MCH-1R Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
SNAP 94847 hydrochloride | 487051-12-7 | sc-311536 sc-311536A | 10 mg 50 mg | $199.00 $825.00 | ||
SNAP 94847 hydrochloride acts as a selective antagonist of the MCH-1R receptor, demonstrating a distinctive binding affinity that disrupts typical receptor activation. Its molecular structure facilitates specific hydrogen bonding and hydrophobic interactions, which modulate receptor conformation. This compound influences the kinetics of receptor-ligand interactions, leading to altered signaling dynamics and downstream effects on cellular processes. Its unique characteristics enhance its role in receptor modulation. | ||||||
ATC 0065 | 510732-84-0 | sc-358785 sc-358785A | 10 mg 50 mg | $350.00 $1200.00 | ||
ATC 0065 functions as a selective modulator of the MCH-1R receptor, exhibiting a unique interaction profile characterized by its ability to stabilize specific receptor conformations. The compound engages in intricate van der Waals forces and electrostatic interactions, which fine-tune the receptor's activity. Its kinetic properties allow for rapid association and dissociation rates, influencing the overall signaling cascade and cellular response mechanisms. This distinct behavior underscores its role in receptor dynamics. | ||||||
ATC0175 | 510733-97-8 | sc-252391 | 10 mg | $520.00 | ||
ATC0175 acts as a selective antagonist of the MCH-1R receptor, showcasing a unique binding affinity that alters receptor dynamics. Its molecular structure facilitates specific hydrogen bonding and hydrophobic interactions, leading to a conformational shift in the receptor. This compound exhibits notable reaction kinetics, with a delayed onset of action that allows for prolonged receptor modulation. The distinct interaction profile of ATC0175 contributes to its nuanced impact on downstream signaling pathways. | ||||||
GW 803430 | 515141-51-2 | sc-363281 sc-363281A | 10 mg 50 mg | $245.00 $982.00 | ||
GW 803430 functions as a selective antagonist of the MCH-1R receptor, characterized by its unique ability to disrupt receptor-ligand interactions. Its molecular architecture promotes specific electrostatic and van der Waals forces, resulting in a significant alteration of receptor conformation. The compound demonstrates a unique kinetic profile, exhibiting a gradual dissociation rate that enhances its modulatory effects on receptor activity, ultimately influencing various intracellular signaling cascades. | ||||||