(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

Cinnamomum verum ingredient 2-methoxycinnamaldehyde: a new antiproliferative drug targeting topoisomerase I and II in human lung squamous cell carcinoma NCI-H520 cells

Chemical Name: N-(3-chlorophenyl)-6

Dehydrocurdione

JC-171 is a selective NLRP3 inflammasome inhibitor

(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