PGF2alphaR Activators
SEE ALSO...
Items 11 to 20 of 24 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(+)-Fluprostenol | 54276-17-4 | sc-205326 sc-205326A | 1 mg 10 mg | $66.00 $398.00 | ||
(+)-Fluprostenol is a potent agonist of the PGF2α receptor, distinguished by its ability to stabilize receptor conformations that favor downstream signaling cascades. Its unique stereochemical arrangement allows for selective binding, enhancing receptor affinity and activation. The compound's hydrophilic characteristics promote effective membrane permeability, while its rapid association and dissociation kinetics facilitate swift biological responses. Additionally, its structural adaptability enhances interactions within diverse cellular environments. | ||||||
Latanoprost | 130209-82-4 | sc-201354 sc-201354A sc-201354A-CW | 1 mg 5 mg 5 mg | $58.00 $230.00 $306.00 | 2 | |
Latanoprost acts as a selective agonist for the PGF2α receptor, characterized by its unique ability to induce conformational changes that enhance receptor activation. Its specific molecular structure allows for high affinity binding, promoting effective signal transduction. The compound exhibits notable lipophilicity, which aids in its interaction with lipid membranes, while its dynamic binding kinetics enable rapid modulation of receptor activity, influencing various intracellular pathways. | ||||||
Fluprostenol isopropyl ester | 157283-68-6 | sc-205327 sc-205327A | 1 mg 5 mg | $80.00 $465.00 | ||
Fluprostenol isopropyl ester functions as a potent agonist for the PGF2α receptor, distinguished by its ability to stabilize receptor conformations that facilitate downstream signaling. Its unique ester moiety enhances membrane permeability, allowing for efficient cellular uptake. The compound's interaction with the receptor is characterized by a rapid association and dissociation rate, promoting swift activation of intracellular pathways. Additionally, its structural features contribute to selective receptor engagement, influencing various physiological responses. | ||||||
AL 8810 | 246246-19-5 | sc-205204 sc-205204A | 1 mg 5 mg | $129.00 $483.00 | 1 | |
AL 8810 acts as a selective agonist for the PGF2α receptor, exhibiting unique binding dynamics that enhance receptor activation. Its structural configuration allows for specific hydrogen bonding interactions, which stabilize the receptor-ligand complex. The compound's kinetic profile reveals a notable affinity for the receptor, leading to efficient signal transduction. Furthermore, AL 8810's lipophilic characteristics facilitate its integration into lipid membranes, optimizing its bioavailability and interaction with cellular targets. | ||||||
Tafluprost | 209860-87-7 | sc-222336 sc-222336A | 500 µg 1 mg | $69.00 $166.00 | ||
Tafluprost functions as a selective agonist for the PGF2α receptor, characterized by its unique stereochemistry that promotes specific conformational changes upon binding. This compound engages in distinct hydrophobic interactions, enhancing receptor affinity and activation. Its rapid kinetics facilitate swift signal propagation, while its ability to penetrate cellular membranes is attributed to its amphiphilic nature, allowing for effective modulation of intracellular pathways. | ||||||
n-Butylidenephthalide, (E)+(Z) | 551-08-6 | sc-279727 | 10 g | $87.00 | 1 | |
Fluprostenol is a synthetic prostaglandin analogue. It can bind to and activate PGF2αR. | ||||||
Bimatoprost, free acid | 38344-08-0 | sc-223818 sc-223818A sc-223818B | 1 mg 5 mg 10 mg | $99.00 $428.00 $617.00 | ||
Bimatoprost, free acid, acts as a potent agonist at the PGF2α receptor, exhibiting a unique binding profile that stabilizes receptor conformations. Its molecular structure allows for specific hydrogen bonding and hydrophobic interactions, which enhance its receptor selectivity. The compound's dynamic behavior in solution promotes efficient receptor activation, while its lipophilic characteristics enable effective membrane permeability, influencing downstream signaling cascades. | ||||||
(+)-15-epi Cloprostenol | 54276-22-1 | sc-205019 sc-205019A | 1 mg 5 mg | $78.00 $352.00 | ||
(+)-15-epi Cloprostenol functions as a selective agonist for the PGF2α receptor, characterized by its unique stereochemistry that influences receptor affinity and activation. The compound engages in specific electrostatic interactions, facilitating a robust conformational change in the receptor. Its distinct hydrophobic regions enhance binding stability, while its kinetic properties allow for rapid receptor engagement, triggering intricate intracellular signaling pathways. | ||||||
Sulprostone | 60325-46-4 | sc-201348 sc-201348A | 1 mg 5 mg | $206.00 $592.00 | 8 | |
Sulprostone is a synthetic prostaglandin E2 (PGE2) analogue. While primarily interacting with PGE2 receptors, it can also activate PGF2αR due to the overlap in ligand specificity among prostaglandin receptors. | ||||||
5-trans Latanoprost (free acid) | 903549-49-5 | sc-205141 sc-205141A | 1 mg 5 mg | $69.00 $315.00 | ||
5-trans Latanoprost (free acid) acts as a potent agonist for the PGF2α receptor, distinguished by its unique structural conformation that optimizes receptor binding. The compound exhibits specific hydrophobic interactions that stabilize its attachment, promoting effective receptor activation. Its dynamic molecular behavior allows for swift engagement with the receptor, initiating complex downstream signaling cascades. The compound's unique stereochemical arrangement further enhances its selectivity and efficacy in receptor modulation. | ||||||