SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
L-748,337 | 244192-94-7 | sc-204044 sc-204044A | 10 mg 50 mg | $258.00 $1068.00 | 4 | |
L-748,337 is a selective beta3-adrenergic receptor agonist characterized by its unique binding affinity and specificity. Its molecular structure enables precise interactions with receptor sites, triggering distinct allosteric effects that modulate downstream signaling pathways. The compound exhibits notable reaction kinetics, with a fast association rate and a gradual dissociation, allowing for sustained receptor engagement. Additionally, its lipophilic nature enhances membrane permeability, influencing its bioavailability and interaction with cellular environments. | ||||||
SR 59230A hydrochloride | 1135278-41-9 | sc-204302 sc-204302A | 10 mg 50 mg | $383.00 $1533.00 | 3 | |
SR 59230A hydrochloride is a selective beta3-adrenergic receptor antagonist known for its unique ability to disrupt receptor activation. Its structural conformation allows for specific interactions with the receptor's binding site, leading to competitive inhibition of agonist activity. The compound demonstrates a slow onset of action, resulting in prolonged receptor occupancy. Its hydrophilic characteristics influence solubility and distribution, impacting its interaction dynamics within biological systems. | ||||||
S(−)-Cyanopindolol hemifumarate salt | 874882-72-1 | sc-253460 sc-253460A | 1 mg 5 mg | $197.00 $758.00 | ||
S(-)-Cyanopindolol hemifumarate salt exhibits selective binding to beta3-adrenergic receptors, characterized by its unique stereochemistry that enhances receptor affinity. This compound engages in distinct molecular interactions, stabilizing the receptor in an inactive conformation. Its kinetic profile reveals a rapid association and a gradual dissociation, allowing for sustained modulation of receptor activity. Additionally, its amphipathic nature influences membrane permeability and cellular uptake, affecting its overall bioavailability. | ||||||