(R)-Elagolix Size:Contact [email protected] for quotation SLC13A5-IN-1 exhibits an IC50 of

SLC13A5-IN-1 exhibits an IC50 of 100 μM in recombinant Human GlyT2/3H-Glycine Uptake Assay

Chemical Name: N-(3-chlorophenyl)-6

Combretastatin A-1 is a microtubule polymerization inhibitor that binds to the colchicine-binding site of tubulin

which is the hormonally active form of vitamin D

Ampicillin-Sulbactam has a wide range of antibacterial activity that includes Gram-positive and Gram-negative aerobic and anaerobic bacteria

(R)-Elagolix Size:Contact [email protected] for quotation SLC13A5-IN-1 exhibits an IC50 ofElagolix is a highly potent, selective, orally active, short duration, non peptide antagonist of the gonadotropin releasing hormone receptor (GnRHR) (KD = 54 pM). Target: GnRHin vitro: Elagolix is a short acting, nonpeptide, GnRH antagonist, administered orally, that unlike injectable depot GnRH agonists and antagonists, produces a dose dependent suppression of ovarian estrogen production, that is, from partial suppression at lower doses to full