SEE ALSO...
Items 11 to 13 of 13 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Raloxifene 6-Glucuronide | 174264-50-7 | sc-222243 sc-222243-CW sc-222243A sc-222243A-CW | 1 mg 1 mg 5 mg 5 mg | $448.00 $562.00 $1977.00 $2081.00 | 1 | |
Raloxifene 6-Glucuronide functions as a selective estrogen receptor modulator, characterized by its ability to engage in specific ligand-receptor interactions that stabilize unique receptor conformations. This compound exhibits distinct binding kinetics, allowing for a nuanced modulation of receptor activity. Its structural features promote effective hydrophilic interactions, enhancing solubility and bioavailability, which can influence downstream signaling pathways and cellular mechanisms. | ||||||
16α-Hydroxy Estrone | 566-76-7 | sc-206281 sc-206281-CW | 2.5 mg 2.5 mg | $220.00 $275.00 | ||
16α-Hydroxy Estrone acts as a potent estrogen receptor ligand, distinguished by its unique hydroxyl group positioning that influences receptor affinity and selectivity. This compound engages in specific hydrogen bonding and hydrophobic interactions, facilitating a distinct conformational change in the receptor. Its metabolic pathways involve conjugation reactions, which can modulate its bioactivity and influence estrogenic signaling cascades, impacting various cellular responses. | ||||||
rac Clomiphene-d5 Citrate | 1217200-17-3 | sc-219815 | 1 mg | $388.00 | ||
Rac Clomiphene-d5 Citrate functions as a selective estrogen receptor modulator, characterized by its deuterated structure that enhances stability and alters metabolic pathways. Its unique binding dynamics involve intricate van der Waals forces and electrostatic interactions, leading to a specific receptor conformation. This compound exhibits distinct kinetic profiles in receptor activation, influencing downstream signaling mechanisms and cellular responses through selective pathway engagement. | ||||||