with diverse biochemical environments, influencing its overall efficacy in modulating receptor behavior. | ||||||